OncoHub.ai
OncoHub.ai
Oncology Scientific Bulletin
ESMO 2026 · Day 1 Summary
ESMO Congress · Day 1 Digest

ESMO 2026 — End-of-Day Summary

An abstract digest clustered by tumour group and ranked by clinical priority. Numerical results (HR, PFS, OS, ORR) are preserved verbatim; reliability caveats are embedded within each study's card.

Date: 23 October 2026 Scope: ~70 ESMO 2026 Day-1 abstracts (Proffered Paper + Rapid Oral) and 15 ESMO/ILCN news items Layout: Disease group → clinical priority

How this digest is organized

  1. Primary axis — disease group: Each item was clustered by tumour group / official ESMO track (🎀 Breast Cancer, 🫁 Thoracic / Lung Cancer, ⚕ Gastrointestinal Cancers, 🔷 Genitourinary Cancers, 🌸 Gynaecological Cancers, ☀ Melanoma & Skin Cancers, 🧠 Sarcoma, CNS & Rare Tumours, 🧪 Developmental Therapeutics & Early Phase, 🧬 Translational Research & Biomarkers, 🤝 Supportive, Palliative & Survivorship).
  2. Secondary axis — clinical priority: Cards and sections were ranked into three tiers (key below).
  3. Reliability inside the card: Hedging present in the source (interim, immature, small n, retrospective, non-ESMO data) is placed as a caveat strip inside the relevant card.
  4. Embargoed titles separated: Late-breaking Plenary / Presidential Symposium abstracts whose results are embargoed until presentation are collected in a dedicated section at the end.
High — practice-changing / -capable positive or negative pivotal Phase 3, plenary dataMedium — long-term / subgroup update, validation, biomarker, promising Phase 2Watch — early phase, preliminary, small n, real-world / health services

Highlights of the Day

practice-changing findings, ranked
resected stage IIB-IV melanoma
INTerpath-001 (LBA1)
resected stage IIB-IV melanoma — 24-mo RFS 82.2% vs 70.0%; HR 0.58 (0.45–0.75); p<0.001; DMFS HR 0.62 (0.45–0.85); p=0.002
ES-SCLC 1L maintenance
DeLLphi-305 (LBA3)
ES-SCLC 1L maintenance — mOS 21.1 vs 12.7 mo; HR 0.42 (0.32–0.54); p<0.001; mPFS 7.4 vs 1.9 mo; HR 0.34; ORR 26.4% vs 4.1%
EGFRm MET-OE/AMP NSCLC post-osi
SAFFRON (LBA6)
EGFRm MET-OE/AMP NSCLC post-osi — mPFS 7.6 vs 5.4 mo; HR 0.55 (0.42–0.72); p<0.001; mOS 17.8 vs 12.9 mo; HR 0.68; p=0.010
cis-ineligible MIBC
VOLGA (LBA2)
cis-ineligible MIBC — durva+EV vs RC: mEFS NR vs 12.1 mo; HR 0.51 (0.38–0.67); p<0.0001; OS HR 0.58 (0.40–0.83); p=0.0027
pretreated KRAS G12C NSCLC
Krascendo 1 (LBA5)
pretreated KRAS G12C NSCLC — mPFS 9.8 vs 5.7 mo; HR 0.58 (0.44–0.76); p<0.0001; mOS 17.7 vs 12.0 mo; HR 0.56; p=0.0005
🎀 Breast Cancer
HORIZON-Breast06 (LBA13)
Pivotal win for a new HER2 ADC in HER2-low advanced BC
HER2-low advanced BC — overall mPFS 16.4 vs 6.8 mo; HR 0.27 (0.21–0.34); p<0.0001; ORR 75.5% vs 41.2%; ILD 2.5%
very high-risk localised/relapsed PC
DASL-HiCaP (LBA4)
very high-risk localised/relapsed PC — 4-yr MFS-CI 95% vs 88%; HR 0.42 (0.27–0.66); p=0.0001
1L advanced biliary tract cancer
HARMONi-GI1 (LBA8)
1L advanced biliary tract cancer — mOS 14.9 vs 12.1 mo; HR 0.75 (0.61–0.92); p=0.0031; PFS HR 0.61; ORR 53.8% vs 32.5%

🎀 Breast Cancer

15 studies

🎀 Breast Cancer

HORIZON-Breast06 — trastuzumab rezetecan vs chemotherapy (HER2-low advanced BC)

LBA13
● High priorityPhase 3HER2 ADCHER2-low

Indication: HER2-low advanced BC with ≤1 prior chemo for metastatic disease

Key finding: Chemo-naïve mPFS 16.6 vs 6.8 mo; HR 0.25 (0.19–0.33); p<0.0001. Overall mPFS 16.4 vs 6.8 mo; HR 0.27 (0.21–0.34); p<0.0001. ORR 75.5% vs 41.2%. Grade ≥3 TRAEs 84.1% vs 67.9%; ILD 2.5%.

Clinical relevance: Pivotal win for a new HER2 ADC in HER2-low advanced BC

OS immature

Source: ESMO 2026 LBA13 · Y. Fan

🎀 Breast Cancer

APEX-Breast01 — TQB2102 vs TPC (HER2-low r/m BC)

LBA27
● High priorityPhase 3Biparatopic HER2 ADC

Indication: HER2-low r/m BC, no prior advanced chemo

Key finding: HR+/HER2-low mPFS 16.4 vs 5.5 mo; HR 0.29 (0.22–0.39); p<0.0001. All HER2-low mPFS 16.4 vs 5.5 mo; HR 0.29 (0.22–0.38); p<0.0001. OS HR 0.44 (HER2-low). ILD 2.2%.

Clinical relevance: Positive pivotal data for biparatopic HER2 ADC

OS immature

Source: ESMO 2026 LBA27 · S. Wang

🎀 Breast Cancer

NATALEE — adjuvant ribociclib + NSAI vs NSAI (HR+/HER2− EBC, 6-y)

LBA25
● High priorityPhase 3CDK4/6iAdjuvant

Indication: High-risk stage II/III HR+/HER2− EBC

Key finding: 6-y OS: RIB+NSAI vs NSAI HR 0.809 (0.661–0.989); nominal 1-sided P=.019; 6-y OS 91.86% vs 89.73%. iDFS HR 0.741 (0.646–0.849); 6-y iDFS 83.23% vs 77.92%. BCSS HR 0.706.

Clinical relevance: Sustained OS/iDFS benefit at 6 y supports adjuvant RIB+NSAI

Source: ESMO 2026 LBA25 · D.J. Slamon

🎀 Breast Cancer

PANKU-Breast01 — izalontamab brengitecan vs TPC (pretreated HR+/HER2− LA/M BC)

LBA50
● High priorityPhase 3EGFR/HER3 BsADC

Indication: Pretreated HR+/HER2− LA/M BC after CDK4/6i and taxane

Key finding: mPFS 8.18 (6.93–8.58) vs 4.01 mo (2.92–4.30); HR 0.41 (0.33–0.53); p<0.0001. cORR 40.5% vs 20.2%; mDOR 6.93 vs 4.21 mo. Discontinuation for TRAEs 1.6%; ILD 1.1%.

Clinical relevance: First-in-class EGFR/HER3 BsADC meets primary PFS endpoint

OS immature; China-only

Source: ESMO 2026 LBA50 · B. Lan

🎀 Breast Cancer

NSABP B-42 — extended letrozole vs placebo (15-y final, HR+ postmenopausal)

LBA24
● Medium priorityPhase 3Extended ET

Indication: Postmenopausal HR+ BC after 5 y AI/sequential ET

Key finding: 15-y DFS HR 0.85 (0.77–0.94); DFS P=61.6% L vs 56.5%. BCFI HR 0.78 (0.67–0.92). DR HR 0.72 (0.57–0.91). OS HR 0.92 (0.82–1.05); 15-y OS 74.0% vs 72.3%.

Clinical relevance: Sustained DFS/DR benefit with extended letrozole; no OS gain

Source: ESMO 2026 LBA24 · E.P. Mamounas

🎀 Breast Cancer

GIM3 FATA — upfront vs switch and A vs E vs L (postmenopausal HR+ EBC)

544RO
● Medium priorityPhase 3Adjuvant AI

Indication: Postmenopausal HR+ EBC

Key finding: Upfront vs switch DFS HR 0.95 (0.82–1.09); OS HR 0.88 (0.74–1.06). 10-y DFS A 79.1%, E 74.2%, L 76.6% (global p=0.028); E vs A HR 1.23 (1.04–1.46). OS not different.

Clinical relevance: No schedule advantage; exemestane inferior for DFS

Source: ESMO 2026 544RO · P. De Placido

🎀 Breast Cancer

DESTINY-Breast11 — T-DXd-THP vs ddAC-THP MRI responses (HER2+ eBC)

543RO
● Medium priorityPhase 3NeoadjuvantHER2+

Indication: High-risk HER2+ eBC neoadjuvant

Key finding: Mid-NAT ORR 77.3% vs 50.8% (ΔORR 26.5%); CR 13.3% vs 2.6%. Median best % change −59% vs −35% (mid-NAT); −81% vs −74% (EOT). PPV of mid-NAT CR for pCR 90.2% vs 87.5%.

Clinical relevance: Deep MRI responses with T-DXd-THP support full regimen

Source: ESMO 2026 543RO · J. Boileau

🎀 Breast Cancer

neoHIP — THP ± pembrolizumab biomarker enrichment (HER2+ EBC)

541RO
● Medium priorityPhase 2NeoadjuvantPD-1

Indication: Stage II/III HER2+ EBC

Key finding: HR− or PDL1+ or sTILs+ (67% positive) enriches pembro benefit: THP+pembro pCR 67% vs THP 31% (+Δ36%); OR 4.7 (1.2–23.0). Unselected pCR 67% vs 48%; +Δ19%.

Clinical relevance: 3-biomarker rule may select HER2+ EBC pts for pembro+THP

Exploratory; needs phase 3 validation

Source: ESMO 2026 541RO · D. Page

🎀 Breast Cancer

TALENT — neoadjuvant T-DXd ± anastrozole or sequence with chemo (HER2-low, HR+ eBC)

LBA23
● WatchPhase 2Neoadjuvant

Indication: HR+/HER2-low early BC, neoadjuvant

Key finding: RCB0: Arm A 3/42 (7%); Arm B 1/29 (3%); Arm C 5/55 (9%). ORR 67%/66%/65%. HER2 higher in RCB0 (2691/1221 amol/mm²) vs RCB1/2/3; ILD rare.

Clinical relevance: Low pCR with neoadjuvant T-DXd regimens in HR+/HER2-low

Low pCR rates

Source: ESMO 2026 LBA23 · S.A. Hurvitz

🎀 Breast Cancer

lidERA BC — giredestrant vs SOC ET PROs (ER+/HER2− eBC)

538RO
● WatchPhase 3AdjuvantPRO

Indication: Adjuvant ER+/HER2− eBC

Key finding: No clinically meaningful HRQoL deterioration either arm; key symptom severity similar (joint pain 43% vs 43%; hot flashes 32% vs 31%). 2–8% more giredestrant pts 'not at all' bothered by side effects.

Clinical relevance: Giredestrant preserves HRQoL vs SOC ET

Source: ESMO 2026 538RO · G. Werutsky

🎀 Breast Cancer

DESTINY-Breast05 PROs — T-DXd vs T-DM1 (high-risk HER2+ eBC)

539RO
● WatchPhase 3PRO

Indication: Post-neoadjuvant HER2+ eBC with residual disease

Key finding: TDD HR vs T-DM1: GHS 1.15; pain 0.77; arm symptoms 0.82; social 1.29. EQ-5D VAS HR 1.05. HRQoL preserved overall.

Clinical relevance: HRQoL maintained with T-DXd vs T-DM1

Source: ESMO 2026 539RO · C.H. Barrios

🎀 Breast Cancer

JCOG1204A1 — postoperative ctDNA surveillance (high-risk BC)

542RO
● WatchctDNASurveillance

Indication: High-risk BC under structured follow-up

Key finding: ctDNA+ in 28/210 (13.3%). 5-y RFS 99.5% (ctDNA−) vs 53.6% (ctDNA+); HR 60.3 (20.5–177.5); time-dependent HR 27.7. ER+/HER2− 7-y RFS 94.1% vs 15.9%. Median lead time 6.9 mo.

Clinical relevance: Supports ctDNA surveillance; ∼7-mo molecular lead time

Source: ESMO 2026 542RO · Y. Ozaki

🎀 Breast Cancer

B-STRONGER-I — ultrasensitive ctDNA during NAT (early TNBC)

540RO
● WatchctDNATNBC

Indication: Stage I–III TNBC on NAT

Key finding: ctDNA+ at baseline 96% (137/142); median LOD 2.19 PPM. 82.1% clearance at T1; stage I 100% clearance vs stage III 50%. Early clearance associated with pCR.

Clinical relevance: Ultrasensitive ctDNA tracks early NAT response

Pre-interim

Source: ESMO 2026 540RO · C.H. Barcenas

🎀 Breast Cancer

AIUR — surgical-glove compression for paclitaxel neuropathy (BC)

LBA28
● WatchRCTSupportive

Indication: Stage II–III BC on paclitaxel

Key finding: Poor outcome 74.5% vs 82.6% (P=0.45; primary not met). Upper-extremity FACT-NTX −3.20 (−4.93 to −1.48; p<0.001); CTCAE ≥G2 sensory neuropathy 58.7% vs 82.2% (P=0.02).

Clinical relevance: Hand-specific signal; feet unprotected

Primary PRO endpoint not met

Source: ESMO 2026 LBA28 · Y.-J. Kang

🎀 Breast Cancer

TOP-1 — RT omission after BCS without ET (older ER+ BC)

545RO
● WatchObservationalDe-escalation

Indication: Age ≥70 low-risk ER+ BC without ET after BCS

Key finding: 5-y LR risk 14.8% (12.3–17.5); contralateral BC 4.0%; BC-related death 2/81 (2.5%). LR surgical in 92.7%; 56.7% received RT and 35.0% ET for LR.

Clinical relevance: RT omission feasible for selected older ER+ pts

LR risk higher than historical with RT

Source: ESMO 2026 545RO · L. Bouwman

🫁 Thoracic / Lung Cancer

1 study

🫁 Thoracic / Lung Cancer

LMD immune checkpoint blockade — advanced NSCLC (multicenter case series)

702RO
● WatchRetrospectiveLMD

Indication: NSCLC leptomeningeal disease

Key finding: Non-AGA (n=79): mLMOS 15.6 mo; PD-1/PD-L1 improved LMOS HR 0.27 (0.18–0.39); p<0.001. AGA+ (n=172): mLMOS 10.6 mo; benefit only in high PD-L1 with combo HR 0.53 (0.23–1.2); p=0.03.

Clinical relevance: Supports selective IO use in LMD

Retrospective

Source: ESMO 2026 702RO · X. Le

⚕ Gastrointestinal Cancers

15 studies

⚕ Gastrointestinal Cancers

G-HOPE-001 — arcotatug tavatecan vs TPC (CLDN18.2+ G/GEJA, 3L+)

LBA77
● High priorityPhase 3CLDN18.2 ADC

Indication: CLDN18.2 IHC ≥2+ in ≥75% cells G/GEJA, 3L+

Key finding: mPFS 5.5 vs 2.9 mo; HR 0.47 (0.34–0.65); p<0.0001. mOS 9.9 vs 7.4 mo; HR 0.63 (0.45–0.89). ORR 23.6% vs 5.3%. Grade ≥3 TEAEs 45.8% vs 57.9%; no ILD.

Clinical relevance: Positive pivotal PFS for CLDN18.2 ADC in 3L+

OS pending IA2

Source: ESMO 2026 LBA77 · K. Shitara

⚕ Gastrointestinal Cancers

HERIZON-GEA-01 IA2 — zanidatamab + chemo ± tislelizumab vs tras + chemo (1L HER2+ mGEA)

LBA79
● High priorityPhase 3HER2 BsAb

Indication: 1L HER2+ advanced/metastatic GEA

Key finding: zani+CT vs tras+CT: mOS 22.9 vs 19.6 mo; HR 0.76 (0.62–0.93); p=0.0088. zani+CT+TIS vs tras+CT: HR 0.65 (0.52–0.80); mOS 27.0 mo. zani+CT+TIS vs zani+CT HR 0.81; P=0.0502.

Clinical relevance: Confirms zani-based regimens as new HER2+ 1L SoC

Source: ESMO 2026 LBA79 · K. Shitara

⚕ Gastrointestinal Cancers

KC-WISE — anbenitamab + chemo vs SoC (HER2+ GC/GEJC post-trastuzumab)

LBA80
● High priorityPhase 3HER2 BsAb

Indication: HER2+ GC/GEJC after trastuzumab failure

Key finding: mOS 19.6 vs 9.6 mo; HR 0.39 (0.28–0.54); p<0.0001. mPFS 7.1 vs 2.7 mo; HR 0.35 (0.26–0.48); p<0.0001. Grade ≥3 TRAEs 69.4% vs 47.9%; 0 vs 5 treatment-related deaths.

Clinical relevance: Dramatic OS win in post-trastuzumab HER2+ GC

Source: ESMO 2026 LBA80 · R. Zhang

⚕ Gastrointestinal Cancers

LOMAC — 4 vs 6 mo adjuvant XELOX (stage II–IIIB gastric cancer)

LBA81
● High priorityPhase 3Non-inferiority

Indication: Stage II–IIIB GC after D2 resection

Key finding: 3-y DFS 69.2% vs 70.8%; HR 1.01 (0.82–1.25); 1-sided P=0.006 for non-inferiority. Grade ≥3 AEs 8.4% vs 15.0%; grade ≥3 neuropathy 0.4% vs 5.9%. Completion 83.6% vs 60.4%.

Clinical relevance: 4 mo XELOX non-inferior with less toxicity

Source: ESMO 2026 LBA81 · D. Xu

⚕ Gastrointestinal Cancers

KEYNOTE-975 — pembro + dCRT vs placebo + dCRT (locally advanced EC/GEJ)

2875O
● High priorityPhase 3Negative

Indication: Unresectable locally advanced EC/GEJ, dCRT

Key finding: PD-L1 CPS ≥10 EFS mPFS 15.2 vs 14.7 mo; HR 0.97 (0.77–1.23); P=0.3994 (not met). mOS 32.2 vs 35.0 mo; HR 1.00 (0.77–1.30). Grade ≥3 AEs 100% both arms.

Clinical relevance: Negative pivotal; pembro+dCRT no benefit

Primary EFS endpoint not met; study stopped

Source: ESMO 2026 2875O · M.A. Shah

⚕ Gastrointestinal Cancers

SANO 5-y — active surveillance vs surgery after nCRT (oesophageal cancer)

LBA78
● High priorityRCTOrgan preservation

Indication: Oesophageal cancer with cCR after nCRT

Key finding: 5-y OS 50% (95%CI 34-57) vs 54% (46-64); HR 1.17 (0.77–1.77). DFS HR 1.39 (0.94–2.06). Distant metastases 46% vs 29% (P<0.01). 43% spared non-beneficial oesophagectomy.

Clinical relevance: Active surveillance feasible with similar OS

Higher distant metastases

Source: ESMO 2026 LBA78 · S.S. Gangaram-Panday

⚕ Gastrointestinal Cancers

RASolute 302 subgroups — daraxonrasib vs chemo (previously treated mPDAC)

LBA82
● Medium priorityPhase 3RAS(ON)

Indication: Previously treated mPDAC

Key finding: Overall mOS 13.2 vs 6.7 mo; HR 0.40. By mut: G12D HR 0.49; G12V HR 0.32; G12R HR 0.61; Q61 HR 0.37; no RAS mut HR 0.43. Across chemo subgroups HR 0.32–0.46.

Clinical relevance: OS benefit consistent across RAS mutation subgroups

Source: ESMO 2026 LBA82 · Z.A. Wainberg

⚕ Gastrointestinal Cancers

DEWI (GERCOR-GONO) — dostarlimab W&W in dMMR/MSI-H localized GEA

2877RO
● Medium priorityPhase 2Organ preservation

Indication: Localized dMMR/MSI-H GEA, cT2–T4

Key finding: First interim (24 pts): 1y-cCR 62.5% (15/24). No events in cCR pts (mFU 16.20 mo). 9/24 operated, all R0; 3 anastomotic fistulas. G3-4 dostarlimab-related AEs 21%.

Clinical relevance: Chemo/surgery-free strategy feasible in dMMR GEA

Interim; small n

Source: ESMO 2026 2877RO · T. André

⚕ Gastrointestinal Cancers

TQB2102 + bemotrizumab ± capecitabine 1L (HER2+ G/GEJC)

2876RO
● Medium priorityPhase 2HER2 BsADC

Indication: 1L HER2+ advanced G/GEJC

Key finding: ORR: A 69.6%, B 80%, C 94.7%; DCR: A 95.7%, B/C 100%; 6-mo PFS: A 71.4%, B 70%, C 92.3%. Grade ≥3 TRAEs 41.67% (C) vs 72.97% (B). TQB2102 6 mg/kg selected RP3D.

Clinical relevance: Deep responses with triple combo in HER2+ GC

Phase 2

Source: ESMO 2026 2876RO · M. Qiu

⚕ Gastrointestinal Cancers

AMPLIFY-7P — camupepimut 7-valent mKRAS amphiphile vs observation (resected PDAC)

LBA83
● Medium priorityPhase 2Vaccine

Indication: Resected stage I–III KRAS-mut PDAC

Key finding: Primary DFS not met: HR 0.85, p=0.539. 6-mo DFS 75.7% vs 61.7%; HR 0.55; p=0.0557. ctDNA(−) subgroup HR 0.51 (0.0280). mKRAS T-cell response 99%.

Clinical relevance: Signal in subgroups; phase 3 planned

Primary endpoint not met

Source: ESMO 2026 LBA83 · E.M. O'Reilly

⚕ Gastrointestinal Cancers

MASTERPLAN — mFOLFIRINOX ± SBRT (high-risk/BRPC/LAPC)

3136RO
● Medium priorityPhase 2SBRT

Indication: High-risk operable, BRPC or LAPC

Key finding: 12-mo LRR 20.2% vs 52.0% (p=0.022). mPFS 11.9 vs 6.3 mo (p=0.002). mOS 22.0 vs 14.0 mo (p=0.006). Grade 3+ toxicity 70.2% vs 64.0%.

Clinical relevance: SBRT improves LRR, PFS and OS without added toxicity

Source: ESMO 2026 3136RO · A. Oar

⚕ Gastrointestinal Cancers

EMT2 — perioperative EPA 4 g vs placebo (CRC liver metastasis surgery)

● Medium priorityPhase 3Supportive

Indication: Patients undergoing CRLM resection

Key finding: 5-y OS 62.0% vs 45.1%; HR 0.68 (0.48–0.96); p=0.03. Median OS NR vs 59.0 mo. mPFS 13.5 vs 12.9 mo; HR 0.89 (0.70–1.13); p=0.33. Well tolerated.

Clinical relevance: OS gain in a nutritional intervention trial

PFS not significant

Source: ESMO press — EMT2 · M.A. Hull

⚕ Gastrointestinal Cancers

RAMIRIS phase III — FOLFIRI+ramucirumab vs paclitaxel+ramucirumab (taxane-pretreated GEA)

2878RO
● WatchPhase 32L

Indication: Taxane-pretreated advanced GEA

Key finding: mOS 8.7 vs 7.5 mo; HR 0.95; p=0.33. ORR 25.3% vs 22.6%; p=0.29. mPFS 5.5 vs 3.7 mo; HR 0.7; p=0.003. Grade 3-5 AEs 70% vs 68%.

Clinical relevance: PFS gain; co-primary endpoints not met

Primary endpoints not met

Source: ESMO 2026 2878RO · M.K. Scheck

⚕ Gastrointestinal Cancers

ARION PRODIGE 67 — durvalumab + dCRT vs dCRT (locally advanced EC)

2879RO
● WatchPhase 2Negative

Indication: Locally advanced non-metastatic EC (SCC/ADK)

Key finding: 12-mo cPFS 48.6% vs 48.9%; HR 0.91; p=0.351. 12-mo PFS 50.1% vs 48.1%. 12-mo OS 75.1% vs 67.9%; HR 0.99; p=0.489.

Clinical relevance: Durvalumab added to CRT no PFS benefit

No benefit

Source: ESMO 2026 2879RO · M.-A. Modesto

⚕ Gastrointestinal Cancers

FORTITUDE-101/102 biomarker — bemarituzumab by FGFR2 amp (FGFR2b+ GC/GEJ)

2883RO
● WatchBiomarkerExploratory

Indication: FGFR2b-overexpressing GC/GEJ

Key finding: FGFR2 amp 18.9% (F101) / 15.9% (F102). F101 OS amp: 19.3 vs 8.0 mo; HR 0.50. F102 amp: 16.6 vs 8.0 mo; HR 0.67. Non-amp HR 0.94 and 0.84.

Clinical relevance: FGFR2 amp may enrich bemarituzumab benefit

Exploratory

Source: ESMO 2026 2883RO · Z.A. Wainberg

🔷 Genitourinary Cancers

14 studies

🔷 Genitourinary Cancers

KEYNOTE-866 — peri-op pembro + cis/gem vs placebo (cis-eligible MIBC)

4735O
● High priorityPhase 3Negative

Indication: cT2-T4a or T1-T4a N1 MIBC, cis-eligible

Key finding: mEFS 74.1 vs NR mo; HR 0.88 (0.71–1.10); P=0.1366 (not met). pCR 44.4% vs 35.8% (Δ 8.9%). mOS NR both; HR 1.00. Grade ≥3 AEs 80.2% vs 75.1%.

Clinical relevance: No EFS benefit from pembro added to cis chemo

Primary EFS endpoint not met

Source: ESMO 2026 4735O · J. Bedke

🔷 Genitourinary Cancers

CA017-078 — neoadj NIVO+GC and adj NIVO vs GC (MIBC)

4736O
● High priorityPhase 3Negative

Indication: Previously untreated cT2-T4aN0M0 MIBC

Key finding: EFS HR 0.94 (0.71–1.25); P=0.67; mEFS NR vs 67.6 mo. pCR 39.1% vs 29.6%; OR 1.54 (99.91% CI 0.88–2.69). OS HR 0.88 (0.64–1.21). Grade ≥3 TRAEs 45.9% vs 49.5%.

Clinical relevance: No EFS/pCR benefit for peri-op NIVO + GC

Primary endpoints not met

Source: ESMO 2026 4736O · A. Necchi

🔷 Genitourinary Cancers

CAPItello-281 updated OS — capivasertib + abiraterone vs placebo (PTEN-def mHSPC)

LBA56
● Medium priorityPhase 3AKTi

Indication: De novo PTEN-deficient mHSPC

Key finding: OS HR 0.82 (0.68–0.99); median 57.4 vs 46.5 mo; P=0.044 (descriptive). rPFS HR 0.83 (0.70–0.99); 35.5 vs 26.0 mo. OS HRs at ≥95%–100% cutoffs 0.76–0.74.

Clinical relevance: Deepening OS trend with capi+abi

Descriptive; alpha not met

Source: ESMO 2026 LBA56 · K. Fizazi

🔷 Genitourinary Cancers

TROPHY-U-01 Cohort 7 — SG + EV + zimberelimab (1L mUC)

4742O
● Medium priorityPhase 1bTROP2+Nectin-4+PD-1

Indication: Treatment-naive mUC

Key finding: n=21; ORR 83% (confirmed 72%), 3 CR. Grade ≥3 TEAEs 62%. SG 7.5 mg/kg selected for expansion.

Clinical relevance: Promising triple combo in 1L mUC

Phase 1b, small n

Source: ESMO 2026 4742O · R. Sweis

🔷 Genitourinary Cancers

KEYNOTE-905/EV-303 ad hoc — pembro or EV+pembro vs cystectomy (cis-ineligible MIBC)

4733O
● Medium priorityPhase 3Peri-op

Indication: MIBC cis-ineligible/declining

Key finding: Prior data: EV+pembro significantly improved EFS, OS, pCR vs control in 344 pts. Pembro vs control arm results to be reported.

Clinical relevance: Expands evidence for peri-op EV+pembro

Ad hoc

Source: ESMO 2026 4733O · A. Ullén

🔷 Genitourinary Cancers

KEYNOTE-B15/EV-304 ctDNA — EV+pembro vs cis/gem (MIBC)

4734O
● Medium priorityctDNAPhase 3

Indication: cT2-T4aN0M0 or T1-T4aN1M0 MIBC

Key finding: Pre-neo ctDNA+ 52.4% vs 56.8%; pre-surg 13.0% vs 19.7%; post-surg 4.8% vs 13.5%. EV+pembro EFS HR 0.54 (ctDNA+) and 0.68 (ctDNA−). Clearance 82.1% vs 66.7%.

Clinical relevance: Supports ctDNA-guided decisions in MIBC

Exploratory

Source: ESMO 2026 4734O · J.A. Chatzkel

🔷 Genitourinary Cancers

TALAPRO-3 ctDNA TF — talazoparib + enza vs placebo + enza (HRR+ mCSPC)

2219RO
● Medium priorityPhase 3ctDNA

Indication: HRR-deficient mCSPC

Key finding: BL ctDNA+ 36% (TALA+ENZA) / 33% (PBO+ENZA). +ve vs −ve rPFS HR 1.59 (TALA) / 2.15 (PBO, p=0.0002). +ve→−ve conversion 82% vs 68%. Persistent −ve HR 0.23 and 0.23.

Clinical relevance: ctDNA TF prognostic in mCSPC

Source: ESMO 2026 2219RO · A.A. Azad

🔷 Genitourinary Cancers

CCTG PR21 QoL — docetaxel vs 177Lu-PSMA (mCRPC)

2221RO
● Medium priorityPhase 2PRO

Indication: mCRPC after prior ARPI

Key finding: TOI worse with doc at wk 24 (−4.1 vs +0.5; p=0.041) and wk 30 (−7.1 vs +2.8; p<0.001). FACT-P worse with doc. GP5 high score 40.7% vs 15.4%.

Clinical relevance: 177Lu-PSMA better tolerated than docetaxel

Source: ESMO 2026 2221RO · D.J. Khalaf

🔷 Genitourinary Cancers

TALAPRO-3 PROs — TALA + ENZA vs ENZA (HRR+ mCSPC)

2222RO
● WatchPhase 3PRO

Indication: HRR-deficient mCSPC

Key finding: No clinically meaningful HRQoL difference (≥5 pts) except appetite loss (+5.2). TTDD GHS/QoL HR 1.16; TTD worst pain HR 0.82 (0.61–1.11).

Clinical relevance: TALA+ENZA preserves PROs

Source: ESMO 2026 2222RO · A.A. Azad

🔷 Genitourinary Cancers

Neoadj toripalimab + TIP in La-PSCC

1209RO
● WatchPhase 2Single-arm

Indication: T4/N2-3M0 penile SCC

Key finding: ORR 84.0% (2 CR, 19 PR); pCR 48.0%. 12-mo EFS 72.0% (56.4–91.9); 12-mo OS 88.0% (76.1–100). Grade 3-4 TRAEs 84.0%.

Clinical relevance: Deep responses in rare penile SCC

Small n

Source: ESMO 2026 1209RO · H. Han

🔷 Genitourinary Cancers

TORL-1-23 (ixotatug vedotin) in CLDN6+ germ cell tumours

1210RO
● WatchPhase 1CLDN6 ADC

Indication: Pretreated advanced GCT

Key finding: n=12; 11 CLDN6+. ORR 50% (95%CI 18.7–81.3); DCR 80%. mDOR 4.5 mo; 1 response 47.4 mo. 3/6 post-SCT had responses.

Clinical relevance: Signal in refractory GCT

Phase 1, small n

Source: ESMO 2026 1210RO · D. Feldman

🔷 Genitourinary Cancers

KEYNOTE-365 Cohort I — pembro + CBDCA/VP-16 vs chemo (NEPC)

2217RO
● WatchPhase 1b/2NEPC

Indication: Metastatic NEPC

Key finding: n=70. ORR 28% vs 15%; mrPFS 5.1 vs 4.0 mo; HR 0.66. mOS 10.2 vs 7.1 mo; HR 0.33 (0.17–0.63). Benefit greatest in CPS ≥1 (OS HR 0.16).

Clinical relevance: Promising addition of pembro to EP in NEPC

No formal testing

Source: ESMO 2026 2217RO · G. von Amsberg

🔷 Genitourinary Cancers

CH vs tumour HRR in liquid biopsy — PARPi outcomes (mCRPC)

2218RO
● WatchLiquid biopsyCH

Indication: mCRPC on PARPi monotherapy

Key finding: 13% of 1368 HRR mutations CH-only. CH-only HRR TTNT HR 3.24 (p=0.022), rwOS HR 3.52 (p=0.036) vs tumour HRR. Post-PARPi enriched for TP53, PTPN11, ASXL1 CH.

Clinical relevance: CH alters PARPi decisions

Retrospective

Source: ESMO 2026 2218RO · E.S. Antonarakis

🔷 Genitourinary Cancers

PROMPT — ctDNA vs tissue genotyping (mCRPC)

2220RO
● WatchLiquid biopsyHRR/PI3K

Indication: mCRPC genotyping at progression

Key finding: BRCA1/2+HRR: OPA 95%, PPV 92%, NPV 95%. ctDNA standalone sensitivity 81%; adjunct +7% yield. PI3K/AKT OPA 80%, PPV 63%; biallelic loss sensitivity 32/81.

Clinical relevance: ctDNA viable for HRR; tissue needed for PI3K/AKT

Source: ESMO 2026 2220RO · N. Mehra

🌸 Gynaecological Cancers

5 studies

🌸 Gynaecological Cancers

ENGOT-OV56/DOVACC — olaparib ± durva ± UV1 (BRCAwt ROC)

LBA39
● Medium priorityPhase 2Vaccine

Indication: BRCAwt recurrent ovarian cancer, maintenance

Key finding: n=188. Arm C vs A mPFS 8.7 vs 5.9 mo; HR 0.83 (0.68–1.01); p=0.066. HRD− HR 0.73; HRD+ HR 1.19. 22-mo RMST +2.5 mo (p=0.043 exploratory).

Clinical relevance: UV1 added to PARPi±IO: PFS signal only

Primary endpoint not met at 0.05

Source: ESMO 2026 LBA39 · T.J. Nøttrup

🌸 Gynaecological Cancers

JSKN033 — SC HER2 BsADC + envafolimab (pretreated cervical cancer)

1243RO
● Medium priorityPhase 1/2SC combo

Indication: Pretreated cervical cancer

Key finding: n=64. 8.4 mg/kg: ORR 52.9% (18/34); DCR 88.2%; mPFS 7.2 mo. 6.7 mg/kg: ORR 17.9%. ILD 1 pt. Grade ≥3 TRAEs 26.6%.

Clinical relevance: Novel SC co-formulation active in CC

Phase 1/2

Source: ESMO 2026 1243RO · X. Wu

🌸 Gynaecological Cancers

SHR-A2102 — nectin-4 ADC (recurrent/metastatic cervical cancer)

1244RO
● Medium priorityPhase 2Nectin-4 ADC

Indication: Recurrent/metastatic cervical cancer

Key finding: n=50; 6 mg/kg confirmed ORR 47.2%; overall 40.0%. mPFS 5.9 mo (6 mg/kg 7.0 mo); mDOR 7.1 mo. Grade ≥3 TRAEs 58.0%.

Clinical relevance: Phase 3 ongoing

Phase 2

Source: ESMO 2026 1244RO · J. Chen

🌸 Gynaecological Cancers

INCB123667 + bevacizumab (recurrent EOC)

1241RO
● Medium priorityPhase 1CDK2i

Indication: Cyclin E1-high recurrent EOC

Key finding: n=23 EOC. ORR 48% (95%CI 26.8–69.4); DCR 91%; mDOR 5.6 mo. Grade 3-4 TEAEs 52%; no discontinuations.

Clinical relevance: Promising CDK2 inhibitor combo

Phase 1

Source: ESMO 2026 1241RO · D. Lorusso

🌸 Gynaecological Cancers

DENALI — azenosertib OS by Cyclin E1 (PROC)

1242RO
● Medium priorityPhase 2WEE1i

Indication: Platinum-resistant ovarian cancer

Key finding: n=102. mOS Cyclin E1+ 15.8 mo (8.7–17.8) vs Cyclin E1− 7.5 mo; overall 12.3 mo. Prior ORR 35% in Cyclin E1+.

Clinical relevance: Cyclin E1 as predictive biomarker

Single-arm

Source: ESMO 2026 1242RO · F. Simpkins

☀ Melanoma & Skin Cancers

4 studies

☀ Melanoma & Skin Cancers

STARBOARD — enco + bini + pembro vs pbo + pembro (1L BRAF V600 melanoma)

2071O
● High priorityPhase 3BRAF/MEK+IO

Indication: 1L unresectable/metastatic BRAF V600 melanoma

Key finding: Confirmed ORR 70.0% vs 32.7%; p<0.0001. mPFS 33.0 vs 3.4 mo; HR 0.33 (0.24–0.46); p<0.0001. 24-mo PFS 55% vs 26%. OS HR 0.71 (0.48–1.05).

Clinical relevance: Triplet dramatically improves PFS/ORR

OS immature

Source: ESMO 2026 2071O · D. Schadendorf

☀ Melanoma & Skin Cancers

HBI-8000-303 — HBI-8000 + nivo vs placebo + nivo (advanced melanoma)

LBA54
● High priorityPhase 3HDACi

Indication: Anti-PD-(L)1 naive advanced melanoma

Key finding: mPFS 11.7 vs 7.4 mo; HR 0.73 (0.56–0.95); P=0.0141. Confirmed ORR 41.4% vs 32.3%. Grade >3 TRAEs 55% vs 18%; discontinuations 14% vs 5%.

Clinical relevance: HDACi+IO improves PFS

Toxicity increased

Source: ESMO 2026 LBA54 · N.I. Khushalani

☀ Melanoma & Skin Cancers

MIZAR-003 — GC101 TIL vs ICC (anti-PD-1 refractory melanoma)

LBA55
● Medium priorityPhase 2TIL

Indication: Anti-PD-1 resistant advanced melanoma

Key finding: mPFS 4.37 vs 1.61 mo; HR 0.44 (0.28–0.70); P=0.0004. ORR 44.0% vs 8.2%; DCR 68.0% vs 40.8%. Grade ≥3 TRAEs 42.0% vs 30.6%.

Clinical relevance: TIL benefit across mucosal/acral

OS immature

Source: ESMO 2026 LBA55 · L. Si

☀ Melanoma & Skin Cancers

IOV-COM-202 — lifileucel + pembro (ICI-naïve advanced melanoma)

2072O
● Medium priorityPhase 2TIL+IO

Indication: Front-line advanced melanoma

Key finding: n=24 at ≥5.6×10^9 cells: ORR 62%; CR 29.2%; PR 33.3%. mPFS 19.8 mo; mDOR not reached (mFU 26.9 mo).

Clinical relevance: Supports phase 3 TILVANCE-301

Small n

Source: ESMO 2026 2072O · A.J. Furness

🧠 Sarcoma, CNS & Rare Tumours

17 studies

🧠 Sarcoma, CNS & Rare Tumours

Vorasidenib early-response predictors (IDHm grade 2 glioma)

695RO
● Medium priorityProspectiveIDHi

Indication: IDH-mut grade 2 glioma post-surgery

Key finding: n=54. 18-mo MRI −55.5%; RANO ORR 27.0%. PET ORR 46%. Plasma D2HG −57.6% at C3. 9/12 pts durable seizure control. 3 hepatotoxicity discontinuations.

Clinical relevance: Early PET/D2HG predict benefit

Single-centre

Source: ESMO 2026 695RO · F. Bruno

🧠 Sarcoma, CNS & Rare Tumours

HSK42360 — brain-penetrant BRAF inhibitor (BRAF V600 glioma)

701RO
● Medium priorityPhase 1BRAFi

Indication: BRAF V600-mutant glioma

Key finding: n=28; ORR 40.7% (HGG 40%, LGG 42.9%); 4 CR; DCR 85.2%. Grade ≥3 TRAEs 14.3%; no SAEs in glioma population.

Clinical relevance: Durable CRs in glioma

Phase 1

Source: ESMO 2026 701RO · W. Li

🧠 Sarcoma, CNS & Rare Tumours

iCer IPI+NIVO ± myDC in resectable rHGG (5-y)

700RO
● Medium priorityPhase 1Local IO

Indication: Recurrent high-grade glioma

Key finding: ICB only (n=69) vs ICB+myDC (n=19): 3-y PFS 2.9% vs 10%; log-rank p=0.008 (PFS) and p=0.018 (OS).

Clinical relevance: Local ICB+DC improves survival

Non-randomised

Source: ESMO 2026 700RO · C. Bertels

🧠 Sarcoma, CNS & Rare Tumours

Debio 0123 + TMZ (recurrent GBM)

699RO
● Medium priorityPhase 1/2WEE1i

Indication: Recurrent/progressive GBM

Key finding: MTD 720 mg. Among 22 evaluable at 400–720 mg: 3 PR, 2 uPR, 8 SD (36.4%); 8/22 ≥5 cycles. 520 and 720 mg selected for expansion.

Clinical relevance: Promising activity in rGBM

Phase 1

Source: ESMO 2026 699RO · M. Vieito

🧠 Sarcoma, CNS & Rare Tumours

ACCOMPLISH — pembrolizumab + lenvatinib (advanced ACC)

1202RO
● Medium priorityPhase 2ACC

Indication: Progressive advanced adrenocortical carcinoma

Key finding: n=30. ORR 30.0% (9 PR); DCR 93.3%; mDOR 9.4 mo. mPFS 10.4 mo; mOS 19.1 mo. Grade ≥3 AEs: hypertension 26.7%.

Clinical relevance: VEGFR-TKI+IO option post-chemo

Single-arm

Source: ESMO 2026 1202RO · I. Park

🧠 Sarcoma, CNS & Rare Tumours

CLERAD-PROBE — I-124 PET-guided risk-adapted RIT (DTC)

4210RO
● Medium priorityRCTDe-escalation

Indication: DTC after thyroidectomy

Key finding: n=324. Blood dose 275 vs 521 mGy (p<0.001); activity 2.5 vs 5.7 GBq. Recurrence HR 0.38 (0.14–1.05); p=0.06. 5-y EFS 96.6% vs 91.5%.

Clinical relevance: Supports PET-guided RIT de-escalation

Few events

Source: ESMO 2026 4210RO · K. Michalski

🧠 Sarcoma, CNS & Rare Tumours

Becotatug vedotin + pucotenlimab (EGFR+ ATC/PDTC)

4211RO
● Medium priorityPhase 2EGFR ADC+IO

Indication: EGFR+ unresectable ATC/PDTC

Key finding: n=30 (25 evaluable). ORR 44.0%; DCR 84%; 2 pCR after surgery. mTTR 43 days. Grade ≥3 TRAEs 26.7%.

Clinical relevance: Signal in aggressive thyroid cancer

Phase 2, small n

Source: ESMO 2026 4211RO · Y. Wang

🧠 Sarcoma, CNS & Rare Tumours

GETNE-CABOTHYROID — cabozantinib (RAIR DTC)

4212RO
● Medium priorityPhase 2Biomarker

Indication: RAIR DTC after lenvatinib/sorafenib

Key finding: n=41; confirmed ORR 25.6%. mTTR 2.7 mo; mDOR 18.4 mo; mPFS 16.1 mo. Grade 3-4 PPE 7%.

Clinical relevance: Confirms activity; methylation biomarkers

Single-arm

Source: ESMO 2026 4212RO · J. Hernando

🧠 Sarcoma, CNS & Rare Tumours

French ENDOCAN-TUTHYREF — BRAFi/MEKi vs standard (BRAF V600 ATC)

4213RO
● Medium priorityReal-world

Indication: BRAF V600E-mutant anaplastic thyroid carcinoma

Key finding: n=150. After MSM-IPTW: BRAFi/MEKi OS HR 0.46 (0.26–0.82); p=0.009. Stage IVc HR 0.57 (0.28–1.16); p=0.10; OS at 437d 26.9% vs 10.1%.

Clinical relevance: Supports early molecular testing

Retrospective

Source: ESMO 2026 4213RO · C. Do Cao

🧠 Sarcoma, CNS & Rare Tumours

Surufatinib + EP + serplulimab (1L advanced extrapulmonary NEC)

2394RO
● Medium priorityPhase 1b/21L NEC

Indication: 1L advanced extrapulmonary NEC

Key finding: n=43. mPFS 9.4 mo (6.5–13.9); ORR 69.8%; DCR 95.3%. CR/PR had PFS 11.5 vs 6.6 mo; p=0.0041. 1 R0 conversion.

Clinical relevance: High ORR in NEC

Phase 2

Source: ESMO 2026 2394RO · Z.Y. Lin

🧠 Sarcoma, CNS & Rare Tumours

RetroSAUNA — SSA continuation with 2L PRRT/TT (GEP-NET)

2395RO
● Medium priorityRetrospective

Indication: Grade 1-2 non-functioning GEP-NET

Key finding: n=394. SSA continuation PFS: PRRT 34.8 vs 27.1 mo (p=0.02); TT 13.3 vs 8.8 mo (p=0.02). Adjusted HR 0.69, 0.66; pooled HR 0.67 (0.53–0.86); p=0.001. OS trend in TT.

Clinical relevance: Supports SSA continuation

Retrospective

Source: ESMO 2026 2395RO · S. Chhajlani

🧠 Sarcoma, CNS & Rare Tumours

[212Pb]VMT-α-NET in SSTR2+ NETs

2396RO
● Medium priorityPhase 1/2Alpha-RLT

Indication: SSTR2-expressing NETs

Key finding: n=67. No DLTs/Grade 4-5 events. Prior Cohort 2 ORR 43.4%. Cohort 3 (6 mCi): 2 PRs after 1-2 cycles.

Clinical relevance: Favourable safety for alpha RLT

Phase 1/2

Source: ESMO 2026 2396RO · T.R. Halfdanarson

🧠 Sarcoma, CNS & Rare Tumours

DAREON-7 — obrixtamig + SoC (1L DLL3+ NEC)

2397RO
● Medium priorityPhase 1bDLL3/CD3

Indication: 1L advanced DLL3+ NEC

Key finding: n=44. Confirmed ORR 77% (DLL3-high 88%, DLL3-low 65%). mPFS 7.7 mo. CRS G1/G2 59/14%; no G≥3.

Clinical relevance: Supports DAREON-NEC-1 phase 3

Phase 1b

Source: ESMO 2026 2397RO · J. Capdevila

🧠 Sarcoma, CNS & Rare Tumours

Finger sweat vorasidenib/D-2HG monitoring (IDHm glioma)

696RO
● WatchBiomarker

Indication: IDHm glioma on vorasidenib

Key finding: Vorasidenib detectable in 13 pts; higher levels with measurable disease (p<0.05). D-2HG decreased in most pts after initiation.

Clinical relevance: Non-invasive monitoring feasible

Exploratory

Source: ESMO 2026 696RO · V. Sunder-Plassmann

🧠 Sarcoma, CNS & Rare Tumours

Dxcover brain cancer liquid biopsy — EMBRACE validation

697RO
● WatchDiagnosticValidation

Indication: Symptomatic brain cancer triage

Key finding: 2324 eligible pts; 697 brain tumours, 395 malignant. Sensitivity 86%, specificity 44%, NPV 99%. GBM detection 86%; CNS lymphoma 94%; brain mets 90%.

Clinical relevance: Triage tool with high NPV

Low specificity

Source: ESMO 2026 697RO · P. Brennan

🧠 Sarcoma, CNS & Rare Tumours

NEO-GLITIPNI — neoadj IV + iCer/iCav IPI+NIVO (resectable rGBM)

698RO
● WatchPhase 1bLocal IO

Indication: Resectable recurrent GBM

Key finding: 18 initiated NADJ; 14 operated; mFU 24w. mPFS 11w (9–13); mOS 39w (29–49). G3/4 TRAEs reversible; no G5.

Clinical relevance: Feasible NADJ+local IO combo

Phase 1b

Source: ESMO 2026 698RO · I. Dirven

🧠 Sarcoma, CNS & Rare Tumours

Progressive BM post-radiotherapy — immune/epigenetic signatures

703RO
● WatchTranslational

Indication: Progressive brain metastases

Key finding: n=153. Post-RT BM: reduced CD3+ (71 vs 494 cells/mm²), CD8+ (44 vs 187), CD45RO+ (104 vs 302); FOXP3+ increased (215 vs 41). Hypermethylation in immunomodulation pathways.

Clinical relevance: Immunosuppressive TME post-RT

Observational

Source: ESMO 2026 703RO · A. Steindl

🧪 Developmental Therapeutics & Early Phase

4 studies

🧪 Developmental Therapeutics & Early Phase

IMA203CD8 — PRAME-directed TCR T-cell therapy

1946O
● Medium priorityPhase 1TCR-T

Indication: PRAME+ R/R solid tumours

Key finding: n=89 treated; confirmed ORR 38% (31/81). Gynaecologic cohort DL4c: ORR 50% (9/18), 89% ongoing. CRS 97% (mostly G1-2).

Clinical relevance: Signal across diverse tumour types

Phase 1

Source: ESMO 2026 1946O · A. Busse

🧪 Developmental Therapeutics & Early Phase

START-001 — invikafusp alfa (ICB-resistant TMB-H tumours)

1948O
● Medium priorityPhase 2Vβ6/10 TCR BiAb

Indication: ICB-resistant TMB-H solid tumours

Key finding: n=97. ORR 17% (11 PR, 1 pCR); DCR 58%. Excluding NSCLC/melanoma: ORR 22%; DCR 65%. CRS mostly low grade; ~8% G3.

Clinical relevance: Novel IO backbone post-ICB

Phase 2

Source: ESMO 2026 1948O · E. Garralda

🧪 Developmental Therapeutics & Early Phase

QLP2117 (anti-CCR8) + QL2107 (anti-PD-1) in solid tumours

1949O
● Medium priorityPhase 1b/2CCR8

Indication: Advanced solid tumours

Key finding: n=149. Overall ORR 23.0%. At 500 mg: ORR 27.1%; CCR8+ pts ORR 37.8% (SQCC 83.3%). G≥3 TRAEs 51.0%; TRAE deaths 3.4%.

Clinical relevance: Anti-CCR8+PD-1 feasible

Phase 1b/2

Source: ESMO 2026 1949O · F. Wang

🧪 Developmental Therapeutics & Early Phase

PREDICT-IO — early immunotherapy KM analysis

1947O
● WatchMethodology

Indication: Immunotherapy KM analytics

Key finding: 104 longitudinal pairs. HR regresses to mean; 47% of early fixed-point differences unconfirmed; 46% false positive cure fraction. RMST most stable (r=0.68–0.79). Mature OS OR 1.50 (1.38–1.64).

Clinical relevance: RMST most robust early metric

Analytical

Source: ESMO 2026 1947O · D. Montero Morenete

🧬 Translational Research & Biomarkers

1 study

🧬 Translational Research & Biomarkers

Pan-cancer BsADC/BsAb+ADC strategies — ESMO Day 1 roundup

● WatchADCBsAb

Indication: Multiple solid tumours

Key finding: Elfe-D + pumitamig phase 2 (n=142): ORRs HNC 38.5%, HCC 42.9%, cervical 50.0%, PROC 80.6% (abs 999O). HS-20122 EGFR/cMET BsADC NSCLC ORR 55.7% (6 mg/kg 61.3%; abs 1000O). IBI3001 EGFR/B7H3 BsADC NSCLC ORR 31.3%, SCLC 62.5% (abs 1001O).

Clinical relevance: Early BsADC/BsAb+ADC signal across tumours

Early phase

Source: ESMO 2026 news — Abstracts 999O, 1000O, 1001O

🤝 Supportive, Palliative & Survivorship

1 study

🤝 Supportive, Palliative & Survivorship

Multispecific agents — CRC/ccRCC early-phase signals

● WatchBsAbTrispecific

Indication: Advanced CRC and ccRCC

Key finding: INCA33890 (TGFβR2×PD-1)+SoC (abs 1954RO): 1L+FOLFOX/bev ORR 71.4% (82.8% in liver mets); 3L+bev ORR 28.2%. XmAb819 (ENPP3 TCE) ccRCC ORR 30–45.5% across doses (abs 3588O). CS2009 (PD-1/VEGF/CTLA-4) 1L mCRC+XELOX ORR 59.1% (abs 1953RO).

Clinical relevance: Multispecifics expand options

Early phase, small n

Source: ESMO 2026 news — Abstracts 1953RO, 1954RO, 3588O

📋 Program Sessions — Invited Talks

no abstracts

Official sessions built from invited talks / pro-con debates. No abstract text is published for these, so no results are reported here — only the programme (talk titles and speakers).
Proffered paper 1: Breast cancer, early and advanced stage
Talks: 1) Invited Discussant LBA23, LBA13 and LBA27 — Barbara Pistilli (Villejuif, France); 2) Q&A and discussion; 3) Invited Discussant LBA24, LBA25 and LBA50 — Fumikata Hara (Nagoya, Japan); 4) Q&A and discussion
Proffered Paper session
Proffered paper 1: Gastrointestinal tumour, upper digestive
Talks: 1) Invited Discussant LBA77, LBA78 and 2875O — Filippo Pietrantonio (Milan, Italy); 2) Q&A and discussion; 3) Invited Discussant LBA82 and LBA83 — Jeroen Dekervel (Leuven, Belgium); 4) Q&A and discussion
Proffered Paper session
Proffered paper: Investigational immunotherapy
Talks: 1) Invited Discussant 1946O and 1947O — Lawrence Fong (Seattle, United States of America); 2) Q&A and discussion; 3) Invited Discussant 1948O and 1949O — Margaret Ottaviano (Naples, Italy); 4) Q&A and discussion
Proffered Paper session
Proffered paper 1: Genitourinary tumour, renal and urothelial
Talks: 1) Invited Discussant 4735O, 4736O and 4742O — Robert Jones (Bearsden, United Kingdom); 2) Q&A and discussion; 3) Invited Discussant 4733O and 4734O — Min Yuen Teo (Dublin, Ireland, NY); 4) Q&A and discussion
Proffered Paper session
Proffered paper: Melanoma and other skin tumours
Talks: 1) Invited Discussant 2071O and LBA54 — Olivier A. Michielin (Geneva, Switzerland); 2) Q&A and discussion; 3) Invited Discussant 2072O and LBA55 — Karijn P.M. Suijkerbuijk (Utrecht, Netherlands); 4) Q&A and discussion
Proffered Paper session
Rapid oral: Genitourinary tumours, prostate, penile and testis
Talks: 1) Invited Discussant 1209RO, 1210RO and 2217RO — Alison H. Reid (Sutton, United Kingdom); 2) Invited Discussant 2218RO, 2219RO and 2220RO — Edmond M. Kwan (Melbourne, Australia); 3) Invited Discussant 2221RO, 2222RO and LBA56 — Thomas Hwang (Boston, United States of America); 4) Q&A and discussion
Rapid Oral session
Rapid oral: CNS tumours
Talks: 1) Invited Discussant 695RO, 696RO and 697RO — Evanthia Galanis (Rochester, United States of America, MN); 2) Invited Discussant 698RO, 699RO, 700RO and 701RO — Mehdi Touat (Paris, France); 3) Invited Discussant 702RO and 703RO — Lizza Hendriks (Maastricht, Netherlands); 4) Q&A and discussion
Rapid Oral session
Rapid oral 1: Gynaecological cancers
Talks: 1) Invited Discussant 1243RO and 1244RO — Patricia Pautier (Villejuif, France); 2) Invited Discussant LBA39, 1241RO and 1242RO — Iain McNeish (London, United Kingdom); 3) Q&A and discussion
Rapid Oral session
Rapid oral: Breast cancer, early stage
Talks: 1) Invited Discussant 544RO, 538RO and 539RO — Sandra Ximena Franco Millan (Bogota, Colombia); 2) Invited Discussant 540RO, 541RO and 542RO — Maria Vittoria Dieci (Padova, Italy); 3) Invited Discussant 543RO, LBA28 and 545RO — Lilit 9. Harutyunyan (Yerevan, Armenia); 4) Q&A and discussion
Rapid Oral session
Rapid oral 1: Gastrointestinal tumour, upper digestive
Talks: 1) Invited Discussant LBA79, LBA80 and 2876RO — Maria Ignez Braghiroli (Sao Paulo, Brazil, SP); 2) Invited Discussant 2877RO, 2878RO and LBA81 — Feng Wang (Guangzhou, China); 3) Invited Discussant 2879RO, 3136RO and 2883RO — Lucjan S. Wyrwicz (Warsaw, Poland); 4) Q&A and discussion
Rapid Oral session
Rapid oral: NETs and endocrine tumours
Talks: 1) Invited Discussant 2394RO, 2395RO, 2396RO and 2397RO — Thomas Walter (Lyon, France); 2) Invited Discussant 1202RO and 4210RO — Alfredo Berruti (Brescia, Italy); 3) Invited Discussant 421RO, 4212RO and 4213RO — Marcia S. Brose (Philadelphia, United States of America); 4) Q&A and discussion
Rapid Oral session
Keynote lecture 1
Talks: 1) Anna Sophie Berghoff (Vienna, Austria) — Anna Sophie Berghoff (Vienna, Austria); 2) CNS disease as the next frontier in oncology care: Glioblastoma, metastases, and leptomeningeal disease — Wolfgang Wick (Heidelberg, Germany)
Keynote lecture
ESMO 2026 Opening session
Talks: 1) ESMO Presidential address — Fabrice André (Villejuif, France); 2) ESMO 2026 Scientific address by Scientific Committee Co-Chairs Yelena Janjigian and James Larkin; 3) ESMO Award - Early detection meets oncology: Lessons from the oesophagus — Rebecca Fitzgerald (Cambridge, United Kingdom); 4) ESMO Award for Translational Research: A glucometer for cancer: Towards a scalable, universal residual disease measurement — Dan Landau (New York, United States of America); 5) ESMO Women for Oncology Award - Gender matters: Shaping better science in oncology — Pilar Garrido Lopez (Madrid, Spain); 6) ESMO Lifetime Achievement Award: Targeted cancer immunotherapy with PD-1 blockade — Antoni Ribas (Los Angeles, United States of America); 7) In case you missed it: 10 critical developments in oncology in 2026 — Karim Fizazi (Lille, France)
Opening session
Melanoma: From standard fit to bespoke care
Talks: 1) What works if neoadjuvant and adjuvant therapy doesn’t? — Dirk Schadendorf (Essen, Germany); 2) Andrew J. Furness (London, United Kingdom) — Andrew J. Furness (London, United Kingdom); 3) Personalising vaccines using peptides, DNA, mRNA and more — Patrick Alexander A. Ott (Boston, United States of America); 4) Autologous cell therapy: Getting the fit right — Chrystal Paulos (Atlanta, United States of America); 5) Q&A and discussion
Special symposium
SCLC: Can we finally tackle it?
Talks: 1) Emerging targets for SCLC: Are molecular classification and treatment selection going to help? (Incl. neversmorkers) — Charles M. Rudin (New York, United States of America); 2) When and how to BiTE SCLC and CAR-T? — Myung-Ju Ahn (Seoul, Republic of Korea); 3) Smart chemotherapy: ADCs and beyond — Noemi Reguart (Barcelona, Spain); 4) Future role of radiation therapy — Bjorn H. Gronberg (Trondheim, Norway); 5) Q&A and discussion
Special symposium
Raising the bar for tumor-agnostic studies
Talks: 1) AI in tumor-agnostic oncology: Hype or hope? — Olivier Elemento (New York, United States of America); 2) Basket trials: When is enough, enough? — Noemie Simon-Tillaux (Villejuif, France); 3) Tumor agnostic drug repurposing trials: Boost or brake? — Emile E. Voest (Amsterdam, Netherlands); 4) Real-world data: The bridge between science and practice — Christopher M. Booth (Kingston, Canada); 5) Q&A and discussion
Special symposium
Emerging therapeutic strategies in advanced prostate cancer
Talks: 1) Novel AR targeted therapies — Alice Bernard-Tessier (Villejuif, France); 2) Emerging immune-based therapies — Niven Mehra (Nijmegen, Netherlands, Surrey); 3) Optimising radioligand therapy — Arun A. Azad (Melbourne, Australia); 4) New targets (ADCs, new biologies) — Ana Aparicio (Houston, United States of America); 5) Q&A and discussion
Special symposium
Beyond traditional therapy: The impact of emerging approaches on sarcoma treatment
Talks: 1) See, target, treat: The power of theranostics — Rainer W. Hamacher (Essen, Germany); 2) T-cell therapy in sarcoma: A hopeful future or unreachable reality? — Sandra P. D'Angelo (New York, United States of America); 3) ADCs: Ready for prime time? — Breelyn Wilky (Aurora, United States of America); 4) Predictive signatures in sarcomas with "damaged" DNA: A matter of caution or excitement? — Sandra Strauss (London, United Kingdom); 5) Q&A and discussion
Special symposium
Quantifying the magnitude of clinical benefit in a changing trial landscape
Talks: 1) How do I read and interpret a cancer clinical trial? Perspectives on critical appraisal from a practising clinician — Bishal Gyawali (Kingston, Canada); 2) Magnitude of benefit in de-escalation trials: Update on the development of a scoring system for “near-equivalence” studies — Dirk Arnold (Hamburg, Germany); 3) Novel trial endpoints: What does the future hold? — Eva Blondeaux (Genova, Italy); 4) ESMO-MCBS: Do we sufficiently distinguish between exceptional curative treatments and those with less pronounced benefits? — Sjoukje F. Oosting (Groningen, Netherlands); 5) Q&A and discussion
Special session
What oncologists should know about mRNA vaccines
Talks: 1) RNA vaccines for cancer: Principles to practice — Vinod Balachandran (New York, United States of America); 2) Perspectives from the medical oncologist — Toni K. Choueiri (Boston, United States of America); 3) Q&A and discussion
Special session
Ensuring compassionate integrated palliative and oncology care: Best practices, approaches, and decision-making
Talks: 1) Jayne E. Wood (London, United Kingdom) — Jayne E. Wood (London, United Kingdom); 2) Overtreatment framework — Karin Jordan (Potsdam, Germany); 3) ESMO Palliative Care Fellowship: Best fellowship project 1 — Mila Petrova (Sofia, Bulgaria); 4) ESMO Palliative Care Fellowship: Best fellowship project 2 — Uddiptya Goswami (Thiruvananthapuram, India); 5) DC programme overview: Where we are and where we are going — Jayne E. Wood (London, United Kingdom); 6) Session conclusion and Designated Centres Awards — Anna K. Reyners (Groningen, Netherlands)
Special session
Invasive lobular carcinoma: Detecting and managing an elusive enemy
Talks: 1) Presentation of case/condition — Marcela Carausu (Anderlecht, Belgium); 2) Overview of lobular breast cancer (incl biology) — Christine Desmedt (Leuven, Belgium); 3) Medical oncology perspective — Meritxell Bellet Ezquerra (Barcelona, Spain); 4) Radiology perspective — Gary Ulaner (Newport Beach, United States of America); 5) Pharmacology perspective — Romano Danesi (Milan, Italy); 6) Q&A and discussion
Multidisciplinary session
Optimising use of local therapy in advanced lung cancer: Why, when, and how
Talks: 1) Presentation of case/condition — Yi-Chen Zhang (Guangzhou, China); 2) Medical oncology perspective — Virginia Calvo de Juan (Majadahonda, Spain); 3) Radiation oncology perspective — Gerard G. Hanna (Dublin, Ireland); 4) Surgery perspective — Yi-Long Wu (Guangzhou, China); 5) Q&A and discussion
Multidisciplinary session
Transforming oncology with generative AI and autonomous tools
Talks: 1) Generative AI, LLMs and AI agents in oncology — Jakob N. Kather (Heidelberg, Germany); 2) Clinical evidence for AI agents: Where are we and what do we need — Daniel Truhn (Aachen, Germany); 3) AI in oncology: Implementing interpretable models for clinical decision-making — Alessandra Pedrocchi (Milan, Italy); 4) Generative AI and AI biomarkers in precision medicine: Advancing regulation and clinical impact in oncology and beyond — Florian Markowetz (Cambridge, United Kingdom); 5) Validating AI for oncology: Navigating the road to clinical implementation — Caroline Chung (Houston, United States of America); 6) Q&A and discussion
Educational session
Key biological concepts and their clinical implication
Talks: 1) Mutational signatures as predictors of response — Geoff Macintyre (Madrid, Spain); 2) Chromosomal instability and structural alterations underpinning tumour development — Simone Zaccaria (London, United Kingdom); 3) Cancer cell plasticity and cancer evolution — Nicholas McGranahan (London, United Kingdom); 4) Spatial cancer immune co-evolution — Ewa Szczurek (Warsaw, Poland); 5) Q&A and discussion
Educational session
Update on the mangement of endometrial cancer in the era of molecular classification
Talks: 1) How to select the optimal adjuvant therapy — Nicole Concin (Vienna, Austria); 2) First-line systemic therapy of patients with metastatic or recurrent EC (dMMR and non-dMMR) — Ramez N. Eskander (La Jolla, United States of America); 3) Current evidence and development of ADCs in EC — Frederik Marmé (Mannheim, Germany); 4) Therapeutic approaches in advanced/recurrent EC beyond CPIs and ADCs — Alexandra Leary (Villejuif, France); 5) Q&A and discussion
Educational session
The evolving standards in the management of chronic lymphocytic leukemia
Talks: 1) Diagnostics and risk stratification of newly diagnosed chronic lymphocytic leukemia — Francesc Bosch Albareda (Barcelona, Spain); 2) Paolo Ghia (Milan, Italy) — Paolo Ghia (Milan, Italy); 3) Mechanisms of CLL relapse and treatment strategies — Stephan Stilgenbauer (Ulm, Germany); 4) From hematologic success to solid tumor challenges: CAR-T therapy and T-cell transformation risk — Gloria Iacoboni (Barcelona, Spain); 5) Q&A and discussion
Educational session
The exorbitant costs of cancer care: What can we do?
Talks: 1) Financial toxicity: Magnitude and solutions — Nirmala Bhoo-Pathy (Kuala Lumpur, Malaysia); 2) Modelling economic impact to deliver population health impact — Kiusiang Tay-Teo (Geneva, Switzerland); 3) Generic drugs and biosimilars: Where do we stand? — E.G. Elisabeth De Vries (Groningen, Netherlands); 4) Optimized approaches to checkpoint inhibitors — Vijay M. Patil (Mumbai, India); 5) Q&A and discussion
Educational session

This report was generated automatically and is not medical advice. Clinical decisions must be verified against official abstract/presentation full texts and current guidelines.