Issued: London, UK

For investors and media only

GSK showcases pipeline momentum across lung, gynaecological and gastrointestinal cancers at ESMO 2026

  • First global Ris-Rez data to show positive anti-tumour activity in relapsed extensive-stage small-cell lung cancer

  • Late-breaking Mo-Rez data will demonstrate clinically meaningful and durable activity in platinum-resistant ovarian cancer

  • AZUR-1 data to show clinically meaningful sustained complete responses with Jemperli (dostarlimab) in MSI-H/dMMR locally advanced rectal cancer

GSK plc (LSE/NYSE: GSK) will present more than 20 abstracts from its expanding solid tumour portfolio at the 2026 European Society for Medical Oncology (ESMO) Congress (23-27 October) in Madrid, Spain. Presentations across lung, gynaecological and gastrointestinal cancers include new investigational data for risvutatug rezetecan (Ris-Rez), mocertatug rezetecan (Mo-Rez) and Jemperli (dostarlimab).

Key presentations include:

  • Ris-Rez in extensive-stage small-cell lung cancer (ES-SCLC): Results from the first global phase I/II EMBOLD PanTumor-101 trial will show positive anti-tumour activity and manageable tolerability at the dose selected for phase III. Together with positive phase III data previously reported in China, the findings support the potential of Ris-Rez to address limited treatment options and poor outcomes for patients with relapsed ES-SCLC. (Abstracts #1071P, #3841P).

  • Ris-Rez in osteosarcoma: GSK’s licensor Hansoh Pharma will present detailed late-breaking phase III ARTEMIS-011 data evaluating Ris-Rez in osteosarcoma. This follows positive topline results announced earlier this year and adds to the body of evidence across multiple difficult-to-treat tumour types (Abstract #LBA9).

  • Mo-Rez in platinum-resistant ovarian cancer (PROC): Late-breaking 13-month follow-up data from the phase I BEHOLD-1 study will demonstrate clinically meaningful, durable responses and encouraging progression-free survival data for Mo-Rez in platinum-resistant ovarian cancer, alongside tolerability data, supporting its potential as a differentiated B7-H4-targeted treatment. (Abstract #LBA41).

  • Jemperli in rectal cancer: Results from the registrational phase II AZUR-1 trial evaluating Jemperli (dostarlimab) in adults with MSI-H/dMMR locally advanced rectal cancer will be presented during a late-breaking oral session. The analysis includes clinically meaningful data on sustained clinical complete responses. (Abstract #LBA87).

Hesham Abdullah, Senior Vice President, Global Head Oncology, R&D, GSK, said: “The data we are presenting at ESMO reflect our progress across some of the most difficult-to-treat cancers. From lung and gynaecological cancers to gastrointestinal tumours, we are building a portfolio of differentiated medicines designed to deliver deep and durable responses, overcome resistance and reduce treatment burden.”

Full list of GSK’s presentations at ESMO:

Ris-Rez

Abstract Name

Presenter

Presentation details

EMBOLD PanTumor-101: Safety and efficacy of Risvutatug Rezetecan (Ris-Rez) monotherapy during dose escalation in a global patient population with advanced/metastatic (A/M) solid tumours (ST)

S. Goel

Abstract #: 1071P

Poster Session

Friday, 23 October, 15:15-16:00 CET

EMBOLD PanTumor-101: Risvutatug Rezetecan (Ris-Rez) dose optimisation in patients with extensive stage small cell lung cancer (ES-SCLC)

H. R. Kim

Abstract #: 3841P

Poster Session

Monday, 26 October, 12:00-12:45 CET

Pooled analysis of interstitial lung disease (ILD) cases among patients (pts) with advanced solid tumours who received risvutatug rezetecan (Ris-Rez) monotherapy

J. Zugazagoitia

Abstract #: 1068P

Poster Session

Friday, 23 October, 15:15-16:00 CET

EMBOLD-SCLC-301: A global, phase 3, randomised study assessing risvutatug rezetecan (Ris-Rez) versus standard of care in patients with relapsed small cell lung cancer (SCLC)

S. Peters

Abstract #: 3861TiP

Poster Session

Monday, 26 October, 12:00-12:45 CET

Real-world treatment patterns among European patients with extensive stage small cell lung cancer (ES-SCLC): Insights from the RESONANCE study

N. Girard

Abstract #: 3836P

Poster Session

Monday, 26 October, 12:00-12:45 CET

Mo-Rez

Abstract Name

Presenter

Presentation details

Mocertatug rezetecan (Mo-Rez) in patients with platinum-resistant ovarian cancer (PROC): Updated results with longer follow-up from the global BEHOLD-1 study

V. Salutari

Abstract #: LBA41

Rapid Oral Session

Saturday, 24 October, 8:30-10:00 CET

BEHOLD-1: Exploratory analysis of biomarkers associated with mocertatug rezetecan (Mo-Rez) response in patients with platinum-resistant ovarian cancer (PROC)

S. Lheureux

Abstract #: 1248RO

Rapid Oral Session

Saturday, 24 October, 8:30-10:00 CET

BEHOLD-Ovarian01: A Phase 3 randomised trial to evaluate mocertatug rezetecan (Mo-Rez) versus standard of care (SoC) in patients (pts) with platinum-resistant ovarian cancer (PROC)

F. Backes

Abstract #: 1341TiP

Poster Session

Monday, 26 October, 12:00-12:45 CET

BEHOLD-Endometrial01: A randomised Phase 3 study evaluating the efficacy and safety of mocertatug rezetecan (Mo-Rez) versus chemotherapy in patients with advanced or recurrent endometrial cancer after platinum-based therapy and immunotherapy

A. Oaknin

Abstract #: 1340TiP

Poster Session

Monday, 26 October, 12:00-12:45 CET

Jemperli (dostarlimab)

Abstract Name

Presenter

Presentation details

Real-world data from the French early access programme of dostarlimab plus chemotherapy in primary advanced or recurrent dMMR/MSI-H endometrial cancer

I. Ray-Coquard

Abstract #: 1285P

Poster Session

Monday, 26 October, 12:00-12:45 CET

Real-world outcomes of dostarlimab plus chemotherapy in US patients with stage III primary advanced endometrial cancer

L. Randall

Abstract #: 1287P

Poster Session

Monday, 26 October, 12:00-12:45 CET

Real-world outcomes of dostarlimab plus chemotherapy in US patients with MMRp/MSS primary advanced or recurrent endometrial cancer (pA/R EC): Subgroup analyses by histology and age

L. Randall

Abstract #: 1286P

Poster Session

Monday, 26 October, 12:00-12:45 CET

Clinical complete response with dostarlimab monotherapy in dMMR/MSI-H locally advanced rectal cancer (LARC): First results from the global registrational AZUR-1 trial

A. Cercek

Abstract #: LBA87

Proffered Paper Session

Sunday, 25 October, 10:15-11:45 CET

A natural history (NH) study of patients (pts) with previously untreated dMMR/MSI-H stage II/III locally advanced rectal cancer (LARC) in Europe

R. V. Garcia

Abstract #: 3115eP

ePoster

Productivity loss, disability and indirect costs associated with locally advanced rectal cancer in the US

T. Bekaii-Saab

Abstract #: 3558eP

ePoster

Velzatinib (IDRX-42)

Abstract Name

Presenter

Presentation details

Molecular Response (MR) in KIT circulating tumour DNA (ctDNA) from StrateGIST 1: A Phase 1/1b study of Velzatinib (IDRX-42) in patients (pts) with advanced gastrointestinal stromal tumours (GIST)

S. Bauer

Abstract #: 3718RO

Rapid Oral Session

Monday, 26 October, 8:35-10:00 CET

Velzatinib exhibits broad c-KIT mutation coverage in a novel panel of Ba/F3 mutant cell models representing the majority of secondary resistance mutations observed clinically in gastrointestinal stromal tumors (GIST)

V. Quereda

Abstract #: 3730P

Poster Session

Monday, 26 October, 12:00-12:45 CET

Zejula (niraparib)

Abstract Name

Presenter

Presentation details

Evaluation of bevacizumab (bev) contribution to efficacy outcome in first-line advanced ovarian cancer phase 3 trial FIRST/ENGOT-OV44

Anne-Claire Hardy-Bessard

Abstract #: 1272P

Presentation

Monday, 26 October, 12:00 - 12:45 CET

GSK5471713

Abstract Name

Presenter

Presentation details

First-time-in-human Phase 1/2 study of GSK5471713, an androgen receptor (AR) degrader, in patients with metastatic castration-resistant prostate cancer (mCRPC)

R. Saleh

Abstract #: 2302TiP

Poster Session

Friday, 23 October, 15:15-16:00 CET

GSK5533524

Abstract Name

Presenter

Presentation details

A phase 1, open-label, multicenter study to investigate the safety and preliminary activity of GSK5533524 alone or in combination in adult patients with advanced solid tumors

V. Samnotra

Abstract #: 1139eTiP

ePoster

CD226

Abstract Name

Presenter

Presentation details

Deep-Learning serial CT imaging predictions of survival compared with RECIST 1.1 objective response rate in immunotherapy-treated NSCLC

D. R. Spigel

Abstract #: 169eP

ePoster

Full list of Alliance studies at ESMO:

Abstract Name

Presenter

Presentation details

Risvutatug rezetecan (Ris-Rez) versus gemcitabine and docetaxel (GD) in heavily pretreated patients (pts) with relapsed or refractory (R/R) osteosarcoma: Primary results from the phase 3 ARTEMIS-011 study

L. Xie

Abstract #: LBA9

Presidential Symposium

Monday, 26 October, 16:30-18:15 CET

Watch-and-wait (W&W) strategy for dostarlimab in localized deficient dMMR/MSI-H gastroesophageal adenocarcinoma (GEA): Results from the first interim analysis of the GERCOR-GONO DEWI phase II study

T. André

Abstract #: 2877RO

Rapid Oral Session

Friday, 23 October, 16:15-17:45 CET

PRODIGE 90 (PREDIR-NEOREC). Neoadjuvant dostarlimab with short course radiotherapy in a watch-and-wait strategy for microsatellite unstable or mismatch repair-deficient locally advanced rectal cancer patients: a randomized phase II trial

M. Karoui

Abstract #: 3548TiP

Poster Session

Sunday, 25 October, 12:00-12:45 CET

RODEO: pReOperative dostarlimab and novel therapies in endometrial cancer

S. Nicum

Abstract #: 1345TiP

Poster Session

Monday, 26 October, 12:00-12:45 CET

Niraparib and dostarlimab plus radiotherapy (RT) in locally advanced head and neck squamous cell carcinoma (LA-HNSCC) patients (TTCC-2022-01 RADIAN)

M. Oliva

Abstract #: LBA46

Rapid Oral Session

Sunday, 25 October, 14:45-16:15 CET

Genotype-Restricted activity of niraparib plus dostarlimab in HRD-positive solid tumours: A translational phase II study

G. A. Vidal

Abstract #: 4361P

Poster Session

Friday, 23 October, 15:15-16:00 CET

About lung cancer

Lung cancer is the most commonly diagnosed cancer and the leading cause of cancer death worldwide, with approximately 2.5 million new cases and 1.88 million deaths annually.1  Non-small cell lung cancer (NSCLC) accounts for approximately 85% of all lung cancer cases, while small cell lung cancer (SCLC) is less common but typically more aggressive.1 Despite advances in treatment, lung cancer is often diagnosed at an advanced stage, when prognosis is poor and risk of disease progression or recurrence is high.1 Extensive-stage SCLC (ES-SCLC) represents the majority of SCLC diagnoses, with most patients presenting after the disease has spread beyond the lungs.2

About ovarian cancer and endometrial cancer

Endometrial cancer affects 1.6 million people globally, with 417,000 new cases each year and 15% to 20% of patients presenting in later stages of the disease. 3,4  Ovarian cancer affects 843,000 people with 240,000 new cases annually.5 70% of these patients present with advanced disease.6 Recurrence is common in advanced cases of disease, up to 67% in endometrial cancer and 70% in ovarian cancer, and survival usually declines after recurrence. 7,8

About stage II/III dMMR/MSI-H locally advanced rectal cancer

Around 5–10% of rectal cancers are mismatch repair-deficient (dMMR) or microsatellite instability-high (MSI-H).9 These tumours have a specific genetic characteristic where they are unable to properly repair DNA damage, leading to an accumulation of mutations. This unique biological feature often makes them responsive to immunotherapies.10, 11 These biomarkers are most commonly found in colorectal, endometrial and other gastrointestinal cancers, but can also be present in other solid tumours.12

About GIST

Gastrointestinal stromal tumours (GIST) are the most common subtype of soft tissue sarcoma, with about 80,000 to 120,000 patients diagnosed with GIST per year worldwide.13 GIST typically presents in the gastrointestinal tract with 80% of cases driven by mutations in the KIT gene that lead to the growth, proliferation and survival of tumour cells (primary or activating mutations in exons 9 and 11).14  Additionally, about 90% of patients treated in the first-line develop new KIT mutations (secondary or resistance mutations in exons 13 and 17) that typically lead to relapse with limited therapeutic options.15  There are currently no approved tyrosine kinase inhibitors (TKIs) that inhibit the full spectrum of clinically relevant primary and secondary mutations in KIT.

About risvutatug rezetecan

Ris-Rez is a novel investigational B7-H3-targeted ADC composed of a fully human anti-B7-H3 monoclonal antibody covalently linked to a topoisomerase inhibitor payload. GSK acquired exclusive worldwide rights (excluding China’s mainland, Hong Kong, Macau and Taiwan) from Hansoh Pharma to progress clinical development and commercialisation of Ris-Rez.

Regulatory designations received for Ris-Rez to date include orphan drug designations from the US Food and Drug Administration (FDA) and Japan’s Ministry of Health, Labour and Welfare in SCLC and the European Medicines Agency (EMA) in a category of cancer that includes SCLC, called pulmonary neuroendocrine carcinoma; Priority Medicines (PRIME) Designation from the EMA for relapsed or refractory ES-SCLC; and Breakthrough Therapy Designations for relapsed or refractory ES-SCLC and relapsed or refractory osteosarcoma from the US FDA. 16, 17, 18, 19, 20, 21 , 22

About mocertatug rezetecan

Mo-Rez is a novel investigational B7-H4-targeted antibody-drug conjugate designed to optimise efficacy and tolerability. It is composed of a fully human anti-B7-H4 monoclonal antibody covalently linked to a topoisomerase inhibitor payload and has a drug-to-antibody ratio (DAR) of 6. GSK acquired exclusive worldwide rights (excluding China’s mainland, Hong Kong, Macau and Taiwan) from Hansoh Pharma to progress clinical development and commercialisation of Mo-Rez globally.

About dostarlimab

Jemperli, a programmed death receptor-1 (PD-1)-blocking antibody, plays an important role in GSK’s immune-oncology research and development programme. A clinical trial programme includes studies of Jemperli alone and in combination with other therapies in gynaecologic, colorectal, and head and neck cancers.

Jemperli was discovered by AnaptysBio, Inc. and licensed to TESARO, Inc., under a collaboration and exclusive license agreement signed in March 2014. Under this agreement, GSK is responsible for the ongoing research, development, commercialisation and manufacturing of Jemperli. 

More information about the product and its currently approved indications is available at EU product information and US product information.

About velzatinib

Velzatinib is a highly selective, investigational small molecule tyrosine kinase inhibitor (TKI) designed to target all key KIT mutations in GIST. The US Food and Drug Administration (FDA) has granted velzatinib Fast Track designation for the treatment of patients with GIST after disease progression on or intolerance to imatinib, and Orphan Drug designations for the treatment of GIST.

GSK in oncology

GSK is focused on developing differentiated medicines for cancers where patients continue to face poor outcomes, treatment resistance, limited options or significant treatment burden. We focus where advances in science and technology offer the greatest opportunity to improve outcomes across haematological, lung, gastrointestinal, genitourinary and gynaecological cancers. Across multiple modalities, including targeted small molecules, antibody-drug conjugates (ADCs) and immunotherapies, GSK applies deep expertise in cancer biology and immune system science to develop differentiated medicines designed to deliver durable responses, overcome resistance and reduce treatment burden.

About GSK

GSK is a global biopharma company with a purpose to unite science, technology, and talent to get ahead of disease together. Find out more at www.gsk.com.

Cautionary statement regarding forward-looking statements

GSK cautions investors that any forward-looking statements or projections made by GSK, including those made in this announcement, are subject to risks and uncertainties that may cause actual results to differ materially from those projected. Such factors include, but are not limited to, those described in the “Risk Factors” section in GSK’s Annual Report on Form 20-F for 2025, and GSK’s Q2 Results for 2026.

References

  1. World Health Organization. Lung cancer Fact Sheet. Updated April 2026. Available at: https://www.who.int/news-room/fact-sheets/detail/lung-cancer

  2. Kim S, Park H, Chiang A. Small Cell Lung Cancer: A Review. JAMA. 2025;333(21):1906-1917.

  3. Sung H, Ferlay J, Siegel R, et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin. 2021;71(3):209-249. doi:10.3322/caac.21660.

  4. CMP: CancerMPact® Patient Metrics Mar-2023, Cerner Enviza.

  5. Ren Y, Xu R, Wang Y, Su L, Su J. Global, regional, and national burden of ovarian cancer in women aged 45 + from 1990 to 2021 and projections for 2050: a systematic analysis based on the 2021 global burden of disease study. J Cancer Res Clin Oncol. 151(8):225. doi:10.1007/s00432-025-06277-9.

  6. Rauh-Hain JA, Krivak TC, Del Carmen MG et al. Ovarian cancer screening and early detection in the general population. Rev Obstet Gynecol. 2011;4(1):15-21.

  7. Shelvin KB, Vincent J, Morron S, Morin M, Mammoser A, Nair N. Recurrent high grade serous endometrial cancer with brain metastases: Immunotherapy confers improved quality of life and survival. Gynecol Oncol Rep. 2024;55:101494. doi:10.1016/j.gore.2024.101494.

  8. Salas Bolívar P, Gonzalez-Benitez C, Carbonell López M, Díez Sebastian J, Hernández Gutiérrez A, Zapardiel I. Prognostic Factors After the First Recurrence of Ovarian Cancer. Journal of Clinical Medicine. 2025; 14(2):470. https://doi.org/10.3390/jcm14020470.

  9. Cercek A, et al. Mismatch Repair-Deficient Rectal Cancer and Resistance to Neoadjuvant Chemotherapy. Clin Cancer Res. 2020 Jul 1;26(13):3271-3279. doi: 1158/1078-0432.CCR-19-3728. Epub 2020 Mar 6. PMID: 32144135; PMCID: PMC7348681

  10. Le DT, et al. PD-1 blockade in tumors with mismatch repair deficiency. N Engl J Med. 2015;372(26):2509-2520.

  11. Andre T, Berton D, Curigliano G, et al. Antitumor Activity and Safety of Dostarlimab Monotherapy in Patients With Mismatch Repair Deficient Solid Tumors: A Nonrandomized Controlled Trial. JAMA Netw Open. 2023;6(11):e2341165. doi:10.1001/jamanetworkopen.2023.41165.

  12. National Cancer Institute at the National Institutes of Health. Definition of mismatch repair deficiency. Accessed June 2026. Available at: https://www.cancer.gov/publications/dictionaries/cancer-terms/def/mismatch-repair-deficiency

  13. Søreide K, Sandvik OM, Søreide JA, Giljaca V, Jureckova A, Bulusu VR. Global epidemiology of gastrointestinal stromal tumours (GIST): A systematic review of population-based cohort studies. Cancer Epidemiol. 2016 Feb;40:39-46.

  14. Bauer S, George S, von Mehren M, Heinrich MC. Early and Next-Generation KIT/PDGFRA Kinase Inhibitors and the Future of Treatment for Advanced Gastrointestinal Stromal Tumor. Front Oncol. 2021 Jul 12;11:672500.

  15. Zhou S, Abdihamid O, Tan F, Zhou H, Liu H, Li Z, Xiao S, Li B. KIT mutations and expression: current knowledge and new insights for overcoming IM resistance in GIST. Cell Commun Signal. 2024 Feb 27;22(1):153.

  16. GSK. GSK receives US FDA Breakthrough Therapy Designation for its B7-H3-targeted antibody-drug conjugate in relapsed or refractory extensive-stage small-cell lung cancer. Available at: https://www.gsk.com/en-gb/media/press-releases/gsk-receives-us-fda-breakthrough-therapy-designation/.

  17. GSK. GSK’s B7-H3-targeted antibody-drug conjugate, risvutatug rezetecan, granted Orphan Drug Designation for small-cell lung cancer in Japan. Available at: https://www.gsk.com/en-gb/media/press-releases/gsk-s-b7-h3-targeted-antibody-drug-conjugate-risvutatug-rezetecan-granted-orphan-drug-designation-for-small-cell-lung-cancer-in-japan/.

  18. GSK. GSK’s B7-H3-targeted antibody-drug conjugate, GSK’227, receives EMA Priority Medicines (PRIME) Designation in relapsed extensive-stage small-cell lung cancer. Available at: https://www.gsk.com/en-gb/media/press-releases/b7-h3-targeted-antibody-drug-conjugate-receives-ema-priority-medicines-designation-in-relapsed-extensive-stage-small-cell-lung-cancer/.

  19. GSK’s B7-H3-targeted antibody-drug conjugate, GSK’227, receives Orphan Drug Designation in the EU. Available at: https://www.gsk.com/en-gb/media/press-releases/gsk-s-b7-h3-targeted-antibody-drug-conjugate-gsk-227-receives-orphan-drug-designation-in-the-eu

  20. GSK. GSK’s B7-H3-targeted antibody-drug conjugate, GSK’227, receives EMA Priority Medicines (PRIME) Designation in relapsed extensive-stage small-cell lung cancer. Available at: https://www.gsk.com/en-gb/media/press-releases/b7-h3-targeted-antibody-drug-conjugate-receives-ema-priority-medicines-designation-in-relapsed-extensive-stage-small-cell-lung-cancer/.

  21. GSK. GSK receives US FDA Breakthrough Therapy Designation for its B7-H3-targeted antibody-drug conjugate in relapsed or refractory extensive-stage small-cell lung cancer. Available at: https://www.gsk.com/en-gb/media/press-releases/gsk-receives-us-fda-breakthrough-therapy-designation/.

  22. GSK. GSK’s B7-H3-targeted antibody-drug conjugate, GSK’227, receives US FDA Breakthrough Therapy Designation in late-line relapsed or refractory osteosarcoma. Available at: https://www.gsk.com/en-gb/media/press-releases/gsk-b7-h3-targeted-antibody-drug-conjugate-gsk227-receives-us-fda-breakthrough-therapy-designation-in-late-line-relapsed-or-refractory-osteosarcoma/.