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Poster session 17

1424P - Maintenance capecitabine plus ramucirumab after first-line platinum-based chemotherapy in advanced oesophagogastric adenocarcinoma (OGA): Final analysis from the PLATFORM trial

Date

14 Sep 2024

Session

Poster session 17

Topics

Clinical Research

Tumour Site

Oesophageal Cancer;  Gastric Cancer;  Gastro-Oesophageal Junction Cancer

Presenters

Anderley Gordon

Citation

Annals of Oncology (2024) 35 (suppl_2): S878-S912. 10.1016/annonc/annonc1603

Authors

A. Gordon1, Z. Rajan2, C.Y.K. Fong1, C. Peckitt2, L. Satchwell2, S. Cromarty1, S. Kidd1, K. Piadel1, B. Leamon1, O. Zhitkov1, M. Davidson1, J. Thompson3, N.R. Maisey4, S. Darby5, T.S. Waddell6, C. Morgan7, A. Bradshaw8, N. Starling1, I. Chau1, D. Cunningham1

Author affiliations

  • 1 Gi/lymphoma Unit, The Royal Marsden Hospital NHS Foundation Trust, SM2 5PT - London/GB
  • 2 Research Data & Statistics Unit, The Royal Marsden Hospital NHS Foundation Trust, SM2 5PT - London/GB
  • 3 Oncology Department, Heartlands Hospital - University Hospitals Birmingham NHS Foundation Trust, B9 5SS - Birmingham/GB
  • 4 Medical Oncology, Guy's Hospital, SE1 9RT - London/GB
  • 5 Oncology Department, Weston Park Hospital - Sheffield Teaching Hospitals NHS Foundation Trust, S10 2SJ - Sheffield/GB
  • 6 Medical Oncology, The Christie NHS Foundation Trust, M20 4BX - Manchester/GB
  • 7 Oncology, Velindre Cancer Centre - Velindre NHS University Trust - NHS Wales, CF14 2TL - Cardiff/GB
  • 8 Clinical Oncology, NUTH - Newcastle Upon Tyne Hospitals NHS Foundation Trust, NE7 7DN - Newcastle-upon-Tyne/GB

Resources

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Abstract 1424P

Background

PLATFORM, a prospective, open-label, multi-centre, adaptive phase II trial assessed maintenance therapy in patients (pts) with advanced OGA after platinum-based first-line induction chemotherapy. We report HER2-negative pts randomised 1:1 to surveillance (control) or maintenance capecitabine plus ramucirumab (cape-ram).

Methods

After 18 weeks of platinum-based chemotherapy, pts with response or stable disease were randomised. Pts had 4- weekly surveillance visits or maintenance cape-ram on day 1 and 8 of a 21-day cycle to progression, death or toxicity. Primary endpoint was progression-free survival (PFS): randomisation to progression or death (pre-specified one-sided p-value 0.025). Key secondary endpoints: overall survival (OS), toxicity. The trial arm closed early in November 2022 due to withdrawal of industry support.

Results

47 pts were randomised. At data cut-off 28 March 2024, 25 control and 22 cape-ram pts were in intention-to- treat (ITT) population. Median follow up was 24.4 mo. Median PFS was 2.5 mo in control arm vs 5.5 mo in cape-ram arm (HR 0.33, 95% CI 0.17 – 0.63, p <0.001) and 6 mo PFS rate was 4% (95% CI 0.3-17.0) vs 42.9% (95% CI 21.9 – 62.3) respectively. Median OS from randomisation of maintenance therapy was 7.1 mo in control arm vs 14.4 mo in cape-ram arm (HR 0.51, 95% CI 0.26-1.00, p=0.025) and median OS from start of induction chemotherapy was 12.1 mo in control arm vs 19.5 mo in cape-ram arm. Of 10 cape-ram pts with measurable disease, 1 had an incremental partial response. 25 control and 21 cape-ram pts were in the safety population. Grade ≥3 adverse events (AEs) were 32% in control arm vs 57% in cape-ram arm. Six cape-ram pts had grade 3 treatment related AEs; hypertension (14%) thromboembolism (10%), anaemia (5%) and hand-foot syndrome (5%). No grade 4+ related AEs or new safety signals were identified.

Conclusions

Maintenance cape-ram after first-line platinum-based chemotherapy for HER2-negative pts significantly improves survival compared to surveillance. To our knowledge, this is the first maintenance study demonstrating survival benefit and should be considered a new option for pts who have not had first-line chemo-immunotherapy.

Clinical trial identification

EudraCT: 2014-002169-30, First opened February 2018.

Editorial acknowledgement

Legal entity responsible for the study

The Royal Marsden GI/Lymphoma Unit.

Funding

Eli Lilly.

Disclosure

C.Y.K. Fong: Financial Interests, Other, Honoraria: BMS. M. Davidson: Financial Interests, Speaker, Consultant, Advisor: Takeda. N.R. Maisey: Financial Interests, Funding: BMS, MSD, Servier. S. Darby: Financial Interests, Invited Speaker: Servier, BMS. T.S. Waddell: Financial Interests, Other, Honoraria, Advisory, Research Funding: Pfizer; Financial Interests, Other, Honoraria, Advisory, Research Funding, Travel/accommodation expenses: BMS, EUSA Pharma; Financial Interests, Other, Advisory, Research Funding: Roche, Eisai Europe; Financial Interests, Other, Advisory, Research Funding,: Merck Sharp & Dohme; Financial Interests, Other, Research Funding, Travel/accommodation: Ipsen. N. Starling: Financial Interests, Personal, Advisory Board: GSK, Novartis, MSD Oncology, Servier, AstraZeneca, Pfizer, Gilead Sciences, Seagen, Janssen, Takeda, Moderna, BMS; Financial Interests, Personal, Invited Speaker: Eli Lilly, Pierre Fabre, Amgen, Merck Serono, Novartis, MSD Oncology, GSK, Servier, Seagen, BMS, AstraZeneca, Astellas; Financial Interests, Institutional, Research Grant, Sept 2017 (24m) Paid to institution research: Merck; Financial Interests, Institutional, Research Grant, Nov 2017 (48m) -Paid to institution research fund: AstraZeneca; Financial Interests, Institutional, Research Grant, Jan 2018 - Paid to institution research fund: Pfizer; Financial Interests, Institutional, Research Grant, July 2018 (36m) Paid to institution research fund: BMS; Financial Interests, Institutional, Research Grant, June 2022 - Paid to institution research fund: Guardant; Financial Interests, Institutional, Research Grant, August 2023 - Paid to institution research fund: Gilead; Non-Financial Interests, Advisory Role, Ad Board uncompensated: Guardant. I. Chau: Financial Interests, Personal, Advisory Board: Bristol Myers Squibb, Eli Lilly, MSD, Roche, Merck-Serono, AstraZeneca, OncXerna, Astella, Incyte, GSK, Sotio, Daiichi Sankyo, Eisai, Taiho, Seagen, Turning Point Therapeutics, Novartis, Takeda, Elevation Oncology; Financial Interests, Personal, Invited Speaker: Eisai, Eli Lilly, Servier, Roche; Financial Interests, Institutional, Coordinating PI: Cilag-Janssen, Eli Lilly. D. Cunningham: Financial Interests, Research Grant: Clovis, Eli Lilly, 4SC, Bayer, Celgene, NIHR EME, Roche; Financial Interests, Other, IMP drug supply: Leap; Financial Interests, Advisory Board: Ovibio. All other authors have declared no conflicts of interest.

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