Abstract 1459P
Background
Gastroesophageal cancer is the fifth most common cancer worldwide and a leading cause of cancer mortality. There is limited real-world evidence (RWE) for the management of patients with gastroesophageal cancer in Norway; specifically, outcomes in patients treated with neoadjuvant chemotherapy versus chemoradiation. This study aimed to report patient demographics, treatment patterns, and overall survival (OS).
Methods
This was a retrospective study of patients with esophageal squamous cell cancer (ESCC), esophageal adenocarcinoma (EAC), gastroesophageal junction cancer (GEJC), and gastric cancer (GC). Data were collected from the Cancer Registry of Norway. The cohort included patients who received initial palliative or curative treatment within 1 year of diagnosis (2010–21). Curative treatments were defined as neoadjuvant systemic anti-cancer therapy (SACT) plus radiotherapy (RT) (any dose) followed by surgery (SACT + RT/surgery), definitive SACT plus RT (≥40Gy) (SACT + RT), SACT followed by surgery (any treatment following surgery allowed) (SACT/surgery), and primary surgery. Palliative treatments were defined as RT (<40Gy) and/or SACT without surgery, or no registered treatment.
Results
The cohort included 8,204 patients (curative n=3,111; 37.9% and palliative n=5,093; 62.1%); ESCC (n=1,120; 13.7%), EAC (n=2,065; 25.2%), GEJC (n=1,538; 18.7%), and GC (n=3,481; 42.4%). Approximately 36.4%–40.4% of patients received curative treatment; predominantly definitive SACT + RT (n=282; 62.3%) in ESCC, SACT + RT/surgery (n=238; 29.9%) in EAC, SACT/surgery (n=295; 49.6%) in GEJC, and primary surgery (n=761; 60.1%) in GC. Patients with EAC and GEJC treated with SACT + RT/surgery had a median OS of 49 months [95% CI: 39.0, 75.1] and 42 months [95% CI: 35.1, NE], respectively, compared with 86 months [95% CI: 51.1, NE] and 75 months [95% CI: 49.1, NE] in those treated with SACT/surgery (Cox regression to be presented).
Conclusions
Patients with GEJC and EAC treated with curative SACT/surgery in Norway may have improved survival outcomes compared with those who received treatment with SACT + RT/surgery. However, these RWE results may be subject to several confounding factors.
Clinical trial identification
Editorial acknowledgement
Editorial assistance and medical writing support was provided by Carla De Villiers and Robert Jenkins of Health Economics and Outcomes Research (HEOR) Ltd.
Legal entity responsible for the study
Bristol Myers Squibb.
Funding
Bristol Myers Squibb.
Disclosure
G.O. Hjortland: Financial Interests, Institutional, Funding, BMS has supported another study with free drug supply: Bristol Myers Squibb. G. Emanuel, M. Ulvestad: Financial Interests, Institutional, Full or part-time Employment: Bristol Myers Squibb. All other authors have declared no conflicts of interest.
Resources from the same session
1468P - cGAS-driven inflammation in chromosomally unstable oesophagogastric adenocarcinoma
Presenter: Eileen Parkes
Session: Poster session 18
1469P - Development of an efficacy prediction model for concurrent chemoradiotherapy in esophageal squamous cell carcinoma using deep learning and multimodal data integration
Presenter: Xin Yang
Session: Poster session 18
1470TiP - Phase I trial of intraperitoneal infusion of GAIA-102 of NK-Like CD3-negative cells for gastric/pancreatic cancer
Presenter: Eiji Oki
Session: Poster session 18
1471TiP - MK-2870-015: A phase III study of trophoblast antigen 2 (TROP2)-directed antibody-drug conjugate (ADC) sacituzumab tirumotecan (sac-TMT) vs treatment of physician’s choice (TPC) for previously treated metastatic gastroesophageal adenocarcinoma (GEA)
Presenter: Zev Wainberg
Session: Poster session 18
1472TiP - Organ preservation with durvalumab-based immunotherapy in combination with chemoradiation as definitive therapy for early stage, cT1 and cT2N0, esophageal adenocarcinoma: A prospective, multicenter study of the FLOT-AIO Gastric Cancer Group – The IKF-057/ PRESTO trial
Presenter: Nils Homann
Session: Poster session 18
1473TiP - Neoadjuvant SOX combined with cadonilimab (AK104) for PD-L1 negative upper GC/GEJC patients
Presenter: Zhen Yuan
Session: Poster session 18
1474TiP - A randomized phase II study of disitamab vedotin (DV) plus toripalimab and chemotherapy versus DV plus toripalimab versus chemotherapy as perioperative treatment for HER2-expressing locally advanced gastric or gastroesophageal junction adenocarcinoma (GC/GEJ)
Presenter: Ziyu Li
Session: Poster session 18
1475TiP - Fruquintinib in combination with sintilimab and CAPEOX as first-line treatment for advanced G/GEJ cancer: A phase Ib/II clinical trial (FUNCTION)
Presenter: Bei-Bei Chen
Session: Poster session 18