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
1455P - Chemotherapy combined with cadonilimab (AK104) as neoadjuvant treatment for locally advanced gastric/gastroesophageal junction cancer: A prospective, single-arm, phase II clinical trial
Presenter: Pengfei Zhang
Session: Poster session 18
Resources:
Abstract
1456P - First in human phase I/II trial of claudin 18.2 ADC RC118 in patients with advanced gastric/gastroesophageal junction cancer
Presenter: Tianshu Liu
Session: Poster session 18
1457P - Tumor immune microenvironment subtypes of esophageal squamous cell carcinoma and their strong ability to predict the efficacy of neoadjuvant immunotherapy
Presenter: Guangyu Yao
Session: Poster session 18
1458P - Impact of 68Ga-FAPI-04 positron emission tomography/computed tomography (PET/CT) on staging and treatment in patients with gastric cancer
Presenter: Shunyu Zhang
Session: Poster session 18
Resources:
Abstract
1460P - Association between effectiveness of treatment with curative intent and outcomes of first-line systemic therapy in metachronous metastatic esophagogastric cancer
Presenter: Denice Kamp
Session: Poster session 18
1462P - A pilot study of hypoxia as a potential resistance mechanism to PD-1 checkpoint blockade therapy in neoadjuvant treatment of esophageal squamous cell carcinoma (HYPERION)
Presenter: Bin Li
Session: Poster session 18
1463P - The presence of liver metastases is associated with systemic immune suppression in gastroesophageal cancer
Presenter: Sebastiaan Siegerink
Session: Poster session 18
1464P - Chemo-radiation alone associated with higher risk of death compared to chemo-radiation plus surgery in esophageal squamous cell carcinoma
Presenter: Brian Housman
Session: Poster session 18
1465P - Potential impact of APC mutation on survival via immune evasion through WNT signaling activation in HER2-positive gastric cancer treated with trastuzumab (tmab), nivolumab (nivo), and chemotherapy
Presenter: Takeru Wakatsuki
Session: Poster session 18