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Poster session 18

1459P - Long-term management and outcomes in gastroesophageal cancer in Norway

Date

14 Sep 2024

Session

Poster session 18

Topics

Tumour Site

Oesophageal Cancer;  Gastric Cancer;  Gastro-Oesophageal Junction Cancer

Presenters

Aleksander Kolstad

Citation

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

Authors

A. Kolstad1, G.O. Hjortland2, Y. Nilssen3, G. Emanuel4, M. Ulvestad5, A. Areffard6, E. Aahlin7

Author affiliations

  • 1 Department Of Clinical Medicine, The Arctic University of Norway, 9020 - Tromsø/NO
  • 2 Department Of Oncology, Oslo University Hospital, 0424 - Oslo/NO
  • 3 Department Of Registration, Cancer Registry of Norway, Norwegian Institute of Public Health, 0379 - Oslo/NO
  • 4 Real World Data Analytics, Bristol Myers Squibb, UB8 1DH - Uxbridge/GB
  • 5 Nordic Medical Department, Bristol Myers Squibb, 1366 - Lysaker/NO
  • 6 Norway Medical Department, Bristol Myers Squibb, 1366 - Lysaker/NO
  • 7 Department Of Gastrointestinal Surgery, University Hospital of North Norway, 9019 - Tromsø/NO

Resources

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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.

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