Chemotherapy switch for localized pancreatic cancer: a systematic review and meta-analysis.

Marjolein Y V Homs, Casper H J van Eijck, Marc G H Besselink, Bas Groot Koerkamp, Motaz Qadan, Eileen M O'Reilly, Roeland F de Wilde, Esther N Dekker, Johanna W Wilmink, Grainne M O'Kane, Raja R Narayan, Mohamed A Ahmami, Anis Meddouch, Eva M M Verkolf, Anne M Gehrels, Bianca Mostert

Journal: The British journal of surgery 2024;111(10):

PMID: 39400008

Abstract

BACKGROUND

Patients with localized (that is non-metastatic) pancreatic ductal adenocarcinoma with an inadequate response or toxicity to first-line chemotherapy may benefit from chemotherapy switch. The aim was to explore the available data on the use and effect of chemotherapy switch, as reported in the literature.

METHODS

A systematic search was conducted in Embase, MEDLINE (Ovid), the Web of Science, Cochrane, and Google Scholar on 1 December 2023. The main outcomes were the proportion of patients who underwent chemotherapy switch and the carbohydrate antigen 19-9 response and resection, R0 resection, and ypN0 resection rates after chemotherapy switch. Data were pooled using a random-effects model.

RESULTS

A total of five retrospective studies, representing 863 patients with localized pancreatic ductal adenocarcinoma, were included and 226 of the 863 patients underwent chemotherapy switch. In four studies, first-line chemotherapy consisted of 5-fluorouracil/leucovorin/irinotecan with oxaliplatin ('FOLFIRINOX') and patients were switched to gemcitabine with nab-paclitaxel. Reasons for chemotherapy switch included an inadequate biochemical, clinical, or radiological response, or toxicity. Three studies compared patients who underwent chemotherapy switch with patients who only received first-line chemotherapy and found that the proportion of patients who underwent chemotherapy switch was 20.5% (95% c.i. 10.5% to 36.3%). The pooled resection rate after chemotherapy switch was 42.0% (95% c.i. 16.6% to 72.5%). Two studies compared the chance of resection after chemotherapy switch versus first-line chemotherapy alone and found a risk ratio of 0.88 (95% c.i. 0.65 to 1.18). Two studies, with a combined total of 576 patients, found similar postoperative survival for patients who underwent chemotherapy switch and patients who only received first-line chemotherapy.

CONCLUSION

One in five patients with localized pancreatic ductal adenocarcinoma underwent chemotherapy switch after an inadequate response or toxicity to first-line chemotherapy. The pooled resection rate after chemotherapy switch was 42% and similar in overall survival compared with first-line chemotherapy only. Three ongoing trials are investigating chemotherapy switch in patients with an inadequate radiological or carbohydrate antigen 19-9 response.

© The Author(s) 2024. Published by Oxford University Press on behalf of BJS Foundation Ltd.

Address: Department of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.; Department of Surgery, Dana-Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.; Cancer Treatment and Quality of Life, Cancer Center Amsterdam, Amsterdam, The Netherlands.; Department of Medical Oncology, Amsterdam UMC, Location University of Amsterdam, Amsterdam, The Netherlands.; Cancer Treatment and Quality of Life, Cancer Center Amsterdam, Amsterdam, The Netherlands.; Department of Surgery, Amsterdam UMC, Location University of Amsterdam, Amsterdam, The Netherlands.; Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.; Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.; Wallace McCain Centre for Pancreatic Cancer, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.; Department of Surgery, Harvard Medical School, Massachusetts General Hospital, Boston, Massachusetts, USA.
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