Journal
JAPANESE JOURNAL OF CLINICAL ONCOLOGY
Volume 52, Issue 12, Pages 1399-1407Publisher
OXFORD UNIV PRESS
DOI: 10.1093/jjco/hyac145
Keywords
pancreatic cancer; chemotherapy; nanoliposomal irinotecan; FOLFIRINOX; gemcitabine with nab-paclitaxel
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This study compared the efficacy and adverse events of nanoliposomal-irinotecan plus fluorouracil and leucovorin and modified FOLFIRINOX as second-line treatment for metastatic and recurrent pancreatic cancer after gemcitabine with nab-paclitaxel. The results showed no significant difference in efficacy between the two treatment options.
Background To compare the treatment outcomes of nanoliposomal-irinotecan (nal-IRI) plus fluorouracil and leucovorin (5-FU/LV) and modified FOLFIRINOX (mFFX) as second-line treatment after gemcitabine with nab-paclitaxel (GnP) for metastatic and recurrent pancreatic cancer. Methods We retrospectively analyzed consecutive patients with metastatic or recurrent pancreatic cancer treated with nal-IRI plus 5-FU/LV or mFFX after first-line GnP treatment between March 2014 and October 2021 in our hospital. Patient characteristics, treatment outcomes and adverse events were extracted for comparison. Results Two hundred sixteen patients were included (nal-IRI plus 5-FU/LV/mFFX: 50/166). Patients in the nal-IRI plus 5-FU/LV group were older, had poorer ECOG PS, and a higher rate of peritoneal metastasis than those in the mFFX group. Median overall survival was 9.5 and 9.8 months (P = 0.97), respectively, and the median progression-free survival was 4.5 vs 4.8 months (P = 0.61), respectively. Anorexia, fatigue and peripheral neuropathy were more common in the mFFX group, but there was no difference in grade 3/4 adverse events between the two groups. Conclusions There was no significant difference in efficacy between nal-IRI plus 5-FU/LV and mFFX after GnP. Nal-IRI plus 5-FU/LV appears to be a viable alternative to mFFX as second-line treatment after GnP. The efficacy of nanoliposomal-irinotecan plus fluorouracil and leucovorin and modified FOLFIRINOX as second-line treatment after gemcitabine with nab-paclitaxel for metastatic and recurrent pancreatic cancer was equivalent.
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