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Comparison Between FOLFIRINOX and nal-IRI/FL as Second-line Treatment After Gemcitabine Plus Nab-paclitaxel for Pancreatic Cancer

Authors :
Tomohisa, Otsu
Yoshikuni, Inokawa
Hideki, Takami
Masamichi, Hayashi
Keisuke, Kurimoto
Nobutake, Tanaka
Haruyoshi, Tanaka
Dai, Shimizu
Norifumi, Hattori
Mitsuro, Kanda
Chie, Tanaka
Goro, Nakayama
Yasuhiro, Kodera
Source :
Anticancer Research. 42:3889-3894
Publication Year :
2022
Publisher :
Anticancer Research USA Inc., 2022.

Abstract

The regimen of nanoliposomal irinotecan plus 5-fluorouracil and leucovorin (Nal-IRI/FL) was approved in Japan as second-line chemotherapy after gemcitabine-based treatment for pancreatic ductal adenocarcinoma (PDAC) in 2020. We examined the difference in outcome between patients treated with second-line folinic acid, fluorouracil, irinotecan hydrochloride and oxaliplatin (FOLFIRINOX) and those treated with nal-IRI/FL after first-line gemcitabine and nab-paclitaxel (GnP).The outcomes of 34 patients with PDAC who received second-line FOLFIRINOX (n=21) or nal-IRI/FL (n=13) after GnP at our Department from January 2016 to June 2021 were reviewed retrospectively.Patient backgrounds did not differ between the groups. Dose reduction was more frequently required for treatment with FOLFIRINOX than with nal-IRI/FL (86% vs. 46%, p=0.022). Pegfilgrastim and aprepitant were used more frequently in the FOLFIRINOX group (both p0.01). Progression-free survival (5.9 vs. 8.3 months) and overall survival (9.1 vs. 11.2 months) did not differ significantly between the groups. The frequency of grade 3 (Common Terminology Criteria for Adverse Events) or higher adverse events was similar between the groups. All-grade peripheral neuropathy was more common in the FOLFIRINOX group (100% vs. 77%, p=0.048).FOLFIRINOX and nal-IRI/FL as second-line therapy after GnP provided similar prognoses, although supportive treatment and dose reduction were more frequently required for FOLFIRINOX.

Details

ISSN :
17917530 and 02507005
Volume :
42
Database :
OpenAIRE
Journal :
Anticancer Research
Accession number :
edsair.doi.dedup.....e98785efcf9160234c4bc49dd47939b4