Journal of Clinical Medicine (Feb 2023)

Correlation of <i>UGT1A1</i> Gene Polymorphisms or Prior Irinotecan Treatment and Treatment Outcomes of Nanoliposomal-Irinotecan plus 5-Fluorouracil/Leucovorin for Pancreatic Ductal Adenocarcinoma: A Multicenter, Retrospective Cohort Study (HGCSG2101)

  • Kazuaki Harada,
  • Takahiro Yamamura,
  • Osamu Muto,
  • Michio Nakamura,
  • Susumu Sogabe,
  • Kentaro Sawada,
  • Shintaro Nakano,
  • Masataka Yagisawa,
  • Tetsuhito Muranaka,
  • Masayoshi Dazai,
  • Miki Tateyama,
  • Yoshimitsu Kobayashi,
  • Sosuke Kato,
  • Kazuteru Hatanaka,
  • Yasuyuki Kawamoto,
  • Satoshi Yuki,
  • Yuh Sakata,
  • Naoya Sakamoto,
  • Yoshito Komatsu

DOI
https://doi.org/10.3390/jcm12041596
Journal volume & issue
Vol. 12, no. 4
p. 1596

Abstract

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The effects of UGT1A1 gene polymorphisms or prior irinotecan treatment on treatment outcomes of nanoliposomal-irinotecan plus 5-fluorouracil/leucovorin (nal-IRI+5-FU/LV) in patients with unresectable pancreatic ductal adenocarcinoma (PDAC) are not established. This multicenter, retrospective cohort study compared treatment outcomes in patients with UGT1A1*1/*1 and those with UGT1A1*1/*6 or *1/*28 genotypes. We also analyzed the impact of prior irinotecan treatment on survival outcomes in 54 patients treated with nal-IRI+5-FU/LV. Comparable effectiveness was found regardless of the UGT1A1 genotypes. While no significant differences were found, grade ≥3 neutropenia and febrile neutropenia were more frequent in patients with UGT1A1*1/*6 or *1/*28 than in those with UGT1A1*1/*1 genotypes (grade ≥3 neutropenia, 50.0% vs. 30.8%, p = 0.24; febrile neutropenia, 9.1% vs. 0.0%, p = 0.20, respectively). No significant difference in progression-free survival (PFS) and overall survival (OS) was observed between irinotecan-naïve-patients and other patients. However, irinotecan-resistant patients showed significantly shorter PFS (hazard ratio (HR) 2.83, p = 0.017) and OS (HR 2.58, p = 0.033) than other patients. Our study indicated that patients with UGT1A1*1/*6 or *1/*28 may be prone to neutropenia, though further study is needed. The survival benefit of nal-IRI+5-FU/LV could be maintained in patients without disease progression after irinotecan therapy.

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