Literature DB >> 35278170

An exploration of trifluridine/tipiracil in combination with irinotecan in patients with pretreated advanced gastric cancer.

Takuro Mizukami1, Keiko Minashi2, Hiroki Hara3, Tomohiro Nishina4, Yusuke Amanuma2, Naoki Takahashi3, Akio Nakasya4, Masaki Takahashi5, Takako Eguchi Nakajima6,7.   

Abstract

BACKGROUND: Trifluridine/tipiracil (FTD/TPI) and irinotecan are treatment options for heavily pretreated patients with advanced gastric cancer, but their efficacies are limited. We investigated the combination of FTD/TPI and irinotecan for such patients.
METHODS: Patients who were refractory to fluoropyrimidine, platinum and taxane were enrolled into four cohorts (Level 1A/1B/2A/2B) and treated with irinotecan (100 [Level 1] or 125 [Level 2] mg/m2 on days 1 and 15) and FTD/TPI (35 mg/m2/dose, twice daily, on days 1-5 and 8-12 [Level A] or on days 1-5 and days 15-19 [Level B]) of a 28-day cycle. The primary endpoints were the maximum tolerated dose, dose-limiting toxicities (DLTs), and recommended phase II dose (RP2D); the secondary endpoint was the disease control rate (DCR).
RESULTS: Eleven patients were enrolled: 2 at Level 1A, 3 at Level 1B, and 6 at Level 2B. DLTs occurred in 2/2 patients at Level 1A and 2/6 patients at Level 2B. Grade 3 or higher treatment-related adverse events were neutropenia (90.9%), leukopenia (54.5%), anemia (45.5%) and febrile neutropenia (18.2%). One patient at Level 2B achieved a partial response, and the DCR was 72.7% (95% CI, 39.0%-94.0%). The median progression-free survival and overall survival periods were 3.0 months (95% CI, 0.92-not reached) and 10.2 months (95% CI, 2.2-not reached), respectively.
CONCLUSION: The RP2D of FTD/TPI combined with irinotecan was determined to be Level 1B; this level was associated with manageable hematologic toxicities and feasible non-hematologic toxicities. Further evaluation of the efficacy of RP2D treatment is necessary.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  CPT-11; Gastric cancer; Irinotecan; TAS-102; Trifluridine/tipiracil

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Substances:

Year:  2022        PMID: 35278170     DOI: 10.1007/s10637-022-01223-9

Source DB:  PubMed          Journal:  Invest New Drugs        ISSN: 0167-6997            Impact factor:   3.651


  3 in total

1.  Efficacy of combination chemotherapy using a novel oral chemotherapeutic agent, TAS-102, with irinotecan hydrochloride on human colorectal and gastric cancer xenografts.

Authors:  Mamoru Nukatsuka; Fumio Nakagawa; Hitoshi Saito; Minoru Sakata; Junji Uchida; Teiji Takechi
Journal:  Anticancer Res       Date:  2015-03       Impact factor: 2.480

2.  A novel antimetabolite, TAS-102 retains its effect on FU-related resistant cancer cells.

Authors:  Tomohiro Emura; Yuko Murakami; Fumio Nakagawa; Masakazu Fukushima; Kenji Kitazato
Journal:  Int J Mol Med       Date:  2004-04       Impact factor: 4.101

3.  An optimal dosing schedule for a novel combination antimetabolite, TAS-102, based on its intracellular metabolism and its incorporation into DNA.

Authors:  Tomohiro Emura; Fumio Nakagawa; Akio Fujioka; Hideyuki Ohshimo; Tatsushi Yokogawa; Hiroyuki Okabe; Kenji Kitazato
Journal:  Int J Mol Med       Date:  2004-02       Impact factor: 4.101

  3 in total

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