Literature DB >> 19730355

A phase II study of a combined biweekly irinotecan and monthly cisplatin treatment for metastatic or recurrent gastric cancer.

Chong Kun Im1, Sun Young Rha, Hei-Cheul Jeung, Joong Bae Ahn, Sang Joon Shin, Sung Hoon Noh, Jae Kyung Roh, Hyun Cheol Chung.   

Abstract

BACKGROUND: There is no universally confirmed standard chemotherapeutic regimen for advanced gastric cancer (AGC). The aim of this study was to investigate the efficacy and safety of combined biweekly irinotecan and monthly cisplatin treatments of patients with AGC. The primary end point was progression-free survival.
MATERIAL AND METHODS: AGC patients with or without measurable lesions received 70 mg/m2 irinotecan on days 1 and 15, and 80 mg/m2 cisplatin on day 1 every 4 weeks.
RESULTS: Of 40 enrolled patients, 21 patients had measurable disease. With a median follow-up duration of 35 weeks, the median progression-free survival and overall survival were 2.2 months and 8.0 months, respectively. The progression-free survival rate at 6 months was 30.0%. The most common adverse event of grade 3 to 4 was neutropenia (32.5%). Grade 3 diarrhea was observed in 2 patients (5.0%). There was no treatment-related death.
CONCLUSION: Current combined biweekly irinotecan and monthly cisplatin treatment did not show activity comparable with other active regimens in AGC.

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Year:  2010        PMID: 19730355     DOI: 10.1097/COC.0b013e31819fe216

Source DB:  PubMed          Journal:  Am J Clin Oncol        ISSN: 0277-3732            Impact factor:   2.339


  2 in total

1.  The UGT1A9*22 genotype identifies a high-risk group for irinotecan toxicity among gastric cancer patients.

Authors:  Choong-Kun Lee; Hong Jae Chon; Woo Sun Kwon; Hyo-Jeong Ban; Sang Cheol Kim; Hyunwook Kim; Hei-Cheul Jeung; Jimyung Chung; Sun Young Rha
Journal:  Genomics Inform       Date:  2022-09-30

2.  Irinotecan monotherapy offers advantage over combination therapy with irinotecan plus cisplatin in second-line setting for treatment of advanced gastric cancer following failure of fluoropyrimidine-based regimens.

Authors:  Masaru Oba; Keisho Chin; Yoshimasa Kawazoe; Koichi Takagi; Mariko Ogura; Eiji Shinozaki; Mitsukuni Suenaga; Satoshi Matsusaka; Nobuyuki Mizunuma; Kiyohiko Hatake
Journal:  Oncol Lett       Date:  2011-01-20       Impact factor: 2.967

  2 in total

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