Impact of peripheral neuropathy induced by platinum in first-line chemotherapy on second-line chemotherapy with paclitaxel for advanced gastric cancer

Background Fluoropyrimidine plus platinum, followed by paclitaxel (PTX) plus ramucirumab is a recommended treatment strategy for advanced gastric cancer (AGC). We investigated how peripheral neuropathy (PN), induced by platinum in first-line chemotherapy, affected the tolerability of second-line che...

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Published inInternational journal of clinical oncology Vol. 25; no. 4; pp. 595 - 601
Main Authors Otsuka, Ryo, Iwasa, Satoru, Yanai, Takako, Hirano, Hidekazu, Shoji, Hirokazu, Honma, Yoshitaka, Okita, Natsuko, Takashima, Atsuo, Kato, Ken, Hashimoto, Hironobu, Sekiguchi, Masatoshi, Makino, Yoshinori, Boku, Narikazu, Yamaguchi, Masakazu
Format Journal Article
LanguageEnglish
Published Singapore Springer Singapore 01.04.2020
Springer Nature B.V
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ISSN1341-9625
1437-7772
1437-7772
DOI10.1007/s10147-019-01598-5

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Summary:Background Fluoropyrimidine plus platinum, followed by paclitaxel (PTX) plus ramucirumab is a recommended treatment strategy for advanced gastric cancer (AGC). We investigated how peripheral neuropathy (PN), induced by platinum in first-line chemotherapy, affected the tolerability of second-line chemotherapy with PTX (2nd-PTX). Methods The subjects were AGC patients who received second-line chemotherapy with PTX (2nd-PTX) after the failure of platinum-based chemotherapy between March 2015 and June 2018. We retrospectively reviewed PN severity, and dose reduction and/or discontinuation due to PN during 2nd-PTX, and compared the cumulative incidence of grade 2 PN between the two groups according to first-line chemotherapy containing oxaliplatin (L-OHP) or cisplatin (CDDP). Results The L-OHP and CDDP groups consisted of 50 patients each. PN severity before 2nd-PTX was grade 1/2 in 46/12% of patients in the L-OHP group, and 100/0% in the CDDP group. The worst grades of chemotherapy-induced PN during 2nd-PTX were grades 1/2/3 in 40/34/14% of patients in the L-OHP group, and 36/18/0% in the CDDP group. Median time to grade 2 PN after starting second-PTX was 2.5 months in the L-OHP group and 8.6 months in the CDDP group (hazard ratio 3.34, p  = 0.002). The frequencies of a PN-related dose reduction and/or discontinuation of PTX were 18% in the L-OHP group and 8% in the CDDP group ( p  = 0.234). Conclusions The severity of PN and tolerability of 2nd-PTX may be affected by first-line chemotherapy with L-OHP or CDDP for AGC.
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ISSN:1341-9625
1437-7772
1437-7772
DOI:10.1007/s10147-019-01598-5