Randomised phase III trial of second-line irinotecan plus cisplatin versus irinotecan alone in patients with advanced gastric cancer refractory to S-1 monotherapy: TRICS trial

被引:44
作者
Nishikawa, Kazuhiro [1 ]
Fujitani, Kazumasa [2 ]
Inagaki, Hitoshi [3 ]
Akamaru, Yusuke [4 ]
Tokunaga, Shinya [5 ]
Takagi, Masakazu [6 ]
Tamura, Shigeyuki [7 ]
Sugimoto, Naotoshi [8 ]
Shigematsu, Tadashi [9 ]
Yoshikawa, Takaki [10 ]
Ishiguro, Tohru [11 ]
Nakamura, Masato [12 ]
Morita, Satoshi [13 ]
Miyashita, Yumi [14 ]
Tsuburaya, Akira [15 ]
Sakamoto, Junichi [16 ]
Tsujinaka, Toshimasa [17 ]
机构
[1] Osaka Natl Hosp, Dept Surg, Chuo Ku, Osaka 5400006, Japan
[2] Osaka Gen Med Ctr, Dept Surg, Sumiyoshi Ku, Osaka 5580056, Japan
[3] Gifu Cent Hosp, Dept Surg, Gifu 5011151, Japan
[4] Osaka Kose Nenkin Hosp, Dept Surg, Fukushima Ku, Osaka 5530007, Japan
[5] Osaka City Gen Hosp, Dept Clin Oncol, Miyakojima Ku, Osaka 5340021, Japan
[6] Shizuoka Prefectural Gen Hosp, Dept Surg, Aoi Ku, Shizuoka 4200881, Japan
[7] Kansai Rosai Hosp, Dept Surg, Amagasaki, Hyogo 5370025, Japan
[8] Osaka Med Ctr Canc & Cardiovasc Dis, Dept Clin Oncol, Higashinari Ku, Osaka 5370025, Japan
[9] Saiseikai Shiga Prefectural Hosp, Dept Gastroenterol, Ritto 5203046, Japan
[10] Kanagawa Canc Ctr, Dept Gastrointestinal Surg, Asahi Ku, Yokohama, Kanagawa 2410815, Japan
[11] Saitama Med Ctr, Dept Digest Tract & Gen Surg, Kawagoe, Saitama 3500844, Japan
[12] Aizawa Hosp, Ctr Comprehens Canc, Matsumoto, Nagano 3900814, Japan
[13] Kyoto Univ, Grad Sch Med, Dept Biomed Stat & Bioinformat, Sakyo Ku, Kyoto 6068397, Japan
[14] Epidemiol & Clin Res Informat Network, Date Ctr, Sakyo Ku, Kyoto 6068392, Japan
[15] Yokohama City Univ, Med Ctr, Dept Gastroenterol Ctr, Minami Ku, Yokohama, Kanagawa 2320024, Japan
[16] Tokai Cent Hosp, Kakamigahara 5048601, Japan
[17] Kaizuka City Hosp, Kaizuka 5970015, Japan
关键词
Phase III; Gastric cancer; Combination chemotherapy; Second-line; Irinotecan; Cisplatin; Fluoropyrimidine; S-1; ADJUVANT CHEMOTHERAPY; SUPPORTIVE CARE; OPEN-LABEL; ADENOCARCINOMA; FLUOROPYRIMIDINE; COMBINATION; PACLITAXEL; DOCETAXEL; THERAPY;
D O I
10.1016/j.ejca.2015.02.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: The optimal second-line regimen for treating advanced gastric cancer (AGC) remains unclear. While irinotecan (CPT-11) plus cisplatin (CDDP) combination therapy and CPT-11 monotherapy have been explored in the second-line setting, the superiority of second-line platinum-based therapies for AGC patients initially treated with S-1 monotherapy has not yet been evaluated; therefore, we aimed to examine the survival benefit of CPT-11/CDDP combination over CPT-11 monotherapy. Methods: AGC patients showing progression after S-1 monotherapy for advanced cancer or recurrence within 6 months after completion of S-1 adjuvant therapy were randomly allocated to CPT-11/CDDP (CPT-11, 60 mg/m(2); CDDP, 30 mg/m(2) , q2w) or CPT-11 (150 mg/m(2), q2w). Results: Sixty-eight advanced and 95 recurrent cases were evaluated. The median overall survivals were 13.9 (95% confidence interval [CI]: 10.8-17.6) and 12.7 (95% CI: 10.3-17.2) months for CPT-11/CDDP and CPT-11, respectively (hazard ratio: 0.834; 95% CI: 0.596-1.167, P = 0.288). No significant differences were observed in the secondary end-points, including progression-free survival (4.6 [95% CI: 3.4-5.9] versus 4.1 [95% CI: 3.3-4.9] months) and response rate (16.9% [95% CI: 8.8-28.3] versus 15.4% [95% CI: 7.6-26.5]). The incidences of grade 3-4 anaemia (16% versus 4%) and elevated serum lactate dehydrogenase levels (5% versus 0%) were higher for CPT-11/CDDP than for CPT-11. Exploratory subgroup analysis revealed that CPT-11/CDDP was significantly more effective for intestinal-type AGC, compared with CPT-11 (overall survival: 15.8 versus 14.0 months; P = 0.019). Conclusion: No survival benefit was observed upon adding CDDP to CPT-11 after S-1 monotherapy failure. (C) 2015 The Authors. Published by Elsevier Ltd. This is an open access article under the CCBY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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收藏
页码:808 / 816
页数:9
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