Improved survival with combined gemcitabine and S-1 for locally advanced pancreatic cancer: pooled analysis of three randomized studies

被引:26
|
作者
Yanagimoto, Hiroaki [1 ]
Ishii, Hiroshi [2 ]
Nakai, Yousuke [3 ]
Ozaka, Masato [2 ]
Ikari, Takaaki [2 ]
Koike, Kazuhiko [3 ]
Ueno, Hideki [4 ]
Ioka, Tatsuya [5 ]
Satoi, Sohei [1 ]
Sho, Masayuki [6 ]
Okusaka, Takuji [4 ]
Tanaka, Masao [7 ]
Shimokawa, Toshio [8 ]
Kwon, A-Hon [1 ]
Isayama, Hiroyuki [3 ]
机构
[1] Kansai Med Univ, Dept Surg, Hirakata, Osaka 5731010, Japan
[2] Canc Inst Hosp, Dept Gastroenterol, Tokyo, Japan
[3] Univ Tokyo, Dept Gastroenterol, Tokyo, Japan
[4] Natl Canc Ctr, Hepatobiliary & Pancreat Oncol Div, Tokyo, Japan
[5] Osaka Med Ctr Canc & Cardiovasc Dis, Dept Screening Canc Digest Organs, Osaka, Japan
[6] Nara Med Univ, Dept Surg, Kashihara, Nara 634, Japan
[7] Kyushu Univ, Grad Sch Med Sci, Dept Surg & Oncol, Fukuoka 812, Japan
[8] Univ Yamanashi, Grad Sch Med & Engn, Kofu, Yamanashi, Japan
关键词
Gemcitabine with S-1; Locally advanced pancreatic cancer; Pooled analysis; PHASE-III TRIAL; ORAL S-1; THERAPY; CHEMORADIOTHERAPY; 5-FLUOROURACIL; CHEMOTHERAPY; FOLFIRINOX; CARCINOMA; RADIATION;
D O I
10.1002/jhbp.130
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background The long-term prognosis for localized pancreatic cancer (PC) remains poor. Three randomized trials (GEST phase III, JACCRO PC-01 phase II and GEMSAP phase II) evaluated gemcitabine (Gem) with or without S-1 for patients with metastatic and locally advanced PC. A pooled analysis based on published data examined whether Gem with S-1 (GS) is superior to Gem alone in overall survival (OS) in patients with locally advanced PC. Methods Data were extracted on 193 patients: 31 (JACCRO), 28 (GEMSAP), and 134 (GEST). OS was used for primary endpoint and progression-free survival (PFS) was used for secondary endpoint. A general variance-based method was used to estimate the pooled HR and 95% CI between GS (n = 96) and Gem (n = 97). Results Meta-analysis demonstrated that the overall risk of death was significantly different between the two chemotherapies (hazard ratio = 0.673, 95% confidence interval: 0.488-0.929, P = 0.016). The median PFSs for GS and GEM in the JACCRO, GEMSAP, and GEST studies were 12.0, 12.6, and 10.7 months, and 4.1, 8.1, and 6.2 months, respectively (P = 0.001). The random-effect pooled estimate for 165 patients showed the objective response rate (ORR) in the GS group (28.4%) was better in the Gem group (8.3%, P = 0.001). Conclusions GS improved ORR, PFS and OS in patients with locally advanced PC over Gem alone. GS could become one of the front-line chemotherapeutic agents.
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收藏
页码:761 / 766
页数:6
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