Irinotecan combined with 5-fluorouracil and leucovorin as second-line chemotherapy for metastatic or relapsed gastric cancer

被引:30
作者
Seo, Myung-Deok [2 ]
Lee, Keun-Wook [1 ]
Lim, Joo Han [3 ]
Yi, Hyeon Gyu [3 ]
Kim, Dae-Young [3 ]
Oh, Do-Youn [3 ]
Kim, Jee Hyun [1 ]
Im, Seock-Ah [3 ]
Kim, Tae-You [3 ]
Lee, Jong Seok [1 ]
Bang, Yung-Jue [3 ]
机构
[1] Seoul Natl Univ, Bundang Hosp, Dept Internal Med, Songnam 463707, Gyeongi Do, South Korea
[2] Cheju Natl Univ Hosp, Dept Internal Med, Cheju, South Korea
[3] Seoul Natl Univ, Dept Internal Med, Seoul, South Korea
关键词
gastric cancer; chemotherapy; second-line; irinotecan; FOLFIRI;
D O I
10.1093/jjco/hyn078
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: We analysed the efficacy and toxicity of irinotecan, leucovorin and 5-fluorouracil (FOLFIRI) chemotherapy as second-line treatment for metastatic or relapsed gastric cancer (MRGC) in a clinical practice setting. Factors to select patients who may benefit from salvage chemotherapy was also analysed. Methods: Patients with MRGC with progression on or within 6 months after discontinuing platinum-based chemotherapy received FOLFIRI as second-line therapy. The FOLFIRI regimen consisted of irinotecan (180 mg/m(2); day 1) combined with leucovorin (200 mg/m(2)), followed by 5-fluorouracil (400 mg/m(2)) as a bolus and 600 mg/m(2) as a 22-h infusion on days 1 and 2 every 2 weeks. Results: Fifty-one patients received a total of 282 courses of chemotherapy. No patients had complete remission (CR), but 9 patients achieved partial remission (PR). Stable disease (SD) was documented in 15 patients. The median progression-free survival (PFS) and overall survival (OS) were 3.2 and 9.1 months, respectively. Toxicities were tolerable and grade 3/4 neutropenia was observed in 49 cycles (17%). In multivariate analysis, patients with less organ involvement by metastasis and good performance status (PS) were independently associated with a longer PFS and OS (P < 0.05). Disease control (CR, PR or SD) after first-line chemotherapy were related to a longer PFS (P = 0.02), but had no effect on OS. Conclusions: FOLFIRI was tolerable and showed modest activity as a second-line therapy in MRGC. Less organ involvement by metastasis or good PS may be optimal selection criteria for patients with MRGC who are suitable for second-line chemotherapy.
引用
收藏
页码:589 / 595
页数:7
相关论文
共 24 条
[1]   Phase II study of irinotecan and 5-fluorouracil/leucovorin in patients with primary refractory or relapsed advanced oesophageal and gastric carcinoma [J].
Assersohn, L ;
Brown, G ;
Cunningham, D ;
Ward, C ;
Oates, J ;
Waters, JS ;
Hill, ME ;
Norman, AR .
ANNALS OF ONCOLOGY, 2004, 15 (01) :64-69
[2]   Randomized multicenter phase II trial of a biweekly regimen of fluorouracil and leucovorin (LV5FU2), LV5FU2 plus cisplatin, or LV5FU2 plus irinotecan in patients with previously untreated metastatic,gastric cancer:: A Federation Francophone de Cancerologie Digestive Group Study -: FFCD 9803 [J].
Bouche, O ;
Raoul, JL ;
Bonnetain, F ;
Giovannini, M ;
Etienne, PL ;
Lledo, G ;
Arsène, D ;
Paitel, JF ;
Guérin-Meyer, V ;
Mitry, E ;
Buecher, B ;
Kaminsky, MC ;
Seitz, JF ;
Rougier, P ;
Bedenne, L ;
Milan, C .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (21) :4319-4328
[3]  
Futatsuki K, 1994, Gan To Kagaku Ryoho, V21, P1033
[4]   Randomized comparison between chemotherapy plus best supportive care with best supportive care in advanced gastric cancer [J].
Glimelius, B ;
Ekstrom, K ;
Hoffman, K ;
Graf, W ;
Sjoden, PO ;
Haglund, U ;
Svensson, C ;
Enander, LK ;
Linne, T ;
Sellstrom, H ;
Heuman, R .
ANNALS OF ONCOLOGY, 1997, 8 (02) :163-168
[5]   Cellular interactions of 5-fluorouracil and the camptothecin analogue CPT-11 (irinotecan) in a human colorectal carcinoma cell line [J].
Guichard, S ;
Hennebelle, I ;
Bugat, R ;
Canal, P .
BIOCHEMICAL PHARMACOLOGY, 1998, 55 (05) :667-676
[6]  
HSIANG YH, 1989, CANCER RES, V49, P5077
[7]   A phase II study of irinotecan with bi-weekly, low-dose leucovorin and bolus and continuous infusion 5-fluorouracil (Modified FOLFIRI) as salvage therapy for patients with advanced or metastatic gastric cancer [J].
Kim, Seong-Geun ;
Oh, Sung Yong ;
Kwon, Hyuk-Chan ;
Lee, Suee ;
Kim, Jung Hwan ;
Kim, Sung-Hyun ;
Kim, Hyo-Jin .
JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2007, 37 (10) :744-749
[8]   Salvage chemotherapy with irinotecan, 5-fluorouracil and leucovorin for taxane- and cisplatin-refractory, metastatic gastric cancer [J].
Kim, ST ;
Kang, WK ;
Kang, JH ;
Park, KW ;
Lee, J ;
Lee, SH ;
Park, JO ;
Kim, K ;
Kim, WS ;
Jung, CW ;
Park, YS ;
Im, YH .
BRITISH JOURNAL OF CANCER, 2005, 92 (10) :1850-1854
[9]   Phase II study of low-dose paclitaxel and cisplatin as a second-line therapy after 5-fluorouracil/platinum chemotherapy in gastric cancer [J].
Lee, Keun-Wook ;
Kim, Jee Hyun ;
Yun, Tak ;
Song, Eun Kee ;
Na, Im Il ;
Shin, Hytinchoon ;
Oh, So Yeon ;
Choi, In Sil ;
Oh, Do-Youn ;
Kim, Dong-Wan ;
Im, Seock-Ah ;
Kim, Tae-You ;
Lee, Jong Seok ;
Heo, Dae Seog ;
Bang, Yung-Jue ;
Kim, Noe Kyeong .
JOURNAL OF KOREAN MEDICAL SCIENCE, 2007, 22 :S115-S121
[10]   Phase II trial of low-dose paclitaxel and cisplatin in patients with advanced gastric cancer [J].
Lee, KW ;
Im, SA ;
Yun, T ;
Song, EK ;
Na, II ;
Shin, H ;
Choi, IS ;
Oh, DY ;
Kim, JH ;
Kim, DW ;
Kim, TY ;
Lee, JS ;
Heo, DS ;
Bang, YJ ;
Kim, NK .
JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2005, 35 (12) :720-726