Weekly administration of irinotecan (CPT-11) plus cisplatin for refractory or relapsed small cell lung cancer

被引:28
作者
Ando, M
Kobayashi, K
Yoshimura, A
Kurimoto, F
Seike, M
Nara, M
Moriyama, G
Mizutani, H
Hibino, S
Gemma, A
Okano, T
Shibuya, M
Kudoh, S
机构
[1] Saitama Canc Ctr, Resp Sect, Ina, Saitama 3620806, Japan
[2] Tuboi Canc Ctr Hosp, Div Internal Med, Fukushima, Japan
[3] Nippon Med Coll, Dept Internal Med 4, Tokyo 113, Japan
关键词
lung neoplasms; CPT-11; diarrhea; enterocolitis;
D O I
10.1016/j.lungcan.2003.10.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Weekly administrations of CPT-11 plus cisplatin together with an anti-diarrheal. program, the Oral Alkalization and Control of Defecation [Int J Cancer 1999;83:491; Int J Cancer 2001;92:269; Cancer Res 2002;62:179], were evaluated in this phase II study for patients with refractory or relapsed small cell lung cancer. Methods: Patients were treated by weekly administrations of 60 mg/m(2) CPT-11 plus 30 mg/m(2) cisplatin on Days 1, 8 and 15 over 4 weeks. Coinciding with the infusions and for 4 days thereafter, the anti-diarrheal program was practiced using orally administered sodium bicarbonate, magnesium oxide and basic water. Results: Twenty-five patients who had prior treatments of etoposide and platinum containing regimens (16 refractory patients and nine relapsed patients) were entered. The mean dose-intensities of CPT-11 and cisplatin were 154.8 and 77.4 mg/m(2) per course, respectively. Therefore, 86% of the planned dose, was delivered. There were 20 partial responses and an overall response rate of 80% (95% confidence interval, 62-96%) was obtained. The median time to progression and the median survival after starting this regimen were 3.6 and 7.9 months, respectively. The major toxicity was myelosuppression. Grades 3 and 4 neutropenia occurred in 24 and 12% of patients, respectively. One patient with febrile neutropenia was experienced, and Grade 3 diarrhea was observed in 8%. But there was no treatment death. Conclusion: Weekly administrations of CPT-11 plus cisplatin together with Oral Alkalization and Control of Defecation provide a practical and well tolerated regimen that was active for refractory or relapsed small cell lung cancer. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:121 / 127
页数:7
相关论文
共 19 条
[1]   Characterisation and clinical management of CPT-11 (irinotecan)-induced adverse events: The European perspective [J].
Bleiberg, H ;
Cvitkovic, E .
EUROPEAN JOURNAL OF CANCER, 1996, 32A :S18-S23
[2]  
Chu XY, 1997, CANCER RES, V57, P1934
[3]   Randomised trial of irinotecan plus supportive care versus supportive care alone after fluorouracil failure for patients with metastatic colorectal cancer [J].
Cunningham, D ;
Pyrhönen, S ;
James, RD ;
Punt, CJA ;
Hickish, TF ;
Heikkila, R ;
Johannesen, TB ;
Starkhammar, H ;
Topham, CA ;
Awad, L ;
Jacques, C ;
Herait, P .
LANCET, 1998, 352 (9138) :1413-1418
[4]  
Ikegami T, 2002, CANCER RES, V62, P179
[5]   IN-VITRO INVESTIGATION OF A COMBINATION OF 2 DRUGS, CISPLATIN AND CARBOPLATIN, AS A FUNCTION OF THE AREA UNDER THE C/T CURVE [J].
KOBAYASHI, K ;
KUDOH, S ;
TAKEMOTO, T ;
HINO, M ;
HAYASHIHARA, K ;
NAKAHIRO, K ;
ANDO, M ;
NIITANI, H .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1995, 121 (12) :715-720
[6]  
Kobayashi K, 1999, INT J CANCER, V83, P491
[7]   Effect of bile acids on the uptake of irinotecan and its active metabolite, SN-38, by intestinal cells [J].
Kobayashi, K ;
Ceryak, S ;
Matsuzaki, Y ;
Kudoh, S ;
Bouscarel, B .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2001, 1525 (1-2) :125-129
[8]   Irinotecan (CPT-11) in combination with weekly administration of cisplatin (CDDP) for non-small-cell lung cancer [J].
Kobayashi, K ;
Shinbara, A ;
Kamimura, M ;
Takeda, Y ;
Kudo, K ;
Kabe, J ;
Hibino, S ;
Hino, M ;
Shibuya, M ;
Kudoh, S .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1998, 42 (01) :53-58
[9]  
LOKIEC F, 1995, CANCER CHEMOTH PHARM, V36, P79
[10]   CPT-11 - A NEW DERIVATIVE OF CAMPTOTHECIN FOR THE TREATMENT OF REFRACTORY OR RELAPSED SMALL-CELL LUNG-CANCER [J].
MASUDA, N ;
FUKUOKA, M ;
KUSUNOKI, Y ;
MATSUI, K ;
TAKIFUJI, N ;
KUDOH, S ;
NEGORO, S ;
NISHIOKA, M ;
NAKAGAWA, K ;
TAKADA, M .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (08) :1225-1229