Amrubicin for treating elderly and poor-risk patients with small-cell lung cancer

被引:11
作者
Igawa, Satoshi [1 ]
Ryuge, Shinichiro [1 ]
Fukui, Tomoya [1 ]
Otani, Sakiko [1 ]
Kimura, Yuka [1 ]
Katono, Ken [1 ]
Takakura, Akira [1 ]
Kubota, Masaru [1 ]
Mitsufuji, Hisashi [1 ]
Katagiri, Masato [2 ]
Yanase, Nobuo [3 ]
Masuda, Noriyuki [1 ]
机构
[1] Kitasato Univ, Sch Med, Dept Resp Med, Kanagawa 2280022, Japan
[2] Kitasato Univ, Dept Clin Physiol, Sch Allied Hlth Sci, Kanagawa 2280022, Japan
[3] Kitasato Univ, Dept Nursing, Kanagawa 2280022, Japan
关键词
Amrubicin; First line; SCLC; Elderly; Poor risk; ONCOLOGY-GROUP WJTOG; PHASE-II; ORAL ETOPOSIDE; CARBOPLATIN; TRIAL; JAPAN; 9-AMINOANTHRACYCLINE; CHEMOTHERAPY; SM-5887;
D O I
10.1007/s10147-010-0085-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study was conducted to evaluate the efficacy of amrubicin as first-line chemotherapy for elderly and poor-risk patients with extensive-disease small-cell lung cancer (ED-SCLC). Untreated SCLC patients who were > 75 years of age or had a performance status of 2 or more were eligible. Amrubicin (35 or 40 mg/m(2) on days 1-3 every 3 weeks) was administered. Between January 2003 and May 2009, 27 patients were evaluated. The median number of treatment cycles was 4 (1-6). Grade 3 or 4 hematologic toxicities comprised neutropenia (63%), leukopenia (56%), thrombocytopenia (15%), and anemia (19%). Febrile neutropenia was observed in four (15%) patients. No treatment-related deaths occurred. The nonhematologic toxicities were mild. The overall response rate was 70%. Progression-free survival, median survival time, and the 1-year survival rate were 6.6 months, 9.3 months, and 30%, respectively. The 40 mg/m(2) dose was feasible and had a tendency to be more effective than the 35 mg/m(2) dose. Amrubicin exhibits activity and acceptable toxicities for elderly and poor-risk patients with ED-SCLC in the first-line treatment setting.
引用
收藏
页码:447 / 452
页数:6
相关论文
共 18 条
[1]   ORAL ETOPOSIDE AND CARBOPLATIN - EFFECTIVE THERAPY FOR ELDERLY PATIENTS WITH SMALL-CELL LUNG-CANCER [J].
EVANS, WK ;
RADWI, A ;
TOMIAK, E ;
LOGAN, DM ;
MARTINS, H ;
STEWART, DJ ;
GOSS, G ;
MAROUN, JA ;
DAHROUGE, S .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1995, 18 (02) :149-155
[2]   A new antitumor agent amrubicin induces cell growth inhibition by stabilizing topoisomerase II-DNA complex [J].
Hanada, M ;
Mizuno, S ;
Fukushima, A ;
Saito, Y ;
Noguchi, T ;
Yamaoka, T .
JAPANESE JOURNAL OF CANCER RESEARCH, 1998, 89 (11) :1229-1238
[3]   Evaluation of the recommended dose and efficacy of amrubicin as second- and third-line chemotherapy for small cell lung cancer [J].
Igawa, Satoshi ;
Yamamoto, Nobuyuki ;
Ueda, Shinya ;
Ono, Akira ;
Nakamura, Yukiko ;
Tsuya, Asuka ;
Murakami, Haruyasu ;
Endo, Masahiro ;
Takahashi, Toshiaki .
JOURNAL OF THORACIC ONCOLOGY, 2007, 2 (08) :741-744
[4]   A phase I study of amrubicin combined with carboplatin for elderly patients with small-cell lung cancer [J].
Inoue, Akira ;
Yamazaki, Koichi ;
Maemondo, Makoto ;
Suzuki, Takuji ;
Kimura, Yuichiro ;
Kanbe, Mariko ;
Isobe, Hiroshi ;
Nishimura, Masaharu ;
Saijo, Yasuo ;
Nukiwa, Toshihiro .
JOURNAL OF THORACIC ONCOLOGY, 2006, 1 (06) :551-555
[5]   STEREOSPECIFIC TOTAL SYNTHESIS OF 9-AMINOANTHRACYCLINES - (+)-9-AMINO-9-DEOXYDAUNOMYCIN AND RELATED-COMPOUNDS [J].
ISHIZUMI, K ;
OHASHI, N ;
TANNO, N .
JOURNAL OF ORGANIC CHEMISTRY, 1987, 52 (20) :4477-4485
[6]  
Kato T, 2006, P AM SOC CLIN ONCOL, V24
[7]   ANTITUMOR ACTIVITIES OF A NOVEL 9-AMINOANTHRACYCLINE (SM-5887) AGAINST MOUSE EXPERIMENTAL-TUMORS AND HUMAN-TUMOR XENOGRAFTS [J].
MORISADA, S ;
YANAGI, Y ;
NOGUCHI, T ;
KASHIWAZAKI, Y ;
FUKUI, M .
JAPANESE JOURNAL OF CANCER RESEARCH, 1989, 80 (01) :69-76
[8]   A statistical study of lung cancer in the Annual of Pathological Autopsy Cases in Japan, from 1958 to 1997, with reference to time trends of lung cancer in the world [J].
Morita, T .
JAPANESE JOURNAL OF CANCER RESEARCH, 2002, 93 (01) :15-23
[9]   Abbreviated treatment for elderly, infirm, or noncompliant patients with limited-stage small-cell lung cancer [J].
Murray, N ;
Grafton, C ;
Shah, A ;
Gelmon, K ;
Kostashuk, E ;
Brown, E ;
Coppin, C ;
Coldman, A ;
Page, R .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (10) :3323-3328
[10]   Chronic effects of a novel synthetic anthracycline derivative (SM-5887) on normal heart and doxorubicin-induced cardiomyopathy in beagle dogs [J].
Noda, T ;
Watanabe, T ;
Kohda, A ;
Hosokawa, S ;
Suzuki, T .
INVESTIGATIONAL NEW DRUGS, 1998, 16 (02) :121-128