Impact of Amrubicin Monotherapy as Second-Line Chemotherapy on Outcomes in Elderly Patients with Relapsed Extensive-Disease Small-Cell Lung Cancer

被引:2
作者
Igawa, Satoshi [1 ]
Ono, Taihei [1 ]
Kasajima, Masashi [1 ]
Manabe, Hideaki [1 ]
Fukui, Tomoya [1 ]
Mitsufuji, Hisashi [2 ]
Yokoba, Masanori [3 ]
Kubota, Masaru [3 ]
Katagiri, Masato [3 ]
Sasaki, Jiichiro [4 ]
Naoki, Katsuhiko [1 ]
机构
[1] Kitasato Univ, Sch Med, Dept Resp Med, Sagamihara, Kanagawa 2520374, Japan
[2] Kitasato Univ, Sch Nursing, Sagamihara, Kanagawa 2520329, Japan
[3] Kitasato Univ, Sch Allied Hlth Sci, Sagamihara, Kanagawa 2520373, Japan
[4] Kitasato Univ, Sch Med, Res & Dev Ctr New Med Frontiers, Sagamihara, Kanagawa 2520374, Japan
关键词
small-cell lung cancer; amrubicin; elderly; second-line chemotherapy; modified Glasgow prognostic score; GLASGOW PROGNOSTIC SCORE; RANDOMIZED PHASE-III; POOR-RISK PATIENTS; SYNTHETIC; 9-AMINOANTHRACYCLINE; TRIAL; JAPAN; TOPOTECAN; SURVIVAL; CARBOPLATIN; ETOPOSIDE;
D O I
10.2147/CMAR.S255552
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Amrubicin (AMR) is an anticancer drug for patients with relapsed small-cell lung cancer (SCLC). However, the efficacy of AMR in elderly patients with relapsed SCLC after chemotherapy by carboplatin plus etoposide (CE) has not been sufficiently evaluated. Patients and Methods: The medical records of patients with relapsed SCLC who received AMR as second-line chemotherapy were retrospectively reviewed, and their treatment outcomes were evaluated. Results: Forty-one patients with a median age of 76 years were analyzed. The overall response rate was 26.8%. Median progression-free survival (PFS) and overall survival (OS) were 3.5 and 8.1 months, respectively. While the median PFS of 4.7 and 2.8 months in the sensitive relapse and the refractory relapse group differed significantly (P=0.043), respectively, the median OS of 10.7 and 6.8 months in the respective relapse groups did not indicate a statistically significant difference (P=0.24). The median PFS in a group with a modified Glasgow prognostic score (mGPS) of 0 and a group with a mGPS 1 or 2 were 4.5 and 1.6 months (P=0.052), respectively, and the median OS in the respective mGPS groups were 10.7 and 4.4 months (P=0.034). Multivariate analysis identified good performance status, limited disease, and mGPS 0 as favorable independent predictors of PFS and OS of AMR monotherapy. Grade 3 or higher neutropenia was observed in 23 patients (56%), and febrile neutropenia was observed in nine patients (22%). Non-hematological toxic effects were relatively mild, and pneumonitis and treatment-related deaths were not observed. Conclusion: AMR is an effective and feasible regimen for elderly patients with relapsed SCLC after CE therapy.
引用
收藏
页码:4911 / 4921
页数:11
相关论文
共 49 条
[1]  
[Anonymous], AM SOC CLIN ONCOL, DOI DOI 10.1200/JC0.2006.24.18
[2]   Phase II study of amrubicin at a dose of 45 mg/m2 in patients with previously treated small-cell lung cancer [J].
Asao, Tetsuhiko ;
Nokihara, Hiroshi ;
Yoh, Kiyotaka ;
Niho, Seiji ;
Goto, Koichi ;
Ohmatsu, Hironobu ;
Kubota, Kaoru ;
Yamamoto, Noboru ;
Sekine, Ikuo ;
Kunitoh, Hideo ;
Fujiwara, Yutaka ;
Ohe, Yuichiro .
JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2015, 45 (10) :941-946
[3]   Evaluation of cumulative prognostic scores based on the systemic inflammatory response in patients with inoperable non-small-cell lung cancer [J].
Forrest, LM ;
McMillan, DC ;
McArdle, CS ;
Angerson, WJ ;
Dunlop, DJ .
BRITISH JOURNAL OF CANCER, 2003, 89 (06) :1028-1030
[4]   Small-cell lung cancer (SCLC): ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up [J].
Frueh, M. ;
De Ruysscher, D. ;
Popat, S. ;
Crino, L. ;
Peters, S. ;
Felip, E. .
ANNALS OF ONCOLOGY, 2013, 24 :99-105
[5]  
García-Luna PP, 2006, NUTR HOSP, V21, P10
[6]   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
[7]   Amrubicin for relapsed small-cell lung cancer: a systematic review and meta-analysis of 803 patients [J].
Horita, Nobuyuki ;
Yamamoto, Masaki ;
Sato, Takashi ;
Tsukahara, Toshinori ;
Nagakura, Hideyuki ;
Tashiro, Ken ;
Shibata, Yuji ;
Watanabe, Hiroki ;
Nagai, Kenjiro ;
Nakashima, Kentaro ;
Ushio, Ryota ;
Ikeda, Misako ;
Kobayashi, Nobuaki ;
Shinkai, Masaharu ;
Kudo, Makoto ;
Kaneko, Takeshi .
SCIENTIFIC REPORTS, 2016, 6
[8]   Topotecan for Relapsed Small-cell Lung Cancer: Systematic Review and Meta-Analysis of 1347 Patients [J].
Horita, Nobuyuki ;
Yamamoto, Masaki ;
Sato, Takashi ;
Tsukahara, Toshinori ;
Nagakura, Hideyuki ;
Tashiro, Ken ;
Shibata, Yuji ;
Watanabe, Hiroki ;
Nagai, Kenjiro ;
Inoue, Miyo ;
Nakashima, Kentaro ;
Ushio, Ryota ;
Shinkai, Masaharu ;
Kudo, Makoto ;
Kaneko, Takeshi .
SCIENTIFIC REPORTS, 2015, 5
[9]   First-Line Atezolizumab plus Chemotherapy in Extensive-Stage Small-Cell Lung Cancer [J].
Horn, L. ;
Mansfield, A. S. ;
Szczesna, A. ;
Havel, L. ;
Krzakowski, M. ;
Hochmair, M. J. ;
Huemer, F. ;
Losonczy, G. ;
Johnson, M. L. ;
Nishio, M. ;
Reck, M. ;
Mok, T. ;
Lam, S. ;
Shames, D. S. ;
Liu, J. ;
Ding, B. ;
Lopez-Chavez, A. ;
Kabbinavar, F. ;
Lin, W. ;
Sandler, A. ;
Liu, S. V. .
NEW ENGLAND JOURNAL OF MEDICINE, 2018, 379 (23) :2220-2229
[10]   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