Alternating Chemotherapy with Amrubicin Plus Cisplatin and Weekly Administration of Irinotecan Plus Cisplatin for Extensive-stage Small Cell Lung Cancer

被引:1
作者
Noro, Rintaro [1 ]
Yoshimura, Akinobu [1 ,2 ]
Yamamoto, Kazuo [1 ]
Miyanaga, Akihiko [1 ]
Mizutani, Hideaki [1 ]
Minegishi, Yuji [1 ]
Seike, Masahiro [1 ]
Kubota, Kaoru [1 ]
Kosaihira, Seiji [3 ]
Hino, Mitsunori [3 ]
Ando, Masahiro [4 ]
Nomura, Koichiro [5 ]
Okano, Tetsuya [6 ]
Kobayashi, Kunihiko [6 ]
Uematsu, Kazutsugu [7 ]
Gemma, Akihiko [1 ]
机构
[1] Nippon Med Sch, Dept Internal Med, Div Pulm Med Infect Dis & Oncol, Tokyo 113, Japan
[2] Tokyo Med Univ Hosp, Dept Clin Oncol, Tokyo 1600023, Japan
[3] Nippon Med Sch, Chiba Hokusoh Hosp, Div Internal Med, Imzai City, Chiba, Japan
[4] Tsuboi Canc Ctr Hosp, Div Internal Med, Koriyama, Fukushima, Japan
[5] Tokyo Metropolitan Hiroo Gen Hosp, Dept Resp Med, Tokyo, Japan
[6] Saitama Med Univ, Saitama Int Med Ctr, Dept Resp Med, Hidaka City, Saitama, Japan
[7] Saitama Med Univ, Saitama Med Ctr, Div Pulm Med, Kawagoe, Saitama, Japan
关键词
Extensive-stage small cell lung cancer; alternating chemotherapy; amrubicin; irinotecan; cisplatin; PHASE-III TRIAL; PREVIOUSLY UNTREATED PATIENTS; TOPOISOMERASE-II; ETOPOSIDE RESISTANCE; ONCOLOGY-GROUP; ETOPOSIDE/CISPLATIN; CYCLOPHOSPHAMIDE; CAMPTOTHECIN; SENSITIVITY; VINCRISTINE;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: A phase II study was conducted in order to determine the tumor efficacy and tolerance of alternating chemotherapy for extensive-stage small cell lung cancer (ED-SCLC). Patients and Methods: Twenty patients with previously-untreated ED-SCLC were enrolled in the study. At least four courses of chemotherapy consisting of alternation of two drug combinations were given: alternating cycles of amrubicin and cisplatin with weekly administration of irinotecan and cisplatin at 3- or 4-week intervals. Results: The overall response rate was 85.0% (17120). The median duration of overall survival and progression-free survival were 359 days and 227 days, respectively. Hematological toxicity was the main adverse event. Grade 3 or 4 neutropenia, thrombocytopenia and anemia were observed in 20 (100%), 4 (20%) and 6 (30%) patients, respectively. With regard to non-hematological adverse events, grade 3 or 4 anorexia, diarrhea, febrile neutropenia and infection were observed in 5 (25%), 2 (10%), 2 (10%) and 2 (10%) patients, respectively. No treatment-related death occurred during either regimen. Conclusion: The novel alternating non-cross-resistant chemotherapy was probably active against ED-SCLC and had acceptable toxicities. Further evaluation of this treatment for ED-SCLC in randomized phase III trials is warranted.
引用
收藏
页码:1117 / 1123
页数:7
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