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KW-2307用于晚期或复发性乳腺癌的II期后期研究。KW-2307合作研究组(乳腺癌组)

[Late phase II study of KW-2307 in advanced or recurrent breast cancer. KW-2307 Cooperative Study Group (Breast Cancer Section)].

作者信息

Tominaga T, Nomura Y, Adachi I, Aoyama H, Nagao K, Mitsuyama S, Nakamura Y, Ogita M, Sano M, Takashima S

机构信息

Dept. of Surgery, Tokyo Metropolitan Komagome Hospital.

出版信息

Gan To Kagaku Ryoho. 1994 May;21(6):809-16.

PMID:8185338
Abstract

A multi-institutional late phase II study of KW-2307 (vinorelbine), a new vinca alkaloid derivative, in advanced or recurrent breast cancer was conducted in 26 nationwide hospitals. KW-2307 was intravenously administered at a dose of 20 mg/m2 once weekly. Eighty among the enrolled 82 patients were eligible. The overall response rate was 30.0% (24/80) with 4 CR, 20 PR, 5 MR, 22 NC, 17 PD and 12 unevaluable patients. The major side effect was leucopenia, which was the dose-limiting factor in this study. Other subjective or objective side effects included general fatigue, nausea-vomiting, anorexia, paresthesia, fever and stomatitis, but none of them was serious.

摘要

一项关于新型长春花生物碱衍生物KW-2307(长春瑞滨)用于晚期或复发性乳腺癌的多机构II期后期研究在全国26家医院开展。KW-2307以20mg/m²的剂量静脉注射,每周一次。82名入组患者中有80名符合条件。总缓解率为30.0%(24/80),其中4例完全缓解,20例部分缓解,5例病情稳定,22例疾病未控,17例疾病进展,12例患者无法评估。主要副作用为白细胞减少,这是本研究中的剂量限制因素。其他主观或客观副作用包括全身乏力、恶心呕吐、厌食、感觉异常、发热和口腔炎,但均不严重。

相似文献

1
[Late phase II study of KW-2307 in advanced or recurrent breast cancer. KW-2307 Cooperative Study Group (Breast Cancer Section)].KW-2307用于晚期或复发性乳腺癌的II期后期研究。KW-2307合作研究组(乳腺癌组)
Gan To Kagaku Ryoho. 1994 May;21(6):809-16.
2
[Early phase II study of KW-2307 in advanced or recurrent breast cancer. KW-2307 Cooperative Study Group (Breast Cancer Section].KW-2307用于晚期或复发性乳腺癌的II期早期研究。KW-2307合作研究组(乳腺癌组)
Gan To Kagaku Ryoho. 1994 May;21(6):801-8.
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[Late phase II clinical study of KW-2307 in advanced/recurrent breast cancer patients (II)].KW-2307用于晚期/复发性乳腺癌患者的II期临床后期研究(II)
Gan To Kagaku Ryoho. 2005 Jul;32(7):983-90.
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[Phase I clinical study on new vinca alkaloid derivative, KW-2307 (vinorelbine). KW-2307 Study Group].新型长春花生物碱衍生物KW-2307(长春瑞滨)的I期临床研究。KW-2307研究组
Gan To Kagaku Ryoho. 1994 Feb;21(2):177-87.
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[Early phase II clinical study of KW-2307 in patients with lung cancer. Lung Cancer Section in KW-2307 Study Group].KW-2307用于肺癌患者的II期早期临床研究。KW-2307研究组肺癌科室
Gan To Kagaku Ryoho. 1994 May;21(6):785-93.
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[A late phase-II trial comparing KW-2307 with vindesine in non-small cell lung cancer (1). Lung cancer section in KW-2307 Study Group].一项在非小细胞肺癌中比较KW-2307与长春地辛的II期晚期试验(1)。KW-2307研究组肺癌部分
Gan To Kagaku Ryoho. 1995 Jan;22(1):67-76.
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Vinorelbine is an active antiproliferative agent in pretreated advanced breast cancer patients: a phase II study.长春瑞滨对经预处理的晚期乳腺癌患者是一种有效的抗增殖药物:一项II期研究。
J Clin Oncol. 1994 Oct;12(10):2094-101. doi: 10.1200/JCO.1994.12.10.2094.
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[Late phase II clinical study of KW-2307 in previously untreated patients with non-small cell lung cancer. KW-2307 Study Group (Lung Cancer Group)].KW-2307用于既往未治疗的非小细胞肺癌患者的II期晚期临床研究。KW-2307研究组(肺癌组)
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Phase II trial of weekly intravenous vinorelbine in first-line advanced breast cancer chemotherapy.长春瑞滨每周静脉注射用于一线晚期乳腺癌化疗的II期试验。
J Clin Oncol. 1993 Jul;11(7):1245-52. doi: 10.1200/JCO.1993.11.7.1245.
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Phase I trial of afatinib plus vinorelbine in Japanese patients with advanced solid tumors, including breast cancer.阿法替尼联合长春瑞滨治疗包括乳腺癌在内的日本晚期实体瘤患者的Ⅰ期试验。
Cancer Chemother Pharmacol. 2015 Oct;76(4):739-50. doi: 10.1007/s00280-015-2826-4. Epub 2015 Aug 8.

引用本文的文献

1
Cost utility in second-line metastatic breast cancer.二线转移性乳腺癌的成本效用
Pharmacoeconomics. 1997 May;11(5):492-7. doi: 10.2165/00019053-199711050-00012.
2
Clinical phase I and pharmacokinetic trial of vinorelbine administered as single intravenous bolus every 21 days in cancer patients.长春瑞滨每21天静脉推注一次用于癌症患者的I期临床和药代动力学试验。
Invest New Drugs. 1996;14(4):371-8. doi: 10.1007/BF00180813.
3
Vinorelbine. A review of its pharmacological properties and clinical use in cancer chemotherapy.长春瑞滨。其药理特性及在癌症化疗中的临床应用综述。
Drugs Aging. 1994 Sep;5(3):200-34. doi: 10.2165/00002512-199405030-00006.