• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

广泛期肺大细胞癌和腺癌的化疗:210例患者的随机试验

Chemotherapy of extensive large cell and adenocarcinoma of the lung: a randomized trial in 210 patients.

作者信息

Vincent R G, Mehta C R, Tucker R D, Mountain C F, Cohen M, Wilson H E, Vogel C

出版信息

Cancer. 1980 Jul 15;46(2):256-60. doi: 10.1002/1097-0142(19800715)46:2<256::aid-cncr2820460206>3.0.co;2-q.

DOI:10.1002/1097-0142(19800715)46:2<256::aid-cncr2820460206>3.0.co;2-q
PMID:6992978
Abstract

Two hundred ten patients with advanced adenocarcinoma of the lung were entered into a two-arm randomized trail. Cytoxan + CCNU + methotrexate was compared to Adriamycin and procarbazine. The tumor response to CCM was significantly higher than the tumor response to Adriamycin and procarbazine. No significant difference existed between the two treatments with respect to survival. Initial performance status, weight loss prior to therapy, and response to therapy were all found to be significant prognostic factors. Median survival time relative to responders in both treatment groups was 31.7 weeks and 15.8 weeks for non-responders.

摘要

210例晚期肺腺癌患者进入一项双臂随机试验。比较了环磷酰胺+洛莫司汀+甲氨蝶呤与阿霉素和丙卡巴肼的疗效。环磷酰胺+洛莫司汀+甲氨蝶呤方案的肿瘤缓解率显著高于阿霉素和丙卡巴肼方案。两种治疗方案在生存率方面无显著差异。初始身体状况、治疗前体重减轻和治疗反应均被发现是重要的预后因素。两个治疗组中,缓解者的中位生存时间为31.7周,未缓解者为15.8周。

相似文献

1
Chemotherapy of extensive large cell and adenocarcinoma of the lung: a randomized trial in 210 patients.广泛期肺大细胞癌和腺癌的化疗:210例患者的随机试验
Cancer. 1980 Jul 15;46(2):256-60. doi: 10.1002/1097-0142(19800715)46:2<256::aid-cncr2820460206>3.0.co;2-q.
2
A randomized clinical trial in bronchogenic small-cell carcinoma evaluating alternating maintenance therapy of vincristine, adriamycin, procarbazine, and etoposide (VAPE) with cyclophosphamide, CCNU, and methotrexate (CCM) versus CCM maintenance alone in complete responders following VAPE induction and late intensification.一项针对支气管源性小细胞癌的随机临床试验,评估长春新碱、阿霉素、丙卡巴肼和依托泊苷(VAPE)与环磷酰胺、洛莫司汀和甲氨蝶呤(CCM)交替维持治疗,与仅在VAPE诱导和晚期强化后完全缓解者中单独使用CCM维持治疗的效果对比。
Am J Clin Oncol. 1994 Dec;17(6):527-37. doi: 10.1097/00000421-199412000-00016.
3
Chemotherapy for bronchogenic carcinoma. Methotrexate, doxorubicin, cyclophosphamide, and lomustine.支气管源性癌的化疗。甲氨蝶呤、阿霉素、环磷酰胺和洛莫司汀。
JAMA. 1977 May 30;237(22):2392-6.
4
Six-drug combination chemotherapy for nonresectable bronchogenic carcinoma.
Cancer Treat Rep. 1979 Aug;63(8):1351-3.
5
"CAMP" combination chemotherapy for unresectable non-oat cell bronchogenic carcinoma.
Cancer Clin Trials. 1979 Winter;2(4):321-6.
6
Chemotherapy for small cell bronchogenic carcinoma: CCNU and doxorubicin compared to CCNU, doxorubicin, vincristine, and procarbazine.小细胞支气管癌的化疗:洛莫司汀与阿霉素联合用药与洛莫司汀、阿霉素、长春新碱及丙卡巴肼联合用药的比较
Cancer Treat Rep. 1980 Aug-Sep;64(8-9):997-1000.
7
Cyclophosphamide, adriamycin, methotrexate, and procarbazine (CAMP) treatment of non-oat cell bronchogenic carcinoma.
Cancer Treat Rep. 1978 Oct;62(10):1595-7.
8
A phase II clinical trial evaluating the use of two sequential, four-drug combination chemotherapy regimens in ambulatory bronchogenic adenocarcinoma patients.一项评估在非卧床支气管源性腺癌患者中使用两种序贯四联化疗方案的II期临床试验。
Am J Clin Oncol. 1992 Dec;15(6):480-6.
9
Cyclic alternating combination chemotherapy for small cell bronchogenic carcinoma.小细胞支气管肺癌的循环交替联合化疗
Cancer Treat Rep. 1979 Feb;63(2):163-70.
10
Metastatic non-small cell bronchogenic carcinoma: a randomized trial of sequential vs combination chemotherapy.转移性非小细胞支气管癌:序贯化疗与联合化疗的随机试验
Eur J Cancer Clin Oncol. 1983 Jan;19(1):33-8. doi: 10.1016/0277-5379(83)90394-2.

引用本文的文献

1
Chemotherapy of lung cancer.肺癌的化疗
Yale J Biol Med. 1981 Jul-Aug;54(4):283-92.
2
Combination chemotherapy for advanced adenocarcinoma of the lung. A review.晚期肺癌腺癌的联合化疗。综述。
Cancer Chemother Pharmacol. 1988;21(2):103-16. doi: 10.1007/BF00257355.