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晚期乳腺癌的化疗。综述

Chemotherapy of advanced breast cancer. A general survey.

作者信息

Lyss A P, Loeb V

出版信息

Cancer. 1984 Feb 1;53(3 Suppl):778-82. doi: 10.1002/1097-0142(19840201)53:3+<778::aid-cncr2820531328>3.0.co;2-7.

DOI:10.1002/1097-0142(19840201)53:3+<778::aid-cncr2820531328>3.0.co;2-7
PMID:6546358
Abstract

Most patients with locally advanced primary breast cancer and almost all patients with disseminated malignancy will ultimately die of their disease. Nevertheless, because breast cancer is one of the most responsive of the solid tumors to cytotoxic drugs, appropriately chosen chemotherapy can relieve symptoms and prolong survival. Adriamycin (doxorubicin) is the most effective among many useful single agents. Combination chemotherapy can augment responses with acceptable toxicity and, along with hormonal manipulation in selected situations, constitutes the standard of care for metastatic disease in 1983. In the interpretation of the clinical oncology literature, meticulous attention to prognostic factors and details of study design is necessary in order to assess the superiority of any particular regimen. Controlled clinical trials of various drug combinations and schedules are especially valuable. The use of an integrated clinical approach involving rational surgical, radiologic, and medical strategies in the management of locally advanced as well as metastatic breast cancer can provide not only meaningful palliation but prolonged disease-free survival for many patients with this common neoplasm.

摘要

大多数局部晚期原发性乳腺癌患者以及几乎所有播散性恶性肿瘤患者最终都会死于其疾病。然而,由于乳腺癌是实体瘤中对细胞毒性药物最敏感的肿瘤之一,适当选择的化疗可以缓解症状并延长生存期。阿霉素(多柔比星)是许多有效单药中最有效的。联合化疗可以在可接受的毒性下增强疗效,并且在某些情况下与激素治疗一起,构成了1983年转移性疾病的标准治疗方法。在解释临床肿瘤学文献时,为了评估任何特定方案的优越性,必须仔细关注预后因素和研究设计细节。各种药物组合和方案的对照临床试验尤其有价值。采用综合临床方法,包括在局部晚期以及转移性乳腺癌的管理中采用合理的手术、放射和医学策略,不仅可以为许多患有这种常见肿瘤的患者提供有意义的姑息治疗,还可以延长无病生存期。

相似文献

1
Chemotherapy of advanced breast cancer. A general survey.晚期乳腺癌的化疗。综述
Cancer. 1984 Feb 1;53(3 Suppl):778-82. doi: 10.1002/1097-0142(19840201)53:3+<778::aid-cncr2820531328>3.0.co;2-7.
2
Combination chemotherapy and adriamycin in patients with advanced breast cancer. A Southwest Oncology Group study.晚期乳腺癌患者的联合化疗与阿霉素治疗。西南肿瘤学组研究。
Cancer. 1976 Jul;38(1):13-20. doi: 10.1002/1097-0142(197607)38:1<13::aid-cncr2820380104>3.0.co;2-5.
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Activity of adriamycin in metastatic breast cancer resistant to a combination regimen with cyclophosphamide, methotrexate, 5-fluorouracil, vincristine, and prdnisone.阿霉素对耐环磷酰胺、甲氨蝶呤、5-氟尿嘧啶、长春新碱和泼尼松联合方案的转移性乳腺癌的活性。
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Variations in responsiveness and survival of clinical subsets of patients with metastatic breast cancer to two chemotherapy combinations.转移性乳腺癌患者临床亚组对两种化疗方案的反应性和生存率差异。
Eur J Cancer (1965). 1980;Suppl 1:141-6.
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Adriamycin plus vincristine compared to and combined with cyclophosphamide, methotrexate, and 5-fluorouracil for advanced breast cancer.阿霉素加长春新碱与环磷酰胺、甲氨蝶呤和5-氟尿嘧啶联合用于晚期乳腺癌的比较及联合应用。
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Chemotherapy for breast cancer.
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Chemotherapy of disseminated breast cancer. Current status and prospects.转移性乳腺癌的化疗。现状与展望。
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Combined chemo- and hormonal therapy in advanced breast cancer.晚期乳腺癌的化疗与激素联合治疗
Cancer. 1977 Jun;39(6 Suppl):2923-33. doi: 10.1002/1097-0142(197706)39:6<2923::aid-cncr2820390679>3.0.co;2-3.
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Combination chemotherapy in disseminated carcinoma of the breast.
Oncology. 1974;29(2):139-46. doi: 10.1159/000224895.

引用本文的文献

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The impact of chemotherapy and radiation therapy on the remodeling of acellular dermal matrices in staged, prosthetic breast reconstruction.化疗和放疗对分期乳房假体再造中脱细胞真皮基质重塑的影响
Plast Reconstr Surg. 2015 Jan;135(1):43e-57e. doi: 10.1097/PRS.0000000000000807.
2
Individual chemosensitivity of in vitro proliferating mammary and ovarian carcinoma cells in comparison to clinical results of chemotherapy.体外增殖的乳腺癌和卵巢癌细胞的个体化学敏感性与化疗临床结果的比较。
J Cancer Res Clin Oncol. 1985;109(3):210-6. doi: 10.1007/BF00390360.
3
Clinical pharmacokinetics of drugs used in the treatment of breast cancer.
Clin Pharmacokinet. 1988 Sep;15(3):180-93. doi: 10.2165/00003088-198815030-00003.
4
Locally advanced breast cancer: report of phase II study and subsequent phase III trial.局部晚期乳腺癌:II期研究及后续III期试验报告
Br J Cancer. 1992 May;65(5):761-5. doi: 10.1038/bjc.1992.160.