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丝裂霉素-C、博来霉素和顺铂化疗治疗晚期或复发性子宫颈鳞状细胞癌。

Treatment of advanced or recurrent squamous cell carcinoma of the uterine cervix with mitomycin-C, bleomycin, and cisplatin chemotherapy.

作者信息

Smith H O, Stringer C A, Kavanagh J J, Gershenson D M, Edwards C L, Wharton J T

机构信息

Department of Gynecology, University of Texas System Cancer Center, M.D. Anderson Hospital and Tumor Institute, Houston 77030.

出版信息

Gynecol Oncol. 1993 Jan;48(1):11-5. doi: 10.1006/gyno.1993.1003.

Abstract

Fifty-nine patients with recurrent/persistent, or advanced local/metastatic squamous cell cancer of the cervix were treated with combination chemotherapy consisting of mitomycin-C, bleomycin, and cisplatin. Response to therapy and survival analysis was determined for 44 of 49 patients who had previously been treated with radiation therapy and/or surgery and for 10 patients with advanced, previously untreated disease. Seven (16%) of the 44 previously treated patients experienced either complete response (CR) or partial response (PR). The median progression-free interval for responders (CR + PR) was 14.5 months, compared with 2.6 months for the nonresponders (significant, P < 0.001). The median survival time for responders (CR + PR) was 15.9 months, compared with 5.9 months for nonresponders (significant, P < 0.01). The 10 previously untreated patients were separately evaluated for response to chemotherapy. Of these, there was 1 CR, 2 PR, 1 < PR, and 6 SD. The 3 responders (CR + PR), who subsequently underwent radiation therapy, were alive and without evidence of disease 7.9, 13.7, and 27.6 months after treatment. Toxicities were mild to moderate, with no treatment-related deaths. In this study, this combination of mitomycin-C, bleomycin, and cisplatin chemotherapy was found to have activity in local, previously untreated disease and in patients with disease recurrence outside pelvic radiation fields.

摘要

59例复发性/持续性或晚期局部/转移性子宫颈鳞状细胞癌患者接受了由丝裂霉素-C、博来霉素和顺铂组成的联合化疗。对49例曾接受过放疗和/或手术治疗的患者中的44例以及10例晚期、既往未接受过治疗的患者进行了治疗反应和生存分析。44例既往接受过治疗的患者中有7例(16%)出现完全缓解(CR)或部分缓解(PR)。缓解者(CR+PR)的无进展生存期(PFI)中位数为14.5个月,而未缓解者为2.6个月(差异有统计学意义,P<0.001)。缓解者(CR+PR)的中位生存时间为15.9个月,未缓解者为5.9个月(差异有统计学意义,P<0.01)。对10例既往未接受过治疗的患者分别评估化疗反应。其中有1例CR、2例PR、1例轻度缓解(<PR)和6例疾病稳定(SD)。3例缓解者(CR+PR)随后接受了放疗,治疗后7.9、13.7和27.6个月时仍存活且无疾病证据。毒性反应为轻至中度,无治疗相关死亡。在本研究中,发现丝裂霉素-C、博来霉素和顺铂联合化疗对局部、既往未接受过治疗的疾病以及盆腔放疗野外疾病复发的患者有活性。

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