Rosenthal C J, Khulpateea N, Boyce J, Mehrotra S, Tamarin S
Cancer. 1983 Dec 1;52(11):2025-30. doi: 10.1002/1097-0142(19831201)52:11<2025::aid-cncr2820521109>3.0.co;2-o.
This study was designed as a Phase II clinical trial in advanced recurrent or metastatic squamous cell carcinoma of the cervix with a combination of bleomycin (B: 10 u/m2/d) and cisplatin (P: 20 mg/m2/d) administered for five consecutive days in intravenous infusion for 7 hours and vincristine (V: 1 mg/m2) and methotrexate (M: 40 mg/m2) administered only on day one of each cycle which was repeated every 28 days up to a maximum of 6 times. Over a period of 2 years, 15 evaluable patients with measurable disease received at least 3 courses of therapy. Six had recurrent disease and nine had distant metastases. All had previous radiation therapy. There were two dropouts after the first course due to nausea and vomiting which was practically universal. Other side effects included: mild paresthesias of the extremities (89%), stomatitis (41%), diarrhea (17%), moderate pancytopenia and hypomagnesemia which was reduced from 65% to 17% when magnesium sulfate 10% was administered with cisplatin. Sixty-six percent of the evaluable patients achieved remission (7 partial and 3 complete) usually before the fourth course of therapy. The disease-free interval was of 29.7 +/- 15 weeks in all responders (40.6 +/- 15.5 weeks in complete responders). The mean survival from the start of BPVM therapy was of 55.8 +/- 33.3 weeks in responders and of only 14 +/- 2.9 weeks in nonresponders (P less than 0.01). It is concluded that BPVM is an effective combination chemotherapy in advanced squamous cell carcinoma of the cervix. These results should be confirmed in a Phase III trial.
本研究设计为一项II期临床试验,针对晚期复发性或转移性宫颈鳞状细胞癌,采用博来霉素(B:10 u/m²/d)和顺铂(P:20 mg/m²/d)联合用药,连续静脉输注5天,每次7小时,长春新碱(V:1 mg/m²)和甲氨蝶呤(M:40 mg/m²)仅在每个周期的第1天给药,每28天重复一个周期,最多重复6次。在2年的时间里,15例可评估的有可测量病灶的患者接受了至少3个疗程的治疗。其中6例为复发性疾病,9例有远处转移。所有患者均曾接受过放疗。第一疗程后有2例因恶心和呕吐(几乎普遍存在)退出研究。其他副作用包括:轻度肢体感觉异常(89%)、口腔炎(41%)、腹泻(17%)、中度全血细胞减少和低镁血症,当顺铂与10%硫酸镁合用时,低镁血症从65%降至17%。66%的可评估患者通常在第4个疗程前实现缓解(7例部分缓解,3例完全缓解)。所有缓解者的无病间期为29.7±15周(完全缓解者为40.6±15.5周)。BPVM治疗开始后的平均生存期,缓解者为55.8±33.3周,未缓解者仅为14±2.9周(P<0.01)。结论是BPVM是晚期宫颈鳞状细胞癌有效的联合化疗方案。这些结果应在III期试验中得到证实。