Rose P G, Blessing J A, Gershenson D M, McGehee R
Case Western Reserve University, Division of Gynecologic Oncology, Department of Reproductive Biology, University Hospitals of Cleveland, Cleveland, OH, USA.
J Clin Oncol. 1999 Sep;17(9):2676-80. doi: 10.1200/JCO.1999.17.9.2676.
On the basis of the activity of paclitaxel as a single agent in chemotherapy-naive squamous cell carcinoma of the cervix in a prior Gynecologic Oncology Group (GOG) trial, a phase II study of paclitaxel and cisplatin as first-line therapy was conducted by the GOG.
Eligibility included squamous cell cancer of the cervix not curable by surgery or radiation, measurable disease, WBC count > or = 3,000/microL, platelet count > or = 100, 000/microL, serum creatinine > or = 2 mg/100 mL, and adequate hepatic function. The starting dose was paclitaxel 135 mg/m(2) infused over 24 hours followed by cisplatin 75 mg/m(2) every 21 days. On the basis of toxicity, a dose escalation of paclitaxel to a maximum dose of 170 mg/m(2)/d was prescribed.
Forty-seven patients were enrolled onto this study; 44 patients were assessable for toxicity and 41 for response. Forty (90.9%) had received prior radiation therapy. A median of six courses of chemotherapy was given (range, one to 10 courses). Neutropenia grade 3 (15.9%) and 4 (61.4%) was the most frequent severe adverse effect and was associated with fever in 13 patients (27.7%). Two patients (4.5%) died from neutropenic sepsis. Grade 4 thrombocytopenia occurred in 6.8% of patients. Of 41 assessable patients, five (12.2%) had complete responses and 14 (34.1%) had partial responses for an overall response rate of 46.3% (95% confidence interval, 30.7% to 62.6%). The median progression-free interval, was 5.4+ months (range, 0.3 to 22+ months) with a median survival of 10.0+ months (range, 0.9 to 22. 2 months). Response was more frequent in patients with disease in nonirradiated sites (70% v 23%, P =.008).
This regimen seems highly active in advanced and recurrent squamous cell carcinoma of the cervix and is currently being evaluated by the GOG in a phase III randomized study comparing the combination of paclitaxel and cisplatin with cisplatin alone.
基于在先前一项妇科肿瘤学组(GOG)试验中,紫杉醇单药对未经化疗的宫颈鳞状细胞癌具有活性,GOG开展了一项紫杉醇和顺铂作为一线治疗的II期研究。
入选标准包括无法通过手术或放疗治愈的宫颈鳞状细胞癌、可测量的病灶、白细胞计数≥3000/μL、血小板计数≥100000/μL、血清肌酐≥2mg/100mL以及肝功能正常。起始剂量为紫杉醇135mg/m²,静脉滴注24小时,随后每21天给予顺铂75mg/m²。根据毒性反应,将紫杉醇剂量递增至最大剂量170mg/m²/d。
47例患者入组本研究;44例患者可评估毒性反应,41例可评估疗效。40例(90.9%)患者曾接受过放疗。化疗疗程中位数为6个(范围1至10个疗程)。3级(15.9%)和4级(61.4%)中性粒细胞减少是最常见的严重不良反应,13例患者(27.7%)伴有发热。2例患者(4.5%)死于中性粒细胞减少性败血症。6.8%的患者发生4级血小板减少。在41例可评估疗效的患者中,5例(12.2%)完全缓解,14例(34.1%)部分缓解,总缓解率为46.3%(可信区间95%,30.7%至62.6%)。无进展生存期中位数为5.4+个月(范围0.3至22+个月),中位生存期为10.0+个月(范围0.9至22.2个月)。未接受放疗部位有病灶的患者缓解率更高(70%对23%,P = 0.008)。
该方案对晚期和复发性宫颈鳞状细胞癌似乎具有高度活性,GOG目前正在开展一项III期随机研究,比较紫杉醇和顺铂联合方案与单纯顺铂方案。