Stehman Frederick B, Ali Shamshad, Keys Henry M, Muderspach Laila I, Chafe Weldon E, Gallup Donald G, Walker Joan L, Gersell Deborah
Department of Obstetrics and Gynecology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Am J Obstet Gynecol. 2007 Nov;197(5):503.e1-6. doi: 10.1016/j.ajog.2007.08.003.
The objective of the study was to confirm that concurrent cisplatin (CT) with radiation therapy (RT) is associated with improved long-term progression-free survival (PFS) and overall survival (OS), compared with RT alone in stage IB bulky carcinoma of the cervix, when both groups' therapy is followed by hysterectomy.
Three hundred seventy-four patients entered this trial. There were 369 evaluable patients; 186 were randomly allocated to receive RT alone and 183 to receive CT plus RT. Radiation dosage was 45 Gray (Gy) in 20 fractions followed by low dose-rate intracavitary application(s) of 30 Gy to point A. Chemotherapy consisted of intravenous cisplatin 40 mg/m2 every week for up to 6 weekly cycles. Total extrafascial hysterectomy followed the completion of RT by 6-8 weeks.
Preliminary results have been published, at which time there were 292 censored observations, and median duration of follow-up was only 36 months. Patient and tumor characteristics were well balanced between the regimens. The median patient age was 41.5 years; 81% had squamous tumors; 59% were white. Median follow-up is now 101 months. The relative risk for progression was 0.61 favoring CT plus RT (95% confidence interval [CI] 0.43 to 0.85, P < .004). At 72 months, 71% of patients receiving CT plus RT were predicted to be alive and disease free when adjusting for age and tumor size, compared with 60% of those receiving RT alone. The adjusted death hazard ratio was 0.63 (95% CI 0.43 to 0.91, P < .015) favoring CT plus RT. At 72 months, 78% of CT plus RT patients were predicted to be alive, compared with 64% of RT patients. An increased rate of early hematologic and gastrointestinal toxicity was seen with CT plus RT. There was no detectable difference in the frequency of late adverse events.
Concurrent weekly cisplatin with RT significantly improves long-term PFS and OS when compared with RT alone. Serious late effects were not increased. The inclusion of hysterectomy has been discontinued on the basis of another trial. Pending further trials, weekly cisplatin with radiation is the standard against which other regimens should be compared.
本研究的目的是证实,对于IB期宫颈巨块型癌患者,在两组治疗后均行子宫切除术的情况下,与单纯放疗相比,顺铂同步放化疗可改善长期无进展生存期(PFS)和总生存期(OS)。
374例患者进入本试验。其中369例可评估;186例随机分配接受单纯放疗,183例接受顺铂同步放化疗。放射剂量为45格雷(Gy),分20次给予,随后对A点进行30 Gy的低剂量率腔内照射。化疗方案为静脉注射顺铂40 mg/m²,每周1次,共6周。放疗结束6 - 8周后行全筋膜外子宫切除术。
初步结果已发表,当时有292例删失观察,中位随访时间仅36个月。各治疗方案间患者和肿瘤特征均衡。患者中位年龄41.5岁;81%为鳞状细胞癌;59%为白人。目前中位随访时间为10l个月。顺铂同步放化疗组进展的相对风险为0.61(95%置信区间[CI] 0.43至0.85,P < 0.004)。校正年龄和肿瘤大小后,72个月时,接受顺铂同步放化疗的患者预计71%存活且无疾病,而单纯放疗组为60%。校正后的死亡风险比为0.63(95%CI 0.43至0.91,P < 0.015),顺铂同步放化疗组更具优势。72个月时,顺铂同步放化疗组预计78%存活,单纯放疗组为64%。顺铂同步放化疗组早期血液学和胃肠道毒性发生率增加。晚期不良事件发生率无显著差异。
与单纯放疗相比,顺铂同步放化疗可显著改善长期PFS和OS。严重晚期效应未增加。基于另一项试验,已不再纳入子宫切除术。在进一步试验之前,顺铂同步放疗是其他治疗方案应与之比较的标准。