Green D M, Breslow N E, Beckwith J B, Finklestein J Z, Grundy P E, Thomas P R, Kim T, Shochat S J, Haase G M, Ritchey M L, Kelalis P P, D'Angio G J
Department of Pediatrics, Roswell Park Cancer Institute, University at Buffalo, State University of New York, 14623, USA.
J Clin Oncol. 1998 Jan;16(1):237-45. doi: 10.1200/JCO.1998.16.1.237.
The National Wilms' Tumor Study (NWTS)-4 was designed to evaluate the efficacy, toxicity, and cost of administration of different regimens for the treatment of Wilms' tumor (WT).
Between August 6, 1986 and September 1, 1994, 1,687 previously untreated children less than 16 years of age with stages I to II/favorable histology (FH) or stage I/anaplastic histology WT (low-risk [LR] group) or stages III to IV/FH WT or stages I to IV/clear cell sarcoma of the kidney (high-risk [HR] group) were randomized to treatment that included vincristine and either divided-dose (standard [STD]) courses (5 days) or single-dose (pulse-intensive [PI]) treatment with dactinomycin. HR patients also received either STD courses (3 days) or PI treatment with doxorubicin.
The 2-year relapse-free survival (RFS) rates for LR patients were 91.3% for 544 randomized to treatment with PI and 91.4% for 556 randomized to treatment with STD chemotherapy (P = .988). The 2-year RFS rates for HR patients were 87.3% for 299 randomized to treatment with PI and 90.0% for 288 randomized to treatment with STD chemotherapy (P = .865).
We conclude that patients treated with PI combination chemotherapy for LR or HR WT or clear cell sarcoma of the kidney have equivalent 2-year RFS to those treated with STD regimens. PI drug administration is recommended as the new standard based on demonstrated efficacy, greater administered dose-intensity, less severe hematologic toxicity, and the requirement for fewer physician and hospital encounters.
国家肾母细胞瘤研究(NWTS)-4旨在评估不同治疗方案治疗肾母细胞瘤(WT)的疗效、毒性及给药成本。
1986年8月6日至1994年9月1日期间,1687例年龄小于16岁、此前未经治疗、处于Ⅰ至Ⅱ期/预后良好组织学类型(FH)或Ⅰ期/间变组织学类型肾母细胞瘤(低危[LR]组)或Ⅲ至Ⅳ期/FH肾母细胞瘤或Ⅰ至Ⅳ期/肾透明细胞肉瘤(高危[HR]组)的患儿被随机分配接受包含长春新碱及放线菌素的分剂量(标准[STD])疗程(5天)或单剂量(脉冲强化[PI])治疗。HR组患者还接受了STD疗程(3天)或阿霉素的PI治疗。
随机接受PI治疗的544例LR组患者的2年无复发生存(RFS)率为91.3%,随机接受STD化疗的556例患者为91.4%(P = 0.988)。随机接受PI治疗的299例HR组患者的2年RFS率为87.3%,随机接受STD化疗的288例患者为90.0%(P = 0.865)。
我们得出结论,LR或HR肾母细胞瘤或肾透明细胞肉瘤患者接受PI联合化疗与接受STD方案治疗的患者2年RFS相当。基于已证实的疗效、更高的给药剂量强度、较轻的血液学毒性以及对医生和医院接触需求较少,推荐PI给药作为新标准。