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放射治疗改善了1岁以上患有儿童肿瘤学组C期神经母细胞瘤患者的预后。

Radiotherapy improves the outlook for patients older than 1 year with Pediatric Oncology Group stage C neuroblastoma.

作者信息

Castleberry R P, Kun L E, Shuster J J, Altshuler G, Smith I E, Nitschke R, Wharam M, McWilliams N, Joshi V, Hayes F A

机构信息

University of Alabama, Birmingham.

出版信息

J Clin Oncol. 1991 May;9(5):789-95. doi: 10.1200/JCO.1991.9.5.789.

Abstract

Children older than 1 year of age who have neuroblastoma with complete or partial removal of the primary tumor and positive intracavitary lymph nodes (Pediatric Oncology Group [POG] stage C) are a small but higher-risk subset of patients. To further evaluate the importance of identifying patients with POG stage C neuroblastoma and to assess the efficacy and toxicity of adding concurrent radiation therapy (RT) to chemotherapy (CT) in these children, a randomized study was conducted. Eligible patients received cyclophosphamide 150 mg/m2 orally days 1 to 7 and Adriamycin (doxorubicin; Adria Laboratories, Columbus, OH) 35 mg/m2 intravenously (IV) on day 8 (CYC/ADR) every 3 weeks for five courses with or without RT to primary tumor and regional lymph nodes (24 to 30 Gy/16 to 20 fractions). Second-look surgery was advised to evaluate response and to remove residual disease. Continuation therapy alternated CYC/ADR every 3 weeks with cisplatin 90 mg/m2 day 1 followed by teniposide 100 mg/m2 day 3 (CDP/VM) for two courses each. Secondary CT with CDP/VM alone was available for patients not achieving complete response (CR) following induction treatment and second-look surgery. Of 29 eligible patients randomized to CT alone, 13 achieved CR, and nine are disease-free (NED) 1 to 52 months (median, 35 months) off therapy. Twenty-two of 33 eligible cases treated with CT/RT attained CR, and 19 are NED 1 to 77 months (median, 23 months) off therapy. Local and metastatic relapses occurred in both arms. Differences in CR, event-free survival, and survival rates were significant, P = .013, .009, and .008, respectively. Surgical compliance was excellent and complications uncommon. Therapy was tolerable in both groups but hematopoietic toxicity was more common in the CT/RT arm. We conclude that POG stage C neuroblastoma in children older than 1 year of age is a higher-risk group that should be identified, that CT/RT provides superior initial and long-term disease control compared with CT alone in this patient subset, and that the occurrence of metastatic failures in both treatment groups suggests a need for more aggressive chemotherapy.

摘要

1岁以上患有神经母细胞瘤且原发肿瘤已完全或部分切除、腔内淋巴结阳性(儿童肿瘤协作组[POG]C期)的儿童是一小部分但风险较高的患者亚组。为了进一步评估识别POG C期神经母细胞瘤患者的重要性,并评估在这些儿童中同步放疗(RT)联合化疗(CT)的疗效和毒性,开展了一项随机研究。符合条件的患者在第1至7天口服环磷酰胺150mg/m²,在第8天静脉注射阿霉素(多柔比星;阿德里亚实验室,俄亥俄州哥伦布市)35mg/m²(CYC/ADR),每3周进行5个疗程,原发肿瘤和区域淋巴结接受或不接受放疗(24至30Gy/16至20次分割)。建议进行二次手术以评估反应并切除残留病灶。维持治疗每3周交替使用CYC/ADR和顺铂90mg/m²第1天,随后替尼泊苷100mg/m²第3天(CDP/VM),各进行2个疗程。对于诱导治疗和二次手术后未达到完全缓解(CR)的患者,可单独使用CDP/VM进行二线CT治疗。在29例随机分配至单纯CT治疗的符合条件患者中,13例达到CR,9例在停止治疗后1至52个月(中位时间35个月)无疾病生存(NED)。在33例接受CT/RT治疗的符合条件病例中,22例达到CR,19例在停止治疗后1至77个月(中位时间23个月)NED。两组均发生局部和远处复发。CR、无事件生存率和生存率的差异具有显著性,P值分别为0.013、0.009和0.008。手术依从性良好且并发症少见。两组治疗耐受性均可,但CT/RT组造血毒性更常见。我们得出结论,1岁以上儿童的POG C期神经母细胞瘤是一个应被识别的高风险组,与单纯CT相比,CT/RT在该患者亚组中提供了更好的初始和长期疾病控制,且两个治疗组中远处转移失败的发生提示需要更积极的化疗。

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