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四期低风险 Wilms 瘤伴肺转移的治疗:来自儿童肿瘤协作组 AREN0533 研究的报告。

Treatment of Stage IV Favorable Histology Wilms Tumor With Lung Metastases: A Report From the Children's Oncology Group AREN0533 Study.

机构信息

David B. Dix, British Columbia Children's Hospital, Vancouver, British Columbia; Paul E. Grundy, University of Alberta, Edmonton, Alberta; Conrad V. Fernandez, Dalhousie University, Halifax, Nova Scotia, Canada; Nita L. Seibel, National Cancer Institute, Bethesda, MD; Yueh-Yun Chi, University of Florida, Gainesville, FL; Geetika Khanna, Washington University School of Medicine, St Louis, MO; Eric Gratias, University of Tennessee College of Medicine Chattanooga, Chattanooga, TN; James R. Anderson, Merck Research Laboratories, North Wales, PA; Elizabeth A. Mullen, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA; James I. Geller, Cincinnati Children's Hospital Medical Center, Cincinnati; Julie M. Gastier-Foster and Elizabeth Wagner, Nationwide Children's Hospital; Julie M. Gastier-Foster, The Ohio State University College of Medicine, Columbus, OH; John A. Kalapurakal, Lurie Comprehensive Cancer Centre of Northwestern University; Elizabeth J. Perlman, Ann and Robert H. Lurie Children's Hospital, Chicago, IL; Arnold C. Paulino, MD Anderson Cancer Center, Houston, TX; Peter F. Ehrlich, University of Michigan, Ann Arbor, MI; Marcio Malogolowkin, University of California at Davis Comprehensive Cancer Center, Sacramento, CA; Jeffrey S. Dome, George Washington University School of Medicine and Health Sciences, Washington, DC; on behalf of the AREN0533 Study Committee.

出版信息

J Clin Oncol. 2018 Jun 1;36(16):1564-1570. doi: 10.1200/JCO.2017.77.1931. Epub 2018 Apr 16.

Abstract

Purpose The National Wilms Tumor Study (NWTS) treatment of favorable histology Wilms tumor with lung metastases was vincristine/dactinomycin/doxorubicin (DD4A) and lung radiation therapy (RT). The AREN0533 study applied a new risk stratification and treatment strategy to improve event-free survival (EFS) while reducing exposure to lung RT. Methods Patients with favorable histology Wilms tumor and isolated lung metastases showing complete lung nodule response (CR) after 6 weeks of DD4A continued receiving chemotherapy without lung RT. Patients with incomplete response (IR) or loss of heterozygosity at chromosomes 1p/16q received lung RT and four cycles of cyclophosphamide/etoposide in addition to DD4A drugs (Regimen M). AREN0533 was designed to preserve a 4-year EFS of 85% for lung nodule CR and improve 4-year EFS from 75% to 85% for lung nodule IR. Results Among 292 assessable patients, 133 had CR and 159 had IR. For patients with CR, 4-year EFS and overall survival (OS) estimates were 79.5% (95% CI, 71.2% to 87.8%) and 96.1% (95% CI, 92.1% to 100%), respectively. Expected versus observed event rates were 15% and 20.2% ( P = .052), respectively. For patients with IR, 4-year EFS and OS estimates were 88.5% (95% CI, 81.8% to 95.3%) and 95.4% (95% CI, 90.9% to 99.8%), respectively. Expected versus observed event rates were 25% and 12.2% ( P < .001), respectively. Overall, 4-year EFS and OS were 85.4% (95% CI, 80.5% to 90.2%) and 95.6% (95% CI, 92.8% to 98.4%) compared with 72.5% (95% CI, 66.9% to 78.1%; P < .001) and 84.0% (95% CI, 79.4% to 88.6%; P < .001), respectively, in the predecessor NWTS-5 study. Conclusion Excellent OS was achieved after omission of primary lung RT in patients with lung nodule CR, although there were more events than expected. EFS was significantly improved, with excellent OS, in patients with lung nodule IR using four cycles of cyclophosphamide/etoposide in addition to DD4A drugs. The overall AREN0533 treatment strategy yielded EFS and OS estimates that were superior to previous studies.

摘要

目的

国家威尔姆斯肿瘤研究(NWTS)对有肺转移的有利组织学 Wilms 肿瘤采用长春新碱/放线菌素 D/多柔比星(DD4A)和肺放疗(RT)治疗。AREN0533 研究应用了一种新的风险分层和治疗策略,在减少肺 RT 暴露的同时提高无事件生存率(EFS)。

方法

有有利组织学 Wilms 肿瘤和孤立性肺转移的患者,在接受 6 周 DD4A 治疗后肺结节完全缓解(CR),继续接受化疗而不接受肺 RT。不完全反应(IR)或 1p/16q 染色体杂合性丢失的患者接受肺 RT 和环磷酰胺/依托泊苷 4 个周期,外加 DD4A 药物(方案 M)。AREN0533 的设计目的是为肺结节 CR 患者保留 4 年 EFS 为 85%,并将肺结节 IR 患者的 4 年 EFS 从 75%提高到 85%。

结果

在 292 例可评估患者中,133 例有 CR,159 例有 IR。对于 CR 患者,4 年 EFS 和总生存率(OS)估计值分别为 79.5%(95%CI,71.2%至 87.8%)和 96.1%(95%CI,92.1%至 100%)。预期与观察到的事件发生率分别为 15%和 20.2%(P=0.052)。对于 IR 患者,4 年 EFS 和 OS 估计值分别为 88.5%(95%CI,81.8%至 95.3%)和 95.4%(95%CI,90.9%至 99.8%)。预期与观察到的事件发生率分别为 25%和 12.2%(P<0.001)。总体而言,与 NWTS-5 研究中 72.5%(95%CI,66.9%至 78.1%;P<0.001)和 84.0%(95%CI,79.4%至 88.6%;P<0.001)相比,4 年 EFS 和 OS 分别为 85.4%(95%CI,80.5%至 90.2%)和 95.6%(95%CI,92.8%至 98.4%)。

结论

在肺结节 CR 患者中省略主要肺 RT 后,获得了优异的 OS,尽管事件发生率高于预期。在肺结节 IR 患者中,使用环磷酰胺/依托泊苷 4 个周期加 DD4A 药物治疗后,EFS 显著改善,同时具有优异的 OS。总体而言,AREN0533 的治疗策略产生的 EFS 和 OS 估计值优于先前的研究。

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