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术前放化疗联合或不联合帕唑帕尼治疗非横纹肌肉瘤软组织肉瘤的结果:来自儿童肿瘤学组和 NRG 肿瘤学的报告。

Outcomes After Preoperative Chemoradiation With or Without Pazopanib in Non-Rhabdomyosarcoma Soft Tissue Sarcoma: A Report From Children's Oncology Group and NRG Oncology.

机构信息

Maine Medical Center, Portland, ME.

Massachusetts General Hospital, Boston, MA.

出版信息

J Clin Oncol. 2023 Nov 1;41(31):4842-4848. doi: 10.1200/JCO.23.00045. Epub 2023 Jul 31.

DOI:10.1200/JCO.23.00045
PMID:37523624
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10852395/
Abstract

JCO ARST1321 was a phase II study designed to compare the near complete pathologic response rate after preoperative chemoradiation with/without pazopanib in children and adults with intermediate-/high-risk chemotherapy-sensitive body wall/extremity non-Rhabdomyosarcoma Soft Tissue Sarcoma (ClinicalTrials.gov identifier: NCT02180867). Enrollment was stopped early following a predetermined interim analysis that found the rate of near complete pathologic response to be significantly greater with the addition of pazopanib. As a planned secondary aim of the study, the outcome data for this cohort were analyzed. Eight-five eligible patients were randomly assigned to receive (regimen A) or not receive (regimen B) pazopanib in combination with ifosfamide and doxorubicin + preoperative radiotherapy followed by primary resection at week 13 and then further chemotherapy at week 25. As of December 31, 2021, at a median survivor follow-up of 3.3 years (range, 0.1-5.8 years), the 3-year event-free survival for all patients in the intent-to-treat analysis was 52.5% (95% CI, 34.8 to 70.2) for regimen A and 50.6% (95% CI, 32 to 69.2) for regimen B ( = .8677, log-rank test); the 3-year overall survival was 75.7% (95% CI, 59.7 to 91.7) for regimen A and 65.4% (95% CI, 48.1 to 82.7) for regimen B ( = .1919, log-rank test). Although the rate of near complete pathologic response was significantly greater with the addition of pazopanib, outcomes were not statistically significantly different between the two regimens.

摘要

JCO ARST1321 是一项 II 期研究,旨在比较术前放化疗联合/不联合帕唑帕尼在儿童和成人中治疗中/高危化疗敏感的体壁/四肢非横纹肌肉瘤软组织肉瘤(ClinicalTrials.gov 标识符:NCT02180867)的近完全病理缓解率。在一项预先确定的中期分析发现添加帕唑帕尼后近完全病理缓解率显著增加后,提前停止了入组。作为该研究的计划次要目标,对该队列的结果数据进行了分析。85 名符合条件的患者被随机分配接受(方案 A)或不接受(方案 B)帕唑帕尼联合异环磷酰胺和多柔比星+术前放疗,然后在第 13 周进行原发性切除,然后在第 25 周进行进一步化疗。截至 2021 年 12 月 31 日,中位随访时间为 3.3 年(范围,0.1-5.8 年),意向治疗分析中所有患者的 3 年无事件生存率为方案 A 的 52.5%(95%CI,34.8-70.2)和方案 B 的 50.6%(95%CI,32-69.2)( =.8677,对数秩检验);方案 A 的 3 年总生存率为 75.7%(95%CI,59.7-91.7),方案 B 的 65.4%(95%CI,48.1-82.7)( =.1919,对数秩检验)。尽管添加帕唑帕尼后近完全病理缓解率显著增加,但两种方案之间的结果无统计学显著差异。

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