间隔压缩化疗方案在儿童尤文氏肉瘤治疗中的安全性和耐受性:来自印度的真实世界经验。

IF 0.8 4区 医学 Q4 HEMATOLOGY
Somdipa Pal, Yamini Krishnan, Krishnan V Parameswaran, Gazel Sainulabdin
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引用次数: 0

摘要

背景和目的:长春新碱-阿霉素-环磷酰胺和异环磷酰胺-依托泊苷交替化疗周期,以及原发性肿瘤手术或放疗或两者结合治疗,构成了尤文氏肉瘤的常用治疗方法。AEWS0031研究显示间隔压缩化疗后的生存获益无明显毒性。这项研究的目的是评估印度等发展中国家对剂量强化化疗的耐受性。方法:回顾性分析2017年12月至2022年12月期间接受治疗的新诊断为尤文氏肉瘤的18岁以下儿童。患儿接受长春新碱(2mg /m2)、阿霉素(75mg /m2)、环磷酰胺(1.2 g/m2)与异环磷酰胺(9g /m2)、依托泊苷(500mg /m2)交替治疗17个周期,非格拉西汀(5µg/kg;最大300µg)周期之间。原发肿瘤治疗采用手术或放疗,或两者兼用。在第12周至第16周进行局部治疗。使用不良事件通用术语标准(CTCAE) 3.0版评估毒性。在非转移性和转移性情况下,分别在6至8个化疗周期后通过重新分期CT或MRI扫描进行放射反应评估。结果:31名儿童入组。23名儿童接受了全部17个周期的化疗。中位周期间隔为18天,41%的儿童在2周间隔内接受化疗。在32%的周期中观察到4级发热性中性粒细胞减少,但未报告与治疗相关的死亡率。在化疗的28个周期(5.6%)和69个周期(13.9%)中分别记录了需要输血支持的贫血和血小板减少。有2例4级心脏毒性事件以心肌病和心律失常的形式出现,需要重症监护管理。手术后,61%的病例实现了良好的坏死。3名儿童复发,无事件生存率(EFS)为87%。结论:在资源有限的情况下,每隔2周给予尤因肉瘤强化化疗是可以忍受的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safety and Tolerability of Interval Compressed Chemotherapy Schedule in Children Receiving Treatment for Ewing Sarcoma: A Real-world Experience From India.

Background and aims: Chemotherapy with alternating cycles of vincristine-doxorubicin-cyclophosphamide and ifosfamide-etoposide, along with primary tumor treatment with surgery or radiotherapy or both, constitute the usual treatment of Ewing sarcoma. The AEWS0031 study demonstrated survival benefits after interval-compressed chemotherapy without significant toxicity. The aim of this study was to assess the tolerability of dose-intensified chemotherapy in developing countries like India.

Methods: This was a retrospective analysis of children younger than 18 years of age with newly diagnosed Ewing sarcoma who came for treatment from December 2017 to December 2022. Children received vincristine (2 mg/m 2 ), doxorubicin (75 mg/m 2 ), and cyclophosphamide (1.2 g/m 2 ) alternating with ifosfamide (9 g/m 2 ), etoposide (500 mg/m 2 ) for 17 cycles, with filgrastim (5 µg/kg; maximum 300 µg) between cycles. Primary tumor treatment was provided with surgery or radiotherapy or both. Local treatment was given between weeks 12 to 16. Toxicity was assessed using the Common Terminology Criteria for Adverse Events (CTCAE) Version 3.0. Radiologic response assessment was carried out with restaging CT or MRI scans after 6 to 8 cycles of chemotherapy in nonmetastatic and metastatic settings, respectively.

Results: Thirty-one children were enrolled. Twenty-three children received all 17 cycles of chemotherapy. The median cycle interval was 18 days and 41% of children received chemotherapy at the 2-week interval. Grade 4 febrile neutropenia was observed in 32% of cycles but no treatment-related mortality was reported. Anemia and thrombocytopenia requiring transfusion support were recorded in 28 (5.6%) and 69 cycles (13.9%) of chemotherapy, respectively. There were 2 events of grade 4 cardiac toxicities in the form of cardiomyopathy and arrhythmia requiring intensive care management. After surgery, good necrosis was achieved in 61% of cases. Three children had a relapse with an event-free survival (EFS) of 87%.

Conclusion: Intensified chemotherapy administered every 2 weeks intervals in Ewing sarcoma, is tolerable with adequate supportive care in resource-constrained settings.

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来源期刊
CiteScore
1.90
自引率
8.30%
发文量
415
审稿时长
2.5 months
期刊介绍: ​Journal of Pediatric Hematology/Oncology (JPHO) reports on major advances in the diagnosis and treatment of cancer and blood diseases in children. The journal publishes original research, commentaries, historical insights, and clinical and laboratory observations.
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