Review of 20 years of adult medulloblastoma treatment: Chemotherapy prescription trends and survival.

IF 2.4 Q2 CLINICAL NEUROLOGY
Marissa Sherwood, Seth Climans, Ronald Ramos, Normand J Laperriere, Andrew F Gao, Barbara-Ann Millar, David B Shultz, Derek S Tsang, Warren P Mason
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Abstract

Background: The historic standard of care for adult medulloblastoma has been considered surgery and radiation, while chemotherapy is increasingly being prescribed. This study reviewed 20-year chemotherapy trends at a high-volume center, as well as overall and progression free-survival.

Methods: Adults with medulloblastoma treated at an academic center from January 1, 1999 to -December 31, 2020 were reviewed. Patient baseline data were summarized and Kaplan-Meier estimators were used for survival.

Results: Forty-nine patients were included; median age was 30 years and male: female ratio was 2:1. Desmoplastic and classical histologies were most common. Of all patients, 23 (47%) were high risk and 7 (14%) metastatic at diagnosis. Only 10 (20%) received initial chemotherapy, of which 70% were high risk and 30% metastatic, with most treated from 2010 to 2020. Forty percent of initial chemotherapy patients received salvage chemotherapy for recurrence or metastases (of all patients, 49% required salvage). Initial chemotherapy regimens were mainly cisplatin/lomustine/vincristine, and at recurrence cisplatin/etoposide. Median overall survival was 8.6 years (95% CI 7.5-∞), with 1-, 5-, and 10-year survival at 95.8%, 72%, and 46.7%. Median overall survival for those who did not receive initial chemotherapy was 12.4 years and 7.4 years for those who did (P-value .2).

Conclusions: Twenty years of adult medulloblastoma treatment was reviewed. Initial chemotherapy patients, most of whom were high risk, trended towards worse survival, but this was nonsignificant. The ideal timing and choice of chemotherapy for adult medulloblastoma is unknown-challenges of administering chemotherapy following photon craniospinal irradiation may have prevented it from becoming routine.

20年成人髓母细胞瘤治疗回顾:化疗处方趋势和生存率。
背景:成人成神经管细胞瘤的历史治疗标准一直被认为是手术和放疗,而化疗越来越多地被开处方。本研究回顾了一个大容量中心20年的化疗趋势,以及总体和无进展生存期。方法:回顾1999年1月1日至2020年12月31日在某学术中心治疗的成神经管细胞瘤成人患者。总结患者基线数据,并使用Kaplan-Meier估计生存率。结果:纳入49例患者;年龄中位数为30岁,男女比例为2:1。结缔组织增生和典型组织学最常见。在所有患者中,23例(47%)为高风险,7例(14%)为诊断转移。只有10例(20%)接受了初始化疗,其中70%为高风险,30%为转移性,大多数治疗时间为2010年至2020年。40%的初始化疗患者因复发或转移接受了补救性化疗(在所有患者中,49%需要补救性化疗)。初始化疗方案以顺铂/洛莫司汀/长春新碱为主,复发时以顺铂/依托泊苷为主。中位总生存期为8.6年(95% CI为7.5-∞),1年、5年和10年生存率分别为95.8%、72%和46.7%。未接受初始化疗的患者的中位总生存期为12.4年,接受初始化疗的患者为7.4年(p值为0.2)。结论:回顾了20年来成人成神经管细胞瘤的治疗。最初的化疗患者,其中大多数是高风险的,倾向于更差的生存,但这并不显著。成人成神经管细胞瘤理想的化疗时机和选择尚不清楚——光子颅脊髓照射后化疗的挑战可能阻止了它成为常规。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neuro-oncology practice
Neuro-oncology practice CLINICAL NEUROLOGY-
CiteScore
5.30
自引率
11.10%
发文量
92
期刊介绍: Neuro-Oncology Practice focuses on the clinical aspects of the subspecialty for practicing clinicians and healthcare specialists from a variety of disciplines including physicians, nurses, physical/occupational therapists, neuropsychologists, and palliative care specialists, who have focused their careers on clinical patient care and who want to apply the latest treatment advances to their practice. These include: Applying new trial results to improve standards of patient care Translating scientific advances such as tumor molecular profiling and advanced imaging into clinical treatment decision making and personalized brain tumor therapies Raising awareness of basic, translational and clinical research in areas of symptom management, survivorship, neurocognitive function, end of life issues and caregiving
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