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World Health Organization 2016 Classification of Central Nervous System Tumors.世界卫生组织 2016 年中枢神经系统肿瘤分类。
Neurol Clin. 2018 Aug;36(3):439-447. doi: 10.1016/j.ncl.2018.04.003.
2
A ten-year follow-up study of treatment outcome of craniopharyngiomas.颅咽管瘤治疗结果的十年随访研究
Swiss Med Wkly. 2018 Feb 7;148:w14521. doi: 10.4414/smw.2018.14521. eCollection 2018.
3
Recent advances in molecular pathology of craniopharyngioma.颅咽管瘤分子病理学的最新进展
F1000Res. 2017 Jul 24;6:1202. doi: 10.12688/f1000research.11549.1. eCollection 2017.
4
Intracystic interferon-alpha in pediatric craniopharyngioma patients: an international multicenter assessment on behalf of SIOPE and ISPN.颅内囊内干扰素-α在小儿颅咽管瘤患者中的应用:代表 SIOPE 和 ISPN 的国际多中心评估。
Neuro Oncol. 2017 Oct 1;19(10):1398-1407. doi: 10.1093/neuonc/nox056.
5
CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2009-2013.CBTRUS统计报告:2009 - 2013年美国原发性脑和其他中枢神经系统肿瘤诊断情况
Neuro Oncol. 2016 Oct 1;18(suppl_5):v1-v75. doi: 10.1093/neuonc/now207.
6
Phase II trial of pegylated interferon alfa-2b in young patients with neurofibromatosis type 1 and unresectable plexiform neurofibromas.聚乙二醇化干扰素α-2b治疗1型神经纤维瘤病年轻患者及不可切除丛状神经纤维瘤的II期试验。
Neuro Oncol. 2017 Feb 1;19(2):289-297. doi: 10.1093/neuonc/now158.
7
Intracystic bleomycin for cystic craniopharyngiomas in children.儿童囊性颅咽管瘤的囊内注射博来霉素治疗
Cochrane Database Syst Rev. 2016 Jul 14;7(7):CD008890. doi: 10.1002/14651858.CD008890.pub4.
8
The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary.2016 年世界卫生组织中枢神经系统肿瘤分类:概述。
Acta Neuropathol. 2016 Jun;131(6):803-20. doi: 10.1007/s00401-016-1545-1. Epub 2016 May 9.
9
Patient-specific dosimetry for intracavitary 32P-chromic phosphate colloid therapy of cystic brain tumours.颅内 32P-膦酸铬胶体腔内治疗囊性脑肿瘤的患者特异性剂量学。
Eur J Nucl Med Mol Imaging. 2013 Oct;40(10):1532-41. doi: 10.1007/s00259-013-2451-6. Epub 2013 Jun 6.
10
Challenges with defining response to antitumor agents in pediatric neuro-oncology: a report from the response assessment in pediatric neuro-oncology (RAPNO) working group.儿童神经肿瘤学中抗肿瘤药物反应定义的挑战:来自儿童神经肿瘤学反应评估(RAPNO)工作组的报告。
Pediatr Blood Cancer. 2013 Sep;60(9):1397-401. doi: 10.1002/pbc.24562. Epub 2013 Apr 26.

聚乙二醇干扰素 α-2b 治疗无法切除或复发性颅咽管瘤患者的 II 期研究:儿科脑瘤联盟报告。

Phase II study of peginterferon alpha-2b for patients with unresectable or recurrent craniopharyngiomas: a Pediatric Brain Tumor Consortium report.

机构信息

Division of Hematology, Oncology, Neuro-Oncology, Stem Cell Transplantation, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois.

Department of Pediatric Neurosurgery, Children's Hospital of Pittsburgh, University of Pittsburgh, Pittsburgh, Pennsylvania.

出版信息

Neuro Oncol. 2020 Nov 26;22(11):1696-1704. doi: 10.1093/neuonc/noaa119.

DOI:10.1093/neuonc/noaa119
PMID:32393959
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7690365/
Abstract

BACKGROUND

Craniopharyngiomas account for approximately 1.2-4% of all CNS tumors. They are typically treated with a combination of surgical resection and focal radiotherapy. Unfortunately, treatment can lead to permanent deleterious effects on behavior, learning, and endocrine function.

METHODS

The Pediatric Brain Tumor Consortium performed a multicenter phase 2 study in children and young adults with unresectable or recurrent craniopharyngioma (PBTC-039). Between December 2013 and November 2017, nineteen patients (median age at enrollment, 13.1 y; range, 2-25 y) were enrolled in one of 2 strata: patients previously treated with surgery alone (stratum 1) or who received radiation (stratum 2).

RESULTS

Eighteen eligible patients (8 male, 10 female) were treated with weekly subcutaneous pegylated interferon alpha-2b for up to 18 courses (108 wk). Therapy was well tolerated with no grade 4 or 5 toxicities. 2 of the 7 eligible patients (28.6%) in stratum 1 had a partial response, but only one response was sustained for more than 3 months. None of the 11 stratum 2 patients had an objective radiographic response, although median progression-free survival was 19.5 months.

CONCLUSIONS

Pegylated interferon alpha-2b treatment, in lieu of or following radiotherapy, was well tolerated in children and young adults with recurrent craniopharyngiomas. Although objective responses were limited, progression-free survival results are encouraging, warranting further studies.

摘要

背景

颅咽管瘤约占所有中枢神经系统肿瘤的 1.2-4%。它们通常采用手术切除和局部放射治疗相结合的方法进行治疗。不幸的是,治疗可能会导致行为、学习和内分泌功能的永久性损害。

方法

儿科脑瘤联盟(Pediatric Brain Tumor Consortium)在无法切除或复发的颅咽管瘤患儿和年轻成人中进行了一项多中心 2 期研究(PBTC-039)。在 2013 年 12 月至 2017 年 11 月期间,19 名患者(中位入组年龄为 13.1 岁;范围,2-25 岁)被纳入 2 个亚组之一:仅接受过手术治疗的患者(亚组 1)或接受过放疗的患者(亚组 2)。

结果

18 名符合条件的患者(8 名男性,10 名女性)接受了每周皮下注射聚乙二醇化干扰素-α-2b 治疗,最多 18 个疗程(108 周)。治疗耐受性良好,无 4 级或 5 级毒性反应。亚组 1 中 7 名符合条件的患者中有 2 名(28.6%)有部分缓解,但只有 1 名缓解持续时间超过 3 个月。11 名亚组 2 患者均无客观影像学反应,但中位无进展生存期为 19.5 个月。

结论

聚乙二醇化干扰素-α-2b 治疗,无论是在放疗之前还是之后,在复发颅咽管瘤的儿童和年轻成人中耐受性良好。虽然客观反应有限,但无进展生存期结果令人鼓舞,值得进一步研究。