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化疗是原发性中枢神经系统黏膜相关淋巴组织淋巴瘤的有效治疗方法。

Chemotherapy is an efficient treatment in primary CNS MALT lymphoma.

机构信息

Neuro-Oncology Department, Hôpital Pitié Salpêtrière, APHP, Sorbonne Université, IHU, ICM, Paris, France.

Neurology Department, Hôpital Pierre Paul Riquet, CHU de Toulouse Purpan, Toulouse, France.

出版信息

J Neurooncol. 2022 Aug;159(1):151-161. doi: 10.1007/s11060-022-04052-1. Epub 2022 Jun 20.

Abstract

BACKGROUND

Mucosae-associated lymphoid tissue (MALT) lymphomas are a rare and poorly understood form of primary central nervous system lymphoma (PCNSL). The aim of this study was to better describe these tumors, their management and their long-term prognosis.

METHODS

Patients with primary CNS MALT lymphoma (PCNSML) were retrospectively selected from the database on PCNSL of the Pitié-Salpêtrière Hospital.

RESULTS

Of 662 PCNSL, 11 (1.7%) PCNSML (9 females and 2 males, median age: 56 years) were selected. The median time from first symptoms to diagnosis was 13 months. Location was dural in 8 cases and parenchymal in 3 cases. The disease was multifocal/diffuse in 7 cases. In first line, all patients received chemotherapy (high-dose methotrexate (HD-MTX) based chemotherapy (n = 4) and non-HD-MTX-based chemotherapy (n = 7)), preceded by surgery in 4 cases. None received radiotherapy. According to the IPCG (International PCNSL Collaborative Group) criteria, the overall response rate was 7/11 (64%). At latest news, 5 patients had persistent contrast enhancement, stable with no treatment since a median of 57 months, raising the question of complete response despite persisting contrast enhancement. No patient developed neurotoxicity except for one patient who subsequently received radiotherapy. The median follow-up was 109 months. The median progression-free survival was 78.0 months and the 10-year overall survival rate was 90%.

CONCLUSION

This is the largest series demonstrating that chemotherapy is an efficient treatment in PCNSML, with an excellent long-term outcome and the absence of neurotoxicity, and calling into question the relevance of the IPCG criteria for the evaluation of response.

摘要

背景

黏膜相关淋巴组织(MALT)淋巴瘤是一种罕见且尚未被充分认识的原发性中枢神经系统淋巴瘤(PCNSL)。本研究旨在更好地描述这些肿瘤及其治疗方法和长期预后。

方法

我们从 Pitié-Salpêtrière 医院的 PCNSL 数据库中回顾性选择了原发性中枢神经系统 MALT 淋巴瘤(PCNSML)患者。

结果

在 662 例 PCNSL 中,选择了 11 例(9 名女性和 2 名男性,中位年龄:56 岁)PCNSML 患者。从首发症状到诊断的中位时间为 13 个月。8 例病变位于硬脑膜,3 例位于脑实质。7 例为多灶性/弥漫性病变。一线治疗中,所有患者均接受了化疗(4 例接受大剂量甲氨蝶呤(HD-MTX)为基础的化疗,7 例接受非 HD-MTX 为基础的化疗),4 例患者在化疗前接受了手术。所有患者均未接受放疗。根据国际 PCNSL 协作组(IPC)标准,总缓解率为 7/11(64%)。在最新的随访中,5 例患者仍有对比增强,尽管有持续的对比增强,但自中位数为 57 个月后无治疗进展,提示存在完全缓解。除 1 例患者随后接受放疗外,无患者出现神经毒性。中位随访时间为 109 个月。无进展生存期的中位数为 78.0 个月,10 年总生存率为 90%。

结论

本研究是最大的系列研究,表明化疗是 PCNSML 的有效治疗方法,具有极好的长期疗效和无神经毒性,这对 IPC 标准用于评估疗效提出了质疑。

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