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利妥昔单抗联合基于噻替派的大剂量化疗及自体干细胞移植治疗新诊断的原发性中枢神经系统淋巴瘤:单中心经验

R-MPV followed by high-dose chemotherapy with thiotepa-based and autologous stem cell transplantation for newly diagnosed primary central nervous system lymphoma: a single-center experience.

作者信息

Lee Ji Yun, Paik Jin Ho, Suh Koung Jin, Kim Ji-Won, Kim Se Hyun, Kim Jin Won, Kim Yu Jung, Lee Keun-Wook, Kim Jee Hyun, Bang Soo-Mee, Lee Jong-Seok, Lee Jeong-Ok

机构信息

Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.

Department of Pathology, Seoul National University Bundang Hospital, Seongnam, Korea.

出版信息

Blood Res. 2021 Dec 31;56(4):285-292. doi: 10.5045/br.2021.2021073.

Abstract

BACKGROUND

High-dose chemotherapy followed by autologous stem cell transplantation (HDC-ASCT) as a consolidation treatment is a promising approach for eligible patients with newly diagnosed primary central nervous system lymphoma (PCNSL).

METHODS

In this retrospective analysis, 22 patients with newly diagnosed PCNSL received chemotherapy with rituximab, methotrexate, procarbazine, and vincristine. Those who showed complete or partial response subsequently received consolidation HDC-ASCT with a thiotepa- based conditioning regimen but did not undergo radiotherapy.

RESULTS

The PCNSL patients had a median age of 57 years (range, 49‒67 yr); of the total patients, 9.1% had a performance status of 2 or higher, and 72.1% had multiple lesions. Approximately 82% of patients received six cycles of induction chemotherapy, which was well tolerated with excellent disease control. The rate of confirmed or unconfirmed complete response increased from 45.5% at the period of interim analysis to 81.8% prior to the initiation of HDC-ASCT. With a median follow-up of 19.6 months (range, 7.5‒56.5 mo), the 2-year progression-free survival and overall survival estimates were 84% and 88%, respectively. No treatment-related deaths occurred. Grade 3 toxicity was recorded in 90.9% of the patients after undergoing the HDC-ASCT, and the most common grade 3 adverse event was febrile neutropenia without sepsis.

CONCLUSION

The discussed treatment approach is feasible in patients with newly diagnosed PCNSL, yielding encouraging results.

摘要

背景

大剂量化疗后行自体干细胞移植(HDC-ASCT)作为巩固治疗,对于新诊断的原发性中枢神经系统淋巴瘤(PCNSL) eligible患者是一种有前景的方法。

方法

在这项回顾性分析中,22例新诊断的PCNSL患者接受了利妥昔单抗、甲氨蝶呤、丙卡巴肼和长春新碱化疗。那些显示完全或部分缓解的患者随后接受了基于噻替派的预处理方案的巩固HDC-ASCT,但未接受放疗。

结果

PCNSL患者的中位年龄为57岁(范围49-67岁);在所有患者中,9.1%的患者体能状态为2或更高,72.1%的患者有多处病灶。约82%的患者接受了六个周期的诱导化疗,耐受性良好,疾病控制良好。在中期分析时确诊或未确诊的完全缓解率从45.5%提高到HDC-ASCT开始前的81.8%。中位随访19.6个月(范围7.5-56.5个月),2年无进展生存率和总生存率估计分别为84%和88%。未发生治疗相关死亡。90.9%的患者在接受HDC-ASCT后记录到3级毒性,最常见的3级不良事件是无败血症的发热性中性粒细胞减少。

结论

所讨论的治疗方法在新诊断的PCNSL患者中是可行的,产生了令人鼓舞的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/801c/8721461/c72881d85b96/br-56-4-285-f1.jpg

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