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无法进行干细胞移植的复发/难治性淋巴瘤患者基于吉西他滨的化疗的疗效和耐受性的回顾性分析。

Retrospective Analysis of the Efficacy and Tolerability of Gemcitabine-Based Chemotherapy in Relapsed/Refractory Lymphoma Patients Not Eligible for Stem Cell Transplant.

机构信息

Waitemata District Health Board, North Shore Hospital, Auckland, New Zealand.

Waitemata District Health Board, North Shore Hospital, Auckland, New Zealand.

出版信息

Clin Lymphoma Myeloma Leuk. 2022 Nov;22(11):835-840. doi: 10.1016/j.clml.2022.06.010. Epub 2022 Jun 29.

DOI:10.1016/j.clml.2022.06.010
PMID:35915036
Abstract

INTRODUCTION

Gemcitabine-based regimens are effective salvage therapy for RR lymphoma patients eligible for ASCT, but there is limited data in transplant-ineligible (TIE) patients. Here, we present a retrospective analysis on the outcome of TIE adult patients with RR lymphoma treated with gemcitabine, cisplatin or carboplatin and dexamethasone (GDP/GDCarboP) +/- rituximab regimen in our center.

PATIENTS

We identified 33 patients: 54.5% diffuse large Bcell lymphoma (DLBCL), 6.1% double/triple hit lymphoma, 15% follicular lymphoma, 18% T-cell lymphoma, and 6% classical Hodgkin lymphoma. Majority of the patients had advanced-stage disease and raised LDH at relapse. The cohort's median age was 71 years. The median number of prior lines of treatment was 2, and 60.6% were refractory to their last line of treatment.

RESULTS

The overall response rate was 33% (complete response 15%) for the entire cohort and 62.5% for DLBCL patients not refractory to prior line of treatment. At median follow-up of 25 months, the median duration of response and overall survival in the responders were not reached. Conversely, the median overall survival for the non-responders was dismal at 5 months. Fifty-five percent required treatment alteration (dose attenuation or omission and treatment delay for >1 week) due to adverse events, 73% needed transfusion, and 70% had at least 1 hospital admission during treatment.

CONCLUSION

Our real-world data showed that GDP/GDCarboP provides meaningful efficacy and durability, especially among the responders. However, dose modification and inpatient support are frequently needed, indicating the need for good supportive care and close follow-up in this frailer population.

摘要

简介

以吉西他滨为基础的方案是适合接受 ASCT 的 RR 淋巴瘤患者的有效挽救性治疗,但在不适合移植(TIE)的患者中数据有限。在此,我们报告了在本中心接受吉西他滨、顺铂或卡铂和地塞米松(GDP/GDCarboP)+/-利妥昔单抗方案治疗的 TIE 成年 RR 淋巴瘤患者的回顾性分析结果。

患者

我们共确定了 33 例患者:54.5%弥漫性大 B 细胞淋巴瘤(DLBCL),6.1%双/三打击淋巴瘤,15%滤泡性淋巴瘤,18% T 细胞淋巴瘤,6%经典霍奇金淋巴瘤。大多数患者为晚期疾病,且复发时乳酸脱氢酶升高。该队列的中位年龄为 71 岁。中位治疗线数为 2 条,60.6%的患者对最后一线治疗耐药。

结果

整个队列的总缓解率为 33%(完全缓解率为 15%),对既往治疗线无耐药的 DLBCL 患者的缓解率为 62.5%。在中位随访 25 个月时,应答者的中位缓解持续时间和总生存期均未达到。相反,无应答者的中位总生存期较差,仅为 5 个月。由于不良反应,55%的患者需要调整治疗(减少剂量或停药超过 1 周),73%需要输血,70%的患者在治疗期间至少有 1 次住院。

结论

我们的真实世界数据表明,GDP/GDCarboP 具有显著的疗效和持久性,尤其是在应答者中。然而,需要经常进行剂量调整和住院支持,这表明在这个更为脆弱的人群中需要良好的支持性护理和密切随访。

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