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改良风险分层序贯治疗(皮下利妥昔单抗联合或不联合化疗)在实体器官移植后 B 细胞移植后淋巴增殖性疾病(PTLD)中的应用:前瞻性多中心 II 期 PTLD-2 试验。

Modified risk-stratified sequential treatment (subcutaneous rituximab with or without chemotherapy) in B-cell Post-transplant lymphoproliferative disorder (PTLD) after Solid organ transplantation (SOT): the prospective multicentre phase II PTLD-2 trial.

机构信息

Department of Hematology and Oncology, DIAKO Ev. Diakonie-Krankenhaus, Bremen, Germany.

Pius-Hospital, University Medicine Oldenburg, Department of Hematology and Oncology, Oldenburg, Germany.

出版信息

Leukemia. 2022 Oct;36(10):2468-2478. doi: 10.1038/s41375-022-01667-1. Epub 2022 Aug 16.

DOI:10.1038/s41375-022-01667-1
PMID:35974101
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9522585/
Abstract

The prospective multicentre Phase II PTLD-2 trial (NCT02042391) tested modified risk-stratification in adult SOT recipients with CD20-positive PTLD based on principles established in the PTLD-1 trials: sequential treatment and risk-stratification. After rituximab monotherapy induction, patients in complete remission as well as those in partial remission with IPI < 3 at diagnosis (low-risk) continued with rituximab monotherapy and thus chemotherapy free. Most others (high-risk) received R-CHOP-21. Thoracic SOT recipients who progressed (very-high-risk) received alternating R-CHOP-21 and modified R-DHAOx. The primary endpoint was event-free survival (EFS) in the low-risk group. The PTLD-1 trials provided historical controls. Rituximab was applied subcutaneously. Of 60 patients enrolled, 21 were low-risk, 28 high-risk and 9 very-high-risk. Overall response was 45/48 (94%, 95% CI 83-98). 2-year Kaplan-Meier estimates of time to progression and overall survival were 78% (95% CI 65-90) and 68% (95% CI 55-80) - similar to the PTLD-1 trials. Treatment-related mortality was 4/59 (7%, 95% CI 2-17). In the low-risk group, 2-year EFS was 66% (95% CI 45-86) versus 52% in the historical comparator that received CHOP (p = 0.432). 2-year OS in the low-risk group was 100%. Results with R-CHOP-21 in high-risk patients confirmed previous results. Immunochemotherapy intensification in very-high-risk patients was disappointing.

摘要

前瞻性多中心 II 期 PTLD-2 试验(NCT02042391)基于 PTLD-1 试验中确立的原则,测试了 CD20 阳性 PTLD 成人 SOT 受者的改良风险分层:序贯治疗和风险分层。利妥昔单抗单药诱导后,完全缓解的患者以及诊断时 IPI<3(低危)的部分缓解患者继续接受利妥昔单抗单药治疗,因此无需化疗。大多数其他患者(高危)接受 R-CHOP-21 治疗。进展的(极高危)胸部 SOT 受者接受交替的 R-CHOP-21 和改良的 R-DHAOx 治疗。主要终点是低危组的无事件生存(EFS)。PTLD-1 试验提供了历史对照。利妥昔单抗皮下给药。60 例患者中,21 例为低危,28 例为高危,9 例为极高危。总缓解率为 45/48(94%,95%CI83-98)。2 年时的无进展时间和总生存率的 Kaplan-Meier 估计值分别为 78%(95%CI65-90)和 68%(95%CI55-80)-与 PTLD-1 试验相似。治疗相关死亡率为 4/59(7%,95%CI2-17)。在低危组中,2 年 EFS 为 66%(95%CI45-86),而历史对照中接受 CHOP 治疗的患者为 52%(p=0.432)。低危组的 2 年 OS 为 100%。高危患者接受 R-CHOP-21 治疗的结果证实了先前的结果。极高危患者的免疫化疗强化令人失望。

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