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伊布替尼作为移植后淋巴增殖性疾病风险分层治疗的一部分:TIDaL 试验的 2 期研究。

Ibrutinib as part of risk-stratified treatment for posttransplant lymphoproliferative disorder: the phase 2 TIDaL trial.

机构信息

Centre for Clinical Haematology, University Hospitals Birmingham National Health System Foundation Trust, Birmingham, United Kingdom.

Cancer Research UK Clinical Trials Unit, Institute of Cancer and Genomics Cancer, University of Birmingham, Birmingham, United Kingdom.

出版信息

Blood. 2024 Jul 25;144(4):392-401. doi: 10.1182/blood.2024023847.

Abstract

Posttransplant lymphoproliferative disorder (PTLD) is a rare complication of solid organ transplantation, and cytotoxic chemotherapy is associated with treatment-related morbidity and mortality. Current treatment takes a sequential, risk-stratified approach, and patients with low-risk disease after initial immunotherapy can avoid escalation to immunochemotherapy. TIDaL is a prospective, single-arm phase 2 trial investigating the activity and tolerability of ibrutinib combined with risk-stratified therapy for first-line treatment of PTLD. Eligible patients were adults with newly diagnosed CD20+ B-cell PTLD after solid organ transplant and performance status 0 to 2. Initial treatment comprised 49 days of ibrutinib 560 mg once daily, with 4 doses of weekly rituximab. Treatment response on interim scan and baseline International Prognostic Index were used to allocate patients to either a low-risk arm (who continued ibrutinib, alongside 4 further doses of 3-weekly rituximab) or high-risk (escalation to rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone [R-CHOP] immunochemotherapy, with ibrutinib continuing in patients aged <65 years). The primary outcome was complete response on interim scan, achieved by 11 of 38 patients (29%; 95% confidence interval [CI], 15-46). This did not reach the prespecified threshold for clinically significant activity. Secondary outcomes included allocation to the low-risk arm (41% of patients), 2-year progression-free survival (58%; 95% CI, 44-76), and 2-year overall survival (76%; 95% CI, 63-91). Adverse events were mostly hematological, gastrointestinal, and infective. Although TIDaL does not support adding ibrutinib into first-line treatment of PTLD, increasing the proportion of patients who can be treated without cytotoxic chemotherapy remains an important aim of future research. This trial was registered at www.clinicaltrials.gov as #ISRCTN32667607.

摘要

移植后淋巴组织增生性疾病(PTLD)是实体器官移植的罕见并发症,细胞毒性化疗与治疗相关的发病率和死亡率有关。目前的治疗采用序贯、分层风险的方法,初始免疫治疗后疾病低危的患者可以避免升级为免疫化疗。TIDaL 是一项前瞻性、单臂 2 期试验,研究伊布替尼联合分层治疗用于初治 PTLD 的活性和耐受性。入组患者为实体器官移植后新诊断的 CD20+ B 细胞 PTLD 且体能状态 0-2 分的成年人。初始治疗包括 49 天伊布替尼 560mg 每日 1 次,联合每周利妥昔单抗 4 次。中期扫描和基线国际预后指数的治疗反应用于将患者分配到低危组(继续伊布替尼,联合 4 次 3 周利妥昔单抗)或高危组(升级为利妥昔单抗、环磷酰胺、阿霉素、长春新碱和泼尼松[R-CHOP]免疫化疗,年龄<65 岁的患者继续伊布替尼)。主要终点是中期扫描的完全缓解,38 例患者中有 11 例(29%;95%置信区间[CI],15-46)达到。这没有达到临床显著活性的预设阈值。次要终点包括低危组的分配(41%的患者)、2 年无进展生存率(58%;95%CI,44-76)和 2 年总生存率(76%;95%CI,63-91)。不良事件主要为血液学、胃肠道和感染。尽管 TIDaL 不支持将伊布替尼添加到 PTLD 的一线治疗中,但增加无需细胞毒性化疗即可治疗的患者比例仍然是未来研究的重要目标。该试验在 www.clinicaltrials.gov 注册,编号为 #ISRCTN32667607。

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