Fante Matthias A, Harrer Dennis C, Zartner Barbara, Lüke Florian, Mayer Stephanie, Menhart Karin, Reichle Albrecht, Herr Wolfgang, Vogelhuber Martin, Heudobler Daniel
Department of Internal Medicine III, Hematology and Internal Oncology, University Hospital Regensburg, Regensburg, Germany.
Division of Personalized Tumor Therapy, Fraunhofer Institute for Toxicology and Experimental Medicine, Regensburg, Germany.
Front Oncol. 2023 May 26;13:1177330. doi: 10.3389/fonc.2023.1177330. eCollection 2023.
Peripheral T-cell lymphoma (PTCL) is a rare and heterogenous hematologic malignancy with poor prognosis especially in elderly and frail patients who are not eligible for intensive treatment. The resulting palliative setting necessitates tolerable but effective schedules for outpatient treatment. TEPIP is a locally developed, all-oral low-dose regimen comprising trofosfamide, etoposide, procarbazine, idarubicin, and prednisolone.
In this observational retrospective, single-center study, the safety and efficacy of TEPIP was evaluated in 12 patients (pts.) with PTCL treated at the University Medical Center Regensburg between 2010 and 2022. The endpoints were overall response rate (ORR) and overall survival (OS), and adverse events were individually reported according to the Common Terminology Criteria for Adverse Events (CTCAE) criteria.
The enrolled cohort was characterized by advanced age (median 70 years), extensive disease (100% Ann Arbor ≥stage 3), and poor prognosis (75% high/high-intermediate international prognostic index). The most common subtype was angioimmunoblastic T-cell lymphoma (8/12), and 11/12 patients had relapsed or refractory disease at TEPIP onset with a median of 1.5 prior treatment regimens. After a median of 2.5 TEPIP cycles (total of 83 cycles), the ORR was 42% (complete remission 25%), and the OS reached a median of 185 days. Any grade of adverse event (AE) occurred in 8/12 patients, with four patients showing AE ≥CTCAE grade 3 (33%), and the AEs were mainly non-hematological.
TEPIP demonstrated competitive efficacy with a tolerable safety profile in a highly palliative cohort of patients with difficult-to-treat PTCL. The all-oral application, which makes outpatient treatment possible, is particularly noteworthy.
外周T细胞淋巴瘤(PTCL)是一种罕见的异质性血液系统恶性肿瘤,预后较差,尤其是对于不适合接受强化治疗的老年体弱患者。在姑息治疗的情况下,需要有可耐受但有效的门诊治疗方案。TEPIP是一种本地研发的全口服低剂量方案,由曲磷胺、依托泊苷、丙卡巴肼、伊达比星和泼尼松龙组成。
在这项观察性回顾性单中心研究中,对2010年至2022年期间在雷根斯堡大学医学中心接受治疗的12例PTCL患者的TEPIP安全性和有效性进行了评估。终点指标为总缓解率(ORR)和总生存期(OS),不良事件根据不良事件通用术语标准(CTCAE)标准单独报告。
入组队列的特点是年龄较大(中位年龄70岁)、疾病广泛(100%Ann Arbor分期≥3期)且预后较差(75%为高/高中间国际预后指数)。最常见的亚型是血管免疫母细胞性T细胞淋巴瘤(8/12),11/12例患者在开始使用TEPIP时已复发或难治,既往治疗方案的中位数为1.5个。经过中位2.5个TEPIP周期(共83个周期)后,ORR为42%(完全缓解率25%),OS的中位数达到185天。8/12例患者发生了任何级别的不良事件(AE),4例患者出现AE≥CTCAE 3级(33%),不良事件主要为非血液学不良事件。
在难以治疗的PTCL高度姑息治疗队列中,TEPIP显示出具有竞争力的疗效和可耐受的安全性。其全口服给药方式使门诊治疗成为可能,这一点尤其值得关注。