Lemonnier François, Safar Violaine, Beldi-Ferchiou Asma, Cottereau Anne-Ségolène, Bachy Emmanuel, Cartron Guillaume, Fataccioli Virginie, Pelletier Laura, Robe Cyrielle, Letourneau Audrey, Missiaglia Edoardo, Fourati Slim, Moles-Moreau Marie-Pierre, Delmer Alain, Bouabdallah Reda, Voillat Laurent, Becker Stéphanie, Bossard Céline, Parrens Marie, Casasnovas Olivier, Cacheux Victoria, Régny Caroline, Camus Vincent, Delfau-Larue Marie-Hélène, Meignan Michel, de Leval Laurence, Gaulard Philippe, Haioun Corinne
Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpitaux Universitaires Henri Mondor, Unité Hémopathies Lymphoïdes, Créteil, France.
Université Paris Est Créteil, INSERM, Institut Médical de Recherche Biomédicale, Créteil, France.
Blood Adv. 2021 Jan 26;5(2):539-548. doi: 10.1182/bloodadvances.2020003081.
Angioimmunoblastic T-cell lymphoma (AITL) is a frequent T-cell lymphoma in the elderly population that has a poor prognosis when treated with cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) therapy. Lenalidomide, which has been safely combined with CHOP to treat B-cell lymphoma, has shown efficacy as a single agent in AITL treatment. We performed a multicentric phase 2 trial combining 25 mg lenalidomide daily for 14 days per cycle with 8 cycles of CHOP21 in previously untreated AITL patients aged 60 to 80 years. The primary objective was the complete metabolic response (CMR) rate at the end of treatment. Seventy-eight of the 80 patients enrolled were included in the efficacy and safety analysis. CMR was achieved in 32 (41%; 95% confidence interval [CI], 30%-52.7%) patients, which was below the prespecified CMR rate of 55% defined as success in the study. The 2-year progression-free survival (PFS) was 42.1% (95% CI, 30.9%-52.8%), and the 2-year overall survival was 59.2% (95% CI, 47.3%-69.3%). The most common toxicities were hematologic and led to treatment discontinuation in 15% of patients. This large prospective and uniform series of AITL treatment data was used to perform an integrative analysis of clinical, pathologic, biologic, and molecular data. TET2, RHOA, DNMT3A, and IDH2 mutations were present in 78%, 54%, 32%, and 22% of patients, respectively. IDH2 mutations were associated with distinct pathologic and clinical features and DNMT3A was associated with shorter PFS. In conclusion, the combination of lenalidomide and CHOP did not improve the CMR in AITL patients. This trial clarified the clinical impact of recurrent mutations in AITL. This trial was registered at www.clincialtrials.gov as #NCT01553786.
血管免疫母细胞性T细胞淋巴瘤(AITL)是老年人群中常见的T细胞淋巴瘤,采用环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP)方案治疗时预后较差。来那度胺已被安全地与CHOP联合用于治疗B细胞淋巴瘤,并且已显示出作为单一药物治疗AITL的疗效。我们进行了一项多中心2期试验,在60至80岁未经治疗的AITL患者中,将来那度胺每日25mg,每周期服用14天,与CHOP21方案联合使用8个周期。主要目标是治疗结束时的完全代谢缓解(CMR)率。80名入组患者中的78名被纳入疗效和安全性分析。32名(41%;95%置信区间[CI],30%-52.7%)患者实现了CMR,低于研究中定义为成功的预先设定的CMR率55%。2年无进展生存期(PFS)为42.1%(95%CI,30.9%-52.8%),2年总生存期为59.2%(95%CI,47.3%-69.3%)。最常见的毒性反应为血液学毒性,导致15%的患者停止治疗。这一大型前瞻性且统一的AITL治疗数据集被用于对临床、病理、生物学和分子数据进行综合分析。分别有78%、54%、32%和22%的患者存在TET2、RHOA、DNMT3A和IDH2突变。IDH2突变与独特的病理和临床特征相关,DNMT3A与较短的PFS相关。总之,来那度胺与CHOP联合使用并未改善AITL患者的CMR。该试验阐明了AITL中复发性突变的临床影响。该试验在www.clincialtrials.gov上注册,注册号为#NCT01553786。