Reboursiere Emilie, Le Bras Fabien, Herbaux Charles, Gyan Emmanuel, Clavert Aline, Morschhauser Franck, Malak Sandra, Sibon David, Broussais Florence, Braun Thorsten, Fornecker Luc-Matthieu, Garidi Reda, Tricot Sabine, Houot Roch, Joly Bertrand, Abarah Wajed, Choufi Bachra, Pham Anne-Dominique, Gac Anne-Claire, Fruchart Christophe, Marin Emilie, Safar Violaine, Parcelier Anne, Maisonneuve Hervé, Bachy Emmanuel, Cartron Guillaume, Jaccard Arnaud, Tournilhac Olivier, Rossi Cédric, Schirmer Luciane, Martignoles Jean-Alain, Gaulard Philippe, Tilly Hervé, Damaj Gandhi
Department of Hematology, University Hospital of Caen, Caen, France.
Department of Hematology, Assistance Publique des Hôpitaux de Paris, Créteil, France.
Oncotarget. 2016 Dec 20;7(51):85573-85583. doi: 10.18632/oncotarget.10764.
Peripheral T-cell lymphoma (PTCL) is a group of diseases with poor outcome and few therapeutic options. We aimed to assess the efficacy of bendamustine in real life cohort of patients.Between November 2009 and March 2015, 138 PTCL patients were treated with bendamustine in 27 centers. Population median age was 64 (28-89) years with male/female ratio of 1.4. There were mainly angio-immunoblastic (AITL = 71), PTCL-not otherwise specified (PTCL-NOS = 40) and anaplastic large cell lymphoma (ALCL = 8). The majority of patients (96%) had disseminated disease and extranodal localizations (77%). Median number of chemotherapy lines prior to bendamustine was 2 (1-8). Median duration of response (DoR) after the last chemotherapy prior to bendamustine was 4.3 months (1-70) and 50% of patients had refractory disease.Median number of administered bendamustine cycles was 2 (1-8) and 72 patients (52%) received less than 3 mostly because of disease progression. Median dose was 90 (50-150) mg/m². Overall response rate (ORR) was 32.6% with complete response (CR) rate of 24.6% and median DoR was 3.3 months (1-39). AITL patients were more sensitive than PTCL-NOS patients (ORR: 45.1 versus 20%, p = 0.01). Median PFS and OS were 3.1 (0.2-46.3) and 4.4 (0.2-55.4) months. On multivariate analysis, refractory disease (p = 0.001) and extranodal localization (p = 0.028) adversely influenced ORR. Grade 3-4 thrombocytopenia, neutropenia and infections were reported in 22, 17 and 23% of cases respectively.Bendamustine as single agent could be considered as a therapeutic option for relapsed or refractory PTCL, particularly in chemosensitive or AITL patients. Combinations of bendamustine with other drugs warrant further evaluation.
外周T细胞淋巴瘤(PTCL)是一组预后较差且治疗选择有限的疾病。我们旨在评估苯达莫司汀在真实世界患者队列中的疗效。2009年11月至2015年3月期间,27个中心的138例PTCL患者接受了苯达莫司汀治疗。总体人群中位年龄为64岁(28 - 89岁),男女比例为1.4。主要病理类型为血管免疫母细胞性淋巴瘤(AITL = 71例)、非特指外周T细胞淋巴瘤(PTCL-NOS = 40例)和间变性大细胞淋巴瘤(ALCL = 8例)。大多数患者(96%)有播散性疾病且有结外侵犯(77%)。苯达莫司汀治疗前化疗线数的中位数为2(1 - 8)。苯达莫司汀治疗前最后一次化疗后的中位缓解持续时间(DoR)为4.3个月(1 - 70),50%的患者为难治性疾病。苯达莫司汀给药周期数的中位数为2(1 - 8),72例患者(52%)接受少于3个周期,主要原因是疾病进展。中位剂量为90(50 - 150)mg/m²。总缓解率(ORR)为32.6%,完全缓解(CR)率为24.6%,中位DoR为3.3个月(1 - 39)。AITL患者比PTCL-NOS患者更敏感(ORR:45.1%对20%,p = 0.01)。中位无进展生存期(PFS)和总生存期(OS)分别为3.1个月(0.2 - 46.3)和4.4个月(0.2 - 55.4)。多因素分析显示,难治性疾病(p = 0.001)和结外侵犯(p = 0.028)对ORR有不利影响。分别有22%、17%和23%的病例报告了3 - 4级血小板减少、中性粒细胞减少和感染。苯达莫司汀单药可被视为复发或难治性PTCL的一种治疗选择,特别是在化疗敏感或AITL患者中。苯达莫司汀与其他药物的联合应用值得进一步评估。