Peyrade Frédéric, Bologna Serge, Delwail Vincent, Emile Jean François, Pascal Laurent, Fermé Christophe, Schiano Jean-Marc, Coiffier Bertrand, Corront Bernadette, Farhat Hassan, Fruchart Christophe, Ghesquieres Herve, Macro Margaret, Tilly Hervé, Choufi Bachra, Delarue Richard, Fitoussi Olivier, Gabarre Jean, Haioun Corinne, Jardin Fabrice
Centre Antoine Lacassagne, Nice, France.
Centre Hospitalier Nancy-Brabois, Vandoeuvre, France.
Lancet Haematol. 2017 Jan;4(1):e46-e55. doi: 10.1016/S2352-3026(16)30171-5.
In 2011 we reported a rituximab plus miniCHOP (reduced-dose cyclophosphamide, doxorubicin, vincristine, and prednisone) combination for patients older than 80 years with diffuse large B-cell lymphoma (DLBCL). The 2-year overall survival was 59% (95% CI 49-67) with an excess of early toxicity. To improve those results we tested the same chemotherapy protocol in combination with ofatumumab and a pre-phase treatment.
For this open-label, multicentre, single-group, phase 2 trial, we recruited patients older than 80 years with untreated histologically-proven CD20-positive DLBCL, Ann Arbor stage I to IV, from 41 academic and hospital centres in France and Belgium. Patients received a pre-phase with oral vincristine (1 mg total dose 1 week before cycle 1 [day -7]) and oral prednisone (60 mg total dose starting 1 week before cycle 1, for 4 days [day -7 to day -4]) before the first cycle of the ofatumumab plus miniCHOP regimen. The regimen consisted of 1000 mg total dose of intravenous ofatumumab, 25 mg/m of intravenous doxorubicin, 400 mg/m of intravenous cyclophosphamide, and 1 mg of intravenous vincristine, on day 1 of each cycle; and 40 mg/m of oral prednisone on days 1-5. Ofatumumab was administered with 1000 mg of paracetamol and 50 mg of diphenhydramine. The primary endpoint was overall survival in the intention-to-treat population. The statistical analysis has been done on an intention-to-treat principle. This study was registered with ClinicalTrials.gov, number NCT01195714.
Between June 2, 2010, and Nov 4, 2011, we enrolled 120 patients. Age-adjusted International Prognostic Index was 2-3 in 68 (57%) of them. The median follow-up time was 26·8 months (IQR 24·5-30·1). The 2-year overall survival was 64·7% (95% CI 55·3-72·7) and median overall survival was not reached (95% CI 30·2-not reached). 45 patients died during the treatment, of whom 28 (62%) died due to lymphoma. The most common side-effect was haematological toxicity. Among the 120 patients, grade 3-4 neutropenia was reported in 24 (21%) patients and thrombocytopenia in two (2%), during the treatment period. Grade 3-4 anaemia was reported in six (5%) patients; seven (6%) patients had one episode of febrile neutropenia. 17 (15%) of 115 patients in the modified intention-to-treat population had red blood cell transfusions and three (3%) had platelet transfusions.
Our result suggest that, in patients older than 80 years with DLBCL, ofatumumab and pre-phase treatment seem to improve overall survival compared with the previously reported data. The combination of pre-phase treatment, a monoclonal antibody against CD20, and miniCHOP can be considered a new treatment platform for use in randomised clinical trial design for DLBCL treatment in patients older than 80 years.
The Lymphoma Study Association, GlaxoSmithKline.
2011年,我们报告了利妥昔单抗联合miniCHOP方案(降低剂量的环磷酰胺、多柔比星、长春新碱和泼尼松)用于80岁以上弥漫性大B细胞淋巴瘤(DLBCL)患者的治疗情况。2年总生存率为59%(95%CI 49 - 67),且早期毒性反应较多。为改善这些结果,我们测试了相同的化疗方案联合奥法木单抗及预治疗阶段的疗效。
在这项开放标签、多中心、单组、2期试验中,我们从法国和比利时的41个学术及医院中心招募了年龄大于80岁、未经治疗且经组织学证实为CD20阳性的DLBCL患者,Ann Arbor分期为I至IV期。在奥法木单抗联合miniCHOP方案的第1周期之前,患者接受一个预治疗阶段,口服长春新碱(总剂量1mg,在第1周期前1周[第 -7天])和口服泼尼松(总剂量60mg,从第1周期前1周开始,共4天[第 -7天至第 -4天])。该方案包括在每个周期的第1天静脉注射奥法木单抗总剂量1000mg、静脉注射多柔比星25mg/m²、静脉注射环磷酰胺400mg/m²和静脉注射长春新碱1mg;以及在第1 - 5天口服泼尼松40mg/m²。奥法木单抗与1000mg对乙酰氨基酚和50mg苯海拉明一起给药。主要终点是意向性治疗人群的总生存率。统计分析按照意向性治疗原则进行。本研究已在ClinicalTrials.gov注册,注册号为NCT01195714。
在2010年6月2日至2011年11月4日期间,我们招募了120例患者。其中68例(57%)的年龄调整国际预后指数为2 - 3。中位随访时间为26.8个月(IQR 24.5 - 30.1)。2年总生存率为64.7%(95%CI 55.3 - 72.7),中位总生存期未达到(95%CI 30.2 - 未达到)。45例患者在治疗期间死亡,其中28例(62%)死于淋巴瘤。最常见的副作用是血液学毒性。在120例患者中,治疗期间有24例(21%)报告发生3 - 4级中性粒细胞减少,2例(2%)发生血小板减少。6例(5%)患者报告发生3 - 4级贫血;7例(6%)患者有1次发热性中性粒细胞减少发作。在改良意向性治疗人群的115例患者中,17例(15%)接受了红细胞输血,3例(3%)接受了血小板输血。
我们的结果表明,对于80岁以上的DLBCL患者,与先前报告的数据相比,奥法木单抗和预治疗阶段似乎能提高总生存率。预治疗阶段、抗CD20单克隆抗体和miniCHOP的联合应用可被视为一个新的治疗平台,用于80岁以上DLBCL患者治疗的随机临床试验设计。
淋巴瘤研究协会,葛兰素史克公司。