Institut de Cancérologie de l'Ouest, Bld Jacques Monod, 44805 Saint-Herblain Cedex, France.
J Clin Oncol. 2012 Nov 1;30(31):3848-53. doi: 10.1200/JCO.2010.33.4474. Epub 2012 Sep 24.
Patients with follicular lymphoma (FL) registered in the F2-study and initially managed without treatment were analyzed to describe the presentation and outcome of a watch and wait (W&W) strategy in the rituximab era, to identify parameters for initiating treatment, and to evaluate whether initial W&W could have deleterious effects on treatment efficacy after progression or relapse.
Between 2003 and 2005, 120 patients selected from the 1,093 treatment-naive patients with FL in the F2-study cohort were initially managed expectantly (W&W), and 107 patients were assessed. Most of these patients (80%) had disseminated disease with a low tumor burden according to Groupe d'Etudes des Lymphomes Folliculaires criteria.
After a median follow-up of 64 months, treatment was initiated in 54 patients (50%), with a median delay of 55 months for the entire cohort. In a univariate analysis, involvement of more than four nodal areas (hazard ratio [HR], 2.26) and serum albumin less than 3.5 g/dL (HR, 3.51) were predictive of a shorter time to lymphoma treatment initiation. In a multivariate analysis, only involvement of more than four nodal areas remained significant (HR, 2.32). The 4-year freedom from treatment failure (FFTF) rate of W&W patients (79%; 95% CI, 69% to 85%) was not inferior to that of a subgroup of 242 patients from the F2-study cohort with good prognosis characteristics who were initially treated with a rituximab-based regimen (69%; 95% CI, 61% to 76%; P = .103).
In the rituximab era, patients with FL in a selected prognostically favorable group can still be managed with W&W. W&W does not seem to have detrimental effects on FFTF and overall survival rates after treatment.
本研究分析了滤泡性淋巴瘤(FL)患者的临床特征和结局,这些患者在 F2 研究中注册,且初始未接受治疗,旨在描述在利妥昔单抗时代观察等待(W&W)策略的表现和结果,确定开始治疗的参数,并评估初始 W&W 是否会对进展或复发后的治疗效果产生不利影响。
在 2003 年至 2005 年期间,从 F2 研究队列中选择了 120 名未经治疗的初治 FL 患者进行初步的期待性治疗(W&W),其中有 107 名患者接受了评估。根据 Groupe d'Etudes des Lymphomes Folliculaires 标准,这些患者中的大多数(80%)有弥漫性疾病且肿瘤负荷低。
中位随访 64 个月后,54 名患者(50%)接受了治疗,整个队列的中位延迟时间为 55 个月。在单因素分析中,淋巴结区受累大于 4 个(危险比[HR],2.26)和血清白蛋白小于 3.5 g/dL(HR,3.51)与淋巴瘤治疗开始时间较短相关。在多因素分析中,只有淋巴结区受累大于 4 个仍然具有显著意义(HR,2.32)。W&W 患者的 4 年无治疗失败(FFTF)率(79%;95%CI,69%85%)并不劣于 F2 研究队列中 242 名预后良好特征的患者亚组(69%;95%CI,61%76%;P=.103)。
在利妥昔单抗时代,对于选择预后良好的滤泡性淋巴瘤患者仍可采用 W&W 策略进行治疗。W&W 似乎不会对治疗后的 FFTF 和总生存率产生不利影响。