JAMA Dermatol. 2014 May;150(5):535-41. doi: 10.1001/jamadermatol.2013.7452.
Primary cutaneous diffuse large B-cell lymphoma, leg type (PCDLBCL-LT), occurs in elderly patients and has been considered as a lymphoma with a poor prognosis, with estimated 5-year specific survival rates of approximately 50%. The hypothesis of an improvement in prognosis over time has not been studied.
To evaluate this hypothesis in a large series of patients and investigate factors associated with prognosis as well as improvement in the prognosis.
DESIGN, SETTING, AND PARTICIPANTS: A retrospective multicenter study was conducted including dermatology departments belonging to the French Study Group on Cutaneous Lymphoma. Participants were 115 patients with PCDLBCL-LT diagnosed between 1988 and 2003 (period 1) or between 2004 and 2010 (period 2).
Age, sex, period of diagnosis, number of skin lesions, tumor stage, tumor location (leg vs nonleg), lactate dehydrogenase level, type of therapy (with or without a combination of rituximab and polychemotherapy [PCT]), and outcome were recorded. Baseline characteristics and outcome were compared according to period of diagnosis and type of therapy. Prognosis factors were identified by univariate and multivariate survival analyses.
The mean age of the patients was 76.9 years, and 47% of the patients were older than 80 years. The 3- and 5-year specific survival rates improved between period 1 and period 2, from 55% to 74% and from 46% to 66%, respectively (P = .01). Patients had similar baseline characteristics during both periods, but rituximab-PCT regimens were administered to 88.5% of the patients in period 2 vs 16.7% in period 1 (P < .001). The 3- and 5-year specific survival rates were 80% and 74%, respectively, in patients who received a rituximab-PCT regimen compared with 48% and 38% in those who received less-intensive therapies. No significant difference was observed between both groups in age and baseline prognostic factors. In multivariate analysis, treatment without rituximab-PCT was the only adverse prognostic factor (odds ratio, 4.6 [95% CI, 2.4-9.1]; P < .001), whereas the number of skin lesions (P = .06) and location on the leg (P = .07) had only borderline significance.
A major improvement in the survival of patients with PCDLBCL-LT has occurred over time in France, mainly as a result of the use of intensive rituximab-PCT regimens in most patients, including very elderly ones. Until further prospective clinical trials are conducted, such regimens should be considered as the standard of care in these patients.
原发性皮肤弥漫性大 B 细胞淋巴瘤,腿型(PCDLBCL-LT)发生于老年患者,被认为是预后不良的淋巴瘤,估计 5 年特异性生存率约为 50%。关于随时间推移预后改善的假设尚未得到研究。
在大量患者中评估这一假设,并调查与预后相关的因素以及预后的改善情况。
设计、地点和参与者:进行了一项回顾性多中心研究,包括属于法国皮肤淋巴瘤研究小组的皮肤科。参与者为 115 名 1988 年至 2003 年(第 1 期)或 2004 年至 2010 年(第 2 期)诊断为 PCDLBCL-LT 的患者。
记录年龄、性别、诊断期、皮损数量、肿瘤分期、肿瘤位置(腿部与非腿部)、乳酸脱氢酶水平、治疗类型(是否联合利妥昔单抗和化疗[PCT])以及结局。根据诊断期和治疗类型比较基线特征和结局。通过单变量和多变量生存分析确定预后因素。
患者的平均年龄为 76.9 岁,47%的患者年龄大于 80 岁。第 1 期和第 2 期的 3 年和 5 年特异性生存率分别提高了 19%和 20%,从 55%提高至 74%和从 46%提高至 66%(P=0.01)。两个时期患者的基线特征相似,但第 2 期 88.5%的患者接受了利妥昔单抗-PCT 方案治疗,而第 1 期仅为 16.7%(P<0.001)。接受利妥昔单抗-PCT 方案治疗的患者 3 年和 5 年的特异性生存率分别为 80%和 74%,而接受非强化治疗的患者分别为 48%和 38%。两组在年龄和基线预后因素方面无显著差异。多变量分析显示,未接受利妥昔单抗-PCT 治疗是唯一的不良预后因素(比值比,4.6[95%CI,2.4-9.1];P<0.001),而皮损数量(P=0.06)和腿部位置(P=0.07)仅具有边缘意义。
法国 PCDLBCL-LT 患者的生存率随时间发生了重大改善,主要是由于大多数患者(包括非常高龄患者)使用了强化的利妥昔单抗-PCT 方案。在进一步开展前瞻性临床试验之前,此类方案应被视为这些患者的标准治疗方法。