Aviles Agustin, Neri Natividad, Fernandez-Diez Jorge, Silva Luis, Nambo Maria-Jesùs
Hematology. 2015 Oct;20(9):538-42. doi: 10.1179/1607845415Y.0000000002. Epub 2015 Jan 16.
Treatment of refractory/relapsed cutaneous T-cell lymphoma (CTCL) remains controversial, most studies included a few patients with a short follow-up. Previously, we performed two small studies employing interferon alpha 2b (IFN) combined with low doses of methotrexate (MTX) or retinoids. Thus, we conducted an open-label clinical trial to assess the benefit and toxicity of the two mentioned regimens in a large number of patients with a longer follow-up of the treatment of refractory/relapsed CTCL.
Three-hundred and seventy-seven patients with refractory/relapsed, pathologically confirmed, CTCL, with advanced stages and at least treated with two previous effective regimens in CTCL, were randomized to receive IFN and low doses of MTX compared with IFN and all trans-retinoid acid during 6 months; if a complete response (CR) was not achieved, treatment was continued until 12 months in both arms. At this time, if patient achieves CR, MTX or retinoid was stopped, and the patient continues to receive IFN until progression disease or toxicity. One-hundred and eight patients received IFN for more than 5 years.
Toxicity was minimal and well tolerated, no patients needed to modify the administration of IFN secondary to toxicity. The overall complete response was achieved 80% in both arms. Actuarial curves at 5 years showed that progression-free survival was 60% in the IFN/MTX group and 62% in the IFN/retinoids group (P = 0.8) that were not statistically different and overall survival (OS) rates were 70 and 67%, respectively (P = 0.03).
Both present schedules showed good tolerance and an excellent OS at 5 years, which is better than the other, more expensive and toxic, regimens. Considering the indolent course of CTCL, we suggested that those regimens, mentioned in this paper, will be regarded as the standard therapy, for patients of this setting.
The use of IFN and retinoids or low dose of cytotoxic drugs will be preferred in patients with refractory/relapse CTCL, because OS is good and toxicity is minimal.
难治性/复发性皮肤T细胞淋巴瘤(CTCL)的治疗仍存在争议,大多数研究纳入的患者数量较少且随访时间短。此前,我们进行了两项小型研究,采用干扰素α2b(IFN)联合低剂量甲氨蝶呤(MTX)或维甲酸。因此,我们开展了一项开放标签的临床试验,以评估上述两种方案对大量难治性/复发性CTCL患者的疗效和毒性,并进行更长时间的随访。
377例经病理证实的难治性/复发性CTCL患者,处于晚期,且至少接受过两种先前有效的CTCL治疗方案,被随机分为两组,分别接受IFN联合低剂量MTX以及IFN联合全反式维甲酸治疗,为期6个月;若未达到完全缓解(CR),两组均继续治疗至12个月。此时,若患者达到CR,则停用MTX或维甲酸,患者继续接受IFN治疗,直至疾病进展或出现毒性反应。108例患者接受IFN治疗超过5年。
毒性极小且耐受性良好,无患者因毒性反应而需要调整IFN的给药方式。两组的总体完全缓解率均达到80%。5年的精算曲线显示,IFN/MTX组的无进展生存率为60%,IFN/维甲酸组为62%(P = 0.8),无统计学差异,总体生存率(OS)分别为70%和67%(P = 0.03)。
两种方案均显示出良好的耐受性,5年时的OS极佳,优于其他更昂贵且毒性更大的方案。考虑到CTCL的惰性病程,我们建议本文提及的这些方案可作为该情况下患者的标准治疗方案。
对于难治性/复发性CTCL患者,首选使用IFN和维甲酸或低剂量细胞毒性药物,因为OS良好且毒性极小。