Avilés Agustin, Nambo M Jesús, Neri Natividad, Castañeda Claudia, Cleto Sergio, Gonzalez Martha, Huerta-Guzmán Judith
Oncology Research Unit, Nacional Medical Center, IMSS, México, D.F. Mexico.
Cancer Biother Radiopharm. 2007 Dec;22(6):836-40. doi: 10.1089/cbr.2007.0402.
Treatment of refractory mycosis fungoides and Sézary syndrome remain unsatisfactory. In this study, we assessed the efficacy and toxicity of low-dose methotrexate (10 mg/m(2), biweekly) and interferon (9.0 MU, three times a week) as induction therapy by 6 or 12 months, followed, if patients achieved a complete remission, by interferon maintenance until toxicity or relapse. In an intent-to-treat analysis, 158 patients were considered evaluable. Complete response (biopsy proven) was observed in 112 patients (49 [31%] at 6 months and 63 [49%] at 12 months); thus, the complete response rate was 74%. With a median follow-up of 155 months (range, 62-181), progression-free disease was 71% and overall survival was 69%. Acute toxicity was mild, treatment was well tolerated, and to date no late toxicity has been observed. We conclude that this regimen is a benefit to this setting of patients, with excellent outcome and mild toxicity.
难治性蕈样肉芽肿和塞扎里综合征的治疗效果仍不尽人意。在本研究中,我们评估了低剂量甲氨蝶呤(10 mg/m²,每两周一次)和干扰素(9.0 MU,每周三次)作为诱导治疗6个月或12个月的疗效和毒性,若患者达到完全缓解,则继续使用干扰素维持治疗,直至出现毒性反应或复发。在意向性分析中,158例患者被视为可评估对象。112例患者观察到完全缓解(活检证实)(6个月时49例[31%],12个月时63例[49%]);因此,完全缓解率为74%。中位随访155个月(范围62 - 181个月),无进展生存期为71%,总生存率为69%。急性毒性反应轻微,治疗耐受性良好,迄今为止未观察到晚期毒性反应。我们得出结论,该方案对这类患者有益,疗效优异且毒性轻微。