Capalbo Silvana, Delia Mario, Dargenio Michela, Liso Arcangelo, Diomede Daniela, Garofalo Lucrezia, Liso Vincenzo
Hematology, University of Bari, Policlinico, Piazza Giulio Cesare 11, 70124 Bari, Italy.
Med Oncol. 2003;20(4):389-96. doi: 10.1385/MO:20:4:389.
We report the use of Alemtuzumab (Campath-1H) as salvage treatment in three patients with advanced mycosis fungoides/Sézary syndrome who had previously been treated with conventional chemotherapy. Two patients (case 1 and case 2), aged 42 and 68 yr, respectively, were heavily pretreated (more than three prior therapy regimens, including autologous transplant in case 2) and refractory to conventional chemotherapy, and the third patient (case 3), aged 80 yr, who had refused any chemotherapy, had been resistant to treatment with cyclosporine and steroids. Campath-1H was administered intravenously, after an escalating dose from 3 to 10 mg, at the dose of 30 mg, three times weekly, to a total dose of 1080, 223, and 480 mg, respectively. The patients with Sézary syndrome (case 2 and case 3) showed clearance of circulating Sézary cells and clinical improvement of the skin lesions after 2 wk of treatment. Two patients (case 1 and case 3) completed the treatment (12 and 6 wk) without significant toxicity, the former achieving a partial response and the latter a clinical complete response. The patient (case 2), who suffered from ischemic cardiopathy and diabetes, quickly achieved a clinical improvement of the Sézary syndrome, but he died because of a myocardial infarction after 3 wk of treatment. Our report shows that the treatment with Campath-1H is active even in patients with advanced refractory mycosis fungoides/Sézary syndrome. Further clinical observations on a larger cohort of patients are needed to establish if Campath-1H may have a role as first line therapy in addition to conventional therapy including chemotherapy.
我们报告了使用阿仑单抗(Campath-1H)对3例晚期蕈样肉芽肿/赛塞里综合征患者进行挽救治疗的情况,这些患者此前接受过传统化疗。两名患者(病例1和病例2),年龄分别为42岁和68岁,接受过大量前期治疗(超过三种先前的治疗方案,病例2包括自体移植)且对传统化疗耐药,第三名患者(病例3),80岁,拒绝任何化疗,对环孢素和类固醇治疗耐药。Campath-1H静脉给药,剂量从3毫克逐步增加至10毫克后,以30毫克的剂量,每周三次,总剂量分别为1080毫克、223毫克和480毫克。赛塞里综合征患者(病例2和病例3)在治疗2周后循环赛塞里细胞清除,皮肤病变临床改善。两名患者(病例1和病例3)完成治疗(分别为12周和6周),无明显毒性,前者达到部分缓解,后者达到临床完全缓解。患有缺血性心脏病和糖尿病的患者(病例2)赛塞里综合征迅速取得临床改善,但在治疗3周后因心肌梗死死亡。我们的报告表明,即使对于晚期难治性蕈样肉芽肿/赛塞里综合征患者,Campath-1H治疗也有活性。需要对更多患者进行进一步临床观察,以确定Campath-1H除了包括化疗在内的传统治疗外是否可作为一线治疗。