Chen Shuanggang, Zhang Xiaoshi, Shen Lujun, Qi Han, Ma Weimei, Cao Fei, Xie Lin, Song Ze, Wu Ying, Li Dandan, Wen Xizhi, Fan Weijun
Department of Minimally Invasive Interventional Therapy; Collaborative Innovation Center of Cancer Medicine, State Key Laboratory of Oncology in South China, Sun Yat-Sen University, Guangzhou, China.
Collaborative Innovation Center of Cancer Medicine, State Key Laboratory of Oncology in South China; Department of Biotherapy Center, Sun Yat-Sen University Cancer Center, Guangzhou, China.
J Cancer Res Ther. 2020;16(2):387-392. doi: 10.4103/jcrt.JCRT_75_20.
Primary anorectal malignant melanoma (ARMM) is an extremely rare but aggressive tumor. We assessed the efficacy and safety of transcatheter arterial infusion (TAI) with anti-PD-1 antibody pembrolizumab at a dosage of 100 mg with 0.9% NaCl at a volume of 100 mL administered over a 30-min period every 3 weeks, combined with temozolomide or albumin-bound paclitaxel (nab-paclitaxel) in four patients with ARMM. Temozolomide was administered orally once per day at a dosage of 200 mg/m2/d for five consecutive days about every 4 weeks. Nab-paclitaxel was administered at a dosage of 200mg/m2/d once about every 3 weeks. Among four patients with a median follow-up of 8.9 months, two cases showed Murine Double Minute 2 (MDM2) amplification. Case 1 with Stage II ARMM showed pathological complete response after four cycles of TAI with pembrolizumab combined with nab-paclitaxel. Case 4 was at Stage II and showed stable disease consistently throughout the treatment. Case 2 was at stage II and Case 3 was at stage III, and they showed partial response after four or three cycles, respectively, of TAI with pembrolizumab combined with temozolomide. No Grades 3-4 adverse reactions were observed. Therefore, a combination of TAI with pembrolizumab and temozolomide or with nab-paclitaxel appears to be a promising option for treating ARMM. However, multicenter clinical trials are required to confirm the efficacy and safety of this procedure.
原发性肛管恶性黑色素瘤(ARMM)是一种极其罕见但侵袭性很强的肿瘤。我们评估了经导管动脉灌注(TAI)联合抗程序性死亡蛋白1(PD-1)抗体帕博利珠单抗(剂量为100mg,溶入100mL 0.9%氯化钠溶液,每3周30分钟内输注完毕),并联合替莫唑胺或白蛋白结合型紫杉醇(纳米紫杉醇)治疗4例ARMM患者的疗效和安全性。替莫唑胺约每4周连续5天每天口服一次,剂量为200mg/m²/d。纳米紫杉醇约每3周一次,剂量为200mg/m²/d。4例患者中位随访8.9个月,其中2例显示鼠双微体2(MDM2)扩增。1例Ⅱ期ARMM患者在接受帕博利珠单抗联合纳米紫杉醇TAI治疗4个周期后出现病理完全缓解。4例患者为Ⅱ期,在整个治疗过程中病情持续稳定。2例患者为Ⅱ期,3例患者为Ⅲ期,分别在接受帕博利珠单抗联合替莫唑胺TAI治疗4个或3个周期后出现部分缓解。未观察到3-4级不良反应。因此,TAI联合帕博利珠单抗和替莫唑胺或纳米紫杉醇似乎是治疗ARMM的一个有前景的选择。然而,需要多中心临床试验来证实该治疗方法的疗效和安全性。