Assessment of Effectiveness and Adverse Effect of New Combination Chemotherapy (irinotecan, cisplatin, and dexamethasone) in Relapse and Refractory Hodgkin Lymphoma.

Mahdi Tabarraee, Atefeh Rezaee, Sara Abolghasemi, Mojtaba Ghadiany, Maria Tavakoli Ardakani, Mahshid Mahdizadeh, Neda Hamidi, Katayoon Ghasemi
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Abstract

Background: Chemotherapy with Adriamycin, Bleomycin, Vinblastine, and Dacarbazine (ABVD regimen) cannot cure all patients with Hodgkin lymphoma. In this study, we evaluated the efficacy and adverse effect of a new regimen consist Irinotecan, Cisplatin, and Dexamethasone (ICD) in relapsed and refractory Hodgkin lymphoma as the second to fifth line of treatment. Materials and Methods: We performed a retrospective study in 26 relapsed or refractory patients with Hodgkin lymphoma receiving at least the first-line chemotherapy regimen (ABVD) and (ICD) as salvage therapy in Thaleghany Hospital from 2012 to 2018. This regimen consisted of Irinotecan 65mg/m2 D1, D8, Cisplatin 30mg/m2 D1, D8, and dexamethasone 40mg D1, 2, 8, and 9 was administered every 3 weeks for 6 cycles.  Treatment was discontinued in cases of disease progression or severe toxicity. Response to treatment was evaluated after two cycles. Patients with complete and partial remission were candidates for high-dose chemotherapy and autologous stem cell transplantation. Twenty-four patients were enrolled in the study. The mean age of 22 patients was 31.5 (19-67) years. Seven patients (29.1%) were in the first recurrence, and 17 (70.8%) were in the second or subsequent recurrence. Results: According to this study, three patients (12.5%) had complete response, 13 (45%) had partial response, four (16.6%) had stable disease, and four (16.6%) had progressive disease. Nine patients (37.5%) received high-dose chemotherapy and autologous stem cell support after ICD regimen. None of the cycles of chemotherapy were delayed due to treatment-related adverse event. Overall survival after six months in all patients was 91%, and mortality rate was 8.3% at the end of the study. Conclusion: The goal of salvage chemotherapy in relapsed or refractory Hodgkin Lymphoma is achieving CR or PR preparation patients for stabilization with BMT. Thus, we recommend ICD as one of the most effective protocols with overall response rate of 66% in this population.

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新联合化疗(伊立替康、顺铂和地塞米松)治疗复发性和难治性霍奇金淋巴瘤的疗效和不良反应评估。
背景:阿霉素、博莱霉素、长春碱和达卡巴嗪(ABVD方案)化疗不能治愈所有霍奇金淋巴瘤患者。在这项研究中,我们评估了伊立替康、顺铂和地塞米松(ICD)作为第二至第五线治疗复发和难治性霍奇金淋巴瘤的新方案的疗效和不良反应。材料和方法:我们对2012年至2018年在Thaleghany医院接受至少一线化疗方案(ABVD)和(ICD)作为挽救治疗的26名复发或难治性霍奇金淋巴瘤患者进行了回顾性研究。该方案由伊立替康65mg/m2 D1、D8、顺铂30mg/m2 D1、CD8和地塞米松40mg D1、2、8和9组成,每3周给药6个周期。在疾病进展或严重毒性的情况下停止治疗。两个周期后评估对治疗的反应。完全和部分缓解的患者是大剂量化疗和自体干细胞移植的候选者。24名患者参与了这项研究。22例患者的平均年龄为31.5(19-67)岁。7名患者(29.1%)首次复发,17名患者(70.8%)第二次或随后复发。结果:根据这项研究,3名患者(12.5%)有完全缓解,13名患者(45%)有部分缓解,4名患者(16.6%)病情稳定,4名(166%)病情进展。9名患者(37.5%)在ICD方案后接受了大剂量化疗和自体干细胞支持。没有一个化疗周期因治疗相关的不良事件而延迟。研究结束时,所有患者6个月后的总生存率为91%,死亡率为8.3%。结论:复发或难治性霍奇金淋巴瘤的挽救性化疗的目标是使CR或PR准备患者用BMT稳定下来。因此,我们推荐ICD作为最有效的方案之一,在该人群中总有效率为66%。
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