Benefits of BV-AVD (Brentuximab vedotin, doxorubicin, vinblastine, and dacarbazine) versus ABVD (doxorubicin hydrochloride, bleomycin sulfate, vinblastine sulfate, dacarbazine) in patients with advanced-stage Hodgkin's lymphoma: an analysis of the ECHELON 1 trial by the GATLA group using the Delphi Method.

Astrid Pavlovsky, Juan Ignacio Garcia Altuve, Amalia Cerutti, Lorena Fiad, Nicolás Kurgansky, Fernando Warley, Florencia Negri Aranguren
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Abstract

Introduction: The BV-AVD (Brentuximab vedotin, doxorubicin, vinblastine, and dacarbazine) combination for first-line treatment of advanced stage Hodgkin's lymphoma has been approved by regulatory authorities and included in international guidelines. However, several factors influence its incorporation as standard of care.

Materials and methods: A group of experts from different institutions was identified and, using the Delphi method, an analysis of the results of the ECHELON 1 trial for the indication of BV-AVD over ABVD (doxorubicin hydrochloride, bleomycin sulfate, vinblastine sulfate, dacarbazine) in patients with Hodgkin's lymphoma Stages III and IV in Argentina was done. The clinical and academic experience of the authors and the context of the Argentine healthcare system were considered.

Results and discussion: Seven statements on general aspects of the management of Hodgkin's lymphoma and nine on specific aspects related to the use of BV-AVD over ABVD reached a consensus of agreement. There was a strong expert consensus in favor of indicating BV-AVD in the presence of extranodal disease or pulmonary disease. Moderate to severe neuropathy, pregnancy and drug allergy were considered absolute contraindications to prescribe BV.

Conclusions: The authors agreed that BV-AVD could be considered a new treatment option in high-risk patients. However health system-dependent factors (such as high cost, lack of availability, reimbursement difficulties, irregular delivery, and issues with granulocyte-colony stimulating factor availability) could pose limitations for this prescription. While awaiting new data from clinical trials and real-world studies, these recommendations can represent a useful tool for hematologists in different parts of the world.

BV-AVD(布伦妥昔单抗韦多汀、多柔比星、长春新碱和达卡巴嗪)与 ABVD(盐酸多柔比星、硫酸博来霉素、硫酸长春新碱和达卡巴嗪)对晚期霍奇金淋巴瘤患者的益处:GATLA 小组使用德尔菲法对 ECHELON 1 试验进行的分析。
简介BV-AVD (Brentuximab vedotin、多柔比星、长春新碱和达卡巴嗪)联合疗法用于晚期霍奇金淋巴瘤的一线治疗,已获得监管机构批准并被纳入国际指南。然而,有几个因素影响着它被纳入标准治疗:确定了一个由来自不同机构的专家组成的小组,并采用德尔菲法分析了 ECHELON 1 试验的结果,该试验的目的是在阿根廷的霍奇金淋巴瘤 III 期和 IV 期患者中将 BV-AVD 用于 ABVD(盐酸多柔比星、硫酸博来霉素、硫酸长春新碱、达卡巴嗪)的适应症。研究考虑了作者的临床和学术经验以及阿根廷医疗系统的背景:就霍奇金淋巴瘤管理的一般方面有七项声明,就使用 BV-AVD 而非 ABVD 的具体方面有九项声明达成了一致意见。专家们一致赞成在出现结节外疾病或肺部疾病时使用 BV-AVD。中度至重度神经病变、妊娠和药物过敏被视为开具 BV 的绝对禁忌症:作者们一致认为,BV-AVD 可被视为高危患者的一种新的治疗选择。然而,医疗系统的相关因素(如费用高昂、缺乏可用性、报销困难、不规则分娩以及粒细胞集落刺激因子的可用性问题)可能会限制这种处方的使用。在等待来自临床试验和实际研究的新数据的同时,这些建议可为世界各地的血液学专家提供有用的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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