Durvalumab-Induced Immune Thrombocytopenia in Patients with Advanced Cholangiocarcinoma Undergoing Yttrium-90 Radioembolization.

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2024-10-18 eCollection Date: 2024-01-01 DOI:10.1159/000541550
Maaz Khan Afghan, Areeb Lutfi, Fatima Qadri, Sahrish Khan, Sana Javaid, Brian Michael Currie, Juan Pablo Rocca, Benjamin Samstein, Erika Hissong, Pashtoon Murtaza Kasi
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引用次数: 0

Abstract

Introduction: Immune thrombocytopenia (ITP) secondary to durvalumab, a programmed cell death ligand 1 inhibitor, is a rare but clinically significant immune-related adverse event. Herein, we present 2 patients with cholangiocarcinoma who developed ITP immediately post-yttrium-90 radioembolization (Y90-RE) while on durvalumab-based systemic therapy. We hypothesize that given the timing, the immunotherapy and the radioembolization combination led to this event. It is not uncommon given the approval of immunotherapy and its role in locoregional therapies, that patients are treated with a combination of systemic immunotherapy and radioembolization or other forms of radiation, thus signifying the importance of potential complications.

Case presentation: Two patients, a 67-year-old female and a 60-year-old man, with biopsy-proven advanced unresectable cholangiocarcinoma, received a combination of systemic therapy with durvalumab, gemcitabine, and cisplatin and subsequently Y90-RE. Both patients developed ITP following in the immediate post-Y90-RE period. All other causes of ITP were comprehensively ruled out and treatment for ITP was initiated in the form of high-dose steroid and intravenous immunoglobulins. Durvalumab was discontinued, and only gemcitabine/cisplatin-based chemotherapy was continued thereafter. Due to recurrence, one of the patients required longer courses of steroids as well as thrombopoietin receptor agonists.

Conclusion: Immunotherapy in the form of durvalumab and now pembrolizumab alongside chemotherapy is an approved first-line standard of care. Furthermore, it is not uncommon for patients to receive Y90-RE to improve patient outcomes. This report highlights the development of ITP in 2 patients who received durvalumab alongside Y90-RE. Awareness of this as a potential immune-mediated event is important to allow for close monitoring of platelet counts and for early intervention/management when this occurs.

接受钇-90放射栓塞治疗的晚期胆管癌患者中杜伐单抗诱发的免疫性血小板减少症
简介:免疫性血小板减少症(ITP)继发于程序性细胞死亡配体 1 抑制剂 durvalumab,是一种罕见但具有临床意义的免疫相关不良事件。在本文中,我们介绍了两名胆管癌患者,他们在接受以杜瓦鲁单抗为基础的全身治疗期间,在钇-90放射栓塞术(Y90-RE)后立即出现了ITP。我们推测,由于时间关系,免疫疗法和放射栓塞疗法的结合导致了这一事件的发生。鉴于免疫疗法的批准及其在局部治疗中的作用,患者同时接受全身免疫疗法和放射栓塞或其他形式的放射治疗的情况并不少见,这表明潜在并发症的重要性:两名经活检证实患有晚期不可切除胆管癌的患者(女性,67 岁;男性,60 岁)接受了杜瓦单抗、吉西他滨和顺铂联合全身治疗,随后又接受了 Y90-RE 治疗。两名患者都在Y90-RE后立即出现了ITP。在全面排除了所有其他ITP病因后,开始以大剂量类固醇和静脉注射免疫球蛋白的形式治疗ITP。停用了 Durvalumab,此后只继续进行以吉西他滨/顺铂为基础的化疗。由于复发,其中一名患者需要使用更长疗程的类固醇和血小板生成素受体激动剂:结论:以durvalumab和现在的pembrolizumab为形式的免疫疗法与化疗一起使用,是已获批准的一线标准治疗方法。此外,患者接受Y90-RE治疗以改善患者预后的情况并不少见。本报告重点介绍了2例在接受Y90-RE的同时接受durvalumab治疗的患者发生ITP的情况。认识到这是一种潜在的免疫介导事件非常重要,以便密切监测血小板计数,并在出现这种情况时及早干预/处理。
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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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
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