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多发性骨髓瘤患者的序贯性骨髓瘤性胸腔和心包积液:一例使用替雷利珠单抗实现长期生存的病例报告

Sequential Myelomatous Pleural and Pericardial Effusions in Multiple Myeloma: A Case Report Demonstrating Extended Survival with Teclistamab.

作者信息

Mudawi Deena, Al-Mashdali Abdulrahman F, Tawalbeh Ahmad, Szabados Lajos, Soliman Dina Sameh, Fareed Shehab

机构信息

Division of Hematology, Department of Medical Oncology, National Center for Cancer Care & Research (NCCCR), Hamad Medical Corporation (HMC), Doha, Qatar.

Department of Medical Education, Hamad Medical Corporation (HMC), Doha, Qatar.

出版信息

Case Rep Oncol. 2025 May 26;18(1):620-629. doi: 10.1159/000545930. eCollection 2025 Jan-Dec.

Abstract

INTRODUCTION

Myelomatous pleural effusion (MPE) and pericardial involvement are rare manifestations of multiple myeloma (MM), occurring in less than 1% of cases and carrying historically poor prognoses. We present a unique case where both these rare serous cavity manifestations occurred sequentially in the same patient, demonstrating the evolving treatment landscape with novel targeted therapies.

CASE PRESENTATION

A 42-year-old Asian female presented with left shoulder pain and swelling, leading to the diagnosis of IgG lambda MM with extensive extramedullary disease. After initial partial response to D-VRD therapy, she developed MPE with complete left lung collapse. Following failure of second-line KPD-PACE therapy, she received teclistamab, achieving complete metabolic and morphological response documented by PET-CT. After maintaining remission for 10 months, she experienced relapse with pericardial involvement presenting as cardiac tamponade.

CONCLUSION

The patient demonstrated an unprecedented response to BCMA-targeted therapy with teclistamab, achieving complete remission that lasted 10 months - more than doubling the historical median survival of 4 months for MPE. Flow cytometry proved instrumental in rapid diagnosis, showing 11% lambda monotypic plasma cells in the pleural fluid. The subsequent pericardial involvement after initial complete response highlighted the persistent challenges in managing extramedullary disease. This case represents the first documented instance of sequential MPE and pericardial involvement in MM, demonstrating the potential of novel targeted therapies, particularly BCMA-directed approaches, in extending survival and improving outcomes in these rare but aggressive disease manifestations.

摘要

引言

骨髓瘤性胸腔积液(MPE)和心包受累是多发性骨髓瘤(MM)的罕见表现,发生率低于1%,历史上预后较差。我们报告了一例独特的病例,同一患者先后出现了这两种罕见的浆膜腔表现,展示了新型靶向治疗带来的不断变化的治疗格局。

病例介绍

一名42岁的亚洲女性因左肩疼痛和肿胀就诊,被诊断为IgG λ型MM,伴有广泛的髓外疾病。在对D-VRD治疗初步产生部分反应后,她出现了MPE,左肺完全萎陷。二线KPD-PACE治疗失败后,她接受了替雷利珠单抗治疗,PET-CT显示达到了完全代谢和形态学缓解。在维持缓解10个月后,她复发并出现心包受累,表现为心脏压塞。

结论

该患者对靶向BCMA的替雷利珠单抗治疗表现出前所未有的反应,实现了持续10个月的完全缓解,这比MPE患者历史中位生存期4个月延长了一倍多。流式细胞术在快速诊断中发挥了重要作用,显示胸腔积液中11%为λ单型浆细胞。初始完全缓解后随后出现的心包受累突出了管理髓外疾病的持续挑战。该病例是MM患者先后出现MPE和心包受累的首个记录实例,证明了新型靶向治疗,特别是针对BCMA的治疗方法,在延长这些罕见但侵袭性疾病表现的生存期和改善预后方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe89/12105835/9a5df508e955/cro-2025-0018-0001-545930_F01.jpg

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