Prognostic implications of splenomegaly in BCMA-directed CAR T-Cell therapy for relapsed myeloma.

IF 3.6 3区 医学 Q2 HEMATOLOGY
Thomas Wiemers, Maximilian Ferle, Jonas Ader, Veronika Sotikova, David Fandrei, Nora Grieb, Luise Fischer, Patrick Born, Heike Weidner, Song Yau Wang, Madlen Jentzsch, Georg-Nikolaus Franke, Carmen Herling, Klaus Metzeler, Marco Herling, Simone Heyn, Timm Denecke, Kristin Reiche, Uwe Platzbecker, Vladan Vucinic, Thomas Neumuth, Hans-Jonas Meyer, Maximilian Merz
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Abstract

Background: B-cell maturation antigen (BCMA)-directed chimeric antigen receptor (CAR) T-cell therapy has shown significant promise for patients with relapsed or refractory multiple myeloma (RRMM). Despite its efficacy, treatment is frequently complicated by adverse events such as cytokine release syndrome and hematologic toxicities, including severe thrombocytopenia. Identifying reliable prognostic markers is essential to improve patient risk stratification, optimizing treatment strategies, and managing complications effectively. While various prognostic markers have been explored, spleen size has not been extensively studied in this context.

Objective: This study aims to evaluate spleen size as a prognostic marker in RRMM patients receiving CAR T-cell therapy. Specifically, we examine its association with thrombocytopenia, metabolic tumor volume, soluble BCMA (sBCMA) levels, progression-free survival (PFS), and overall survival (OS). Additionally, we compare spleen size to other established prognostic markers, including sBCMA, EASIX, and CAR-HEMATOTOX scores, to determine its predictive value.

Study design: Data from RRMM patients (N=73) treated with either Idecabtagene vicleucel or Ciltacabtagen autoleucel were analyzed. The association of spleen size, assessed via computed tomography imaging, with clinical outcomes was analyzed.

Results: Splenomegaly (spleen size > 340 cm³) was found to be significantly associated with severe and prolonged thrombocytopenia, higher metabolic tumor volumes, and elevated sBCMA levels. In our cohort, splenomegaly emerged as an independent prognostic factor for both PFS and OS, showing stronger associations than other markers such as sBCMA, EASIX, and CAR-HEMATOTOX scores.

Conclusions: Spleen size may serve as a promising prognostic marker in CAR T-cell therapy for RRMM patients, providing a simple and readily accessible tool for enhancing risk stratification. This finding could inform monitoring strategies and optimize healthcare resource management for these patients.

脾肿大在bcma定向CAR - t细胞治疗复发性骨髓瘤中的预后意义。
背景:b细胞成熟抗原(BCMA)靶向嵌合抗原受体(CAR) t细胞疗法对复发或难治性多发性骨髓瘤(RRMM)患者显示出显著的前景。尽管其疗效显著,但治疗中经常出现不良事件,如细胞因子释放综合征和血液学毒性,包括严重的血小板减少症。确定可靠的预后标记对于改善患者风险分层、优化治疗策略和有效管理并发症至关重要。虽然已经探索了各种预后标志物,但脾脏大小尚未在此背景下进行广泛研究。目的:本研究旨在评估脾脏大小作为接受CAR - t细胞治疗的RRMM患者的预后指标。具体来说,我们研究了它与血小板减少症、代谢性肿瘤体积、可溶性BCMA (sBCMA)水平、无进展生存期(PFS)和总生存期(OS)的关系。此外,我们将脾脏大小与其他已建立的预后指标(包括sBCMA、EASIX和CAR-HEMATOTOX评分)进行比较,以确定其预测价值。研究设计:对接受Idecabtagene vicleucel或Ciltacabtagen autotolucel治疗的RRMM患者(N=73)的数据进行分析。通过计算机断层成像评估脾脏大小与临床结果的关系进行了分析。结果:脾肿大(脾体积约为340cm³)与严重和延长的血小板减少症、较高的代谢性肿瘤体积和升高的sBCMA水平显著相关。在我们的队列中,脾肿大成为PFS和OS的独立预后因素,与sBCMA、EASIX和CAR-HEMATOTOX评分等其他指标相比,其相关性更强。结论:脾脏大小可能作为一种有希望的RRMM患者CAR - t细胞治疗预后指标,提供了一种简单且易于获取的工具来加强风险分层。这一发现可以为这些患者的监测策略提供信息,并优化医疗资源管理。
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
7.00
自引率
15.60%
发文量
1061
审稿时长
51 days
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