Pranav Pramod Patwardhan, Joseph Franz, Mounzer Agha, Bryan Rea
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引用次数: 0
摘要
目的:本研究试图分析抗 B 细胞成熟抗原(BCMA)嵌合抗原受体(CAR)T 细胞输注后的骨髓检查结果及其与全血细胞减少症的相关性:研究了 12 例接受抗 BCMA CAR T 细胞治疗的患者的相关临床病理数据,包括全血细胞计数、中性粒细胞计数、相关治疗史以及治疗前后的骨髓评估:结果:12 例患者中有 6 例在接受 CAR T 细胞疗法后进行了骨髓检查,其中 3 例患者的骨髓细胞明显减少,造血功能明显减弱或基本丧失。一个病例显示骨髓细胞减少,但有三系造血,其余两个病例显示浆细胞骨髓瘤持续受累。网织红细胞染色未发现明显的纤维化。治疗后第90天,10名患者出现贫血,8名患者出现白细胞和血小板减少。长期随访显示,12例患者中有10例病情持续存在:大多数患者在接受BCMA CAR T细胞治疗后会出现长期细胞减少症,骨髓评估显示相关的细胞明显减少,造血功能极低或没有,但纤维化没有增加。
Persistent cytopenias after anti-BCMA CAR T-cell therapy are associated with reduced hematopoietic activity in posttreatment bone marrows.
Objectives: We attempt to analyze bone marrow findings and correlation with cytopenia(s) after anti-B-cell maturation antigen (BCMA) chimeric antigen receptor (CAR) T-cell infusion in this study.
Methods: Relevant clinicopathologic data, including complete blood counts, neutrophil counts, relevant therapy history, and pre- and posttherapy bone marrow evaluations, were studied in 12 patients who received anti-BCMA CAR T-cell therapy.
Results: Bone marrow findings after CAR T-cell therapy were available in 6 of 12 cases, 3 of which showed markedly hypocellular marrow with either markedly reduced or essentially absent hematopoiesis. One case showed a hypocellular marrow with trilineage hematopoiesis, while the remaining 2 cases showed persistent involvement by plasma cell myeloma. Reticulin stains did not reveal significant fibrosis. Ten patients had anemia, and 8 patients had leukopenia and thrombocytopenia at day 90 posttherapy. Long-term follow-up showed persistent disease in 10 of 12 cases.
Conclusions: Prolonged cytopenias occur in most patients after BCMA CAR T-cell therapy with bone marrow evaluations demonstrating associated marked hypocellularity with minimal or no hematopoiesis without an increase in fibrosis.