Vainstein Vladimir, Avni Batia, Grisariu Sigal, Kfir-Erenfeld Shlomit, Asherie Nathalie, Nachmias Boaz, Auman Shlomtzion, Saban Revital, Zimran Eran, Assayag Miri, Filanovsky Kalman, Horowitz Netanel A, Lebel Eyal, Shaulov Adir, Gur Michal, Rosenbluh Chaggai, Krichevsky Svetlana, Stepensky Polina, Gatt Moshe E
Department of Hematology, Hadassah Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem 91121, Israel.
Department of Bone Marrow Transplantation and Cancer Immunotherapy, Hadassah Medical Center, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem 91121, Israel.
Cancers (Basel). 2023 Jul 3;15(13):3471. doi: 10.3390/cancers15133471.
Multiple myeloma (MM) is characterized by recurrent relapses. Consequently, patients receive multiple therapy lines, including alkylating agents and immune modulators, which have been associated with secondary malignancies such as myelodysplastic syndrome (MDS). Anti-B-cell maturation antigen (BCMA) chimeric antigen receptor T cell (CART) therapy is efficacious in patients with relapsed/refractory (R/R) MM. However, the long-term complications, particularly MDS, are not well understood. Whether CART therapy causes or promotes MDS has not been thoroughly investigated. In this study, we explored the causal relationship between MDS and CART therapy. We retrospectively examined the prevalence of MDS-related morphological and mutational changes before and after administration of CART therapy in five patients. Among them, four developed MDS after CART therapy, while one had pre-existing MDS prior to CART. None of the four patients who developed post-CART MDS showed morphological MDS changes prior to CART therapy. However, all four patients exhibited molecular alterations associated with MDS in their pre-CART as well as post-CART therapy bone marrow. No new mutations were observed. Our findings provide initial evidence suggesting that anti-BCMA CART therapy in MM may promote expansion of pre-existing MDS clones rather than causing development of new clones.
多发性骨髓瘤(MM)的特点是反复复发。因此,患者会接受多线治疗,包括烷化剂和免疫调节剂,这些治疗与继发性恶性肿瘤如骨髓增生异常综合征(MDS)有关。抗B细胞成熟抗原(BCMA)嵌合抗原受体T细胞(CART)疗法对复发/难治性(R/R)MM患者有效。然而,其长期并发症,尤其是MDS,目前尚不清楚。CART疗法是否会导致或促进MDS尚未得到充分研究。在本研究中,我们探讨了MDS与CART疗法之间的因果关系。我们回顾性检查了5例患者在接受CART治疗前后MDS相关形态学和突变变化的发生率。其中,4例在CART治疗后发生MDS,而1例在CART治疗前就已存在MDS。4例CART治疗后发生MDS的患者在CART治疗前均未出现MDS形态学改变。然而,所有4例患者在CART治疗前及治疗后的骨髓中均表现出与MDS相关的分子改变。未观察到新的突变。我们的研究结果提供了初步证据,表明MM中的抗BCMA CART疗法可能促进已存在的MDS克隆的扩增,而不是导致新克隆的产生。