PMID- 37670301 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20231121 IS - 1475-2867 (Print) IS - 1475-2867 (Electronic) IS - 1475-2867 (Linking) VI - 23 IP - 1 DP - 2023 Sep 5 TI - Safety and efficacy of T-cell-redirecting bispecific antibodies for patients with multiple myeloma: a systematic review and meta-analysis. PG - 193 LID - 10.1186/s12935-023-03045-y [doi] LID - 193 AB - BACKGROUND: In recent years, several bispecific antibodies (BsAbs) have been introduced that revolutionized the treatment approach for patients with multiple myeloma (MM). In the present study, we sought for conducting a systematic review and meta-analysis with the aim of evaluating the safety and efficacy of BsAbs in MM patients. METHODS: PubMed, Scopus, Web of Science, and Embase databases were systematically searched on June 10, 2022. Two steps of title/abstract and full-text screening were performed for selecting the relevant articles. The primary endpoint was considered to evaluate the safety of BsAbs by examining the rate of hematologic and non-hematologic adverse effects (AEs). The secondary outcome was set at the efficacy of BsAbs through pooling objective response rate (ORR), (stringent) complete response (sCR/CR), very good partial response (VGPR), and partial response (PR). RESULTS: Eleven publications with a total of nine evaluable BsAbs were included for qualitative and quantitative data synthesis. Hematologic AEs were more common among patients than non-hematologic events, with the most frequent events being anemia (41.4%), neutropenia (36.4%), and thrombocytopenia (26.3%). The most common non-hematological AE was infection, which occurred in 39.9% of patients, followed by dysgeusia (28.3%), fatigue (26.5%), and diarrhea (25.8%). Besides, 8.1% of patients experienced immune effector cell-associated neurotoxicity syndrome and neurotoxicity occurred in 5.1% of them. Moreover, 59.8% of patients experienced cytokine release syndrome. The pooled rate of deaths attributable to BsAbs was estimated at 0.1%. In terms of efficacy measures, the ORR was achieved in 62.6% of MM patients, and the pooled rates of sCR/CR, VGPR, and PR were 22.7%, 23.0%, and 12.1%, respectively. CONCLUSIONS: In an era with several emerging promising treatments for MM, BsAbs have achieved a high ORR and tolerable AEs in heavily pretreated patients. However, there is still room for developing BsAbs with a lower rate of AEs and capable of bypassing tumor evasion mechanisms. CI - (c) 2023. BioMed Central Ltd., part of Springer Nature. FAU - Noori, Maryam AU - Noori M AD - Student Research Committee, School of Medicine, Iran University of Medical Sciences, Tehran, Iran. AD - Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Tehran, Iran. FAU - Yazdanpanah, Niloufar AU - Yazdanpanah N AD - Research Center for Immunodeficiencies, Children's Medical Center Hospital, Tehran University of Medical Sciences, Dr. Qarib St, Keshavarz Blvd, 14194, Tehran, Iran. AD - Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Tehran, Iran. AD - Student Research Committee, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran. FAU - Rezaei, Nima AU - Rezaei N AD - Research Center for Immunodeficiencies, Children's Medical Center Hospital, Tehran University of Medical Sciences, Dr. Qarib St, Keshavarz Blvd, 14194, Tehran, Iran. rezaei_nima@tums.ac.ir. AD - Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Tehran, Iran. rezaei_nima@tums.ac.ir. AD - Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran. rezaei_nima@tums.ac.ir. LA - eng PT - Journal Article PT - Review DEP - 20230905 PL - England TA - Cancer Cell Int JT - Cancer cell international JID - 101139795 PMC - PMC10478206 OTO - NOTNLM OT - Bispecific antibodies OT - BsAbs OT - Hematological OT - Multiple myeloma OT - Neutropenia OT - Relapse OT - anemia COIS- The authors declare no competing interests. EDAT- 2023/09/06 00:41 MHDA- 2023/09/06 00:42 PMCR- 2023/09/05 CRDT- 2023/09/05 23:43 PHST- 2023/06/24 00:00 [received] PHST- 2023/08/28 00:00 [accepted] PHST- 2023/09/06 00:42 [medline] PHST- 2023/09/06 00:41 [pubmed] PHST- 2023/09/05 23:43 [entrez] PHST- 2023/09/05 00:00 [pmc-release] AID - 10.1186/s12935-023-03045-y [pii] AID - 3045 [pii] AID - 10.1186/s12935-023-03045-y [doi] PST - epublish SO - Cancer Cell Int. 2023 Sep 5;23(1):193. doi: 10.1186/s12935-023-03045-y.