[The efficacy and safety of daratumumab in relapsed and refractory multiple myeloma].

Autor: Liu J; Department of Hematology, Changzheng Hospital, the Second Military Medical University, Shanghai 200003, China., He HY; Department of Hematology, Changzheng Hospital, the Second Military Medical University, Shanghai 200003, China., Li L; Department of Hematology, Changzheng Hospital, the Second Military Medical University, Shanghai 200003, China., Lu J; Department of Hematology, Changzheng Hospital, the Second Military Medical University, Shanghai 200003, China., Qiang WT; Department of Hematology, Changzheng Hospital, the Second Military Medical University, Shanghai 200003, China., Guo P; Department of Hematology, Changzheng Hospital, the Second Military Medical University, Shanghai 200003, China., Hou N; Department of Hematology, Changzheng Hospital, the Second Military Medical University, Shanghai 200003, China., Jiang H; Department of Hematology, Changzheng Hospital, the Second Military Medical University, Shanghai 200003, China., Du J; Department of Hematology, Changzheng Hospital, the Second Military Medical University, Shanghai 200003, China., Fu WJ; Department of Hematology, Changzheng Hospital, the Second Military Medical University, Shanghai 200003, China.
Jazyk: čínština
Zdroj: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi [Zhonghua Xue Ye Xue Za Zhi] 2021 Jan 14; Vol. 42 (1), pp. 27-32.
DOI: 10.3760/cma.j.issn.0253-2727.2021.01.006
Abstrakt: Objective: To investigate the efficacy and safety of daratumumab in relapsed and refractory multiple myeloma (RRMM) . Methods: The clinical characteristics, adverse reactions, efficacy, and prognosis of 46 patients with RRMM treated with daratumumab in Shanghai Changzheng Hospital from September 2017 to March 2020 were retrospectively analyzed. Results: All patients were treated with daratumumab-based regimen: 8 in the Dd group, 35 in the DRd group, and 3 in the DVd group. With a median follow-up of 9.6 months, the overall response rate (ORR) was 75% [complete remission (CR) rate 18.2% ] among the 44 patients available for evaluation. The ORRs of patients resistant to bortezomib, lenalidomide, and both were 70.6% , 69.2% , and 63.6% , respectively. The CR rates of patients resistant to bortezomib, lenalidomide, and both were 17.6% , 11.5% , and 13.6% , respectively. No significant difference was observed in ORR and CR rates among the three groups. The ORRs of the DRd, DVd, and Dd groups were 85.3% , 66.7% , and 28.6% , respectively ( P =0.007) . The median PFS of 46 patients was 8.9 months, the median OS was not reached, and the 1-year OS rate was 74% . The median PFS and OS in the DRd group were longer than those in the Dd group (PFS: 14.4 months vs 2.0 months; OS: not reached vs 5.2 months) . After treatment with daratumumab, neutropenia is the most common hematological adverse reaction above grade 3. Non-hematological adverse reactions are mainly infusion-related adverse reactions and infections. Prognostic analysis showed that patients with extramedullary invasion had shorter PFS and OS compard with patients without extramedullary invasion (PFS: 5.7 vs 14.4 months, P =0.033; OS: 6.3 months vs not reached, P =0.029) . The OS of patients with an ECOG score of 3-4 was significantly shorter than patients with an ECOG score of 1-2 (5.9 months vs not reached, P =0.004) . Conclusion: Daratumumab-based regimens have good efficacy and safety in the treatment of RRMM.
Databáze: MEDLINE