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来那度胺治疗复发难治性多发性骨髓瘤57例临床观察

OBJECTIVE: To investigate the clinical efficacy and safety of lenalidomide (Revlimid, R) - based chemotherapy in the treatment of relapsed/refractory multiple myeloma (MM) patients. METHODS: 57 consecutively relapsed/refractory MM patients were retrospectively analyzed from June 2013 to February 201...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342977/
https://www.ncbi.nlm.nih.gov/pubmed/28655091
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2017.06.005
Descripción
Sumario:OBJECTIVE: To investigate the clinical efficacy and safety of lenalidomide (Revlimid, R) - based chemotherapy in the treatment of relapsed/refractory multiple myeloma (MM) patients. METHODS: 57 consecutively relapsed/refractory MM patients were retrospectively analyzed from June 2013 to February 2016. All the patients received lenalidomide-based chemotherapy. RESULTS: ①60.4% patients had international staging system (ISS) stage Ⅲ, 37.9% patients had revised international staging system (R-ISS) stage Ⅲ, and 53.3% patients harbored at least one of the high-risk cytogenetic abnormalities[del (17p) and/or t(4;14) and/or t(14;16)]. ②The patients received median 6 cycles of R (range: 1–32). The overall response rate (ORR) was 58.9% (33/56), among which 8.9% was complete response (CR), 19.8% was very good partial response (VGPR), and 30.4% was partial response (PR). In addition, 10.7% patients attained minor response (MR). Total clinical benefit was 69.6%. Patients with more than 1 line of prior therapy, or previously thalidomide-resistance, or R-ISS stage Ⅲ disease showed significantly lower ORR. ③With a median follow-up of 27 months, the median progression free survival (PFS), the median interval to PR, the median duration of response (DOR), and the median overall survival (OS) was 8 months, 2 months, 8 months, and 19 months, respectively. Univariate prognostic analysis showed that abnormal karyotype, R-ISS stage Ⅲ and response inferior to PR were negative prognostic factors for PFS and OS. While the multivariate prognostic analysis showed that abnormal karyotype and R-ISS stage Ⅲ were independent prognostic factors. ④In the safety aspect, the most common grade 3–4 non-hematology adverse events (AEs) were infection (17.5%), rash (1.8%) and thromboembolism (1.8%), and the most common grade 3–4 hematology AEs were neutropenia (7.0%) and thrombocytopenia (3.5%). Totally 3 patients (5.3%) discontinued R because of AEs, and 2 cases (3.5%) of secondary primary malignancies were observed. CONCLUSION: The R-based treatment is effective and safe in the treatment of relapsed/refractory MM patients in China. Abnormal karyotype and R-ISS stage Ⅲ were independent negative prognosis factors in this cohort.