Effect of Chemotherapy with Alkylating Agents on the Yield of CD34+ Cells in Patients with Multiple Myeloma. Results of the Spanish Myeloma Group (GEM) Study
Overview
Authors
Affiliations
Background And Objectives: Although alkylating agents are clearly beneficial in multiple myeloma (MM), their deleterious effect on bone marrow hematopoietic progenitor cells usually precludes their use as front-line therapy in patients scheduled to undergo autologous stem cell transplantation (ASCT). We analyzed the impact of first-line chemotherapy with alkylating agents on stem cell collection in MM patients.
Design And Methods: Seven hundred and eighty-nine patients included in the Spanish multicenter protocol GEM-2000 underwent mobilization therapy after four courses of alternating VBMCP/VBAD chemotherapy.
Results: The mobilization regimens consisted of standard or high-dose granulocyte colony-stimulating factor (G-CSF) in 551 (70%) patients, and chemotherapy and G-CSF in 206 (26%) patients. The CD34+ cell yield was lower than 4x10(6)/kg in 388 patients (49%), and equal or greater than 4x10(6)/kg in 401 patients (51%). Multivariate analysis indicated that advanced age (p<0.0001) and longer interval between diagnosis and mobilization (p=0.012) were the two variables associated with a lower CD34+ cell yield. Significant differences in CD34+ cell yield were not observed between the mobilization regimens. Of the 789 patients included in the protocol, 726 (92%) underwent the planned ASCT, whereas 25 (3%) patients did not because of the low number of CD34+ cells collected. Following ASCT, 0.5x10(9) neutrophils/L could be recovered after 11 days (median time; range, 5-71 days) and 20x10(9) platelets/L could be recovered after 12 days (median time; range, 6-69 days).
Interpretation And Conclusions: A short-course of therapy with alkylating agents according to the GEM-2000 protocol was associated with an appropriate CD34+ cell collection, and allowed the planned ASCT to be performed in the majority of MM patients.
Lemieux C, Muffly L, Iberri D, Craig J, Johnston L, Lowsky R Bone Marrow Transplant. 2021; 56(11):2664-2671.
PMID: 34163014 PMC: 8715953. DOI: 10.1038/s41409-021-01371-1.
Wang L, Xiang H, Yan Y, Deng Z, Li H, Li X Ann Hematol. 2021; 100(2):563-573.
PMID: 33404694 PMC: 7817584. DOI: 10.1007/s00277-020-04376-w.
Outcomes and Cost-Effectiveness of Autologous Hematopoietic Cell Transplant for Multiple Sclerosis.
Dunn-Pirio A, Heyman B, Kaufman D, Kinkel R Curr Treat Options Neurol. 2019; 21(10):53.
PMID: 31624926 DOI: 10.1007/s11940-019-0588-8.
Sunami K, Matsumoto M, Fuchida S, Omoto E, Takamatsu H, Adachi Y Int J Clin Oncol. 2019; 24(8):966-975.
PMID: 30937622 DOI: 10.1007/s10147-019-01436-8.
Song G, Jung S, Ahn S, Jung S, Yang D, Ahn J BMC Cancer. 2019; 19(1):59.
PMID: 30642286 PMC: 6332580. DOI: 10.1186/s12885-019-5285-1.