[1] Fonseca R, Abouzaid S, Bonafede M, et al. Trends in overall survival and costs of multiple myeloma, 2000-2014 [J]. Leukemia, 2017, 31(9): 1915-1921. [2] Gay F, Oliva S, Petrucci M T, et al. Chemotherapy plus lenalidomide versus autologous transplantation, followed by lenalidomide plus prednisone versus lenalidomide maintenance, in patients with multiple myeloma: a randomised, multicentre, phase 3 trial [J]. Lancet Oncol, 2015, 16(16): 1617-1629. [3] Attal M, Lauwers-Cances V, Hulin C, et al. Lenalidomide, bortezomib, and dexamethasone with transplantation for myeloma [J]. N Engl J Med, 2017, 376(14): 1311-1320. [4] Moreau P, San Miguel J, Sonneveld P, et al. Multiple myeloma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up [J]. Ann Oncol, 2017, 28(suppl 4): iv52-iv61. [5] Rajkumar S V, Kumar S. Multiple myeloma: diagnosis and treatment [J]. Mayo Clin Proc, 2016, 91(1): 101-119. [6] Kumar S K, Callander N S, Adekola K, et al. Multiple myeloma, Version 3.2021, NCCN clinical practice guidelines in oncology [J]. J Natl Compr Canc Netw, 2020, 18(12): 1685-1717. [7] International Myeloma Working G. Criteria for the classification of monoclonal gammopathies, multiple myeloma and related disorders: a report of the International Myeloma Working Group [J]. Br J Haematol, 2003, 121(5): 749-757. [8] Rajkumar S V, Dimopoulos M A, Palumbo A, et al. International Myeloma Working Group updated criteria for the diagnosis of multiple myeloma [J]. Lancet Oncol, 2014, 15(12): e538-548. [9] Durie B G, Harousseau J L, Miguel J S, et al. International uniform response criteria for multiple myeloma [J]. Leukemia, 2006, 20(9): 1467-1473. [10] Anderson K C, Kyle R A, Rajkumar S V, et al. Clinically relevant end points and new drug approvals for myeloma [J]. Leukemia, 2008, 22(2): 231-239. [11] Jackson G H, Davies F E, Pawlyn C, et al. Response-adapted intensification with cyclophosphamide, bortezomib, and dexamethasone versus no intensification in patients with newly diagnosed multiple myeloma (Myeloma XI): a multicentre, open-label, randomised, phase 3 trial [J]. Lancet Haematol, 2019, 6(12): e616-e629. [12] Figueiredo A, Atkins H, Mallick R, et al. Cyclophosphamide-bortezomib-dexamethasone compared with bortezomib-dexamethasone in transplantation-eligible patients with newly diagnosed multiple myeloma [J]. Curr Oncol, 2020, 27(2): e81-e85. [13] Einsele H, Engelhardt M, Tapprich C, et al. Phase II study of bortezomib, cyclophosphamide and dexamethasone as induction therapy in multiple myeloma: DSMM XI trial [J]. Br J Haematol, 2017, 179(4): 586-597. [14] Rosinol L, Oriol A, Rios R, et al. Bortezomib, lenalidomide, and dexamethasone as induction therapy prior to au-tologous transplant in multiple myeloma [J]. Blood, 2019, 134(16): 1337-1345. [15] Uttervall K, Borg Bruchfeld J, Gran C, et al. Upfront bortezomib, lenalidomide, and dexamethasone compared to bortezomib, cyclophosphamide, and dexamethasone in multiple myeloma [J]. Eur J Haematol, 2019, 103(3): 247-254. [16] Dosani T, Covut F, Pinto R, et al. Impact of lenalidomide on collected hematopoietic myeloid and erythroid progenitors: peripheral stem cell collection may not be affected [J]. Leuk Lymphoma, 2019, 60(9): 2199-2206. [17] Paripati H, Stewart A K, Cabou S, et al. Compromised stem cell mobilization following induction therapy with lenalidomide in myeloma [J]. Leukemia, 2008, 22(6): 1282-1284. [18] Laurent V, Fronteau C, Antier C, et al. Autologous stem-cell collection following VTD or VRD induction therapy in multiple myeloma: a single-center experience [J]. Bone Marrow Transplant, 2021, 56(2): 395-399. |