Complete remission in IgG kappa multiple myeloma with initially unfavorable prognosis after bortezomib-thalidomide-dexamethasone induction and autologous hematopoietic stem cell transplantation
DOI:
https://doi.org/10.5281/zenodo.21896222Keywords:
multiple myeloma, immunoglobulin G, autologous hematopoietic stem cell transplantation, residual neoplasm, remission induction, case reportAbstract
Introduction: Multiple myeloma is a hematologic neoplasm characterized by clonal proliferation of plasma cells in the bone marrow and production of a monoclonal immunoglobulin, with a usually aggressive clinical course when extensive bone disease is present.
Objective: To describe a case of IgG kappa multiple myeloma with multiple vertebral osteolytic lesions at diagnosis that achieved complete remission without minimal residual disease after induction and autologous hematopoietic stem cell transplantation.
Case presentation: We present the case of a 59-year-old man, former smoker, with no known baseline medical conditions, who had a six-month history of stabbing lumbar pain partially relieved by common analgesics, accompanied by 5 kg weight loss over the same period. Because symptoms persisted, laboratory studies and computed tomography of the chest, abdomen and pelvis were performed. Laboratory findings showed anemia, a monoclonal gamma peak on protein electrophoresis, elevated beta-2-microglobulin, positive immunofixation for IgG kappa monoclonal protein, and flow cytometry with a population of atypical monoclonal kappa plasma cells. Imaging showed disseminated vertebral osteolytic lesions with wedging. Multiple myeloma was confirmed and induction with bortezomib-thalidomide-dexamethasone was started, followed by autologous hematopoietic stem cell transplantation after mobilization and collection. The post-transplant course included transient neutropenia and thrombocytopenia resolving within the first ten days, self-limited diarrhea without mucositis, and associated hypocalcemia and hypokalemia. The patient was discharged in good general condition. Follow-up flow cytometry showed complete remission without evidence of minimal residual disease.
Conclusions: This case illustrates that an integrated diagnostic approach and timely induction and intensification therapy can achieve complete remission in multiple myeloma even when the initial presentation —with extensive bone disease— suggests an unfavorable prognosis, and it underscores the value of minimal residual disease as a marker of deep treatment response.
References
Kyle RA, Rajkumar SV. Multiple myeloma. N Engl J Med. 2004;351(18):1860-1873. https://doi.org/10.1056/NEJMra041875
Ríos R, Sánchez Rodríguez D, Sánchez Pérez MJ. Epidemiology of Multiple Myeloma. En: Update on Multiple Myeloma. IntechOpen; 2019. https://doi.org/10.5772/intechopen.75396
Kyle RA, Therneau TM, Rajkumar SV, Plevak MF, Melton LJ. Incidence of multiple myeloma in Olmsted County, Minnesota. Cancer. 2004;101(11):2667-2674. https://doi.org/10.1002/cncr.20652
Curado MP, Oliveira MM, Silva DRM, Souza DLB. Epidemiology of multiple myeloma in 17 Latin American countries: an update. Cancer Med. 2018;7(5):2101-2108. https://doi.org/10.1002/cam4.1347
Rajkumar SV, Dimopoulos MA, Palumbo A, Blade J, Merlini G, Mateos MV, et al. International Myeloma Working Group updated criteria for the diagnosis of multiple myeloma. Lancet Oncol. 2014;15(12):e538-e548. https://doi.org/10.1016/S1470-2045(14)70442-5
Durie BGM, Salmon SE. A clinical staging system for multiple myeloma correlation of measured myeloma cell mass with presenting clinical features, response to treatment, and survival. Cancer. 1975;36(3):842-854. https://doi.org/10.1002/1097-0142(197509)36:3%3C842::AID-CNCR2820360303%3E3.0.CO;2-U
Greipp PR, San Miguel J, Durie BGM, Crowley JJ, Barlogie B, Bladé J, et al. International staging system for multiple myeloma. J Clin Oncol. 2005;23(15):3412-3420. https://doi.org/10.1200/JCO.2005.04.242
Kaufman JL, Nooka AK, Vrana M, Levine B, Nain S, Lonial S, et al. Bortezomib, thalidomide, and dexamethasone as induction therapy for patients with symptomatic multiple myeloma. Cancer. 2010;116(13):3143-3151. https://doi.org/10.1002/cncr.25143
Palumbo A, Gay F, Falco P, Crippa C, Montefusco V, Patriarca F, et al. Bortezomib as induction before autologous transplantation, followed by lenalidomide as consolidation-maintenance in untreated multiple myeloma patients. J Clin Oncol. 2010;28(5):800-807. https://doi.org/10.1200/JCO.2009.22.7561
Mohty M, Malard F. Induction prior to autologous haematopoietic cell transplantation in multiple myeloma. Br J Haematol. 2024;205(6):2193-2197. https://doi.org/10.1111/bjh.19753
Steiner N. Induction therapy with bortezomib, thalidomide and dexamethasone (VTD) in Caucasian patients with multiple myeloma: a single center experience. J Blood Disord Transfus. 2015;6(4):296. https://doi.org/10.4172/2155-9864.1000296
Munshi NC, Avet-Loiseau H, Rawstron AC, Owen RG, Child JA, Thakurta A, et al. Association of minimal residual disease with superior survival outcomes in patients with multiple myeloma. JAMA Oncol. 2017;3(1):28-35. https://doi.org/10.1001/jamaoncol.2016.3160
Valdivieso-Herrera MA, Vargas-Ruiz LO, Morales D, Piscoya Rivera JA, del Carpio Jayo DR. Mieloma múltiple con osteoesclerosis difusa: reporte de caso. Gac Mex Oncol. 2016;15(3):177-180. https://doi.org/10.1016/j.gamo.2016.05.011
De la Peña-Celaya JA, Aguilar-Luévano J, Alcivar-Cedeño LM, Álvarez-Vera JL, Anaya-Cuellar I, Añorve-Hernández E, et al. Mexican Consensus of Multiple Myeloma. Gac Med Mex. 2023;156(92):1-49. https://doi.org/10.24875/gmm.m20000392
Borggrefe J, Giravent S, Campbell GM, Heller M, Panzer S, Kroeger H, et al. Association of osteolytic lesions, bone mineral loss and trabecular sclerosis with prevalent vertebral fractures in patients with multiple myeloma. Eur J Radiol. 2015;84(11):2269-2274. https://doi.org/10.1016/j.ejrad.2015.07.024
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Copyright (c) 2024 Fabiana Giménez Chamorro, Vivian Gayoso Álvarez, Nelly Gómez Larrosa, Isamar Fabiola Ferreira, Zara Escobar Benítez (Autor/a)

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