Objectives: To describe the clinical and subclinical characteristics of patients with multiple
myeloma. Subjects and methods: A retrospective and prospective descriptive study on 96 patients
with multiple myeloma diagnosed, treated and autologous stem cell transplantation at the Ho Chi
Minh City Blood Transfusion Hematology Hospital from 2018 to 2021. Results: The most common
form of multiple myeloma was monoclonal IgG (62.8%), followed by IgA monoclonal increase
(18.75%) and light chain (18.75%). The group of multiple myeloma patients in stage II accounted
for the highest percentage (69.8%), followed by stage I (18.7%). The number of patients hospitalized
in stage III accounted for the lowest rate (11.5%). The mean hemoglobin concentration was 94.1 ±
20.4 (g/l), white blood cell count (6.42 ± 2.38 G/l), platelet count (186.4 ± 75.3 G/l) l), bone marrow
cell count (71.16 ± 68.7 G/l), percentage of plasma cell lineage in the marrow (35.6 ± 21.3 %). IgG
(6281.0 ± 2938.6 mg/L), IgA (3521.4 ± 1405.3 mg/L), Free Kappa (1201.5 ± 1422.1), Free Lambda
(2194.7 ± 2421) ,1), ß2 microglobulin (4.24 ± 6.67 mg/L). Conclusion: The most common type of
multiple myeloma was monoclonal IgG. The group of patients with multiple myeloma in stage II
accounted for the highest percentage.
2. CLINICAL AND SUBCLINICAL CHARACTERISTICS OF MULTIPLE MYELOMA PATIENTS
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Keywords
Multiple myeloma, clinical and subclinical characteristics.
Abstract
References
[1]
Emerson SG, Zhu J, Hematopoietic cytokines,
Google Scholar
[2]
transcription factors and lineage commitment.
Google Scholar
[3]
Oncogene, 21: 3295-3313, 2002.
Google Scholar
[4]
Amadori S, TribaltoM, Cudillo L et al.,
Google Scholar
[5]
Autologous peripheral blood stem cell
Google Scholar
[6]
transplantation as first linetreatment of
Google Scholar
[7]
multiple myeloma: an Italian multicenter study.
Google Scholar
[8]
Haematologica, 85: 52–58, 2000.16
Google Scholar
[9]
Caballero MD, Rodriguez J, Gutierrez A,
Google Scholar
[10]
Autologous stem-cell transplantation in diffuse
Google Scholar
[11]
large B-cell non-Hodgkin’s lymphoma not
Google Scholar
[12]
achieving complete response after induction
Google Scholar
[13]
chemotherapy: the GEL/TAMO experience.
Google Scholar
[14]
Annals of Oncology, 15: 1504–1509, 2018.
Google Scholar
[15]
Noone AHN, KrapchoM, Neyman N et al., Seer
Google Scholar
[16]
CancerStatistics Review, 1975–2009 (Vintage 2009
Google Scholar
[17]
Populations). National Cancer Institute, 2012.
Google Scholar
[18]
Nguyễn Thị Mai, Nghiên cứu hiệu quả điều
Google Scholar
[19]
trị Đa u tủy xương bằng bortezomib kết hợp
Google Scholar
[20]
dexamethasone tại Viện Huyết học và Truyền
Google Scholar
[21]
máu Trung ương, Luận văn Thạc sỹ Y học, Đại
Google Scholar
[22]
học Y Hà Nội, 2011.
Google Scholar
[23]
Storer BE, Rotta M, Sahebi F et al., Long-term
Google Scholar
[24]
outcome of patients with multiple myeloma after
Google Scholar
[25]
autologous hematopoietic cell transplantation and
Google Scholar
[26]
nonmyeloablative allografting. Blood, 113: 3383-
Google Scholar
[27]
, 2009.
Google Scholar
[28]
Durie BGM, Harousseau J-L, Miguel JS et al.,
Google Scholar
[29]
International uniform response criteria for multiple
Google Scholar
[30]
myeloma. Leukemia, 20: 1467–1473, 2006.
Google Scholar
[31]
Nguyễn Thị Mai, Nghiên cứu hiệu quả điều
Google Scholar
[32]
trị Đa u tủy xương bằng bortezomib kết hợp
Google Scholar
[33]
dexamethasone tại Viện Huyết học và Truyền
Google Scholar
[34]
máu Trung ương. Luận văn Thạc sỹ Y học, 2011.
Google Scholar
[35]
Nguyễn Lan Phương, Nghiên cứu đặc điểm giai
Google Scholar
[36]
đoạn bệnh theo hệ thống phân loại quốc tế ISS
Google Scholar
[37]
trong bệnh Đa u tủy xương. Luận văn Thạc sỹ Y
Google Scholar
[38]
học, 2010.
Google Scholar
[39]
Caballero MD, Rodriguez J, Gutierrez A et al.,
Google Scholar
[40]
Autologous stem-cell transplantation in diffuse
Google Scholar
[41]
large B-cell non-Hodgkin’s lymphoma not
Google Scholar
[42]
achieving complete response after induction
Google Scholar
[43]
chemotherapy: the GEL/TAMO experience.
Google Scholar
[44]
Annals of Oncology, 15: 1504–1509, 2004.
Google Scholar