ID:2035 Chromosomal abnormalities and treatment response in Multiple myeloma patients at Cho Ray hospital

Authors

  • Thanh Thanh Suzanne Cho Ray Hospital, Ho Chi Minh City
  • Oanh Hoang Le Cho Ray Hospital, Ho Chi Minh City
  • Xinh Thi Phan Cho Ray Hospital, Ho Chi Minh City
  • Tung Thanh Tran Cho Ray Hospital, Ho Chi Minh City
  • Cuong Kim Nguyen Cho Ray Hospital, Ho Chi Minh City
  • Thang Thanh Phan Cho Ray Hospital, Ho Chi Minh City
  • Hoa Hong Huynh Cho Ray Hospital, Ho Chi Minh City

DOI:

https://doi.org/10.15419/bmrat.v4iS.274

Keywords:

Biology, Multiple myeloma, Karyotyping, Chromosomal abnormalities

Abstract

Multiple myeloma (MM) is a malignant plasma cell, generating abnormal immunoglobulins in the blood and urin. From January 2012 to December 2014, we performed chromosome analysis and treatment for 44 MM patients with the regimens containing Bortezomib (VD, VMP, VD plus autologus hematopoietic stem cell transplantation) at the Hematology department, Cho Ray hospital. The patient median of age was 64 year old, with the proportion of male/female was 0.83. IgG and IgA were two most common M-protein with accounting for 44.7% and 22.7%, respectively. Patients were usually admitted to the hospital late in phase II and III of disease. 43 of 44 MM patient haboring chromosomal abnormalities. Karyotyping analysis results showed that 3.7% cases with hypodiploidy and 14.8% cases hyperdiploidy. Translocation t(4;14), t(6;14), t(11;14) and t(14;16) were found in 6.8%, 4.5%, 11.3% and 4.5% of cases, respectively. Del(13q) and del(17p) accounted for 31.8% and 29.5% of cases. High risk group was found in 40.9% of cases. Patients carrying the translocation t(4;14) had the worse prognosis than other abnormalities with low response rate and overall survival, whereas higher rate of mortality. Results of our study showed that chromosomal abnormalities in MM are diversity and high percentage that affect the prognosis. Therefore, we need to indentify chromosomal abnormalities before treatment to select appropriate therapy regiments.

References

1. Avet-Loiseau H, Attal M, Moreau P, Charbonnel C, et al. Genetic abnormalities and survival in multiple myeloma: the experience of the Intergroupe Francophone du Myelome. Blood 2007; 109(8):3489-95.
2. Fonseca R, Blood EA, Oken MM, et al. Myeloma and the t(11;14) (q13;q32); evidence for a biologically defined unique subset of patients. Blood 2002; 99(10):3735-41.
3. Greipp PR, San Miguel J, Durie BG, et al. International staging system for multiple myeloma. J Clin Oncol 2005; 23(15):3412-20.
4. Kyle RA, Gertz MA, Witzig TE, et al. Review of 1027 patients with newly diagnosed multiple myeloma. Myo Clin Proc 2003; 78(1):21-33.

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Published

2017-09-05

How to Cite

ID:2035 Chromosomal abnormalities and treatment response in Multiple myeloma patients at Cho Ray hospital. (2017). Biomedical Research and Therapy, 4(S), S66. https://doi.org/10.15419/bmrat.v4iS.274

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