The presence of minimal residual disease (MRD) is an important prognostic factor for multiple myeloma, while copy number variation (CNV) is a widely accepted biomarker used for multiple myeloma (MM). Detecting MRD and monitoring clonal evolution by monitoring CNV using low-pass whole genome sequencing is promising due to its high analytical sensitivity. To evaluate the correlation between MRD detected by flow cytometry and low-pass whole genome sequencing, nearly 200 samples were collected for this study. We applied ultrasensitive chromosomal aberrations detection to detect CNV for each patient. The follow-up samples were then collected and sequencing used the same method.
Study Type
OBSERVATIONAL
Enrollment
80
InsituteHBDH
Tianjin, Tianjin Municipality, China
Detection of copy number variation
Time frame: From May 1, 2023 to December 31, 2023
Serial monitoring of treatment response
Time frame: From January 1, 2024 to May 31, 20224
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