Lab Med Online.  2023 Oct;13(4):356-363. 10.47429/lmo.2023.13.4.356.

Current Status of BCR::ABL1 Quantitative PCR Analysis in Korea (2022)

Affiliations
  • 1Department of Laboratory Medicine, Inje University Busan Paik Hospital, Busan, Korea
  • 2Department of Laboratory Medicine, Pusan National University Yangsan Hospital, Yangsan, Korea
  • 3Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
  • 4Department of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Korea
  • 5Department of Laboratory Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea

Abstract

Background
BCR::ABL1 real-time quantitative PCR (RQ-PCR) is the optimal test for monitoring patients with chronic myeloid leukemia after treatment; however, standardization among testing institutions is required to assess molecular response. We performed an online survey to investigate the actual status and standardization of the BCR::ABL1 RQ-PCR test in Korea.
Methods
The survey was provided by e-mail to the laboratory experts in molecular genetic testing at university hospitals, tertiary medical institutions, and specialized testing institutions. Questionnaires covered each institution’s BCR::ABL1 RQ-PCR test (eight questions), reporting format (six questions), verification of the lower limit of detection and quantitation (seven questions), and internal and external quality control (two questions).
Results
Responses were received from 15 institutions. Every institution utilized RQ-PCR kits that were commercially available. All of them used the ABL1 gene as a reference gene and had a copy number range of at least 10,000, which is necessary for determining a deep molecular response (DMR). The majority of laboratories established their own laboratory detection limits suitable for determining a DMR. The reporting of results and internal and external quality control procedures differed by institution.
Conclusions
The survey confirmed that testing institutions are implementing standardized RQ-PCR methods, but it is necessary to perform detection limit verification and internal and external quality control to improve the precision and sensitivity of the results. Standardization and guidelines are required to enhance the consistency of testing result reports across institutions.

Keyword

BCR::ABL1; Real-time PCR; quantitative; Chronic myeloid leukemia; Surveys and questionnaires

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