A new score including CD43 and CD180: Increased diagnostic value for atypical chronic lymphocytic leukemia

Yi Li1, Xiwen Tong1, Lifang Huang1

  • 1Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Cancer Medicine
|June 1, 2021
PubMed

Insights

A new diagnostic score using CD43 and CD180 improves chronic lymphocytic leukemia (CLL) detection, especially in Asian patients with atypical immunophenotypes. This score offers higher sensitivity and specificity compared to existing methods.

Area of Science:

  • Hematology
  • Immunophenotyping
  • Diagnostic Biomarkers

Background:

  • The Moreau score is used to distinguish chronic lymphocytic leukemia (CLL) from other mature B-cell neoplasms.
  • The Moreau score has demonstrated limitations, particularly in Asian patient populations.
  • A need exists for a more accurate diagnostic tool for CLL, especially in diverse ethnic groups.

Purpose of the Study:

  • To develop and evaluate a novel scoring system for the diagnosis of CLL.
  • To replace CD5 and CD23 with CD43 and CD180 in the diagnostic criteria for CLL.
  • To assess the diagnostic performance of the new score in differentiating CLL from other mature B-cell neoplasms, particularly in Asian patients.

Main Methods:

  • Collected 237 untreated mature B-cell neoplasm samples, divided into exploratory (2:1 ratio) and validation cohorts.
  • Analyzed the expression of CD5, CD19, CD20, CD23, CD43, CD79b, CD180, CD200, FMC7, and surface immunoglobulin (SmIg).
  • Developed a new CLL score using a logistic regression model and evaluated its sensitivity and specificity via ROC curves.

Main Results:

  • The new CLL score, incorporating CD43/CD180, CD200, FMC7, and CD79b, achieved 91.8% sensitivity and 83.1% specificity in the exploratory cohort.
  • Validation cohort confirmed the score's performance with 90.5% sensitivity and 79.5% specificity.
  • The new score demonstrated significantly improved sensitivity (79.4%) in CD5/CD23 negative and atypical CLL cases compared to Moreau and CLLflow scores.

Conclusions:

  • The proposed CLL score, utilizing CD43 and CD180, offers improved diagnostic accuracy for CLL.
  • This novel score is particularly valuable for differentiating CLL in cases with atypical immunophenotypes and in Asian populations.
  • The new scoring system, combined with morphological and molecular methods, enhances the accurate diagnosis of CLL.

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