Related Experiment Video
Updated: May 18, 2026

09:02
Immunoglobulin Gene Sequence Analysis In Chronic Lymphocytic Leukemia: From Patient Material To Sequence Interpretation
Published on: November 26, 2018
Chronic lymphocytic leukemia and prognostic factors
Zahra Mozaheb1, Mohamad Hasan Hasanzadeh NazarAbadi, Monavar Afzal Aghaee
1Department of hematology-oncology, Mashhad University of Medical Science, Iran. mozahebz@mums.ac.ir
Asian Pacific Journal of Cancer Prevention : APJCP
|September 22, 2012
Summary
Beta-2 microglobulin (β2-MG) and lymphocyte doubling time (LDT) are significant prognostic factors for chronic lymphocytic leukemia (CLL). These markers can help predict disease progression and outcome in CLL patients, complementing existing staging systems.
Area of Science:
- Hematology
- Oncology
- Clinical Pathology
Background:
- Chronic lymphocytic leukemia (CLL) exhibits variable clinical courses, making prognosis challenging with current staging systems.
- Early-stage CLL patients require reliable prognostic markers to predict disease progression.
- Previous research identified lymphocyte doubling time (LDT), β2-microglobulin (β2-MG), and cytogenetic analysis as potential prognostic indicators.
Purpose of the Study:
- To evaluate a comprehensive range of prognostic factors in patients diagnosed with CLL.
- To determine the relationship between various clinical and laboratory markers and disease outcome in CLL.
- To identify reliable predictors of disease progression and prognosis in CLL.
Main Methods:
- Seventy CLL patients were enrolled and assessed at diagnosis.
- Evaluated prognostic factors included Binet staging, LDT, β2-MG, ESR, LDH, peripheral blood smudge cells, absolute lymphocyte count, and conventional cytogenetics (CC).
- Patients were followed up to ascertain outcomes, and factors were compared against each other and Binet staging.
Main Results:
- β2-microglobulin (β2-MG) levels and lymphocyte doubling time (LDT) showed a significant direct relationship with CLL staging and patient outcome (p<0.0001 and p<0.001, respectively).
- No significant correlation was found between LDH, ESR, smudge cells, or absolute lymphocyte count and disease stage or prognosis.
- Conventional cytogenetic (CC) analysis detected alterations in 19% of patients.
Conclusions:
- Conventional cytogenetics (CC) alone is insufficient for detecting all chromosomal alterations in CLL; fluorescence in situ hybridization (FISH) is recommended.
- Due to the cost and limited availability of FISH, β2-microglobulin (β2-MG) is proposed as a viable and accessible prognostic marker for CLL.
- β2-MG should be considered for integration into the Binet staging system to improve prognostic subgrouping and patient management in CLL.

