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Updated: Jan 28, 2026

Immunoglobulin Gene Sequence Analysis In Chronic Lymphocytic Leukemia: From Patient Material To Sequence Interpretation
Published on: November 26, 2018
Improving risk-stratification of patients with chronic lymphocytic leukemia using multivariate patient similarity
Peter Turcsanyi1, Eva Kriegova2, Milos Kudelka3
1Department of Hemato-Oncology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Olomouc, Olomouc, Czech Republic.
Insights
This study used patient similarity networks to identify ultra-high-risk chronic lymphocytic leukemia (CLL) patient subsets. This approach refines risk stratification for precision medicine in CLL treatment.
Area of Science:
- Hematology
- Oncology
- Genetics
Background:
- Accurate risk stratification is crucial for chronic lymphocytic leukemia (CLL) patients.
- Identifying ultra-high-risk (HR)-CLL subsets is essential given new therapeutic options.
Purpose of the Study:
- To apply multivariate patient similarity networks for prognostic assessment in HR-CLL.
- To identify distinct subsets of ultra-HR-CLL patients using routine clinical, genetic, and laboratory data.
Main Methods:
- A cohort of 116 HR-CLL patients with del(11q), del(17p)/TP53 mutations, and/or complex karyotype (CK) was analyzed.
- Multivariate patient similarity network and clustering were employed to assess prognostic factors.
- Patient subsets were defined based on genetic aberrations, lymphadenopathy, splenomegaly, and gender.
Main Results:
- Three major patient subsets (P-I, P-II, P-III) were identified based on prognostic variables.
- Subanalysis revealed three ultra-HR-CLL groups, including men with TP53 disruption and women with TP53 disruption and CK, experiencing poor short-term outcomes.
- The patient similarity network refined HR-CLL subsets, suggesting potential for targeted drug selection.
Conclusions:
- Multivariate patient similarity networks are useful for stratifying HR-CLL patients.
- This approach supports the clinical implementation of precision medicine in CLL.
- The findings are particularly relevant with the availability of novel targeted therapies for CLL.
Background:
Better risk-stratification of patients with chronic lymphocytic leukemia (CLL) and identification of subsets of ultra-high-risk (HR)-CLL patients are crucial in the contemporary era of an expanded therapeutic armamentarium for CLL.
Methods:
A multivariate patient similarity network and clustering was applied to assess the prognostic values of routine genetic, laboratory, and clinical factors and to identify subsets of ultra-HR-CLL patients. The study cohort consisted of 116 HR-CLL patients (F/M 36/80, median age 63 yrs) carrying del(11q), del(17p)/TP53 mutations and/or complex karyotype (CK) at the time of diagnosis.
Results:
Three major subsets based on the presence of key prognostic variables as genetic aberrations, bulky lymphadenopathy, splenomegaly, and gender: profile (P)-I (n = 34, men/women with CK + no del(17p)/TP53 mutations), P-II (n = 47, predominantly men with del(11q) + no CK + no del(17p)/TP53 mutations), and P-III (n = 35, men/women with del(17p)/TP53 mutations, with/without del(11q) and CK) were revealed. Subanalysis of major subsets identified three ultra-HR-CLL groups: men with TP53 disruption with/without CK, women with TP53 disruption with CK and men/women with CK + del(11q) with poor short-term outcomes (25% deaths/12 mo). Besides confirming the combinations of known risk-factors, the used patient similarity network added further refinement of subsets of HR-CLL patients who may profit from different targeted drugs.
Conclusions:
This study showed for the first time in hemato-oncology the usefulness of the multivariate patient similarity networks for stratification of HR-CLL patients. This approach shows the potential for clinical implementation of precision medicine, which is especially important in view of an armamentarium of novel targeted drugs.
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