Conference Coverage

Variant not linked to CLL in Southeast Europe


 

REPORTING FROM LEUKEMIA AND LYMPHOMA 2018

– New research suggests there is no association between the PTPN22 R620W polymorphism and chronic lymphocytic leukemia (CLL) or autoimmune hematologic disorders in patients from the Republic of Macedonia.

Past studies have shown an association between the PTPN22 R620W variant and both CLL and autoimmune diseases in patients from Northwest Europe. However, a new study of Macedonian patients suggests there is no association between the variant and CLL, autoimmune hemolytic anemia (AIHA), or idiopathic thrombocytopenic purpura (ITP) for patients from Southeast Europe.

Irina Panovska-Stavridis, PhD, of Ss. Cyril and Methodius University in Skopje, Republic of Macedonia, and her colleagues presented this finding at Leukemia and Lymphoma, a meeting jointly sponsored by the University of Texas MD Anderson Cancer Center and the School of Medicine at the University of Zagreb, Croatia.

“A lot of data from the literature suggests [the PTPN22 R620W variant ] has a role in developing multiple immune diseases, but it is validated just in patients from Northwest Europe,” Dr. Panovska-Stavridis noted.

She and her colleagues decided to assess the frequency of the PTPN22 R620W variant (C1858T, rs2476601) in individuals from Southeast Europe, particularly the Republic of Macedonia.

The researchers evaluated 320 patients – 168 with CLL, 66 with AIHA, and 86 with ITP – and 182 age- and sex-matched control subjects with no history of malignant or autoimmune disease.

The team found a similar frequency of the minor T allele and genotype distribution in control subjects and patients. For example, minor T allele was 0.107 in CLL, 0.067 in AIHA, 0.036 in ITP, and 0.05 in controls. Similarly, the frequency of the CC genotype was 0.809 in CLL, 0.166 in AIHA, 0.023 in ITP, and 0.901 in controls.

Dr. Panovska-Stavridis said these results suggest the PTPN22 R620W variant is not a risk factor for the development of CLL, AIHA, or ITP in patients from Southeast Europe.

She also said the results suggest the influence of the variant on lymphocytic homeostasis is affected by certain genetic and environmental factors, and the development of CLL and autoimmune diseases is influenced by race/ethnicity-based variations in the germline composition of the IGHV locus in correlation with environmental factors.

Dr. Panovska-Stavridis did not declare any conflicts of interest.

The Leukemia and Lymphoma meeting is organized by Jonathan Wood & Associates, which is owned by the parent company of this news organization.

Recommended Reading

RESONATE-2 update: First-line ibrutinib has sustained efficacy in older CLL patients
MDedge Hematology and Oncology
Venetoclax label now includes MRD data
MDedge Hematology and Oncology
FDA approves new hairy cell leukemia drug
MDedge Hematology and Oncology
FDA approves new drug for CLL/SLL and follicular lymphoma
MDedge Hematology and Oncology
Real-world clues for optimal sequencing of CLL novel agents
MDedge Hematology and Oncology
Novel options for treating hairy cell leukemia
MDedge Hematology and Oncology
Some mutation testing can be useful at CLL diagnosis
MDedge Hematology and Oncology
Ibrutinib plus obinutuzumab gets priority review in CLL/SLL
MDedge Hematology and Oncology
Ibrutinib discontinuation harms survival in CLL
MDedge Hematology and Oncology
Sandoz halts pursuit of U.S. approval for rituximab biosimilar
MDedge Hematology and Oncology