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Evaluation of Second Primary Cancer Risk Among Chronic Lymphocytic Leukemia Patients: Multicenter Study.
Selim Sayin1, Emrah Kiliacslan2, Murat Yildirim1
1Gülhane Educational and Research Hospital, Department of Hematology, Ankara, Turkey.
Patients with chronic lymphocytic leukemia (CLL) have a 9.2% risk of developing second primary cancers (SPC), particularly epithelial tumors. The 13q deletion genetic abnormality was significantly more common in CLL patients who developed SPC.
Area of Science:
- Hematology
- Oncology
- Cancer Epidemiology
Background:
- Patients with chronic lymphocytic leukemia (CLL) face an elevated risk of second primary cancers (SPC).
- Understanding the incidence and risk factors for SPC in CLL is crucial for patient management.
Purpose of the Study:
- To determine the frequency of SPC in CLL patients.
- To investigate the relationship between SPC and treatment status, cytogenetic factors, and other risk factors.
Main Methods:
- Multicenter, retroprospective study design.
- Involved 553 patients diagnosed with CLL.
- Data collected between August 2016 and May 2021.
Main Results:
- A 9.2% incidence rate of SPC was observed in 51 out of 553 CLL patients.
- Epithelial tumors were the most frequent SPC, followed by skin, lymphoma, and renal cancers.
- The 13q deletion was the most common genetic abnormality, found significantly more often in patients with SPC.
Conclusions:
- Higher rates of SPC in CLL were associated with age at diagnosis, 13q deletion, CD38 positivity, and treatment with fludarabine and monoclonal antibodies.
- SPC risk was independent of most genetic mutations (except 13q), hemogram values (except hemoglobin), and treatment lines.
- CLL patients with SPC exhibited higher mortality rates and were diagnosed at more advanced stages.
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