Risk factors for second primary malignancies (SPM) in patients with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL): A real-world study.
Abstract
e19022 Background: Patients with CLL/SLL are at increased risk of developing SPM. Identification of key clinical risk factors associated with SPM is critical to inform long-term surveillance strategies and optimize disease management. Methods: Adult patients diagnosed with CLL/SLL from Jan 1, 2019 to May 31, 2023 were identified from the Symphony open claims database. Patients were categorized into three cohorts: (1) treated with first-line covalent BTK inhibitor (cBTKi), (2) treated with first-line chemoimmunotherapy (CIT), and (3) those who are managed with active observation. The 36-month incidence of SPM (excl. nonmelanoma skin cancer [NMSC] and hematologic malignancies [HM]) was estimated. Multivariable logistic regressions were used to assess associations between baseline characteristics (demographics; region; obesity; 3-factor risk estimate scale [TRES], a validated comorbidity risk score; and select comorbidities) and SPM occurrence. Results: In total 86,654 patients with CLL/SLL were identified (cBTKi treated, n=11,352; CIT treated, n=12,589; and on active observation, n=62,713). Over 36-month follow-up, the incidence of SPM (excl. NMSC and HM) was 13.1% with cBTKi, 16.6% with CIT, and 11.8% managed with active observation ( P <.0001). In the overall population, age ≥70 yr (odds ratio [OR], 1.43; 95% CI, 1.36-1.50), male sex (OR, 1.32; 95% CI, 1.26-1.38), higher TRES score (OR, 1.11; 95% CI, 1.05-1.18), chronic pulmonary disease (OR, 1.26; 95% CI, 1.19-1.34) and liver disease (OR, 1.30; 95% CI, 1.19-1.41) were independently associated with increased risk of SPM. Similar risk factors were identified when cBTKi, CIT, and patients on active observation, were assessed individually. Conclusions: Older age, male sex, higher disease burden, and chronic comorbidities were associated with increased SPM risk in patients with CLL/SLL. Treatment with CIT was linked to a higher SPM risk compared with cBTKi therapy or observation. Patients with these risk factors should be monitored for the development of SPM during CLL/SLL management. Risk factors, OR (95% CI) Overall CLL/SLL (N=86,654) cBTKi (n=11,352) CIT (n=12,589) Observation (n=62,713) Age (yr) ≥70 vs <70 1.43 (1.36-1.50) 1.35 (1.19-1.54) 1.22 (1.09-1.36) 1.52 (1.43-1.61) Sex Male vs female 1.32 (1.26-1.38) 1.33 (1.17-1.51) 1.19 (1.07-1.33) 1.34 (1.27-1.42) Race/ethnicity Non-Hispanic Black vs Non-Hispanic White 1.07 (0.99-1.16) 1.07 (0.87-1.30) 0.92 (0.75-1.12) 1.11 (1.01-1.23) Hispanic vs Non-Hispanic White 1.05 (0.95-1.16) 0.83 (0.61-1.13) 1.21 (0.98-1.49) 1.04 (0.92-1.17) TRES Scores 2-3 vs scores 0-1 1.11 (1.05-1.18) 1.25 (1.07-1.47) 1.24 (1.09-1.41) 1.05 (0.98-1.13) Select comorbidities Chronic pulmonary disease 1.26 (1.19-1.34) 1.13 (0.96-1.34) 1.22 (1.06-1.39) 1.29 (1.21-1.39) Liver disease 1.30 (1.19-1.41) 1.08 (0.82-1.42) 1.20 (1.01-1.43) 1.32 (1.18-1.47)
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (6)
Lili Zhou
School of Integrated Circuits and Electronics, MIIT Key Laboratory for Low-Dimensional Quantum Structure and Devices
Ayad K. Ali
3BeOne Medicines Ltd, San Carlos, United States
Qianhong Fu
2BeOne Medicines Ltd, San Carlos, United States
Wassim Aldairy
4BeOne Medicines Ltd, San Carlos, United States
Vanthana Bharathi
1The University of Texas MD Anderson Cancer Center, Houston, United States
Alessandra Ferrajoli
1University of Texas MD Anderson Cancer Center, Leukemia, Houston, United States