CLL-153: Evaluation of Second Primary Cancer Risk Among Chronic Lymphocytic Leukemia Patients: Multicenter Study

2021 ◽  
Vol 21 ◽  
pp. S320
Author(s):  
Selim Sayın ◽  
Emrah Kılıçaslan ◽  
Murat Yıldırım ◽  
Hacer Berna Afacan Öztürk ◽  
Esra Şafak Yılmaz ◽  
...  
2021 ◽  
Vol 21 ◽  
pp. S222
Author(s):  
Selim Sayın ◽  
Emrah Kılıçaslan ◽  
Murat Yıldırım ◽  
Hacer Berna Afacan Öztürk ◽  
Esra Şafak Yılmaz ◽  
...  

2018 ◽  
Vol 2 (21) ◽  
pp. 3025-3034 ◽  
Author(s):  
Inger Lise Gade ◽  
Signe Juul Riddersholm ◽  
Ilse Christiansen ◽  
Annika Rewes ◽  
Mikael Frederiksen ◽  
...  

Abstract Venous thromboembolism (VTE) is associated with inferior survival in cancer patients. The risk of VTE and its effect on survival in chronic lymphocytic leukemia (CLL) patients remains unclear. The present study investigated the impact of patient-related factors, CLL prognostic markers, and CLL treatment on the risk of VTE and assessed overall survival relative to VTE. All patients in the Danish National CLL Registry (2008-2015) were followed from the date of CLL diagnosis to death, VTE, emigration, or administrative censoring. Hazard ratios (HRs) were estimated using Cox models, and second primary cancers and anticoagulation treatment were included as time-varying exposures. During a median follow-up of 2.6 years, 92 VTEs occurred among 3609 CLL patients, corresponding to a total incidence rate of 8.2 VTEs per 1000 person-years (95% confidence interval [CI], 6.7-10.1). A history of VTE or second primary cancer was associated with HRs of VTE of 5.09 (95% CI, 2.82-9.17) and 3.72 (95% CI, 2.15-6.34), respectively, while β2-microglobulin >4 mg/L, unmutated immunoglobulin HV and unfavorable cytogenetics had lower HRs. CLL patients with VTE had marginally higher mortality, which was most pronounced among patients <60 years of age (HR, 7.74; 95% CI, 2.12-28.29). Our findings suggest that markers of unfavorable CLL prognosis contribute to an increased risk of VTE; however, previous VTE or a second primary cancer is more strongly associated with the risk of VTE than any CLL-specific marker. Focusing attention on this preventable complication may improve survival in young CLL patients.


BMC Cancer ◽  
2014 ◽  
Vol 14 (1) ◽  
Author(s):  
Jérémie Jégu ◽  
Marc Colonna ◽  
Laetitia Daubisse-Marliac ◽  
Brigitte Trétarre ◽  
Olivier Ganry ◽  
...  

Thyroid ◽  
2017 ◽  
Vol 27 (2) ◽  
pp. 261-270 ◽  
Author(s):  
Nilton Lavatori Corrêa ◽  
Lidia Vasconcellos de Sá ◽  
Rossana Corbo Ramalho de Mello

2019 ◽  
Vol 28 (5) ◽  
Author(s):  
Linda Aagaard Rasmussen ◽  
Henry Jensen ◽  
Line Flytkjær Virgilsen ◽  
Alina Zalounina Falborg ◽  
Henrik Møller ◽  
...  

2017 ◽  
Vol 35 (15_suppl) ◽  
pp. e18090-e18090
Author(s):  
Amir Bista ◽  
Dipesh Uprety ◽  
Subash Ghimire ◽  
Megha Giri ◽  
Binay Kumar Shah

e18090 Background: There has been significant improvement in survival among patients with primary Chronic Lymphocytic Leukemia (CLL) in recent years but, not much is known about survival among CLL developed after a first primary malignancy. Methods: SEER 18 database, 2015 submission, was used to calculate 5 and 10 year relative survival (RS) by period survival modeling method for 1993 to 2012, with division of the period into 4 cohorts of 5 years each. SEER*Stat software from National Cancer Institute was used to calculate relative survival (RS) for 4 different periods of 5 years duration. The trend in survival for cases with CLL as second primary cancer (CLLSPC) was evaluated using COX proportional hazard method using Cansurv software and also compared with that of primary CLL cases. Results: A total of 8731 patients with CLLSPC were included in the study, which represents 14.5% of all cases of CLL. The median age at diagnosis was 75 years. Median time to diagnosis of CLL was 50 months after diagnosis of first primary malignancy. Prostate cancer, breast cancer and colorectal cancer were 3most common primary cancers. 5-year and 10-year RS improved significantly in the year 2008-2012 compared to 1993-1997 (59.3% to 70.2%,P 0.044 and 40.1% to 50.6%, p 0.045). In subgroup analysis, significant improvement in 5-year and 10-year RS was seen in females and ≥ 80 years age group but no significant improvement was observed in males and age group 60-79 years. Survival among CLLSPC was significant worse compared to first primary CLL in all periods, even after adjusting for age and sex. Conclusions: CLLSPC represents about 14.5% of all CLL cases. Relative survival among patients with CLLSPC is gradually improving but still lags behind that of CLL as first primary cancer.


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