P120 | CHRONIC LYMPHOCYTIC LEUKEMIA AND RENAL CELL CARCINOMA: A CASE SERIES OF TWELVE PATIENTS

Background: Chronic lymphocytic leukemia (CLL) is the most common leukemia in adults, with a median age at diagnosis of 72 years. CLL patients (pts) have an increased risk of second malignancies due to multiple synergistic factors: genetic, environmental, treatment-induced and immunomodulatory effects. Renal cell carcinoma (RCC) has an annual incidence of 14.9 per 100,000 people, with a median age at diagnosis of 65 years. In 6-9% of cases, it is associated with germline mutations in genes linked to cancer predisposition. Despite nephrectomy, 30% of RCC pts develop metastatic disease, requiring systemic therapy and carrying a high mortality risk. No association on the epidemiology and genetics of the two diseases has been reported so far. Results: Out of 740 CLL pts followed at our center in the last 25 years, we found 12 pts (1.62%) with a diagnosis of RCC (Table 1). Eleven (92%) were male. The median age at diagnosis was 61 (43–73) years for CLL, and 61 (42–73) for RCC. In 3 pts (25%), RCC was diagnosed prior to CLL; in 6 pts (50%), the malignancies were detected concurrently; finally, 3 pts (25%) developed RCC after CLL. Our pts did not show other malignancies and family history revealed no tumours clustering. Nine pts (75%) had RCC at early stage (I, II) and received surgical resection. After an average follow-up of 6.5 years since RCC diagnosis, 9/12 (75%) pts are alive. Discussion: Currently, this is the largest single-center series of pts with CLL and RCC. An increased incidence of RCC in pts with NHL has been reported7, but its concomitance with CLL remains a sporadic finding. The young age at diagnosis for both malignancies might suggest a genetic predisposition. Del(13q), a common lesion in CLL, was present in 7 pts, but its specific role is unclear. In our cohort, almost all RCC diagnoses occurred before or concurrently with CLL, excluding CLL treatment toxicity as a cause. Six pts were smokers, an established risk factor for RCC (RR 1.5–2.0). Regular medical check-ups and abdominal ultrasounds, routinely performed by our CLL pts, likely increased the incidental finding of renal lesions. Early detection may explain why our pts were successfully treated with surgery, without the need for systemic therapies. Conclusion: Our study suggests a potential link between CLL and RCC, warranting further study. Frequent CLL follow-up may aid early detection of other cancers, improving quality of life and survival of our pts.

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SHILAP Revista de lepidopterología
Published
2025-09-01
Primary Topic
History and Developments in Astronomy
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P120 | CHRONIC LYMPHOCYTIC LEUKEMIA AND RENAL CELL CARCINOMA: A CASE SERIES OF TWELVE PATIENTS

SHILAP Revista de lepidopterología
History and Developments in Astronomy
article

P120 | CHRONIC LYMPHOCYTIC LEUKEMIA AND RENAL CELL CARCINOMA: A CASE SERIES OF TWELVE PATIENTS

article en

Abstract

Background: Chronic lymphocytic leukemia (CLL) is the most common leukemia in adults, with a median age at diagnosis of 72 years. CLL patients (pts) have an increased risk of second malignancies due to multiple synergistic factors: genetic, environmental, treatment-induced and immunomodulatory effects. Renal cell carcinoma (RCC) has an annual incidence of 14.9 per 100,000 people, with a median age at diagnosis of 65 years. In 6-9% of cases, it is associated with germline mutations in genes linked to cancer predisposition. Despite nephrectomy, 30% of RCC pts develop metastatic disease, requiring systemic therapy and carrying a high mortality risk. No association on the epidemiology and genetics of the two diseases has been reported so far. Results: Out of 740 CLL pts followed at our center in the last 25 years, we found 12 pts (1.62%) with a diagnosis of RCC (Table 1). Eleven (92%) were male. The median age at diagnosis was 61 (43–73) years for CLL, and 61 (42–73) for RCC. In 3 pts (25%), RCC was diagnosed prior to CLL; in 6 pts (50%), the malignancies were detected concurrently; finally, 3 pts (25%) developed RCC after CLL. Our pts did not show other malignancies and family history revealed no tumours clustering. Nine pts (75%) had RCC at early stage (I, II) and received surgical resection. After an average follow-up of 6.5 years since RCC diagnosis, 9/12 (75%) pts are alive. Discussion: Currently, this is the largest single-center series of pts with CLL and RCC. An increased incidence of RCC in pts with NHL has been reported7, but its concomitance with CLL remains a sporadic finding. The young age at diagnosis for both malignancies might suggest a genetic predisposition. Del(13q), a common lesion in CLL, was present in 7 pts, but its specific role is unclear. In our cohort, almost all RCC diagnoses occurred before or concurrently with CLL, excluding CLL treatment toxicity as a cause. Six pts were smokers, an established risk factor for RCC (RR 1.5–2.0). Regular medical check-ups and abdominal ultrasounds, routinely performed by our CLL pts, likely increased the incidental finding of renal lesions. Early detection may explain why our pts were successfully treated with surgery, without the need for systemic therapies. Conclusion: Our study suggests a potential link between CLL and RCC, warranting further study. Frequent CLL follow-up may aid early detection of other cancers, improving quality of life and survival of our pts.

SHILAP Revista de lepidopterología
Università Cattolica del Sacro Cuore (IT), Università degli Studi della Tuscia (IT), Friedrich-Alexander-Universität Erlangen-Nürnberg (DE), Agostino Gemelli University Polyclinic (IT)
Good health and well-being
Openalex Percentile: Top 47%
History and Developments in Astronomy
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