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Updated: Jun 14, 2026

HPLC-based Assay to Monitor Extracellular Nucleotide/Nucleoside Metabolism in Human Chronic Lymphocytic Leukemia Cells
Published on: July 20, 2016
It is feasible and safe to stop specialized follow-up of asymptomatic lower-risk chronic lymphocytic leukemia
Christian Brieghel1, Caspar da Cunha-Bang1, Jindrich Mourek1
1Department of Hematology, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Insights
Ending specialized follow-up (sFU) for low-risk chronic lymphocytic leukemia (CLL) patients is safe and feasible. This approach reduces healthcare visits without compromising overall survival or increasing treatment need.
Area of Science:
- Hematology
- Oncology
- Clinical Medicine
Background:
- Chronic lymphocytic leukemia (CLL) patients often require lifelong specialized follow-up (sFU), straining healthcare resources.
- Many CLL patients, particularly those asymptomatic and low-risk, may not benefit from continuous sFU.
Purpose of the Study:
- To evaluate the feasibility and safety of discontinuing sFU in asymptomatic, low-to-intermediate risk CLL patients.
- To assess clinical outcomes, healthcare utilization, and treatment initiation rates after ending sFU.
Main Methods:
- A comparative study involving 112 patients ending sFU and 88 patients continuing sFU.
- Analysis of 3-year clinical outcomes, including overall survival, hospital visits, infection rates, and treatment initiation.
Main Results:
- Similar 3-year overall survival (87% vs. 80%) between groups.
- Patients ending sFU had significantly fewer hospital visits (median 0.7 vs. 4.3 per year) and longer time to first infection.
- Lower 3-year first treatment rate (4% vs. 23%) in patients who ended sFU.
Conclusions:
- Discontinuing sFU for selected low-to-intermediate risk CLL patients is feasible and safe.
- This strategy can optimize healthcare resource allocation without adverse clinical outcomes.
Abstract:
Approximately half of patients with chronic lymphocytic leukemia (CLL) will never require treatment; nonetheless, they are recommended life-long specialized follow-up (sFU). To prioritize health care resources, local hospital management implemented ending sFU in asymptomatic patients with CLL International Prognostic Index (CLL-IPI) and CLL without need of treatment (CLL-WONT) low-to-intermediate risk, who were covered by universal health care. To evaluate the feasibility and safety of ending sFU, we investigated 3-year clinical outcomes among 112 patients selected by clinical assessment to end sFU as compared with 88 patients selected to continue sFU. Patients who ended sFU were older, but otherwise lower risk compared with patients continuing sFU. Overall survival (OS) was similar in patients ending and continuing sFU (3-year OS, 87% and 80%, respectively; P = .16). Hospital visits per patient-year were lower (median 0.7 vs 4.3, P < .0001) and time to first infection was longer (P = .035) in patients ending sFU compared with those who continued sFU, including shorter in-hospital antimicrobial treatment (median 4 vs 12 days, respectively; P = .026). Finally, 1 in 6 patients were rereferred, including 4 patients meeting international workshop on CLL criteria for need of treatment. This also resulted in a lower 3-year first treatment rate for patients ending sFU compared with patients continuing sFU (4% vs 23%, respectively; P < .0001). In conclusion, it is feasible and safe to end sFU for patients with CLL who have low-to-intermediate risk CLL-IPI and CLL-WONT scores upon thorough clinical evaluation before ending sFU.
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