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Published on: October 19, 2014
Comorbidities predict inferior outcomes in chronic lymphocytic leukemia treated with ibrutinib
Max J Gordon1, Michael Churnetski2, Hamood Alqahtani3
1Oregon Health and Science University, Portland, Oregon.
Insights
Comorbidities negatively impact outcomes for chronic lymphocytic leukemia (CLL) patients treated with ibrutinib. Higher comorbidity scores predict worse event-free survival and overall survival in CLL patients receiving targeted therapy.
Area of Science:
- Hematology
- Oncology
- Clinical Research
Background:
- Most chronic lymphocytic leukemia (CLL) patients have multiple comorbidities.
- Comorbidities negatively impact outcomes in chemoimmunotherapy-treated CLL patients.
- The effect of comorbidities on outcomes with targeted therapies in CLL is not well understood.
Purpose of the Study:
- To evaluate the significance of comorbidities in CLL patients treated with ibrutinib.
- To assess the impact of comorbidity burden on event-free survival (EFS) and overall survival (OS).
Main Methods:
- Multicenter, retrospective analysis of 145 CLL patients treated with ibrutinib.
- Comorbidities assessed using the Cumulative Illness Rating Scale (CIRS).
- Analysis included patients in frontline and relapsed/refractory settings.
Main Results:
- High comorbidity burden (CIRS score ≥ 7) associated with inferior median EFS (24 vs 37 months) and 2-year OS (79% vs 100%).
- Increased CIRS score correlated with worse EFS and OS in adjusted Cox models.
- Comorbidities linked to higher risk of ibrutinib dose reduction and treatment discontinuation.
Conclusions:
- Comorbidities indicate a poor prognosis for CLL patients receiving ibrutinib.
- CIRS score is a predictive factor for outcomes in both frontline and relapsed CLL.
- Further prospective studies are needed to optimize treatment strategies for CLL patients with comorbidities.
Background:
Most patients with chronic lymphocytic leukemia (CLL) present with multiple comorbidities. Although comorbidities negatively affect outcomes for patients treated with chemoimmunotherapy, their impact on patients who receive targeted therapies is unknown.
Methods:
This multicenter, retrospective analysis evaluated the significance of comorbidities, as assessed by the Cumulative Illness Rating Scale (CIRS), among patients with CLL treated with ibrutinib.
Results:
One hundred forty-five patients received ibrutinib (80% in a relapsed/refractory setting). A high burden of comorbidities (CIRS score ≥ 7) was associated with inferior median event-free survival (EFS; 24 vs 37 months; P = .003) and 2-year overall survival (OS; 79% vs 100%; P = .005). In an adjusted Cox model, both EFS and OS worsened with an incremental increase in the CIRS score. Furthermore, comorbidities were associated with an increased risk of ibrutinib dose reduction and therapy discontinuation. CIRS was predictive in both frontline and relapsed CLL, regardless of patient age.
Conclusions:
Comorbidities portend a poor prognosis among patients with CLL treated with ibrutinib. Prospective studies are needed to optimize the treatment of patients with CLL who have comorbidities. Cancer 2018. © 2018 American Cancer Society.
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