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Competitive Transplants to Evaluate Hematopoietic Stem Cell Fitness
Published on: August 31, 2016
Late congestive heart failure after hematopoietic cell transplantation
Saro H Armenian1, Can-Lan Sun, Liton Francisco
1Division of Hematology/Oncology, Childrens Hospital Los Angeles, USA.
Insights
Pre-transplant chemotherapy and comorbidities significantly increase late congestive heart failure risk after hematopoietic cell transplantation (HCT). Conditioning therapy plays a minor role, highlighting the need for targeted surveillance and comorbidity management.
Area of Science:
- Hematology
- Oncology
- Cardiology
Background:
- Late congestive heart failure (CHF) is a serious complication following hematopoietic cell transplantation (HCT).
- Identifying risk factors for late CHF is crucial for patient management and outcomes.
Purpose of the Study:
- To investigate the independent contributions of pre-HCT therapeutic exposures, conditioning regimens, and comorbidities to the development of late CHF post-HCT.
Main Methods:
- A nested case-control study was conducted using a cohort of 2,938 1+ year survivors of HCT.
- Sixty patients with late CHF (diagnosed >= 1 year post-HCT) were matched with controls without CHF.
Main Results:
- Patients who developed late CHF received more pre-HCT chemotherapy cycles, had higher lifetime anthracycline exposure, and were more likely to have multiple comorbidities.
- Multivariable analysis identified pre-HCT chemotherapy cycles, anthracycline dose (>= 250 mg/m2), and multiple comorbidities as independent predictors of late CHF.
Conclusions:
- Pre-HCT anthracycline exposure and pre-existing comorbidities are primary drivers of late CHF risk after HCT.
- Transplantation conditioning regimens do not significantly contribute to late CHF risk.
- Findings support targeted surveillance and aggressive comorbidity management for high-risk HCT survivors.
Purpose:
To examine the independent roles of pre-hematopoietic cell transplantation (HCT) therapeutic exposures, transplantation-related conditioning, and comorbidities (pre- and post-HCT) in the development of late congestive heart failure (CHF) after HCT.
Methods:
This was a nested case-control design. Individuals with late CHF (diagnosed >or= 1 year after HCT) were identified from a cohort of 2,938 1+ year survivors who underwent transplantation at City of Hope National Medical Center, Duarte, CA. This cohort formed the sampling frame for selecting controls (without CHF) matched for age and year of HCT, donor source (allogeneic v autologous), and length of follow-up.
Results:
Sixty patients with late CHF were identified; median age at HCT was 45.3 years (range, 16.6 to 68.6 years); median time to CHF was 3.0 years (range, 1.03 to 18.9 years); 68% received autologous HCT. Median ejection fraction was 36.9% (range, 15% to 53%). Compared with matched controls (n = 166), patients with late CHF received more cycles of pre-HCT chemotherapy (8.6 v 4.9 cycles; P < .01), had greater body mass index at HCT (28.4 v 26.2 kg/m(2); P = .01), greater lifetime anthracycline exposure (285.3 v 175.6 mg/m(2); P < .01), and were more likely to have multiple chronic comorbidities (30.0% v 13.9%; P < .01). Multivariable analysis revealed number of pre-HCT chemotherapy cycles (odds ratio [OR] = 1.2; P < .01), anthracycline dose >/= 250 mg/m(2) (OR = 3.2; P = .05), and two or more chronic comorbidities (OR = 4.3; P = .01) to be independently associated with late CHF.
Conclusion:
Pre-HCT exposure to anthracyclines and presence of comorbidities are primarily responsible for the risk associated with late CHF after HCT. Conditioning-related therapeutic exposure does not contribute significantly to the risk. These results form the basis for identifying high-risk individuals for targeted surveillance, as well as developing preventive strategies in the form of aggressive management of comorbidities.
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