4.7 Article

Hematopoietic cell transplantation-comorbidity index and Karnofsky performance status are independent predictors of morbidity and mortality after allogeneic nonmyeloablative hematopoietic cell transplantation

Journal

CANCER
Volume 112, Issue 9, Pages 1992-2001

Publisher

WILEY
DOI: 10.1002/cncr.23375

Keywords

hematopoietic cell transplantation-specific comorbidity index; Karnofsky performance status; hematologic malignancies; nonmyeloablative conditioning; allogeneic hematopoietic cell transplantation; post-transplantation toxicities; nonrelapse mortality; survival

Categories

Funding

  1. NCI NIH HHS [CA 78902, P01 CA078902, P01 CA018029, CA 15704, CA 18029] Funding Source: Medline
  2. NHLBI NIH HHS [HL 36444, HL 088021] Funding Source: Medline

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BACKGROUND. Elderly and medically infirm cancer patients are increasingly offered allogeneic nonmyeloablative hematopoietic cell transplantation (HCT). A better understanding of the impact of health status on HCT outcomes is warranted. Herein, a recently developed HCT-specific comorbidity index (HCT-CI) was compared with a widely acceptable measure of health status, the Karnofsky performance status (KPS). METHODS. The outcomes of 341 patients were evaluated, conditioned for either related or unrelated HCT by 2-gray (Gy) total body irradiation given alone or 2 combined with fludarabine at a dose of 90 mg/m(2). Comorbidities were assessed retrospectively by the HCT-CI. Performance status before and toxicities after HCT were graded prospectively using the KPS and National Cancer Institute Common Toxicity criteria, respectively. RESULTS. Weak Spearman rank correlations were noted between HCT-CI and KPS and between the 2 measures and age, number of prior chemotherapy regimens, and intervals between diagnosis and HCT (all r < 0.20). High-risk diseases correlated significantly with higher mean HCT-CI scores (P =.009) but not low KPS (P=.37). In multivariate models, the HCT-CI had significantly greater independent predictive power for toxicities (P =.004), nonrelapse mortality (P =.0002), and overall mortality (P =.0002) compared with the KPS (P =.05,.13, and .05, respectively). Using consolidated HCT-CI and KPS scores, patients were stratified into 4 risk groups with 2-year survivals of 68%, 58%, 41%, and 32%, respectively. CONCLUSIONS. HCT-CI and KPS should be assessed simultaneously before HCT. The use of both tools combined likely refines risk-stratification for HCT outcomes. Novel guidelines for assessment of performance status among HCT patients are warranted.

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