4.2 Article

Hematopoietic Cell Transplant Comorbidity Index Is Predictive of Survival after Autologous Hematopoietic Cell Transplantation in Multiple Myeloma

期刊

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
卷 20, 期 3, 页码 402-408

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2013.12.557

关键词

Autologous hematopoietic cell transplantation; Multiple myeloma; Comorbidity; Transplant outcome

资金

  1. Public Health Service from the National Cancer Institute (NCI) [U24 CA076518]
  2. National Heart, Lung and Blood Institute (NHLBI)
  3. National Institute of Allergy and Infectious Diseases
  4. NHLBI [U10 HL069294]
  5. NCI
  6. Health Resources and Services Administration [HHSH250201200016C]
  7. Office of Naval Research [N00014-12-1-0142, N00014-13-1-0039]
  8. Alias Therapeutics, Inc.
  9. Amgen, Inc.

向作者/读者索取更多资源

Autologous hematopoietic stem cell transplantation (AHCT) improves survival in patients with multiple myeloma (MM) but is associated with morbidity and nonrelapse mortality (NRM). Hematopoietic cell transplant comorbidity index (HCT-CI) was shown to predict risk of NRM and survival after allogeneic transplantation. We tested the utility of HCT-CI as a predictor of NRM and survival in patients with MM undergoing AHCT. We analyzed outcomes of 1156 patients of AHCT after high-dose melphalan reported to the Center for International Blood and Marrow Transplant Research. Individual comorbidities were prospectively collected at the time of AHCT. The impact of HCT-CI and other potential prognostic factors, including Karnofsky performance score (KPS), on NRM and survival were studied in multivariate Cox regression models. HCT-CI score was 0, 1, 2, 3, and >3 in 42%, 18%, 13%, 13%, and 14% of the study cohort, respectively. Subjects were stratified into 3 risk groups: HCT-CI score of 0(42%) versus HCT-CI score of 1 to 2(32%) versus HCT-CI score > 2 (26%). Higher HCT-CI was associated with lower KPS < 90 (33% of subjects score of 0 versus 50% in HCT-CI score > 2). HCT-CI score > 2 was associated with melphalan dose reduction (22% versus 10% in score 0 cohort). One-year NRM was low at 2% (95% confidence interval, 1% to 4%) and did not correlate with HCT-CI score (P = .9). On multivariate analysis, overall survival was inferior in groups with HCT-CI score of 1 to 2 (relative risk, 1.37, [95% confidence interval, 1.01 to 1.87], P = .04) and HCT-CI score > 2 (relative risk, 1.5 [95% confidence interval, 1.09 to 2.08], P = .01). Overall survival was also inferior with KPS < 90 (P < .001), IgA subtype (P <= .001), those receiving >1 pretransplant induction regimen (P = .007), and those with resistant disease at the time of AHCT (P < .001), AHCT for MM is associated with low NRM, and death is predominantly related to disease progression. Although a higher HCT-CI score did not predict NRM, it was associated with inferior survival. (C) 2014 American Society for Blood and Marrow Transplantation.

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