Journal Home
Search for

Volume 15, Issue 10, Pages 1265-1270 (October 2009)


View previous. 10 of 22 View next.

Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Patients with Low Left Ventricular Ejection Fraction

Muzaffar H. Qazilbash1Corresponding Author Informationemail address, Ali Imran Amjad2, Suhail Qureshi1, Sofia R. Qureshi1, Rima M. Saliba1, Ziad U. Khan3, Chitra Hosing1, Sergio A. Giralt1, Marcos J. De Lima1, Uday R. Popat1, Syed W. Yusuf4, Richard E. Champlin1

Received 9 March 2009; accepted 3 June 2009. published online 03 August 2009.

A high risk of regimen-related toxicity with allogeneic hematopoietic stem cell transplantation (allo-HSCT) limits this potentially curative treatment for patients with a left ventricular ejection fraction (LVEF) of ≥50%. We evaluated the frequency of cardiac complications and 100-day nonrelapse mortality (NRM) in 56 patients with a LVEF of ≤45%, who received allo HCT at our institution. The results were retrospectively compared with a matched control group with LVEF of ≥50%, which received an allogeneic stem cell transplantation (allo-SCT). After a median follow-up of 29 months in the study group, grade ≥2 cardiac complications were seen in 7 of 56 (12.5%) patients and cumulative incidence of 100-day NRM was 12.5% with no deaths from cardiac causes. In contrast, after a median follow-up of 49 months in the control group, grade >2 cardiac complications were seen in 19 of 161 patients (11.8%; P = 1.00) and cumulative incidence of 100-day NRM was 14.9% (P = .82). The presence of at least 1 of the 7 pretransplant cardiac risk factors (past history of smoking, hypertension, hyperlipidemia, coronary artery disease, arrhythmia, prior myocardial infarction, and congestive heart failure) was associated with a higher cardiac complication rate in the study group (P = .03). In conclusion, selected patients with a LVEF of ≤45% can safely receive allo-HCT without a significant increase in cardiac toxicity or NRM.

1 Stem Cell Transplantation and Cellular Therapy, University of Texas M.D. Anderson Cancer Center, Houston, Texas

2 Department of Internal Medicine, University of Pittsburgh, Pennsylvania

3 Department of Internal Medicine, University of Texas at Houston, Houston, Texas

4 Department of Cardiology, University of Texas M.D. Anderson Cancer Center, Houston, Texas

Corresponding Author InformationCorrespondence and reprint requests: Muzaffar H. Qazilbash, MD, Department of Stem Cell Transplantation and Cellular Therapy—423, University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX, 77030.

 Financial disclosure: See Acknowledgments on page 1269.

PII: S1083-8791(09)00274-2

doi:10.1016/j.bbmt.2009.06.001


View previous. 10 of 22 View next.