4.2 Article

Lymphocyte Recovery Is a Major Determinant of Outcome after Matched Unrelated Myeloablative Transplantation for Myelogenous Malignancies

Journal

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
Volume 15, Issue 9, Pages 1108-1115

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2009.05.015

Keywords

Hematopoietic stem cell transplantation (HSCT); Lymphocytes; Relapse-free survival (RFS); Graft-versus-host disease (GVHD)

Funding

  1. Swedish Cancer Society [07 0132, 07 0529, 07 0117]
  2. Children's Cancer Foundation [05/007, 06/094]
  3. Swedish Research Council [K2006-32X-14716-04-1, K2005-32P-15457-01A, K2008-64X-20742-01-3, K2008-64X-05971-28-3, K2008-64P-15457-04-3]
  4. Tobias Foundation
  5. Cancer Society in Stockholm
  6. Swedish Society of Medicine
  7. Stockholm County Council
  8. Sven and Ebba-Christina Hagbergs Foundation
  9. Cancer and Allergy Foundation
  10. Karolinska Institutet

Ask authors/readers for more resources

A higher absolute lymphocyte count I month (LC30) after allogeneic hematopoietic stem cell transplantation (HSCT) is associated with better outcome in patients transplanted from a matched sibling. We studied 102 SCT patients with unrelated donor and matched unrelated donors and the relationship between LC30 and outcome in patients with myelogenous leukemia. Conditioning was myeloablative using cyclophosphamide (Cy) with busulfan (Bu; n = 61) or total body irradiation (TBI; n = 41). LC30 was low (<0.2 x 10(9)/L) in 18 patients, intermediate (0.2-1.0 x 10(9)L) in 67, and high (>1.0 x 10(9)/L) in 17 patients. In multivariate analysis, independent factors associated with high relapse-free survival (RFS) were high LC30, high CD34 cell-dose, and absence of acute graft-versus-host disease (aGVHD) grades II-IV. When analyzed as a continuous variable in multivariate analysis, a higher LC30 was associated with a lower transplant-related mortality (TRM; relative hazard [RH] = 0.87, P < .05), higher relapse-free survival (RH = 3.42, P = .036), and improved survival (RH = 4.53, P = .016, excluding GVHD). In patients with high, intermediate, and low LC30, overall survival (OS) was 91% versus 60%, versus 36% (P = .02 and .001, respectively). This significant relationship was maintained in patients who did not develop GVHD by day 30. Significant risk factors to develop low LC30 was chronic myelogenous leukemia (CML; hazard ratio [HR] 0.73, P = .001), prophylaxis with granulocyte colony-stimulating factor (G-CSF; HR 0.81, P = .02) and aGVHD (HR 0.84, P = .05). These results indicate that LC30 is an independent prognostic factor for transplant outcome in matched unrelated SCT for myelogenous malignancies. Biol Blood Marrow Transplant 15: 1108-1115 (2009) (C) 2009 Elsevier Inc. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available