4.2 Article

Outcomes among patients with recurrent high-risk hematologic malignancies after allogeneic hematopoietic cell transplantation

期刊

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
卷 13, 期 10, 页码 1160-1168

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2007.06.007

关键词

transplantation; acute leukemia; Myelodysplastic syndromes; relapse; survival

资金

  1. NCI NIH HHS [P01 CA078902, CA15704, CA78902, CA18029] Funding Source: Medline
  2. NHLBI NIH HHS [HL36444] Funding Source: Medline
  3. NIDDK NIH HHS [DK064715] Funding Source: Medline

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We retrospectively analyzed outcomes among 307 consecutive patients who had recurrent or persistent acute leukemia (n = 244), chronic myclogenous leukemia in blast phase (CML; n = 28), or advanced myelodysplastic syndromes (AIDS; n = 35) after allogeneic hematopoietic cell transplantation and who received at least 1 relapse-directed intervention: withdrawal of immunosuppression, chemotherapy, or donor lymphocyte infusion (DLI). Transplants were performed at a single institution between 1995 and 2004, and outcomes were analyzed according to time intervals from transplantation to detection of malignancy: early, < 100 days (n = 111); intermediate, 100-200 days (n = 73); and late, >200 days (n = 123). The overall remission rate was 30%. Compared to early recurrence, intermediate recurrence and late recurrence were associated with increasing probabilities of remission (hazard ratios, 1.89 and 2.16; P = .05 and .02) and decreasing risks of overall mortality (hazard ratios, 0.73 and 0.33; P = .05 and <.0001). The 2-year overall survival (OS) estimates for patients with early, intermediate, and late recurrence were 3%, 9%, and 19%, respectively. Remission was associated with a median survival prolongation of 9.5 months. Individual types or combinations of these nonrandomly assigned relapse-directed interventions were not associated with higher or lower probabilities of remission or survival. More effective intervention strategies are needed for treatment of recurrent high-risk hematologic malignancies after hematopoietic cell transplantation. In the absence of innovative clinical trials, patients with early recurrence might wish to forego further interventions in favor of palliative care. (C) 2007 American Society for Blood and Marrow Transplantation.

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