Transplant‐related mortality following allogeneic hematopoeitic stem cell transplantation for pediatric acute lymphoblastic leukemia: 25‐year retrospective review. Issue 9 (3rd June 2013)

• Record Type: Journal Article
• Authors: Mateos, Marion K.; O'Brien, Tracey A.; Oswald, Cecilia; Gabriel, Melissa; Ziegler, David S.; Cohn, Richard J.; Russell, Susan J.; Barbaric, Draga; Marshall, Glenn M.; Trahair, Toby N.
• Is Part Of: Pediatric blood & cancer. Volume 60:Issue 9(2013:Sep.)
• Page Start: 1520
• Page End: 1527
• Publication Date: 2013-06-03
• Subjects: Tumors in children -- Periodicals; Blood -- Diseases -- Periodicals; Cancer in children -- Periodicals; 618.92
• DOI: 10.1002/pbc.24559
• Languages: English
• ISSNs: 1545-5009

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="pbc24559-sec-0001" sec-type="section"> <title>Background</title> <p>Over the last 25 years, donor source, conditioning, graft‐versus‐host disease prevention and supportive care for children undergoing hematopoeitic stem cell transplantation (HSCT) have changed dramatically. HSCT indications for acute lymphoblastic leukemia (ALL) now include high‐risk patients in first and subsequent remission. There is a large burden of infectious and pre‐HSCT morbidities, due to myelosuppressive therapy required for remission induction. We hypothesized that, despite these trends, overall survival (OS) had increased.</p> </sec> <sec id="pbc24559-sec-0002" sec-type="section"> <title>Procedure</title> <p>A retrospective audit of allogeneic pediatric HSCT for ALL was performed in our institution over 25 years. Outcomes for 136 HSCTs were analyzed in three consecutive 8‐year periods (Period 1: 1/1/1984–31/8/1992, Period 2: 1/9/1992–30/4/2001, Period 3: 1/5/2001–31/12/2009).</p> </sec> <sec id="pbc24559-sec-0003" sec-type="section"> <title>Results</title> <p>Despite a significant increase in unrelated donor HSCT, event‐free and OS over 25 years improved significantly. (EFS 31.6–64.8%, <italic>P</italic> = 0.0027; OS 41.8–78.9%, <italic>P</italic> < 0.0001) Concurrently, TRM dropped from 33% to 5% (<italic>P</italic> = 0.0004) whilst relapse rate was static (<italic>P</italic> = 0.07). TRM reduced significantly for matched sibling and unrelated cord blood transplantation (UCT) in Period 3 compared with earlier periods (<italic>P</italic> = 0.036, <italic>P</italic> = 0.0098, respectively). Factors leading to improved survival in patients undergoing UCT include better matching, higher total nucleated cell doses, and significantly faster neutrophil engraftment. Length of initial HSCT admission was similar over time.</p> </sec> <sec id="pbc24559-sec-0004" sec-type="section"> <title>Conclusion</title> <p>EFS and OS have increased significantly despite heightened HSCT complexity. This survival gain was due to TRM reduction. Contemporary patients have benefited from refined donor selection and improved supportive care. Overall rates of leukemic relapse post‐HSCT are unchanged, and remain the focus for improvement. Pediatr Blood Cancer 2013;160:1520–1527. © 2013 Wiley Periodicals, Inc.</p> </sec> </abstract>