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Survival Trends in Infants Undergoing Allogeneic Hematopoietic Cell Transplant.
Parikh, Suhag H; Satwani, Prakash; Ahn, Kwang Woo; Sahr, Natasha A; Fretham, Caitrin; Abraham, Allistair A; Agrawal, Vaibhav; Auletta, Jeffery J; Abdel-Azim, Hisham; Copelan, Edward; Diaz, Miguel-Angel; Dvorak, Christopher C; Frangoul, Haydar A; Freytes, Cesar O; Gadalla, Shahinaz M; Gale, Robert Peter; George, Biju; Gergis, Usama; Hashmi, Shahrukh; Hematti, Peiman; Hildebrandt, Gerhard C; Keating, Amy K; Lazarus, Hillard M; Myers, Kasiani C; Olsson, Richard F; Prestidge, Timothy; Rotz, Seth J; Savani, Bipin N; Shereck, Evan B; Williams, Kirsten M; Wirk, Baldeep; Pasquini, Marcelo C; Loren, Alison W.
Affiliation
  • Parikh SH; Department of Pediatric Blood and Marrow Transplant, Duke University Medical Center, Durham, North Carolina.
  • Satwani P; Division of Pediatric Hematology, Oncology and Stem Cell Transplantation, Department of Pediatrics, Columbia University Medical Center, New York, New York.
  • Ahn KW; Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee.
  • Sahr NA; St Jude Children's Research Hospital, Memphis, Tennessee.
  • Fretham C; Center for International Blood and Marrow Transplant Program, National Marrow Donor Program/Be the Match, Minneapolis, Minnesota.
  • Abraham AA; Division of Blood and Marrow Transplantation, Center for Cancer and Blood Disorders, Children's National Health System, Washington, DC.
  • Agrawal V; Indiana University, Indianapolis.
  • Auletta JJ; Blood and Marrow Transplant Program and Host Defense Program, Divisions of Hematology, Oncology, Bone Marrow Transplant and Infectious Diseases, Nationwide Children's Hospital, Columbus, Ohio.
  • Abdel-Azim H; Division of Hematology, Oncology and Blood and Marrow Transplantation, Children's Hospital of Los Angeles, Los Angeles.
  • Copelan E; Levine Cancer Institute, Atrium Health, Carolinas HealthCare System, Charlotte, North Carolina.
  • Diaz MA; Department of Hematology/Oncology, Hospital Infantil Universitario Niño Jesús, Madrid, Spain.
  • Dvorak CC; Division of Pediatric Allergy, Immunology and Bone Marrow Transplantation, Benioff Children's Hospital, University of California, San Francisco.
  • Frangoul HA; The Children's Hospital at TriStar Centennial Medical Center, Nashville, Tennessee.
  • Freytes CO; Sarah Cannon Research Institute, Nashville, Tennessee.
  • Gadalla SM; Texas Transplant Institute, San Antonio.
  • Gale RP; National Cancer Institute, Bethesda, Maryland.
  • George B; Division of Cancer Epidemiology & Genetics, National Cancer Institute, Clinical Genetics Branch, Rockville, Maryland.
  • Gergis U; Hematology Research Centre, Division of Experimental Medicine, Department of Medicine, Imperial College London, London, United Kingdom.
  • Hashmi S; Christian Medical College, Vellore, India.
  • Hematti P; Hematologic Malignancies & Bone Marrow Transplant, Department of Medicial Oncology, New York-Presbyterian Hospital/Weill Cornell Medical Center, New York.
  • Hildebrandt GC; King Faisal Specialist Hospital, Riyadh, Saudi Arabia.
  • Keating AK; Division of Hematology/Oncology/ Bone Marrow Transplantation, Department of Medicine, University of Wisconsin Hospital and Clinics, University of Wisconsin, Madison.
  • Lazarus HM; Markey Cancer Center, University Kentucky HealthCare, Lexington.
  • Myers KC; Children's Hospital Colorado, Denver.
  • Olsson RF; University of Colorado, Denver.
  • Prestidge T; Case Western Reserve University, Cleveland, Ohio.
  • Rotz SJ; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
  • Savani BN; Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital, Cincinnati, Ohio.
  • Shereck EB; Karolinska Institute, Stockholm, Sweden.
  • Williams KM; Blood and Cancer Centre, Starship Children's Health, Central Auckland, New Zealand.
  • Wirk B; Department of Pediatric Hematolgy, Oncology and Blood and Marrow Transplantation, Cleveland Clinic Children's Hospital, Cleveland, Ohio.
  • Pasquini MC; Vanderbilt University, Nashville, Tennessee.
  • Loren AW; Oregon Health & Science University, Portland.
JAMA Pediatr ; 173(5): e190081, 2019 05 01.
Article in En | MEDLINE | ID: mdl-30882883
ABSTRACT
Importance Studies demonstrating improved survival after allogeneic hematopoietic cell transplant generally exclude infants.

Objective:

To analyze overall survival trends and other outcomes among infants who undergo allogeneic hematopoietic cell transplant. Design, Setting, and

Participants:

In this cohort study, we used time-trend analysis to evaluate 3 periods 2000 through 2004, 2005 through 2009, and 2010 through 2014. The study was conducted in a multicenter setting through the Center for International Blood and Marrow Transplant Research, which is made up of a voluntary working group of more than 450 transplant centers worldwide. Two groups of infants aged 1 year or younger in 2 cohorts were included those with malignant conditions, such as leukemia, and those with nonmalignant disorders, including immunodeficiencies. Data analysis was conducted from July 2017 to December 2018. Exposures Allogeneic hematopoietic cell transplant. Main Outcomes and

Measures:

Survival trends, disease relapse, and toxicity.

Results:

A total of 2498 infants with a median age of 7 months (range, <1-12 months) were included. In the nonmalignant cohort (n = 472), survival rates improved from the first to the second period (hazard ratio, 0.77 [95% CI, 0.63-0.93]; P = .007) but did not change after 2004. Compared with infants with nonmalignant diseases (n = 2026; 3-year overall survival 2000-2004, 375/577 [65.0%]; 2005-2009, 503/699 [72.0%]; and 2010-2014, 555/750 [74.0%]), those with malignant conditions had poorer survival rates, without improvement over time (3-year overall survival 2000-2004, 109/199 [54.8%]; 2005-2009, 104/161 [64.6%]; and 2010-2014, 66/112 [58.9%]). From 2000 through 2014, relapse rates increased in infants with malignant conditions (3-year relapse rate 2000-2004, 19% [95% CI, 14%-25%]; 2005-2009, 23% [95% CI, 17%-30%]; 2010-2014, 36% [95% CI, 27%-46%]; P = .01). Sinusoidal obstruction syndrome was frequent, occurring with a cumulative incidence of 13% (95% CI, 11%-16%) of infants with nonmalignant diseases and 32% (95% CI, 22%-42%) of those with malignant diseases. Generally, recipients of human leukocyte antigen-identical sibling bone marrow grafts had the best outcomes. Conclusions and Relevance Survival rates have not improved for infants with malignant diseases over the 15-year study period. Infants with nonmalignant diseases had improved survival rates in the earlier but not the later study period. Higher relapses for the malignant cohort and toxicities for all infants remain significant challenges. Strategies to reduce relapse and toxicity and optimize donor and graft selection may improve outcomes in the future.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leukemia / Hematopoietic Stem Cell Transplantation / Immunologic Deficiency Syndromes Type of study: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Infant / Male / Newborn Language: En Journal: JAMA Pediatr Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leukemia / Hematopoietic Stem Cell Transplantation / Immunologic Deficiency Syndromes Type of study: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Infant / Male / Newborn Language: En Journal: JAMA Pediatr Year: 2019 Document type: Article