Predictors of Loss to Follow-Up Among Pediatric and Adult Hematopoietic Cell Transplantation Survivors: A Report from the Center for International Blood and Marrow Transplant Research

Follow-up is integral for hematopoietic cell transplantation (HCT) care to ensure surveillance and intervention for complications. We characterized the incidence of and predictors for being lost to follow-up. Two-year survivors of first allogeneic HCT (10,367 adults and 3865 children) or autologous...

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Veröffentlicht in:BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION 2020-03, Vol.26 (3), p.553-561
Hauptverfasser: Buchbinder, David, Brazauskas, Ruta, Bo-Subait, Khalid, Ballen, Karen, Parsons, Susan, Johns, Tami, Hahn, Theresa, Sharma, Akshay, Steinbergs, Amir, D'Souza, Anita, Kumar, Anita J, Yoshimi, Ayami, Wirk, Baldeep, Shawl, Bronwen, Freytes, Cesar, LeMaistre, Charles, Bredeson, Christopher, Dandoy, Christopher, Almaguer, David, Marks, David I, Szwajcer, David, Hale, Gregory, Schouten, Harry, Hashem, Hasan, Schoemans, Helene, Murthy, Hemant S, Lazarus, Hillard M, Cerny, Jan, Tay, Jason, Yared, Jean A, Adekola, Kehinde, Schultz, Kirk R, Lehmann, Leslie, Burns, Linda, Aljurf, Mahmoud, Diaz, Miguel Angel, Majhail, Navneet, Farhadfar, Nosha, Kamble, Rammurti, Olsson, Richard, Schears, Raquel, Seo, Sachiko, Beattie, Sara, Chhabra, Saurabh, Savani, Bipin N, Badawy, Sherif, Ganguly, Siddhartha, Ciurea, Stefan, Marino, Susana, Gergis, Usama, Kuwatsuka, Yachiyo, Inamoto, Yoshihiro, Khera, Nandita, Hashmi, Shahrukh, Wood, William, Saber, Wael
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container_title BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
container_volume 26
creator Buchbinder, David
Brazauskas, Ruta
Bo-Subait, Khalid
Ballen, Karen
Parsons, Susan
Johns, Tami
Hahn, Theresa
Sharma, Akshay
Steinbergs, Amir
D'Souza, Anita
Kumar, Anita J
Yoshimi, Ayami
Wirk, Baldeep
Shawl, Bronwen
Freytes, Cesar
LeMaistre, Charles
Bredeson, Christopher
Dandoy, Christopher
Almaguer, David
Marks, David I
Szwajcer, David
Hale, Gregory
Schouten, Harry
Hashem, Hasan
Schoemans, Helene
Murthy, Hemant S
Lazarus, Hillard M
Cerny, Jan
Tay, Jason
Yared, Jean A
Adekola, Kehinde
Schultz, Kirk R
Lehmann, Leslie
Burns, Linda
Aljurf, Mahmoud
Diaz, Miguel Angel
Majhail, Navneet
Farhadfar, Nosha
Kamble, Rammurti
Olsson, Richard
Schears, Raquel
Seo, Sachiko
Beattie, Sara
Chhabra, Saurabh
Savani, Bipin N
Badawy, Sherif
Ganguly, Siddhartha
Ciurea, Stefan
Marino, Susana
Gergis, Usama
Kuwatsuka, Yachiyo
Inamoto, Yoshihiro
Khera, Nandita
Hashmi, Shahrukh
Wood, William
Saber, Wael
description Follow-up is integral for hematopoietic cell transplantation (HCT) care to ensure surveillance and intervention for complications. We characterized the incidence of and predictors for being lost to follow-up. Two-year survivors of first allogeneic HCT (10,367 adults and 3865 children) or autologous HCT (7291 adults and 467 children) for malignant/nonmalignant disorders between 2002 and 2013 reported to the Center for International Blood and Marrow Transplant Research were selected. The cumulative incidence of being lost to follow-up (defined as having missed 2 consecutive follow-up reporting periods) was calculated. Marginal Cox models (adjusted for center effect) were fit to evaluate predictors. The 10-year cumulative incidence of being lost to follow-up was 13% (95% confidence interval [CI], 12% to 14%) in adult allogeneic HCT survivors, 15% (95% CI, 14% to 16%) in adult autologous HCT survivors, 25% (95% CI, 24% to 27%) in pediatric allogeneic HCT survivors, and 24% (95% CI, 20% to 29%) in pediatric autologous HCT survivors. Factors associated with being lost to follow-up include younger age, nonmalignant disease, public/no insurance (reference: private), residence farther from the tranplantation center, and being unmarried in adult allogeneic HCT survivors; older age and testicular/germ cell tumor (reference: non-Hodgkin lymphoma) in adult autologous HCT survivors; older age, public/no insurance (reference: private), and nonmalignant disease in pediatric allogeneic HCT survivors; and older age in pediatric autologous HCT survivors. Follow-up focusing on minimizing attrition in high-risk groups is needed to ensure surveillance for late effects.
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We characterized the incidence of and predictors for being lost to follow-up. Two-year survivors of first allogeneic HCT (10,367 adults and 3865 children) or autologous HCT (7291 adults and 467 children) for malignant/nonmalignant disorders between 2002 and 2013 reported to the Center for International Blood and Marrow Transplant Research were selected. The cumulative incidence of being lost to follow-up (defined as having missed 2 consecutive follow-up reporting periods) was calculated. Marginal Cox models (adjusted for center effect) were fit to evaluate predictors. The 10-year cumulative incidence of being lost to follow-up was 13% (95% confidence interval [CI], 12% to 14%) in adult allogeneic HCT survivors, 15% (95% CI, 14% to 16%) in adult autologous HCT survivors, 25% (95% CI, 24% to 27%) in pediatric allogeneic HCT survivors, and 24% (95% CI, 20% to 29%) in pediatric autologous HCT survivors. 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We characterized the incidence of and predictors for being lost to follow-up. Two-year survivors of first allogeneic HCT (10,367 adults and 3865 children) or autologous HCT (7291 adults and 467 children) for malignant/nonmalignant disorders between 2002 and 2013 reported to the Center for International Blood and Marrow Transplant Research were selected. The cumulative incidence of being lost to follow-up (defined as having missed 2 consecutive follow-up reporting periods) was calculated. Marginal Cox models (adjusted for center effect) were fit to evaluate predictors. The 10-year cumulative incidence of being lost to follow-up was 13% (95% confidence interval [CI], 12% to 14%) in adult allogeneic HCT survivors, 15% (95% CI, 14% to 16%) in adult autologous HCT survivors, 25% (95% CI, 24% to 27%) in pediatric allogeneic HCT survivors, and 24% (95% CI, 20% to 29%) in pediatric autologous HCT survivors. Factors associated with being lost to follow-up include younger age, nonmalignant disease, public/no insurance (reference: private), residence farther from the tranplantation center, and being unmarried in adult allogeneic HCT survivors; older age and testicular/germ cell tumor (reference: non-Hodgkin lymphoma) in adult autologous HCT survivors; older age, public/no insurance (reference: private), and nonmalignant disease in pediatric allogeneic HCT survivors; and older age in pediatric autologous HCT survivors. Follow-up focusing on minimizing attrition in high-risk groups is needed to ensure surveillance for late effects.</abstract><pub>ELSEVIER SCIENCE INC</pub><oa>free_for_read</oa></addata></record>
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ispartof BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2020-03, Vol.26 (3), p.553-561
issn 1083-8791
language eng
recordid cdi_kuleuven_dspace_123456789_668830
source Lirias (KU Leuven Association); Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; ScienceDirect Journals (5 years ago - present); Alma/SFX Local Collection
title Predictors of Loss to Follow-Up Among Pediatric and Adult Hematopoietic Cell Transplantation Survivors: A Report from the Center for International Blood and Marrow Transplant Research
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