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Author Notes:

Corresponding author: Mehdi Hamadani, MD, Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, 9200 W. Wisconsin Avenue, Suite C5500, Milwaukee, WI 53226, USA; Phone: 414-805-0643; Fax: 414-805-0714; mhamadani@mcw.edu.

Conception and design: Praskash Satwani & Mehdi Hamadani.

Collection and assembly of data: Kwang Woo Ahn, Jeanette Carreras and Mehdi Hamadani.

Data analysis: Kwang Woo Ahn, Jeanette Carreras with final approval on fidelity of analysis by CIBMTR statistical center in Milwaukee, WI.

Data Interpretation: Prakash Satwani, Kwang Woo Ahn, Jeanette Carreras and Mehdi Hamadani. All remaining authors provided written comments on interpretation of data.

Manuscript writing: Prakash Satwani and Mehdi Hamadani prepared the first manuscript draft. All authors critically reviewed the study and provided detailed written comments initially at the conception of study protocol, after results of analysis were available, and finally helped revise/write the final draft of the manuscript.

We would like to acknowledge the patients and centers reporting to CIBMTR and CIBMTR Lymphoma. We would also like to acknowledge the following committee members for their scientific input: Baldeep Wirk, Basem M. William, Harry C. Schouten, Nishitha M. Reddy, David Rizzieri, Mahmoud Aljurf, Reinhold Munker, Brandon Hayes-Lattin, Victor A. Lewis, and Maggie M. Simaytis for administrative support.

No conflict of interests.

Subjects:

Research Funding:

The CIBMTR is supported by Public Health Service Grant/Cooperative Agreement U24-CA076518 from the National Cancer Institute (NCI), the National Heart, Lung and Blood Institute (NHLBI) and the National Institute of Allergy and Infectious Diseases (NIAID); a Grant/Cooperative Agreement 5U10HL069294 from NHLBI and NCI; a contract HHSH250201200016C with Health Resources and Services Administration (HRSA/DHHS); two Grants N00014-12-1-0142 and N00014-13-1-0039 from the Office of Naval Research.

For the full list of donors, see Acknowledgments in the full article.

Keywords:

  • Life Sciences & Biomedicine
  • Biophysics
  • Oncology
  • Hematology
  • Immunology
  • Transplantation
  • STEM-CELL TRANSPLANTATION
  • HIGH-DOSE CHEMOTHERAPY
  • EVENT-FREE SURVIVAL
  • SALVAGE THERAPY
  • CONDITIONING REGIMEN
  • RECURRENT
  • CYCLOPHOSPHAMIDE

A prognostic model predicting autologous transplantation outcomes in children, adolescents and young adults with Hodgkin lymphoma

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Journal Title:

Bone Marrow Transplantation

Volume:

Volume 50, Number 11

Publisher:

, Pages 1416-1423

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Autologous hematopoietic cell transplantation (AutoHCT) is a potentially curative treatment modality for relapsed/refractory Hodgkin lymphoma (HL). However, no large studies have evaluated pretransplant factors predictive of outcomes of AutoHCT in children, adolescents and young adults (CAYA, age <30 years). In a retrospective study, we analyzed 606 CAYA patients (median age 23 years) with relapsed/refractory HL who underwent AutoHCT between 1995 and 2010. The probabilities of PFS at 1, 5 and 10 years were 66% (95% confidence interval (CI): 62-70), 52% (95% CI: 48-57) and 47% (95% CI: 42-51), respectively. Multivariate analysis for PFS demonstrated that at the time of AutoHCT patients with Karnofsky/Lansky score ≥90, no extranodal involvement and chemosensitive disease had significantly improved PFS. Patients with time from diagnosis to first relapse of <1 year had a significantly inferior PFS. A prognostic model for PFS was developed that stratified patients into low-, intermediate- and high-risk groups, predicting for 5-year PFS probabilities of 72% (95% CI: 64-80), 53% (95% CI: 47-59) and 23% (95% CI: 9-36), respectively. This large study identifies a group of CAYA patients with relapsed/refractory HL who are at high risk of progression after AutoHCT. Such patients should be targeted for novel therapeutic and/or maintenance approaches post-AutoHCT.

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© 2015 Macmillan Publishers Limited. All rights reserved.

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