Volume 51, Issue 2 pp. 216-221
Research Article

Serum protein expression profiling in pediatric Hodgkin lymphoma: A report from the Children's Oncology Group

Lining Qi PhD

Lining Qi PhD

Department of Microbiology and Molecular Cell Biology, Eastern Virginia Medical School, Norfolk, Virginia

Center for Biomedical Proteomics, Eastern Virginia Medical School, Norfolk, Virginia

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Lisa Cazares BS

Lisa Cazares BS

Department of Microbiology and Molecular Cell Biology, Eastern Virginia Medical School, Norfolk, Virginia

Center for Biomedical Proteomics, Eastern Virginia Medical School, Norfolk, Virginia

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Cris Johnson MD

Cris Johnson MD

Departments of Microbiology and Pediatrics, University of Virginia, Charlottesville, Virginia

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Pedro de Alarcon MD

Pedro de Alarcon MD

Saint Jude Children's Research Hospital, Memphis, Tennessee

Hodgkin Lymphoma Committee, Children's Oncology Group, Arcadia, California

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Gary M. Kupfer MD

Corresponding Author

Gary M. Kupfer MD

Departments of Microbiology and Pediatrics, University of Virginia, Charlottesville, Virginia

Hodgkin Lymphoma Committee, Children's Oncology Group, Arcadia, California

LMP 2074, Yale University School of Medicine, 333 Cedar St. New Haven, CT 06520.===Search for more papers by this author
O. John Semmes PhD

O. John Semmes PhD

Department of Microbiology and Molecular Cell Biology, Eastern Virginia Medical School, Norfolk, Virginia

Center for Biomedical Proteomics, Eastern Virginia Medical School, Norfolk, Virginia

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First published: 17 April 2008
Citations: 11

Abstract

Background

The prognosis for children with Hodgkin lymphoma (HL) treated with a risk adjusted combination of radiation therapy and multi-drug chemotherapy has markedly improved. There remains a group of patients whose disease either recurs or does not respond to therapy. Protein expression profiling has been used to define protein characteristics of serum from adult patients in order to improve screening for early diagnosis. However, profiling for the purpose of staging and defining prognostic characteristics of childhood diseases is not well studied. The current stage-based risk assignment of HL cannot predict the patients within a risk group that are destined to recur or do not respond to therapy. Thus, a need exists to develop new methodologies to better stratify the risk classification of pediatric HL.

Procedure

We have completed a preliminary project to identify characteristic serum protein peaks determined by protein expression profiling in serum of 22 subjects with HL, 13 with stage II HL and 9 with stage III or IV.

Results

Protein profiling successfully discriminated between high grade (III/IV) HL and low grade (II) HL.

Conclusion

These data lay the basis for prospective studies to identify protein expression profiles useful for diagnosis, prognosis, treatment stratification, and the follow-up of minimal residual disease. Pediatr Blood Cancer © 2008 Wiley-Liss, Inc.

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