Rare Pediatric Non-Hodgkin Lymphomas: A Report From Children's Oncology Group Study ANHL 04B1
Background Non‐Hodgkin lymphoma (NHL) is a relatively common malignancy in pediatric patients; however, a small subgroup have unusual lymphoma subtypes for the pediatric population. Procedure The Children's Oncology Group Rare and Cutaneous NHL registry's (protocol ANHL 04B1) main objectiv...
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| Published in | Pediatric blood & cancer Vol. 63; no. 5; pp. 794 - 800 |
|---|---|
| Main Authors | , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
United States
Blackwell Publishing Ltd
01.05.2016
Wiley Subscription Services, Inc |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1545-5009 1545-5017 |
| DOI | 10.1002/pbc.25881 |
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| Abstract | Background
Non‐Hodgkin lymphoma (NHL) is a relatively common malignancy in pediatric patients; however, a small subgroup have unusual lymphoma subtypes for the pediatric population.
Procedure
The Children's Oncology Group Rare and Cutaneous NHL registry's (protocol ANHL 04B1) main objectives were to determine the pathologic, biologic, and clinical features of rare and cutaneous pediatric NHL and establish a bank of centrally reviewed tissue specimens. We report the clinical data, treatment data, and outcome for rare pediatric NHL.
Results
In 101 lymphomas, there is a 97.8% concordance between the reviewing study pathologists and an 87.6% concordance between the central and institutional pathology review. Samples in the specimen bank include primary tumor tissue that is snap frozen, in paraffin blocks, or H&E‐stained and unstained paraffin slides as well as blood, serum, and bone marrow. This descriptive analysis shows that children with pediatric follicular lymphoma, mucosa‐associated lymphoid tissue, nodal marginal zone lymphoma, primary cutaneous, primary central nervous system lymphoma, and subcutaneous panniculitis‐like T‐cell lymphomas have 100% survival at a median of 2 years from enrollment. There are early deaths, mostly from progressive disease, in subjects with peripheral T‐cell (not otherwise specified), NKT, and hepatosplenic T‐cell lymphomas.
Conclusions
This registry provides high‐quality biologic specimens with clinical data to investigators working on the biology of these unusual pediatric diseases. |
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| AbstractList | Background Non-Hodgkin lymphoma (NHL) is a relatively common malignancy in pediatric patients; however, a small subgroup have unusual lymphoma subtypes for the pediatric population. Procedure The Children's Oncology Group Rare and Cutaneous NHL registry's (protocol ANHL 04B1) main objectives were to determine the pathologic, biologic, and clinical features of rare and cutaneous pediatric NHL and establish a bank of centrally reviewed tissue specimens. We report the clinical data, treatment data, and outcome for rare pediatric NHL. Results In 101 lymphomas, there is a 97.8% concordance between the reviewing study pathologists and an 87.6% concordance between the central and institutional pathology review. Samples in the specimen bank include primary tumor tissue that is snap frozen, in paraffin blocks, or H&E-stained and unstained paraffin slides as well as blood, serum, and bone marrow. This descriptive analysis shows that children with pediatric follicular lymphoma, mucosa-associated lymphoid tissue, nodal marginal zone lymphoma, primary cutaneous, primary central nervous system lymphoma, and subcutaneous panniculitis-like T-cell lymphomas have 100% survival at a median of 2 years from enrollment. There are early deaths, mostly from progressive disease, in subjects with peripheral T-cell (not otherwise specified), NKT, and hepatosplenic T-cell lymphomas. Conclusions This registry provides high-quality biologic specimens with clinical data to investigators working on the biology of these unusual pediatric diseases. BACKGROUNDNon-Hodgkin lymphoma (NHL) is a relatively common malignancy in pediatric patients; however, a small subgroup have unusual lymphoma subtypes for the pediatric population.PROCEDUREThe Children's Oncology Group Rare and Cutaneous NHL registry's (protocol ANHL 04B1) main objectives were to determine the pathologic, biologic, and clinical features of rare and cutaneous pediatric NHL and establish a bank of centrally reviewed tissue specimens. We report the clinical data, treatment data, and outcome for rare pediatric NHL.RESULTSIn 101 lymphomas, there is a 97.8% concordance between the reviewing study pathologists and an 87.6% concordance between the central and institutional pathology review. Samples in the specimen bank include primary tumor tissue that is snap frozen, in paraffin blocks, or H&E-stained and unstained paraffin slides as well as blood, serum, and bone marrow. This descriptive analysis shows that children with pediatric follicular lymphoma, mucosa-associated lymphoid tissue, nodal marginal zone lymphoma, primary cutaneous, primary central nervous system lymphoma, and subcutaneous panniculitis-like T-cell lymphomas have 100% survival at a median of 2 years from enrollment. There are early deaths, mostly from progressive disease, in subjects with peripheral T-cell (not otherwise specified), NKT, and hepatosplenic T-cell lymphomas.CONCLUSIONSThis registry provides high-quality biologic specimens with clinical data to investigators working on the biology of these unusual pediatric diseases. Background Non‐Hodgkin lymphoma (NHL) is a relatively common malignancy in pediatric patients; however, a small subgroup have unusual lymphoma subtypes for the pediatric population. Procedure The Children's Oncology Group Rare and Cutaneous NHL registry's (protocol ANHL 04B1) main objectives were to determine the pathologic, biologic, and clinical features of rare and cutaneous pediatric NHL and establish a bank of centrally reviewed tissue specimens. We report the clinical data, treatment data, and outcome for rare pediatric NHL. Results In 101 lymphomas, there is a 97.8% concordance between the reviewing study pathologists and an 87.6% concordance between the central and institutional pathology review. Samples in the specimen bank include primary tumor tissue that is snap frozen, in paraffin blocks, or H&E‐stained and unstained paraffin slides as well as blood, serum, and bone marrow. This descriptive analysis shows that children with pediatric follicular lymphoma, mucosa‐associated lymphoid tissue, nodal marginal zone lymphoma, primary cutaneous, primary central nervous system lymphoma, and subcutaneous panniculitis‐like T‐cell lymphomas have 100% survival at a median of 2 years from enrollment. There are early deaths, mostly from progressive disease, in subjects with peripheral T‐cell (not otherwise specified), NKT, and hepatosplenic T‐cell lymphomas. Conclusions This registry provides high‐quality biologic specimens with clinical data to investigators working on the biology of these unusual pediatric diseases. Non-Hodgkin lymphoma (NHL) is a relatively common malignancy in pediatric patients; however, a small subgroup have unusual lymphoma subtypes for the pediatric population. The Children's Oncology Group Rare and Cutaneous NHL registry's (protocol ANHL 04B1) main objectives were to determine the pathologic, biologic, and clinical features of rare and cutaneous pediatric NHL and establish a bank of centrally reviewed tissue specimens. We report the clinical data, treatment data, and outcome for rare pediatric NHL. In 101 lymphomas, there is a 97.8% concordance between the reviewing study pathologists and an 87.6% concordance between the central and institutional pathology review. Samples in the specimen bank include primary tumor tissue that is snap frozen, in paraffin blocks, or H&E-stained and unstained paraffin slides as well as blood, serum, and bone marrow. This descriptive analysis shows that children with pediatric follicular lymphoma, mucosa-associated lymphoid tissue, nodal marginal zone lymphoma, primary cutaneous, primary central nervous system lymphoma, and subcutaneous panniculitis-like T-cell lymphomas have 100% survival at a median of 2 years from enrollment. There are early deaths, mostly from progressive disease, in subjects with peripheral T-cell (not otherwise specified), NKT, and hepatosplenic T-cell lymphomas. This registry provides high-quality biologic specimens with clinical data to investigators working on the biology of these unusual pediatric diseases. |
| Author | Welch, Jennifer J. G. Smith, Lynette M. Gross, Thomas G. Bollard, Catherine M. Galardy, Paul J. Perkins, Sherrie L. O'Suoji, Chibuzo Weitzman, Sheila Simko, Stephen J. Termuhlen, Amanda M. |
| Author_xml | – sequence: 1 givenname: Chibuzo surname: O'Suoji fullname: O'Suoji, Chibuzo organization: Division of Pediatric Hematology/Oncology, West Virginia University, West Virginia, Charleston – sequence: 2 givenname: Jennifer J. G. surname: Welch fullname: Welch, Jennifer J. G. email: atermuhlen@chla.usc.edu organization: Division of Pediatric Hematology/Oncology, Hasbro Children's Hospital, Alpert Medical School Brown University, Rhode Island, Providence – sequence: 3 givenname: Sherrie L. surname: Perkins fullname: Perkins, Sherrie L. organization: Department of Pathology, University of Utah Health Sciences, Utah, Salt Lake City – sequence: 4 givenname: Lynette M. surname: Smith fullname: Smith, Lynette M. organization: Department of Biostatistics, University of Nebraska Medical Center, Nebraska, Omaha – sequence: 5 givenname: Sheila surname: Weitzman fullname: Weitzman, Sheila organization: Division of Pediatric Hematology/Oncology, Hospital for Sick Children, Ontario, Toronto, Canada – sequence: 6 givenname: Stephen J. surname: Simko fullname: Simko, Stephen J. organization: Texas Children's Cancer Center, Baylor College of Medicine, Texas, Houston – sequence: 7 givenname: Paul J. surname: Galardy fullname: Galardy, Paul J. organization: Division of Pediatric Hematology/Oncology, Mayo Clinic, Minnesota, Rochester – sequence: 8 givenname: Catherine M. surname: Bollard fullname: Bollard, Catherine M. organization: Children's National Health System, The George Washington University, District of Columbia, Washington – sequence: 9 givenname: Thomas G. surname: Gross fullname: Gross, Thomas G. organization: National Cancer Institute, Maryland, Rockville – sequence: 10 givenname: Amanda M. surname: Termuhlen fullname: Termuhlen, Amanda M. organization: Department of Pediatrics, Keck School of Medicine, University of Southern California, California, Los Angeles |
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| Keywords | Non-Hodgkin lymphoma follicular lymphoma cutaneous lymphoma |
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| Notes | COG Chair's - No. U10CA098543 Human Specimen Banking in NCI-Sponsored Clinical Trials; Grant number: - No. U24CA114766; Grant sponsor Statistics & Data Center - No. U10CA098413 ark:/67375/WNG-R34ZC4N1-N Statistics & Data Center; Grant number: - No. U10CA098413. istex:F8E60FDC11D1B0000005191345C348E33D0E13B9 COG Chair's; Grant number: - No. U10CA098543; Grant sponsor ArticleID:PBC25881 Human Specimen Banking in NCI-Sponsored Clinical Trials - No. U24CA114766 Grant sponsor: COG Chair's; Grant number: U10CA098543; Grant sponsor: Human Specimen Banking in NCI‐Sponsored Clinical Trials; Grant number: U24CA114766; Grant sponsor: Statistics & Data Center; Grant number: U10CA098413. Chibuzo O'Suoji and Jennifer Welch are co‐first authors. Conflict of interest: S.J.S. is currently employed by Genentech/Roche. The authors report no relevant conflicts of interest related to the work presented here. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Feature-1 content type line 23 |
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database publication-title: Cancer – volume: 45 start-page: 21 year: 2006 end-page: 24 article-title: Subcutaneous panniculitis‐like T‐cell lymphoma: Successful initial treatment with prednisolone and cyclosporin A publication-title: Intern Med – volume: 32 start-page: 1169 year: 2013 end-page: 1175 article-title: The presenting manifestations of subcutaneous panniculitis‐like T‐cell lymphoma and T‐cell lymphoma and cutaneous gammadelta T‐cell lymphoma may mimic those of rheumatic diseases: A report of 11 cases publication-title: Clin Rheumatol – volume: 14 start-page: 741 year: 2008 end-page: 747 article-title: Long‐term results of autologous hematopoietic cell transplantation for peripheral T cell lymphoma: The Stanford experience publication-title: Biol Blood Marrow Transplant – volume: 50 start-page: 784 year: 2008 end-page: 787 article-title: Peripheral T‐cell lymphoma in childhood: Population‐based experience in the United Kingdom over 20 years publication-title: Pediatr BloodCancer – volume: 21 start-page: E8 year: 2006 article-title: Primary central nervous system lymphoma in children publication-title: Neurosurg Focus – start-page: 439 year: 2008 – volume: 40 start-page: 924 year: 2013 end-page: 934 article-title: Hypopigmented mycosis fungoides in childhood and adolescence: A long‐term retrospective study publication-title: J Cutan Pathol – volume: 120 start-page: 2395 year: 2012 end-page: 2404 article-title: Pediatric‐type nodal follicular lymphoma: An indolent clonal proliferation in children and adults with high proliferation index and no BCL2 rearrangement publication-title: Blood – volume: 16 start-page: 2780 year: 1998 end-page: 2795 article-title: New approach to classifying non‐Hodgkin's lymphomas: Clinical features of the major histologic subtypes. Non‐Hodgkin's Lymphoma Classification Project publication-title: J Clin Oncol – volume: 20 start-page: 1080 year: 2009 end-page: 1085 article-title: Hepatosplenic gamma‐delta T‐cell lymphoma: Clinicopathological features and treatment publication-title: Ann Oncol – volume: 92 start-page: 258 year: 2012 end-page: 263 article-title: Ten‐year experience of bexarotene therapy for cutaneous T‐cell lymphoma in Finland publication-title: Acta Derm Venereol – volume: 27 start-page: 1378 year: 2012 end-page: 1384 article-title: Successful treatment of primary central nervous system lymphoma without irradiation in children: Single center experience publication-title: J Korean Med Sci |
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Non‐Hodgkin lymphoma (NHL) is a relatively common malignancy in pediatric patients; however, a small subgroup have unusual lymphoma subtypes for the... Non-Hodgkin lymphoma (NHL) is a relatively common malignancy in pediatric patients; however, a small subgroup have unusual lymphoma subtypes for the pediatric... Background Non-Hodgkin lymphoma (NHL) is a relatively common malignancy in pediatric patients; however, a small subgroup have unusual lymphoma subtypes for the... BACKGROUNDNon-Hodgkin lymphoma (NHL) is a relatively common malignancy in pediatric patients; however, a small subgroup have unusual lymphoma subtypes for the... |
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| Title | Rare Pediatric Non-Hodgkin Lymphomas: A Report From Children's Oncology Group Study ANHL 04B1 |
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