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Dive into the research topics where Burton Appel is active.

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Featured researches published by Burton Appel.


Pediatric Blood & Cancer | 2013

Children's Oncology Group's 2013 blueprint for research: Hodgkin lymphoma

Kara M. Kelly; David R. W. Hodgson; Burton Appel; Lu Chen; Peter D. Cole; Terzah M. Horton; Frank G. Keller

In childhood Hodgkin lymphoma, estimated 5 years survival rates exceed 90%. Long‐term survival continues to decline from delayed toxicities. Key findings from recent Childrens Oncology Group trials include: (1) Radiotherapy selection may be based on early chemotherapy response assessed by both FDG‐PET and CT imaging, (2) A new prognostic factor score stratifies patients into risk categories; and (3) novel retrieval regimens were identified. A phase I/II trial is investigating Brentuximab vedotin (Bv) with gemcitabine in relapsed patients. A phase 3 trial will modify conventional chemotherapy and radiotherapy approaches through the addition of Bv, while incorporating translational biology to identify molecular targets. Pediatr Blood Cancer 2013; 60: 972–978.


Pediatric Blood & Cancer | 2012

Impact of low‐dose involved‐field radiation therapy on pediatric patients with lymphocyte‐predominant Hodgkin lymphoma treated with chemotherapy: A report from the Children's Oncology Group

Burton Appel; Lu Chen; Allen Buxton; Suzanne L. Wolden; David C. Hodgson; James Nachman

Treatment of pediatric lymphocyte‐predominant Hodgkin lymphoma (LPHL) is controversial but has typically consisted of both chemotherapy and radiation. Radiation therapy is associated with potential late effects in children and adolescents. We examined the impact of radiation therapy on long‐term outcome of patients with LPHL treated on CCG‐5942, a large pediatric cooperative group study of Hodgkin lymphoma (HL).


British Journal of Haematology | 2017

Outcomes of adults and children with primary mediastinal B-cell lymphoma treated with dose-adjusted EPOCH-R

Lisa Giulino-Roth; Tara O'Donohue; Zhengming Chen; Nancy L. Bartlett; Ann S. LaCasce; William Martin-Doyle; Matthew J. Barth; Kimberly Davies; Kristie A. Blum; Beth Christian; Carla Casulo; Sonali M. Smith; James Godfrey; Amanda M. Termuhlen; Matthew J. Oberley; Sarah Alexander; Sheila Weitzman; Burton Appel; Benjamin Mizukawa; Jakub Svoboda; Zeinab Afify; Melinda Pauly; Hema Dave; Rebecca A. Gardner; Deborah M. Stephens; William A. Zeitler; Jennifer Levine; Michael E. Williams; Jody L. Sima; Catherine M. Bollard

Treatment with dose‐adjusted EPOCH (etoposide, doxorubicin, cyclophosphamide, vincristine, prednisone) chemotherapy and rituximab (DA‐EPOCH‐R) has become the standard of care for primary mediastinal B‐cell lymphoma (PMBCL) at many institutions despite limited data in the multi‐centre setting. We report a large, multi‐centre retrospective analysis of children and adults with PMBCL treated with DA‐EPOCH‐R to characterize outcomes and evaluate prognostic factors. We assessed 156 patients with PMBCL treated with DA‐EPOCH‐R across 24 academic centres, including 38 children and 118 adults. All patients received at least one cycle of DA‐EPOCH‐R. Radiation therapy was administered in 14·9% of patients. With median follow‐up of 22·6 months, the estimated 3‐year event‐free survival (EFS) was 85·9% [95% confidence interval (CI) 80·3–91·5] and overall survival was 95·4% (95% CI 91·8–99·0). Outcomes were not statistically different between paediatric and adult patients. Thrombotic complications were reported in 28·2% of patients and were more common in paediatric patients (45·9% vs. 22·9%, P = 0·011). Seventy‐five per cent of patients had a negative fluorodeoxyglucose positron emission tomography (FDG‐PET) scan at the completion of DA‐EPOCH‐R, defined as Deauville score 1–3. Negative FDG‐PET at end‐of‐therapy was associated with improved EFS (95·4% vs. 54·9%, P < 0·001). Our data support the use of DA‐EPOCH‐R for the treatment of PMBCL in children and adults. Patients with a positive end‐of‐therapy FDG‐PET scan have an inferior outcome.


Journal of Clinical Oncology | 2016

Minimal Treatment of Low-Risk, Pediatric Lymphocyte-Predominant Hodgkin Lymphoma: A Report From the Children's Oncology Group

Burton Appel; Lu Chen; Allen Buxton; Robert E. Hutchison; David C. Hodgson; Peter F. Ehrlich; Louis S. Constine; Cindy L. Schwartz

PURPOSE Childrens Oncology Group study AHOD03P1 was designed to determine whether excellent outcomes can be maintained for patients with low-risk, pediatric lymphocyte-predominant Hodgkin lymphoma (LPHL) with a strategy of resection alone or minimal chemotherapy. PATIENTS AND METHODS Patients with stage IA LPHL in a single node that was completely resected were observed without further therapy; recurrences were treated with three cycles of doxorubicin/vincristine/prednisone/cyclophosphamide (AV-PC). Patients with unresected stage IA or stage IIA LPHL were treated with three cycles of AV-PC. Patients with less than a complete response (CR) to AV-PC received 21-Gy involved-field radiation therapy (IFRT). RESULTS A total of 183 eligible patients were enrolled; 178 were evaluable. Of these, 52 patients underwent complete resection of a single node. There were 13 relapses at a median of 11.5 months; 5-year event-free survival (EFS) was 77% (range, 62% to 87%). A total of 135 patients received AV-PC; 126 were treated at diagnosis and nine at relapse after surgery alone. Eleven patients receiving AV-PC had less than CR and received IFRT. Fourteen first events occurred among 135 patients (12 relapses and two second malignancies). Two relapses occurred in patients who had received IFRT. Five-year EFS was 88.8% (95% CI, 81.8% to 93.2%). Five-year EFS for the entire cohort was 85.5% (95% CI, 79.2% to 90.1%); overall survival was 100%. CONCLUSION Some 75% of highly selected pediatric patients with LPHL may be spared chemotherapy after surgical resection alone. Pediatric LPHL has excellent EFS with chemotherapy that is less intensive than standard regimens; > 90% of patients can avoid radiation therapy. The salvage rate for the few relapses is high, with 100% survival overall.


Pediatric Blood & Cancer | 2018

Variant histology, IgD and CD30 expression in low-risk pediatric nodular lymphocyte predominant Hodgkin lymphoma: A report from the Children's Oncology Group

Ramona Vesna Untanu; Jason Back; Burton Appel; Qinglin Pei; Lu Chen; Allen Buxton; David C. Hodgson; Peter F. Ehrlich; Louis S. Constine; Cindy L. Schwartz; Robert E. Hutchison

Histologic prognostic factors have been described for nodular lymphocyte predominant Hodgkin lymphoma (NLPHL). This study examines histologic and immunophenotypic variants in a clinical trial for pediatric NLPHL.


Pediatric Blood & Cancer | 2018

Outcomes in intermediate-risk pediatric lymphocyte-predominant Hodgkin lymphoma: A report from the Children's Oncology Group

Lianna J. Marks; Qinglin Pei; Rizvan Bush; Allen Buxton; Burton Appel; Kara M. Kelly; Cindy L. Schwartz; Debra L. Friedman

Optimal management of patients with intermediate‐risk lymphocyte‐predominant Hodgkin lymphoma (LPHL) is unclear due to their small numbers in most clinical trials. Childrens Oncology Group AHOD0031, a randomized phase III trial of pediatric patients with intermediate‐risk Hodgkin lymphoma (HL), included patients with LPHL. We report the outcomes of these patients and present directions for future therapeutic strategies.


ASCO Meeting Abstracts | 2013

Treatment of pediatric lymphocyte predominant Hodgkin lymphoma (LPHL): A report from the Children's Oncology Group.

Burton Appel; Lu Chen; Robert E. Hutchison; David C. Hodgson; Peter F. Ehrlich; Louis S. Constine; Cindy L. Schwartz


Hematological Oncology | 2017

OUTCOMES OF ADULTS, ADOLESCENTS, AND CHILDREN WITH PRIMARY MEDIASTINAL B-CELL LYMPHOMA TREATED WITH DOSE-ADJUSTED EPOCH-R THERAPY: a MULTICENTER RETROSPECTIVE ANALYSIS

L.G. Roth; T. O'Donohue; Zhengming Chen; Nancy L. Bartlett; William Martin-Doyle; Matthew J. Barth; Kimberly Davies; Beth Christian; Carla Casulo; James Godfrey; Matthew J. Oberley; Sarah Alexander; Sheila Weitzman; Burton Appel; Jakub Svoboda; Zeinab Afify; Melinda Pauly; Hema Dave; Rebecca A. Gardner; Deborah M. Stephens; W.A. Zeitler; Jennifer Levine; Michael E. Williams; Catherine M. Bollard; John P. Leonard


Journal of Pediatric Hematology Oncology | 2018

Surgeon concordance in the assessment of resectability for stage ia nodular lymphocyte predominant hodgkin lymphoma

Jennifer H. Aldrink; Burton Appel; Joel Kaplan; Robert E. Hutchison; Cindy L. Schwartz; Kara M. Kelly; Kathleen McCarten; Peter F. Ehrlich


International Journal of Radiation Oncology Biology Physics | 2018

Patterns of Involved-Field Radiation Therapy Protocol Deviations in Pediatric Versus Adolescent and Young Adults With Hodgkin Lymphoma: A Report From the Children's Oncology Group AHOD0031

Aaron S. Parzuchowski; Rizvan Bush; Qinglin Pei; Debra L. Friedman; Thomas J. Fitzgerald; Suzanne L. Wolden; Kavita V. Dharmarajan; Louis S. Constine; Fran Laurie; Sandy Kessel; Burton Appel; Karen S. Fernández; Angela Punnett; Cindy L. Schwartz; Jacob T. Cox; Stephanie A. Terezakis

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Cindy L. Schwartz

University of Texas MD Anderson Cancer Center

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Lu Chen

Children's Oncology Group

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Allen Buxton

Children's Oncology Group

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Robert E. Hutchison

State University of New York Upstate Medical University

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Suzanne L. Wolden

Memorial Sloan Kettering Cancer Center

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David C. Hodgson

Princess Margaret Cancer Centre

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Kara M. Kelly

Roswell Park Cancer Institute

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