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Originally published as JCO Early Release 10.1200/JCO.2007.15.1001 on October 6 2008 © 2008 American Society of Clinical Oncology. Involved-Nodal Radiation Therapy As a Component of Combination Therapy for Limited-Stage Hodgkin's Lymphoma: A Question of Field Size
From the Departments of Radiation Oncology, Pathology, and Medical Oncology, British Columbia Cancer Agency; and the University of British Columbia, Vancouver, Canada Corresponding author: Belinda A. Campbell, MBBS, FRANZCR, British Columbia Cancer Agency, 600 West 10th Ave, Vancouver, British Columbia, Canada; e-mail: Bcampbell3{at}bccancer.bc.ca Purpose Combined-modality therapy is the standard of care for limited-stage Hodgkin's lymphoma (HL). Radiation therapy has evolved from extended-field radiation therapy (EFRT) to involved-field radiation therapy (IFRT), reducing toxicity while maintaining high cure rates. Recent publications recommend a further reduction to involved-nodal radiation therapy (INRT), however, this has not been clinically validated.
Patients and Methods We identified 325 patients with limited-stage HL, diagnosed between May 1, 1989 and April 1, 2005, and treated with chemotherapy and radiation therapy following era-specific guidelines: EFRT until 1996; IFRT from 1996 to 2001; INRT
Results At diagnosis, median age was 35 years; 52% male; stage IA 29%; stage IIA 71%. Ninety-five percent of patients received two chemotherapy cycles. The three radiation therapy groups were: EFRT, 39%; IFRT, 30%; and INRT
Conclusion Reduction in field size appears to be safe, without an increased risk of LRR in patients receiving INRT published online ahead of print atwww.jco.org on October 6, 2008 Supported in part by generous donations from the Turner Family Fund for Lymphoma Research, the Porte Endowment for Lymphoma Research, and the Centre for Lymphoid Cancer of the British Columbia Cancer Agency. Presented in part at the 14th European Cancer Conference, Barcelona, Spain, September 23-27, 2007. Authors disclosures of potential conflicts of interest and author contributions are found at the end of this article.
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Copyright © 2008 by the American Society of Clinical Oncology, Online ISSN: 1527-7755. Print ISSN: 0732-183X
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