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Cited by 406

The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.

ABVD Alone versus Radiation-Based Therapy in Limited-Stage Hodgkin's Lymphoma

Open access
Meyer, Ralph M., Gospodarowicz, Mary K., Connors, Joseph M., Pearcey, Robert G., Wells, Woodrow A., Winter, Jane N., Horning, Sandra J., Dar, A. Rashid, Shustik, Chaim, Stewart, Douglas A., Crump, Michael, Djurfeldt, Marina S., Chen, Bingshu E., Shepherd, Lois E.·2012·New England Journal of Medicine

Abstract

BACKGROUND: Chemotherapy plus radiation treatment is effective in controlling stage IA or IIA nonbulky Hodgkin's lymphoma in 90% of patients but is associated with late treatment-related deaths. Chemotherapy alone may improve survival because it is associated with fewer late deaths. METHODS: We randomly assigned 405 patients with previously untreated stage IA or IIA nonbulky Hodgkin's lymphoma to treatment with doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) alone or to treatment with subtotal nodal radiation therapy, with or without ABVD therapy. Patients in the ABVD-only group, both those with a favorable risk profile and those with an unfavorable risk profile, received four to six cycles of ABVD. Among those assigned to subtotal nodal radiation therapy, patients who had a favorable risk profile received subtotal nodal radiation therapy alone and patients with an unfavorable risk profile received two cycles of ABVD plus subtotal nodal radiation therapy. The primary end point was 12-year overall survival. RESULTS: The median length of follow-up was 11.3 years. At 12 years, the rate of overall survival was 94% among those receiving ABVD alone, as compared with 87% among those receiving subtotal nodal radiation therapy (hazard ratio for death with ABVD alone, 0.50; 95% confidence interval [CI], 0.25 to 0.99; P=0.04); the rates of freedom from disease progression were 87% and 92% in the two groups, respectively (hazard ratio for disease progression, 1.91; 95% CI, 0.99 to 3.69; P=0.05); and the rates of event-free survival were 85% and 80%, respectively (hazard ratio for event, 0.88; 95% CI, 0.54 to 1.43; P=0.60). Among the patients randomly assigned to ABVD alone, 6 patients died from Hodgkin's lymphoma or an early treatment complication and 6 died from another cause; among those receiving radiation therapy, 4 deaths were related to Hodgkin's lymphoma or early toxic effects from the treatment and 20 were related to another cause. CONCLUSIONS: Among patients with Hodgkin's lymphoma, ABVD therapy alone, as compared with treatment that included subtotal nodal radiation therapy, was associated with a higher rate of overall survival owing to a lower rate of death from other causes. (Funded by the Canadian Cancer Society and the National Cancer Institute; HD.6 ClinicalTrials.gov number, NCT00002561.).

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Metadata

Authors
Meyer, R. M., Gospodarowicz, M. K., Connors, J. M., Pearcey, R. G., Wells, W. A., Winter, J. N., Horning, S. J., Dar, A. R., Shustik, C., Stewart, D. A., Crump, M., Djurfeldt, M. S., Chen, B. E., & Shepherd, L. E.
Venue
New England Journal of Medicine
Published
2012-02-02
Volume
366
Issue
5
Pages
399-408
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2099126154
Cited by
406
References
18
FWCI
23.81
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: ABVD Alone versus Radiation-Based Therapy in Limited-Stage Hodgkin's Lymphoma. https://app.cochat.ai/papers/10.1056/nejmoa1111961
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Meyer, R. M., Gospodarowicz, M. K., Connors, J. M., Pearcey, R. G., Wells, W. A., Winter, J. N., Horning, S. J., Dar, A. R., Shustik, C., Stewart, D. A., Crump, M., Djurfeldt, M. S., Chen, B. E., & Shepherd, L. E. (2012). ABVD Alone versus Radiation-Based Therapy in Limited-Stage Hodgkin's Lymphoma. New England Journal of Medicine. https://doi.org/10.1056/nejmoa1111961

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.