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Ibritumomab consolidation after 3 cycles of CHOP plus radiotherapy in high-risk limited-stage aggressive B-cell lymphoma: SWOG S0313.
Persky, Daniel O; Miller, Thomas P; Unger, Joseph M; Spier, Catherine M; Puvvada, Soham; Stea, B Dino; Press, Oliver W; Constine, Louis S; Barton, Kevin P; Friedberg, Jonathan W; LeBlanc, Michael; Fisher, Richard I.
Afiliación
  • Persky DO; University of Arizona Cancer Center, University of Arizona, Tucson, AZ;
  • Miller TP; University of Arizona Cancer Center, University of Arizona, Tucson, AZ;
  • Unger JM; SWOG Statistical Center, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Spier CM; Department of Pathology, University of Arizona, Tucson, AZ;
  • Puvvada S; University of Arizona Cancer Center, University of Arizona, Tucson, AZ;
  • Stea BD; University of Arizona Cancer Center, University of Arizona, Tucson, AZ;
  • Press OW; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Constine LS; James P. Wilmot Cancer Center, University of Rochester, Rochester, NY;
  • Barton KP; Loyola University Medical Center, Maywood IL; and.
  • Friedberg JW; James P. Wilmot Cancer Center, University of Rochester, Rochester, NY;
  • LeBlanc M; SWOG Statistical Center, Fred Hutchinson Cancer Research Center, Seattle, WA;
  • Fisher RI; Fox Chase Cancer Center-Temple Health, Philadelphia, PA.
Blood ; 125(2): 236-41, 2015 Jan 08.
Article en En | MEDLINE | ID: mdl-25395425
ABSTRACT
In the S0313 trial, we evaluated the impact of adding ibritumomab tiuxetan consolidation to 3 cycles of standard cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) chemotherapy plus involved field radiotherapy (IFRT) in patients with limited-stage aggressive B-cell non-Hodgkin lymphoma (LD-NHL). Patients with at least 1 stage-modified adverse risk factor (nonbulky stage II, age >60 years, elevated lactate dehydrogenase, or World Health Organization performance status of 2) were treated with CHOP on days 1, 22, and 43, followed 3 weeks later by 40 to 50 Gy of IFRT. An ibritumomab tiuxetan regimen was initiated 3 to 6 weeks following IFRT. Forty-six patients were registered and eligible, with median follow-up of 7.3 years. The progression-free survival estimate is 89% at 2 years, 82% at 5 years, and 75% at 7 years. The overall survival estimate is 91% at 2 years, 87% at 5 years, and 82% at 7 years. Grade 4 adverse events occurring more than once included neutropenia (8), leukopenia (5), and lymphopenia (2). Febrile neutropenia was observed in 4 patients. No cases of treatment-related myeloid neoplasms were noted. In conclusion, patients with high-risk LD-NHL treated with 3 cycles of CHOP plus IFRT followed by ibritumomab tiuxetan consolidation had outcomes that compare favorably to our historical experience. The clinical trial was registered at www.clinicaltrials.gov as #NCT00070018.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Linfoma de Células B / Quimioradioterapia / Quimioterapia de Consolidación / Anticuerpos Monoclonales Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Año: 2015 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Linfoma de Células B / Quimioradioterapia / Quimioterapia de Consolidación / Anticuerpos Monoclonales Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Año: 2015 Tipo del documento: Article