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A phase II study of cetuximab and radiation in elderly and/or poor performance status patients with locally advanced non-small-cell lung cancer (N0422).
Jatoi, A; Schild, S E; Foster, N; Henning, G T; Dornfeld, K J; Flynn, P J; Fitch, T R; Dakhil, S R; Rowland, K M; Stella, P J; Soori, G S; Adjei, A A.
Afiliação
  • Jatoi A; Mayo Clinic Rochester, Rochester, MN. Electronic address: jatoi.aminah@mayo.edu.
  • Schild SE; Mayo Clinic Arizona, Scottsdale, AZ.
  • Foster N; Mayo Clinic Rochester, Rochester, MN.
  • Henning GT; Michigan Cancer Consortium, Ann Arbor, MI.
  • Dornfeld KJ; Duluth City Clinical Oncology Program, Duluth, MN.
  • Flynn PJ; Metro-Minnesota Community Oncology Program, St Louis Park, MN.
  • Fitch TR; Mayo Clinic Arizona, Scottsdale, AZ.
  • Dakhil SR; Wichita Community Clinical Oncology Program, Wichita, KS.
  • Rowland KM; Carle Cancer Center City Clinical Oncology Program, Urbana, IL.
  • Stella PJ; Michigan Cancer Consortium, Ann Arbor, MI.
  • Soori GS; Missouri Valley Cancer Consortium, Omaha, NE.
  • Adjei AA; Roswell Park Cancer Institute, Buffalo, NY, USA.
Ann Oncol ; 21(10): 2040-2044, 2010 Oct.
Article em En | MEDLINE | ID: mdl-20570832
ABSTRACT

BACKGROUND:

Non-small-cell lung cancer (NSCLC) is a disease of the elderly. Seeking a tolerable but effective regimen, we tested cetuximab + radiation in elderly and/or poor performance status patients with locally advanced NSCLC. PATIENTS AND

METHODS:

Older patients [≥ 65 years with an Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2] or younger patients (performance status of 2) received cetuximab 400 mg/m(2) i.v. on day 1 followed by weekly cetuximab 250 mg/m(2) i.v. with concomitant radiation of 6000 cGy in 30 fractions. The primary end point was the percentage who lived 11+ months.

RESULTS:

This 57-patient cohort had a median age (range) of 77 years (60-87), and 12 (21%) had a performance status of 2. Forty of 57 (70%) lived 11+ months, thus exceeding the anticipated survival rate of 50%. The median survival was 15.1 months [95% confidence interval (CI) 13.1-19.3 months], and the median time to cancer progression was 7.2 months (95% CI 5.8-8.6 months). No treatment-related deaths occurred, but 31 patients experienced grade 3+ adverse events, most commonly fatigue, anorexia, dyspnea, rash, and dysphagia, each of which occurred in <10% of patients.

CONCLUSION:

This combination merits further study in this group of patients.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares / Anticorpos Monoclonais / Antineoplásicos Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2010 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares / Anticorpos Monoclonais / Antineoplásicos Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2010 Tipo de documento: Article