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Induction chemotherapy followed by gefitinib and concurrent thoracic radiotherapy for unresectable locally advanced adenocarcinoma of the lung: a multicenter feasibility study (JCOG 0402).
Niho, S; Ohe, Y; Ishikura, S; Atagi, S; Yokoyama, A; Ichinose, Y; Okamoto, H; Takeda, K; Shibata, T; Tamura, T; Saijo, N; Fukuoka, M.
Afiliación
  • Niho S; Division of Thoracic Oncology, National Cancer Center Hospital East, Kashiwa. Electronic address: siniho@east.ncc.go.jp.
  • Ohe Y; Division of Thoracic Oncology, National Cancer Center Hospital East, Kashiwa.
  • Ishikura S; Department of Radiology, Nagoya City University Graduate School of Medical Sciences, Nagoya.
  • Atagi S; Department of Thoracic Oncology, Division of Internal Medicine, NHO Kinki-Chuo Chest Medical Center, Sakai.
  • Yokoyama A; Department of Internal Medicine, Niigata Cancer Center, Niigata.
  • Ichinose Y; Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka.
  • Okamoto H; Department of Respiratory Medicine, Yokohama Municipal Citizen's Hospital, Yokohama.
  • Takeda K; Department of Clinical Oncology, Osaka City General Hospital, Osaka.
  • Shibata T; Japan Clinical Oncology Group Data Center, Multi-institutional Clinical Trial Support Center, National Cancer Center, Tokyo.
  • Tamura T; Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo.
  • Saijo N; Department of Medical Oncology, Kinki University School of Medicine, Osaka, Japan.
  • Fukuoka M; Department of Medical Oncology, Kinki University School of Medicine, Osaka, Japan.
Ann Oncol ; 23(9): 2253-2258, 2012 Sep.
Article en En | MEDLINE | ID: mdl-22357446
ABSTRACT

BACKGROUND:

We conducted a feasibility study of induction chemotherapy followed by gefitinib and thoracic radiotherapy (TRT) for unresectable locally advanced adenocarcinoma of the lung. PATIENTS AND

METHODS:

Patients received induction chemotherapy with cisplatin (80 mg/m(2), days 1 and 22) and vinorelbine (25 mg/m(2), days 1, 8, 22, and 29) followed by gefitinib (250 mg daily, beginning on day 43, for 1 year) and TRT (60 Gy/30 fractions, days 57-98). The primary end point was feasibility, which was defined as the proportion of patients who completed 60 Gy of TRT and received >75% of the planned dose of gefitinib without developing grade 2 or worse pneumonitis.

RESULTS:

Of the 38 enrolled patients, 23 patients [60.5% ; 80% confidence interval (CI) 48.8-71.3] completed treatment without experiencing grade 2 or worse pneumonitis. During the chemoradiation phase, grade 3-4 alanine aminotransferase elevations were observed in 37.1% of the patients. The overall response rate was 73.0% . The median survival time was 28.5 months (95% CI 22.5-38.2), and the 2-year survival rate was 65.4% .

CONCLUSIONS:

Although the results did not meet our criterion for feasibility, the toxicity was acceptable. This treatment warrants further evaluation among patients with locally advanced non-small-cell lung cancer harboring epidermal growth factor receptor mutations.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Adenocarcinoma / Protocolos de Quimioterapia Combinada Antineoplásica / Quimioterapia de Inducción / Neoplasias Pulmonares Tipo de estudio: Clinical_trials Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2012 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Adenocarcinoma / Protocolos de Quimioterapia Combinada Antineoplásica / Quimioterapia de Inducción / Neoplasias Pulmonares Tipo de estudio: Clinical_trials Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2012 Tipo del documento: Article