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Intercalated Dosing Schedule of Erlotinib and Docetaxel as a Therapeutic Strategy to Avoid Antagonism and Optimize Its Benefits in Advanced Non-Small-Cell Lung Cancer. A Randomized Phase II Clinical Trial.
Juan, Óscar; Aparisi, Francisco; Sánchez-Hernández, Alfredo; Muñoz-Langa, José; Esquerdo, Gaspar; García-Sánchez, José; López, Antonio; Garde, Javier; Giner, Vicente.
Afiliação
  • Juan Ó; Hospital Universitari i Politècnic La Fe, Medical Oncology Department, Valencia, Spain. Electronic address: juan_osc@gva.es.
  • Aparisi F; Hospital Virgen de los Lirios, Medical Oncology Department, Alcoy, Spain.
  • Sánchez-Hernández A; Consorcio Hospitalario Provincial de Castellón, Medical Oncology Department, Castellón, Spain.
  • Muñoz-Langa J; Hospital Universitario Dr Peset, Medical Oncology Department, Valencia, Spain.
  • Esquerdo G; ITIC-Clínica Benidorm, Benidorm, Alicante, Spain.
  • García-Sánchez J; Hospital Arnau de Vilanova, Medical Oncology Department, Valencia, Spain.
  • López A; Hospital Universitari Sant Joan de Alicante, Medical Oncology Department, Alicante, Spain.
  • Garde J; Hospital Arnau de Vilanova, Medical Oncology Department, Valencia, Spain.
  • Giner V; Hospital de Sagunto, Medical Oncology Department, Sagunto, Spain.
Clin Lung Cancer ; 16(3): 193-9, 2015 May.
Article em En | MEDLINE | ID: mdl-25547902
ABSTRACT

INTRODUCTION:

The purpose of this study was to assess whether an intercalated dosing schedule of erlotinib and docetaxel could avoid possible negative interactions and optimize the benefit obtained as second-line therapy in non-small-cell lung cancer (NSCLC) patients. PATIENTS AND

METHODS:

A phase II randomized clinical trial was designed for advanced NSCLC patients in whom previous chemotherapy treatment had failed. The experimental arm with 33 patients consisted of erlotinib 150 mg/d orally, intermittent administration on days 2 to 16 every 21 days, combined with docetaxel 75 mg/m(2) every 21 days; the control arm with 35 patients consisted of erlotinib 150 mg/d orally, administered continuously. The study's primary end point was the proportion of patients who remained progression-free at 6 months in the 2 arms.

RESULTS:

The proportion of patients who remained progression-free at 6 months was of 5 patients (15%) in the intercalated arm and 3 patients (9%) in the erlotinib monotherapy arm respectively. Median progression-free survival (PFS) was 3.0 versus 2.1 months (hazard ratio [HR], 0.65; 95% confidence interval [CI], 0.39-1.06; P = .086). Median overall survival (OS) was 7.5 and 5.2 months (HR, 0.70; 95% CI, 0.41-1.19; P = .19). Disease control rates were 51.7% and 36.4%, respectively. No new safety signals were observed.

CONCLUSION:

Erlotinib and docetaxel with intermittent administration of erlotinib improved PFS, OS, and disease control rates compared with erlotinib alone. All of our results indicated that an intercalated dosing schedule of erlotinib and docetaxel could be more efficient than erlotinib treatment alone. Therefore, further studies should be developed in a larger number of patients. This study has shown the absence of antagonism between docetaxel and erlotinib when given in an intercalated fashion.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Idioma: En Ano de publicação: 2015 Tipo de documento: Article