Concurrent gemcitabine and 3D radiotherapy in patients with stage III unresectable non-small cell lung cancer
Autor: | RM Pieterman, Gerald S. M. A. Kerner, Ellen M Driever, Thijo J N Hiltermann, Edwin Blokzijl, Marc J F Mertens, Harry J.M. Groen, John W. G. van Putten, Erwin M. Wiegman, Jeroen J W Liesker, Leon F. A. van Dullemen, Tineke E. J. Renkema, Joachim Widder |
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Přispěvatelé: | Guided Treatment in Optimal Selected Cancer Patients (GUTS), Translational Immunology Groningen (TRIGR) |
Jazyk: | angličtina |
Rok vydání: | 2014 |
Předmět: |
Male
Oncology Radiation-Sensitizing Agents Lung Neoplasms medicine.medical_treatment Kaplan-Meier Estimate PACLITAXEL Deoxycytidine chemistry.chemical_compound CHEMORADIATION CONSOLIDATION DOCETAXEL Carcinoma Non-Small-Cell Lung Antineoplastic Combined Chemotherapy Protocols INDUCTION CHEMOTHERAPY ONCOLOGY-GROUP THORACIC RADIOTHERAPY Aged 80 and over Chemoradiotherapy Middle Aged I TRIAL Concurrent chemoradiotherapy Treatment Outcome Radiology Nuclear Medicine and imaging Female medicine.drug Adult medicine.medical_specialty Vinblastine Disease-Free Survival Internal medicine medicine Humans Radiology Nuclear Medicine and imaging Lung cancer Aged CARBOPLATIN Radiotherapy business.industry Research Induction chemotherapy RANDOMIZED PHASE-III medicine.disease Gemcitabine Carboplatin Radiation therapy chemistry RADIATION Cisplatin Radiotherapy Conformal Stage III NSCLC business Esophagitis |
Zdroj: | Radiation oncology, 9:190. BMC Radiation Oncology (London, England) |
ISSN: | 1748-717X |
Popis: | Background: Stage III unresectable non-small cell lung cancer (NSCLC) is preferably treated with concurrent schedules of chemoradiotherapy, but none is clearly superior Gemcitabine is a radiosensitizing cytotoxic drug that has been studied in phase 1 and 2 studies in this setting. The aim of this study was to describe outcome and toxicity of low-dose weekly gemcitabine combined with concurrent 3-dimensional conformal radiotherapy (3D-CRT).Patients & methods: Treatment consisted of two cycles of a cisplatin and gemcitabine followed by weekly gemcitabine 300 mg/m(2) during 5 weeks of 3D-CRT, 60 Gy in 5 weeks (hypofractionated-accelerated). Overall survival (OS), progression-free survival (PFS), and treatment related toxicity according to Common Toxicity Criteria of Adverse Events (CTCAE) version 3.0 were assessed.Results: Between February 2002 and August 2008, 318 patients were treated. Median age was 64 years (range 36-86); 72% were male, WHO PS 0/1/2 was 44/53/3%. Median PFS was 15.5 months (95% confidence interval [CI], 12.9-18.1) and median OS was 24.6 months (95% CI., 21.0-28.1). Main toxicity (CTCAE grade >= 3) was dysphagia (12.6%), esophagitis (9.6%), followed by radiation pneumonitis (3.0%). There were five treatment related deaths (1.6%), two due to esophagitis and three due to radiation pneumonitis.Conclusion: Concurrent low-dose gemcitabine and 3D-CRT provides a comparable survival and toxicity profile to other available treatment schemes for unresectable stage III. |
Databáze: | OpenAIRE |
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