Interim Analysis of a Phase III Trial Comparing Cisplatin, Gemcitabine, and Vinorelbine vs. Either Cisplatin and Gemcitabine or Cisplatin and Vinorelbine in Advanced Non–Small-Cell Lung Cancer. A Southern Italy Cooperative Oncology Group Study

التفاصيل البيبلوغرافية
العنوان: Interim Analysis of a Phase III Trial Comparing Cisplatin, Gemcitabine, and Vinorelbine vs. Either Cisplatin and Gemcitabine or Cisplatin and Vinorelbine in Advanced Non–Small-Cell Lung Cancer. A Southern Italy Cooperative Oncology Group Study
المؤلفون: Luigi Maiorino, Giuseppe De Cataldis, G.P. Nicolella, Vito Lorusso, A Lamberti, R. Cioffi, Angelo Di Nota, Giuseppe Frasci, S. Mancarella, E. Micillo, Pasquale Comella, Domenico Bilancia, N. Panza, Luigi Manzione, Michele Di Natale, Giuseppe Comella
المصدر: Clinical Lung Cancer. 1:202-207
بيانات النشر: Elsevier BV, 2000.
سنة النشر: 2000
مصطلحات موضوعية: Pulmonary and Respiratory Medicine, Oncology, Cisplatin, Cancer Research, Chemotherapy, medicine.medical_specialty, business.industry, medicine.medical_treatment, Vinorelbine, Interim analysis, medicine.disease, Gemcitabine, law.invention, Regimen, Randomized controlled trial, law, Internal medicine, medicine, business, Lung cancer, medicine.drug
الوصف: In a previous phase II randomized study, a cisplatin/gemcitabine/vinorelbine (PGV) regimen produced a 50-week median survival time (MST) in advanced non–small-cell lung cancer (NSCLC) patients. The present trial was planned to randomly compare the outcome of patients treated with this new triplet regimen with those of patients receiving either cisplatin plus vinorelbine (PV) or cisplatin plus gemcitabine (PG) doublet combinations. One hundred eighty patients with stage IIIB (76) or IV (104) disease, aged ≤ 70 years, and with Eastern Cooperative Oncology Group performance status (ECOG PS) ≤ 1, were randomly allocated to receive: cisplatin, 50 mg/m 2 plus gemcitabine, 1000 mg/m 2 plus vinorelbine, 25 mg/m 2 (PGV) on days 1 and 8 every 3 weeks; cisplatin, 100 mg/m 2 on day 1 plus gemcitabine, 1000 mg/m 2 (PG) on days 1, 8, and 15 every 4 weeks; cisplatin, 120 mg/m 2 on days 1 and 29 plus vinorelbine, 30 mg/m 2 /week (PV). At the planned interim analysis, the MST of patients in the PGV, PG, and PV arms was 51, 42, and 35 weeks, respectively. The hazard of death (Cox analysis) for patients receiving PGV compared with those receiving PV was 0.35 (95% confidence index [CI], 0.16–0.77, P = 0.0058). The response rate was 47% in the PGV arm, 30% in the PG arm, and 25% in the PV arm. Severe neutropenia (75% vs. 45%), and vomiting (50% vs. 15%) significantly affected more patients in the PV than in the PGV arm. Since the difference in survival met early stopping rules, accrual to the PV arm was suspended. Enrollment still continues in the PGV and PG arms to ascertain whether the triplet regimen has a more significant effect on survival than that produced with the PG regimen.
تدمد: 1525-7304
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::706ccae4a7957e34b0bbf602fe0ed78e
https://doi.org/10.3816/clc.2000.n.003
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....706ccae4a7957e34b0bbf602fe0ed78e
قاعدة البيانات: OpenAIRE