The role of concurrent chemoradiotherapy (CRT) in patients with non-small-cell lung cancer (NSCLC) unsuitable for radical therapy but who require locoregional treatment has not been defined. The aims of this phase I trial were thus to develop a novel regimen of weekly chemotherapy concurrent with high-dose palliative RT (40 Gy/20 fractions) and assess its tolerability, objective and symptomatic response rates. Eligible patients had stage I-IIIB NSCLC unsuitable for radical RT or limited stage IV disease, ECOG PS<or=1 and required locoregional therapy. Treatment was RT (40 Gy/20 fractions/5 per week) and weekly Vinorelbine plus Cisplatin escalated in six planned dose levels (DLs). At 4 weeks post-RT, patients received two cycles of Cisplatin...
International audienceINTRODUCTION: Cisplatin in combination with vinorelbine has reported an optima...
The aim of the study was to evaluate the activity of cisplatin (CDDP) plus vinorelbine (VNR) in pati...
Background: In this open-label phase I study, the maximum-tolerated dose of cetuximab with concurren...
Aim: Despite recent advances, outcomes for patients with stage III non–small cell lung cancer (NSCLC...
IntroductionConcurrent chemoradiotherapy with full doses of cisplatin-based chemotherapy is standard...
Background: Concurrent chemoradiotherapy is the current standard treatment for inoperable stage III ...
Introduction:The aim of this multicenter phase II trial was to evaluate the combination of oral vino...
[[abstract]]Weekly vinorelbine injection with cisplatin had been used in treatment of non-small-cell...
This is phase II study evaluating a non-platinum-containing regimen, used in conjunction with radiot...
BACKGROUND: Intravenous vinorelbine plus cisplatin is widely prescribed for the treatment of NSCLC. ...
Purpose: To evaluate the efficacy of a novel multiday schedule of vinorelbine and cisplatin in patie...
Thirty consecutive patients with stage IIIB-IV non small cell lung cancer were treated with a combin...
IntroductionThe optimal treatment for patients with stage IIIA to IIIB non-small cell lung cancer (N...
BACKGROUND: To determine the activity and safety of a sequential regimen of cisplatin and vinorelbin...
IntroductionCisplatin in combination with vinorelbine has reported an optimal activity/tolerance rat...
International audienceINTRODUCTION: Cisplatin in combination with vinorelbine has reported an optima...
The aim of the study was to evaluate the activity of cisplatin (CDDP) plus vinorelbine (VNR) in pati...
Background: In this open-label phase I study, the maximum-tolerated dose of cetuximab with concurren...
Aim: Despite recent advances, outcomes for patients with stage III non–small cell lung cancer (NSCLC...
IntroductionConcurrent chemoradiotherapy with full doses of cisplatin-based chemotherapy is standard...
Background: Concurrent chemoradiotherapy is the current standard treatment for inoperable stage III ...
Introduction:The aim of this multicenter phase II trial was to evaluate the combination of oral vino...
[[abstract]]Weekly vinorelbine injection with cisplatin had been used in treatment of non-small-cell...
This is phase II study evaluating a non-platinum-containing regimen, used in conjunction with radiot...
BACKGROUND: Intravenous vinorelbine plus cisplatin is widely prescribed for the treatment of NSCLC. ...
Purpose: To evaluate the efficacy of a novel multiday schedule of vinorelbine and cisplatin in patie...
Thirty consecutive patients with stage IIIB-IV non small cell lung cancer were treated with a combin...
IntroductionThe optimal treatment for patients with stage IIIA to IIIB non-small cell lung cancer (N...
BACKGROUND: To determine the activity and safety of a sequential regimen of cisplatin and vinorelbin...
IntroductionCisplatin in combination with vinorelbine has reported an optimal activity/tolerance rat...
International audienceINTRODUCTION: Cisplatin in combination with vinorelbine has reported an optima...
The aim of the study was to evaluate the activity of cisplatin (CDDP) plus vinorelbine (VNR) in pati...
Background: In this open-label phase I study, the maximum-tolerated dose of cetuximab with concurren...