Objectives: Induction chemotherapy followed by cetuximab and RT (IBRT) (Arm A) was compared to cisplatin/RT (CRT) (Arm B) in a randomized phase III study. Patients and methods: Na\uefve patients with stage III-IVa, histologically proven locally advanced head and neck cancer (LASCCHN) were eligible. Arm A (IBRT): 3 TPF induction followed by cetuximab-RT (equivalent daily dose 2 Gy up to 70 Gy); Arm B: 3 cisplatin concurrent with the same RT scheduling. Due to slow accrual and incomplete data collection a futility analysis was performed. Results: 236/282 patients were evaluable. Therefore, no formal analyses can be made between the two arms. OS was 45.2/53.6 months in Arm A/B. Complete responses were achieved in 64% of patients in both arms. ...
Purpose: This study describes the long-term survival and toxicity outcomes of a multicenter randomiz...
B490 (EudraCT# 2011-002564-24) is a randomized, phase 2b, noninferiority study investigating the eff...
[[abstract]]Background: To evaluate the therapeutic efficacy of sequential regimen using cetuximab-b...
International audiencePurposeBoth concurrent chemoradiotherapy (CT-RT) and cetuximab radiotherapy (c...
Purpose Both concurrent chemoradiotherapy (CT-RT) and cetuximab radiotherapy (cetux-RT) have been es...
PURPOSE We performed an open-label randomized controlled phase III study comparing treatment outcome...
PURPOSE: To study the feasibility of induction chemotherapy added to concomitant cisplatin-based che...
PURPOSE: This was an open, randomized, multicenter, phase I/II study to investigate the safety and t...
PURPOSE: Despite the lack of evidence to support its implementation in the clinical practice, induct...
Background: Platinum-based chemoradiation (CCRT) is the standard treatment for Locally Advanced Head...
OBJECTIVE: To analyze the outcome of N3 patients treated with very accelerated radiotherapy (VART) o...
International audiencePurposeTo investigate the effect of adding concurrent chemotherapy (CT) to cet...
PurposeCombining cisplatin or cetuximab with radiation improves overall survival (OS) of patients wi...
PURPOSE: To evaluate the feasibility and efficacy of moderately accelerated intensity-modulated radi...
Cetuximab is active in the treatment of squamous cell carcinoma of the head and neck (SCCHN), enhanc...
Purpose: This study describes the long-term survival and toxicity outcomes of a multicenter randomiz...
B490 (EudraCT# 2011-002564-24) is a randomized, phase 2b, noninferiority study investigating the eff...
[[abstract]]Background: To evaluate the therapeutic efficacy of sequential regimen using cetuximab-b...
International audiencePurposeBoth concurrent chemoradiotherapy (CT-RT) and cetuximab radiotherapy (c...
Purpose Both concurrent chemoradiotherapy (CT-RT) and cetuximab radiotherapy (cetux-RT) have been es...
PURPOSE We performed an open-label randomized controlled phase III study comparing treatment outcome...
PURPOSE: To study the feasibility of induction chemotherapy added to concomitant cisplatin-based che...
PURPOSE: This was an open, randomized, multicenter, phase I/II study to investigate the safety and t...
PURPOSE: Despite the lack of evidence to support its implementation in the clinical practice, induct...
Background: Platinum-based chemoradiation (CCRT) is the standard treatment for Locally Advanced Head...
OBJECTIVE: To analyze the outcome of N3 patients treated with very accelerated radiotherapy (VART) o...
International audiencePurposeTo investigate the effect of adding concurrent chemotherapy (CT) to cet...
PurposeCombining cisplatin or cetuximab with radiation improves overall survival (OS) of patients wi...
PURPOSE: To evaluate the feasibility and efficacy of moderately accelerated intensity-modulated radi...
Cetuximab is active in the treatment of squamous cell carcinoma of the head and neck (SCCHN), enhanc...
Purpose: This study describes the long-term survival and toxicity outcomes of a multicenter randomiz...
B490 (EudraCT# 2011-002564-24) is a randomized, phase 2b, noninferiority study investigating the eff...
[[abstract]]Background: To evaluate the therapeutic efficacy of sequential regimen using cetuximab-b...