Patients with recurrent or metastatic cancer commonly suffer from debilitating toxicity associated with conventional treatment modalities, as well as disease-related symptoms, often with a concomitant negative impact on health-related quality of life (HRQoL). Patient-reported outcomes (PROs) provide important insights into the patient experience in clinical trials. Nivolumab is a programmed death-1 receptor inhibitor that extends survival in patients with recurrent or metastatic disease in multiple tumor types. In this review, we summarize published PRO analyses from eight phase II-IV clinical trials with nivolumab for the treatment of melanoma, non-small cell lung cancer, renal cell carcinoma (RCC), and squamous cell carcinoma of the head ...
Nivolumab is a programmed death receptor-1 (PD-1) blocking antibody approved for the treatment of ad...
Aim To assess diseases outcomes and tolerability of reallife second-line nivolumab in a series of me...
Objectives: We report 2-year results from CheckMate 141 to establish the long-term efficacy and safe...
BACKGROUND: Patients with platinum-refractory recurrent or metastatic squamous cell carcinoma of th...
In the era of value-based oncology care, stakeholders are increasingly using patient reported outcom...
BACKGROUND:Response patterns with immune checkpoint inhibitors may be different from those with chem...
Recently, a global phase III study demonstrated that nivolumab markedly improved patient outcomes in...
BACKGROUND: Nivolumab, a programmed death 1 inhibitor, has been approved as second-line treatment fo...
Background: The Italian Renal Cell Cancer Early Access Program was an expanded access program that a...
OBJECTIVES:We report 2-year results from CheckMate 141 to establish the long-term efficacy and safet...
Background: The Italian Renal Cell Cancer Early Access Program was an expanded access program that a...
BACKGROUND: Response patterns with immune checkpoint inhibitors may be different from those with che...
BACKGROUND: Nivolumab, a programmed death 1 inhibitor, has been approved as second-line treatment fo...
Nivolumab is an anti-PD-1 monoclonal antibody currently used as immunotherapy for patients with recu...
Blockade of the immune checkpoint PD-1 is a new and promising strategy for the treatment of advanced...
Nivolumab is a programmed death receptor-1 (PD-1) blocking antibody approved for the treatment of ad...
Aim To assess diseases outcomes and tolerability of reallife second-line nivolumab in a series of me...
Objectives: We report 2-year results from CheckMate 141 to establish the long-term efficacy and safe...
BACKGROUND: Patients with platinum-refractory recurrent or metastatic squamous cell carcinoma of th...
In the era of value-based oncology care, stakeholders are increasingly using patient reported outcom...
BACKGROUND:Response patterns with immune checkpoint inhibitors may be different from those with chem...
Recently, a global phase III study demonstrated that nivolumab markedly improved patient outcomes in...
BACKGROUND: Nivolumab, a programmed death 1 inhibitor, has been approved as second-line treatment fo...
Background: The Italian Renal Cell Cancer Early Access Program was an expanded access program that a...
OBJECTIVES:We report 2-year results from CheckMate 141 to establish the long-term efficacy and safet...
Background: The Italian Renal Cell Cancer Early Access Program was an expanded access program that a...
BACKGROUND: Response patterns with immune checkpoint inhibitors may be different from those with che...
BACKGROUND: Nivolumab, a programmed death 1 inhibitor, has been approved as second-line treatment fo...
Nivolumab is an anti-PD-1 monoclonal antibody currently used as immunotherapy for patients with recu...
Blockade of the immune checkpoint PD-1 is a new and promising strategy for the treatment of advanced...
Nivolumab is a programmed death receptor-1 (PD-1) blocking antibody approved for the treatment of ad...
Aim To assess diseases outcomes and tolerability of reallife second-line nivolumab in a series of me...
Objectives: We report 2-year results from CheckMate 141 to establish the long-term efficacy and safe...