Immune checkpoint inhibitors for metastatic bladder cancer
•Atezolizumab and Pembrolizumab showed in phase II (Atezolizumab and Pembrolizumab) and phase III (Pembrolizumab) trials to improve clinical outcome of patients progressed to platinum based therapy.•Atezolizumab failed to show OS benefit over chemotherapy in a phase III trial for patients progressed...
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Published in | Cancer treatment reviews Vol. 64; pp. 11 - 20 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier Ltd
01.03.2018
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Subjects | |
Online Access | Get full text |
ISSN | 0305-7372 1532-1967 1532-1967 |
DOI | 10.1016/j.ctrv.2017.12.007 |
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Abstract | •Atezolizumab and Pembrolizumab showed in phase II (Atezolizumab and Pembrolizumab) and phase III (Pembrolizumab) trials to improve clinical outcome of patients progressed to platinum based therapy.•Atezolizumab failed to show OS benefit over chemotherapy in a phase III trial for patients progressed to platinum based therapy.•Immunotherapy improve clinical outcome of patients unfit to standard first line platinum therapy.•We describe the active or ongoing clinical trials involving Programmed Death Ligand 1 (PD-L1), Programmed Death receptor 1 (PD-1) and Cytotoxic-T Lymphocyte Antigen 4 (CTLA 4) inhibitors in urothelial carcinoma focusing our attention on the developing new immune-agents and combination strategies with immune-checkpoint inhibitors.
Chemotherapy has represented the standard therapy for unresectable or metastatic urothelial carcinoma for more than 20 years. The growing knowledge of the interaction between tumour and immune system has led to the advent of new classes of drugs, the immune-checkpoints inhibitors, which are intended to change the current scenario.
To date, immunotherapy is able to improve the overall responses and survival. Moreover, thanks to its safety profile immune-checkpoint inhibitors could be proposed also to patients unfit for standard chemotherapy.
No doubts that these agents have started a revolution expected for years, but despite this encouraging results it appears clear that not all subjects respond to these agents and requiring the development of reliable predictive response factors able to isolate patients who can more benefit from these treatments as well as new strategies aimed to improve immunotherapy clinical outcome.
In this review we describe the active or ongoing clinical trials involving Programmed Death Ligand 1 (PD-L1), Programmed Death receptor 1 (PD-1) and Cytotoxic-T Lymphocyte Antigen 4 (CTLA 4) inhibitors in urothelial carcinoma focusing our attention on the developing new immune-agents and combination strategies with immune-checkpoint inhibitors. |
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AbstractList | •Atezolizumab and Pembrolizumab showed in phase II (Atezolizumab and Pembrolizumab) and phase III (Pembrolizumab) trials to improve clinical outcome of patients progressed to platinum based therapy.•Atezolizumab failed to show OS benefit over chemotherapy in a phase III trial for patients progressed to platinum based therapy.•Immunotherapy improve clinical outcome of patients unfit to standard first line platinum therapy.•We describe the active or ongoing clinical trials involving Programmed Death Ligand 1 (PD-L1), Programmed Death receptor 1 (PD-1) and Cytotoxic-T Lymphocyte Antigen 4 (CTLA 4) inhibitors in urothelial carcinoma focusing our attention on the developing new immune-agents and combination strategies with immune-checkpoint inhibitors.
Chemotherapy has represented the standard therapy for unresectable or metastatic urothelial carcinoma for more than 20 years. The growing knowledge of the interaction between tumour and immune system has led to the advent of new classes of drugs, the immune-checkpoints inhibitors, which are intended to change the current scenario.
To date, immunotherapy is able to improve the overall responses and survival. Moreover, thanks to its safety profile immune-checkpoint inhibitors could be proposed also to patients unfit for standard chemotherapy.
No doubts that these agents have started a revolution expected for years, but despite this encouraging results it appears clear that not all subjects respond to these agents and requiring the development of reliable predictive response factors able to isolate patients who can more benefit from these treatments as well as new strategies aimed to improve immunotherapy clinical outcome.
In this review we describe the active or ongoing clinical trials involving Programmed Death Ligand 1 (PD-L1), Programmed Death receptor 1 (PD-1) and Cytotoxic-T Lymphocyte Antigen 4 (CTLA 4) inhibitors in urothelial carcinoma focusing our attention on the developing new immune-agents and combination strategies with immune-checkpoint inhibitors. Chemotherapy has represented the standard therapy for unresectable or metastatic urothelial carcinoma for more than 20 years. The growing knowledge of the interaction between tumour and immune system has led to the advent of new classes of drugs, the immune-checkpoints inhibitors, which are intended to change the current scenario. To date, immunotherapy is able to improve the overall responses and survival. Moreover, thanks to its safety profile immune-checkpoint inhibitors could be proposed also to patients unfit for standard chemotherapy. No doubts that these agents have started a revolution expected for years, but despite this encouraging results it appears clear that not all subjects respond to these agents and requiring the development of reliable predictive response factors able to isolate patients who can more benefit from these treatments as well as new strategies aimed to improve immunotherapy clinical outcome. In this review we describe the active or ongoing clinical trials involving Programmed Death Ligand 1 (PD-L1), Programmed Death receptor 1 (PD-1) and Cytotoxic-T Lymphocyte Antigen 4 (CTLA 4) inhibitors in urothelial carcinoma focusing our attention on the developing new immune-agents and combination strategies with immune-checkpoint inhibitors.Chemotherapy has represented the standard therapy for unresectable or metastatic urothelial carcinoma for more than 20 years. The growing knowledge of the interaction between tumour and immune system has led to the advent of new classes of drugs, the immune-checkpoints inhibitors, which are intended to change the current scenario. To date, immunotherapy is able to improve the overall responses and survival. Moreover, thanks to its safety profile immune-checkpoint inhibitors could be proposed also to patients unfit for standard chemotherapy. No doubts that these agents have started a revolution expected for years, but despite this encouraging results it appears clear that not all subjects respond to these agents and requiring the development of reliable predictive response factors able to isolate patients who can more benefit from these treatments as well as new strategies aimed to improve immunotherapy clinical outcome. In this review we describe the active or ongoing clinical trials involving Programmed Death Ligand 1 (PD-L1), Programmed Death receptor 1 (PD-1) and Cytotoxic-T Lymphocyte Antigen 4 (CTLA 4) inhibitors in urothelial carcinoma focusing our attention on the developing new immune-agents and combination strategies with immune-checkpoint inhibitors. Chemotherapy has represented the standard therapy for unresectable or metastatic urothelial carcinoma for more than 20 years. The growing knowledge of the interaction between tumour and immune system has led to the advent of new classes of drugs, the immune-checkpoints inhibitors, which are intended to change the current scenario. To date, immunotherapy is able to improve the overall responses and survival. Moreover, thanks to its safety profile immune-checkpoint inhibitors could be proposed also to patients unfit for standard chemotherapy. No doubts that these agents have started a revolution expected for years, but despite this encouraging results it appears clear that not all subjects respond to these agents and requiring the development of reliable predictive response factors able to isolate patients who can more benefit from these treatments as well as new strategies aimed to improve immunotherapy clinical outcome. In this review we describe the active or ongoing clinical trials involving Programmed Death Ligand 1 (PD-L1), Programmed Death receptor 1 (PD-1) and Cytotoxic-T Lymphocyte Antigen 4 (CTLA 4) inhibitors in urothelial carcinoma focusing our attention on the developing new immune-agents and combination strategies with immune-checkpoint inhibitors. |
Author | Di Nunno, Vincenzo Cubelli, Marta Montironi, Rodolfo Lopez-Beltran, Anto Battelli, Nicola Ardizzoni, Andrea Santoni, Matteo Massari, Francesco Cheng, Liang Fiorentino, Michelangelo |
Author_xml | – sequence: 1 givenname: Francesco surname: Massari fullname: Massari, Francesco email: francesco.massari@aosp.bo.it organization: Division of Oncology, S.Orsola-Malpighi Hospital, Bologna, Italy – sequence: 2 givenname: Vincenzo surname: Di Nunno fullname: Di Nunno, Vincenzo organization: Division of Oncology, S.Orsola-Malpighi Hospital, Bologna, Italy – sequence: 3 givenname: Marta surname: Cubelli fullname: Cubelli, Marta organization: Division of Oncology, S.Orsola-Malpighi Hospital, Bologna, Italy – sequence: 4 givenname: Matteo surname: Santoni fullname: Santoni, Matteo organization: Oncology Unit, Macerata Hospital, Macerata, Italy – sequence: 5 givenname: Michelangelo surname: Fiorentino fullname: Fiorentino, Michelangelo organization: Pathology Service, Addarii Institute of Oncology, S-Orsola-Malpighi Hospital, Bologna, Italy – sequence: 6 givenname: Rodolfo surname: Montironi fullname: Montironi, Rodolfo organization: Section of Pathological Anatomy, Polytechnic University of the Marche Region, School of Medicine, United Hospitals, Ancona, Italy – sequence: 7 givenname: Liang surname: Cheng fullname: Cheng, Liang organization: Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN, USA – sequence: 8 givenname: Anto surname: Lopez-Beltran fullname: Lopez-Beltran, Anto organization: Unit of Anatomical Pathology, Faculty of Medicine, Cordoba University, Cordoba, Spain – sequence: 9 givenname: Nicola surname: Battelli fullname: Battelli, Nicola organization: Oncology Unit, Macerata Hospital, Macerata, Italy – sequence: 10 givenname: Andrea surname: Ardizzoni fullname: Ardizzoni, Andrea organization: Division of Oncology, S.Orsola-Malpighi Hospital, Bologna, Italy |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29407369$$D View this record in MEDLINE/PubMed |
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Keywords | Pembrolizumab Durvalumab Nivolumab Ipilimumab Avelumab Urothelial carcinoma Combination therapy Immune-checkpoint inhibitors Atezolizumab |
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Snippet | •Atezolizumab and Pembrolizumab showed in phase II (Atezolizumab and Pembrolizumab) and phase III (Pembrolizumab) trials to improve clinical outcome of... Chemotherapy has represented the standard therapy for unresectable or metastatic urothelial carcinoma for more than 20 years. The growing knowledge of the... |
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SubjectTerms | Animals Antibodies, Monoclonal - pharmacology Atezolizumab Avelumab B7-H1 Antigen - antagonists & inhibitors Combination therapy Durvalumab Humans Immune-checkpoint inhibitors Immunotherapy Ipilimumab Molecular Targeted Therapy Nivolumab Pembrolizumab Urinary Bladder Neoplasms - drug therapy Urinary Bladder Neoplasms - immunology Urinary Bladder Neoplasms - metabolism Urinary Bladder Neoplasms - secondary Urothelial carcinoma |
Title | Immune checkpoint inhibitors for metastatic bladder cancer |
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