Cited by 601Cancer Immunotherapy and BiomarkersImmunotherapy and Immune ResponsesT-cell and B-cell Immunology

Development of immuno-oncology drugs — from CTLA4 to PD1 to the next generations

Hoos, Axel·2016·Nature Reviews Drug Discovery

Abstract

Since the regulatory approval of ipilimumab in 2011, the field of cancer immunotherapy has been experiencing a renaissance. This success is based on progress in both preclinical and clinical science, including the development of new methods of investigation. Immuno-oncology has become a sub-specialty within oncology owing to its unique science and its potential for substantial and long-term clinical benefit. Immunotherapy agents do not directly attack the tumour but instead mobilize the immune system - this can be achieved through various approaches that utilize adaptive or innate immunity. Therefore, immuno-oncology drug development encompasses a broad range of agents, including antibodies, peptides, proteins, small molecules, adjuvants, cytokines, oncolytic viruses, bi-specific molecules and cellular therapies. This Perspective summarizes the recent history of cancer immunotherapy, including the factors that led to its success, provides an overview of novel drug-development considerations, summarizes three generations of immunotherapies that have been developed since 2011 and, thus, illustrates the breadth of opportunities these new generations of immunotherapies represent.

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Crossref · 10.1038/nrd.2015.35

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Authors
Hoos, A.
Affiliations
GlaxoSmithKline (United States) (US)
Corresponding author
Hoos, Axel
Venue
Nature Reviews Drug Discovery
Published
2016-03-11
Volume
15
Issue
4
Pages
235-247
ISSN
  • 1474-1776 (ISSN-L)
  • 1474-1784
OpenAlex
W2296047035
Cited by
601
References
14
Citations by year
2026: 20 · 2025: 37 · 2024: 66 · 2023: 55 · 2022: 54 · 2021: 74 · 2020: 86 · 2019: 66 · 2018: 58 · 2017: 62 · 2016: 21 · 2015: 1
FWCI
6.98
Type
journal article
Language
en
Open access
closed
Locations
  • Nature Reviews Drug Discovery (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • American Association for Cancer Research
  • Sabin Vaccine Institute
Topics
  • Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
  • Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
Keywords
cancer immunotherapy, CTLA-4 inhibitors, PD-1 inhibitors, ipilimumab, drug development, history of cancer immunotherapy, immune checkpoint inhibitors, bispecific molecules, oncolytic viruses, cell therapy, cytokines, adjuvants
MeSH terms
Ipilimumab, Antibodies, Monoclonal, Antineoplastic Agents, Humans, Immunity, Immunotherapy, Neoplasms, Treatment Outcome, Medication Therapy Management, CTLA-4 Antigen, Programmed Cell Death 1 Receptor, Antibodies, Monoclonal, Humanized

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