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CA A Cancer Journal for Clinicians
Article . 2012 . Peer-reviewed
License: Wiley Online Library User Agreement
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Immunotherapy of cancer in 2012

Authors: John M, Kirkwood; Lisa H, Butterfield; Ahmad A, Tarhini; Hassane, Zarour; Pawel, Kalinski; Soldano, Ferrone;

Immunotherapy of cancer in 2012

Abstract

Abstract The immunotherapy of cancer has made significant strides in the past few years due to improved understanding of the underlying principles of tumor biology and immunology. These principles have been critical in the development of immunotherapy in the laboratory and in the implementation of immunotherapy in the clinic. This improved understanding of immunotherapy, enhanced by increased insights into the mechanism of tumor immune response and its evasion by tumors, now permits manipulation of this interaction and elucidates the therapeutic role of immunity in cancer. Also important, this improved understanding of immunotherapy and the mechanisms underlying immunity in cancer has fueled an expanding array of new therapeutic agents for a variety of cancers. Pegylated interferon‐α2b as an adjuvant therapy and ipilimumab as therapy for advanced disease, both of which were approved by the United States Food and Drug Administration for melanoma in March 2011, are 2 prime examples of how an increased understanding of the principles of tumor biology and immunology have been translated successfully from the laboratory to the clinical setting. Principles that guide the development and application of immunotherapy include antibodies, cytokines, vaccines, and cellular therapies. The identification and further elucidation of the role of immunotherapy in different tumor types, and the development of strategies for combining immunotherapy with cytotoxic and molecularly targeted agents for future multimodal therapy for cancer will enable even greater progress and ultimately lead to improved outcomes for patients receiving cancer immunotherapy. CA Cancer J Clin 2012. © 2012 American Cancer Society.

Keywords

T-Lymphocytes, Genetic Vectors, Programmed Cell Death 1 Receptor, Gene Transfer Techniques, Antibodies, Monoclonal, Cetuximab, Angiogenesis Inhibitors, Antineoplastic Agents, Dendritic Cells, Antibodies, Monoclonal, Humanized, Cancer Vaccines, Erb-b2 Receptor Tyrosine Kinases, Bevacizumab, ErbB Receptors, Nivolumab, Histocompatibility Antigens, Neoplasms, Humans, Immunotherapy, Alemtuzumab

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    selected citations
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    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    405
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 1%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 1%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 0.1%
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
405
Top 1%
Top 1%
Top 0.1%
Published in a Diamond OA journal
Related to Research communities
Cancer Research