Novel cancer immunotherapy agents with survival benefit: recent successes and next steps
By Padmanee Sharma, K. Wagner, J. Wolchok, James P. Allison. Nature Reviews. Cancer, 2011
639 citations recorded by the source corpus.
The US Food and Drug Administration (FDA) recently approved two novel immunotherapy agents, sipuleucel-T and ipilimumab, which showed a survival benefit for patients with metastatic prostate cancer and melanoma, respectively. The mechanisms by which these agents provideclinical benefit are not completely understood. However, knowledge of these mechanisms will be crucial for probing human immune responses and tumour biology in order to understand what distinguishes responders from non-responders. The following next steps are necessary: first, the development of immune-monitoring strategies for the identification of relevant biomarkers; second, the establishment of guidelines for the assessment of clinical end points; and third, the evaluation of combination therapy strategies to improve clinical benefit.
Subfields: Immunology, Oncology
View Paper: https://www.semanticscholar.org/paper/76e2da35635a487d493d0518f03f8735025bf63d
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In Immunology
- Kristen E. Pauken
- D. Pardoll
- James P. Allison
- E. Wherry
- H. Nishikawa
- Padmanee Sharma
- Shimon Sakaguchi
- S. Farkona
In Oncology
- D. Pardoll
- Kristen E. Pauken
- Padmanee Sharma
- James P. Allison
- E. Wherry
- S. Topalian
- Eleftherios P. Diamandis
- S. Farkona
Citations in the corpus
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- Immune Checkpoint Targeting in Cancer Therapy: Towards Combination Strategies with Curative Potential (2015, background): “The clinical success of anti-CTLA-4 opened a new field termed ‘‘immune checkpoint therapy’’ as additional T cell intrinsic pathways were identified and targeted for clinical development (Sharma et al., 2011; Pardoll, 2012).”
- Molecular and genetic properties of tumors associated with local immune cytolytic activity (2015, positive): “With the recent success of checkpoint blockade therapy (against CTLA4 or PD1/PDL1) in inducing durable control of diverse tumors (Hinrichs and Rosenberg, 2014; Sharma et al., 2011), it has become critical to understand why some tumors are not responsive or develop resistance to therapy.”
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