Literature DB >> 27663893

Improved Efficacy of Neoadjuvant Compared to Adjuvant Immunotherapy to Eradicate Metastatic Disease.

Jing Liu1,2,3, Stephen J Blake1, Michelle C R Yong1, Heidi Harjunpää1,3, Shin Foong Ngiow2, Kazuyoshi Takeda4, Arabella Young2,3, Jake S O'Donnell1,2,3, Stacey Allen1, Mark J Smyth2,3, Michele W L Teng5,3.   

Abstract

Immunotherapy has recently entered a renaissance phase with the approval of multiple agents for the treatment of cancer. Immunotherapy stands ready to join traditional modalities, including surgery, chemotherapy, radiation, and hormone therapy, as a pillar of cancer treatment. Although immunotherapy has begun to have success in advanced cancer treatment, its scheduling and efficacy with surgery to treat earlier stages of cancer and prevent distant metastases have not been systematically examined. Here, we have used two models of spontaneously metastatic breast cancers in mice to illustrate the significantly greater therapeutic power of neoadjuvant, compared with adjuvant, immunotherapies in the context of primary tumor resection. Elevated and sustained peripheral tumor-specific immune responses underpinned the outcome, and blood sampling of tumor-specific CD8+ T cells immediately prior to and post surgery may provide a predictor of outcome. These data now provide a strong rationale to extensively test and compare neoadjuvant immunotherapy in humans. SIGNIFICANCE: We demonstrate the significantly greater therapeutic efficacy of neoadjuvant, compared with adjuvant, immunotherapies to eradicate distant metastases following primary tumor resection. Elevated and sustained peripheral tumor-specific immune responses underpinned the outcome, and blood sampling of tumor-specific CD8+ T cells immediately prior to and post surgery may provide a predictor of outcome. Cancer Discov; 6(12); 1382-99. ©2016 AACR.See related commentary by Melero et al., p. 1312This article is highlighted in the In This Issue feature, p. 1293. ©2016 American Association for Cancer Research.

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Year:  2016        PMID: 27663893     DOI: 10.1158/2159-8290.CD-16-0577

Source DB:  PubMed          Journal:  Cancer Discov        ISSN: 2159-8274            Impact factor:   39.397


  191 in total

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Journal:  N Engl J Med       Date:  2018-04-16       Impact factor: 91.245

Review 4.  Making Checkpoint Inhibitors Part of Treatment of Patients With Locally Advanced Lung Cancers: The Time Is Now.

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6.  CD96 targeted antibodies need not block CD96-CD155 interactions to promote NK cell anti-metastatic activity.

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Journal:  Oncoimmunology       Date:  2018-02-01       Impact factor: 8.110

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Review 8.  Adjuvant Therapy Options in Renal Cell Carcinoma: Where Do We Stand?

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Review 9.  Combination immunotherapy strategies for glioblastoma.

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Review 10.  Radiotherapy and Immunotherapy Combinations for Lung Cancer.

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