CAR T Cells Targeting B7-H3, a Pan-Cancer Antigen, Demonstrate Potent Preclinical Activity Against Pediatric Solid Tumors and Brain Tumors

Clinical Cancer Research - Tập 25 Số 8 - Trang 2560-2574 - 2019
Robbie G. Majzner1, Johanna Theruvath1, Anandani Nellan2, Sabine Heitzeneder1, Yongzhi Cui3, Christopher W. Mount4, Skyler P. Rietberg1, Miles H. Linde5,6, Peng Xu1, Christopher Rota3, Elena Sotillo1, Louai Labanieh7, Daniel W. Lee8, Rimas J. Orentas9, Dimiter S. Dimitrov10, Zhongyu Zhu11, Brad St. Croix12, Alberto Delaidelli13,14, Alla Sekunova13,14, Ezio Bonvini15, Siddhartha S. Mitra16,2, Martha Quezado17, Ravindra Majeti18,19,6, Michelle Monje4, Poul H. Sorensen13,14, John M. Maris20, Crystal L. Mackall18,19,1
11Department of Pediatrics, Stanford University School of Medicine, Palo Alto, California.
22Department of Pediatrics, University of Colorado, Denver Anschutz Medical Center, Denver, Colorado.
33Pediatric Oncology Branch, NCI, Bethesda, Maryland.
44Department of Neurology, Stanford University School of Medicine, Palo Alto, California.
55Immunology Graduate Program, Stanford University School of Medicine, Palo Alto, California.
66Institute for Stem Cell Biology and Regenerative Medicine, Palo Alto, California.
77Department of Bioengineering, Stanford University School of Medicine, Palo Alto, California.
88Division of Pediatric Hematology/Oncology, Department of Pediatrics, University of Virginia, Charlottesville, Virginia.
99Department of Pediatrics, University of Washington School of Medicine, Seattle, Washington.
1010Center for Antibody Therapeutics, University of Pittsburgh Medical School, Pittsburgh, Pennsylvania.
1111Cancer and Inflammation Program, NCI, NIH, Frederick, Maryland.
1212Tumor Angiogenesis Unit, Mouse Cancer Genetics Program (MCGP), NCI, NIH, Frederick, Maryland.
1313Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
1414Department of Molecular Oncology, British Columbia Cancer Agency, Vancouver, British Columbia, Canada.
1515MacroGenics, Inc., Rockville, Maryland.
1616Department of Neurosurgery, Stanford University School of Medicine, Palo Alto, California.
1717Laboratory of Pathology, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
1818Department of Medicine, Stanford University School of Medicine, Palo Alto, California.
1919Stanford Cancer Institute, Stanford University School of Medicine, Palo Alto, California.
2020Children's Hospital of Philadelphia and Department of Pediatrics, University of Pennsylvania, Philadelphia, Pennsylvania.

Tóm tắt

Abstract Purpose:

Patients with relapsed pediatric solid tumors and CNS malignancies have few therapeutic options and frequently die of their disease. Chimeric antigen receptor (CAR) T cells have shown tremendous success in treating relapsed pediatric acute lymphoblastic leukemia, but this has not yet translated to treating solid tumors. This is partially due to a paucity of differentially expressed cell surface molecules on solid tumors that can be safely targeted. Here, we present B7-H3 (CD276) as a putative target for CAR T-cell therapy of pediatric solid tumors, including those arising in the central nervous system.

Experimental Design:

We developed a novel B7-H3 CAR whose binder is derived from a mAb that has been shown to preferentially bind tumor tissues and has been safely used in humans in early-phase clinical trials. We tested B7-H3 CAR T cells in a variety of pediatric cancer models.

Results:

B7-H3 CAR T cells mediate significant antitumor activity in vivo, causing regression of established solid tumors in xenograft models including osteosarcoma, medulloblastoma, and Ewing sarcoma. We demonstrate that B7-H3 CAR T-cell efficacy is largely dependent upon high surface target antigen density on tumor tissues and that activity is greatly diminished against target cells that express low levels of antigen, thus providing a possible therapeutic window despite low-level normal tissue expression of B7-H3.

Conclusions:

B7-H3 CAR T cells could represent an exciting therapeutic option for patients with certain lethal relapsed or refractory pediatric malignancies, and should be tested in carefully designed clinical trials.

Từ khóa


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