Tumor B7-H3 expression in diagnostic biopsy specimens and survival in patients with metastatic prostate cancer

Background Prostate cancer spans a broad spectrum from indolent to deadly disease. In the management of prostate cancer, diagnostic biopsy specimens are important sources of data that inform the selection of treatment. B7-H3 (CD276), an immune checkpoint molecule, has emerged as a promising immunoth...

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Veröffentlicht in:Prostate cancer and prostatic diseases 2021-09, Vol.24 (3), p.767-774
Hauptverfasser: Amori, Gulanbar, Sugawara, Emiko, Shigematsu, Yasuyuki, Akiya, Masashi, Kunieda, Junko, Yuasa, Takeshi, Yamamoto, Shinya, Yonese, Junji, Takeuchi, Kengo, Inamura, Kentaro
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Sprache:eng
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Zusammenfassung:Background Prostate cancer spans a broad spectrum from indolent to deadly disease. In the management of prostate cancer, diagnostic biopsy specimens are important sources of data that inform the selection of treatment. B7-H3 (CD276), an immune checkpoint molecule, has emerged as a promising immunotherapy target. B7-H3 expression is related to adverse clinical outcomes in various types of cancer; however, little is known concerning the association between tumor B7-H3 expression in diagnostic biopsy specimens and clinical outcome in patients with metastatic prostate cancer. Methods We evaluated tumor B7-H3 expression levels in diagnostic biopsy specimens from 135 patients with metastatic prostate cancer and 113 patients with localized prostate cancer. Results High B7-H3 expression was more frequently observed in patients with metastatic cancer than in those with localized cancer (31 vs. 12%; p  = 0.0003). In patients with localized cancer, the B7-H3 expression status was not associated with biochemical recurrence-free survival. However, among patients with metastatic cancer, high B7-H3 expression was independently associated with high disease-specific mortality (multivariable hazard ratio [HR] = 2.72; p  = 0.047) and overall mortality rates (multivariable HR = 2.04; p  = 0.025). Conclusions Tumor B7-H3 expression in diagnostic biopsy specimens may be a useful biomarker for identifying highly aggressive metastatic prostate cancer. Given the potential utility of anti-B7-H3 immunotherapy, this information may aid in stratifying prostate cancer based on its responsiveness to B7-H3-targeted treatment.
ISSN:1365-7852
1476-5608
DOI:10.1038/s41391-021-00331-6