Background: Alterations in the PI3K/AKT/mTOR signaling pathway represent a mechanism of resistance to endocrine therapy in advanced HR+/HER2-breast cancer. The identification of activating mutations in PIK3CA has gained therapeutic relevance, guiding the use of PIK3CA-targeted inhibitors such as alpelisib and inavolisib. Methods: A multidisciplinary panel of Italian experts conducted a structured consensus process to develop shared recommendations for molecular testing of PIK3CA in advanced HR+/HER2-breast cancer, addressing preanalytical, analytical, and clinical-therapeutic areas of concern. Results: A total of 23 out of 29 statements reached complete agreement (100%). The resulting recommendations encompass sample selection, analytical methodologies, sensitivity thresholds, result reporting, and clinical interpretation and integration. Additional guidance is provided for the management of non-canonical gene variants and for other genes involved in the PI3K/AKT/mTOR pathway. Conclusions: This consensus document provides operational and interpretative guidelines aimed at standardizing PIK3CAtesting and assessing related genes in clinical practice. These recommendations promote a harmonized approach to patient care, in line with the latest scientific evidence.

Integrating PIK3CA Testing into Clinical Practice for Advanced HR+/HER2- Breast Cancer: An Expert Consensus / De Angelis, C., De Biase, D., Gerratana, L., Arpino, G., Bianchini, G., Castellano, I., Curigliano, G., Del Mastro, L., Fabi, A., Fusco, N., Gennari, A., Guarneri, V., Zamagni, C., Zambelli, A., Malapelle, U., Puglisi, F.. - In: THE BREAST. - ISSN 0960-9776. - 87:(2026). [10.1016/j.breast.2026.104786]

Integrating PIK3CA Testing into Clinical Practice for Advanced HR+/HER2- Breast Cancer: An Expert Consensus

Bianchini G.;
2026-01-01

Abstract

Background: Alterations in the PI3K/AKT/mTOR signaling pathway represent a mechanism of resistance to endocrine therapy in advanced HR+/HER2-breast cancer. The identification of activating mutations in PIK3CA has gained therapeutic relevance, guiding the use of PIK3CA-targeted inhibitors such as alpelisib and inavolisib. Methods: A multidisciplinary panel of Italian experts conducted a structured consensus process to develop shared recommendations for molecular testing of PIK3CA in advanced HR+/HER2-breast cancer, addressing preanalytical, analytical, and clinical-therapeutic areas of concern. Results: A total of 23 out of 29 statements reached complete agreement (100%). The resulting recommendations encompass sample selection, analytical methodologies, sensitivity thresholds, result reporting, and clinical interpretation and integration. Additional guidance is provided for the management of non-canonical gene variants and for other genes involved in the PI3K/AKT/mTOR pathway. Conclusions: This consensus document provides operational and interpretative guidelines aimed at standardizing PIK3CAtesting and assessing related genes in clinical practice. These recommendations promote a harmonized approach to patient care, in line with the latest scientific evidence.
2026
Inglese
Elsevier Ltd
87
104786
10
Pubblicato
https://www.thebreastonline.com/article/S0960-9776(26)00096-2/fulltext
Esperti anonimi
Internazionale
Goal 3: Good health and well-being
Expert consensus
HR+/HER2− breast cancer
Liquid biopsy
NGS
PIK3CA
No
Integrating PIK3CA Testing into Clinical Practice for Advanced HR+/HER2- Breast Cancer: An Expert Consensus / De Angelis, C., De Biase, D., Gerratana, L., Arpino, G., Bianchini, G., Castellano, I., Curigliano, G., Del Mastro, L., Fabi, A., Fusco, N., Gennari, A., Guarneri, V., Zamagni, C., Zambelli, A., Malapelle, U., Puglisi, F.. - In: THE BREAST. - ISSN 0960-9776. - 87:(2026). [10.1016/j.breast.2026.104786]
open
16
info:eu-repo/semantics/article
262
De Angelis, C.; De Biase, D.; Gerratana, L.; Arpino, G.; Bianchini, G.; Castellano, I.; Curigliano, G.; Del Mastro, L.; Fabi, A.; Fusco, N.; Gennari, ...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/206342
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