A human breast cancer-derived xenograft and organoid platform for drug discovery and precision oncology

Author:

Guillen Katrin P.,Fujita Maihi,Butterfield Andrew J.,Scherer Sandra D.ORCID,Bailey Matthew H.,Chu Zhengtao,DeRose Yoko S.,Zhao Ling,Cortes-Sanchez Emilio,Yang Chieh-Hsiang,Toner Jennifer,Wang Guoying,Qiao Yi,Huang Xiaomeng,Greenland Jeffery A.,Vahrenkamp Jeffery M.,Lum David H.ORCID,Factor Rachel E.,Nelson Edward W.,Matsen Cindy B.,Poretta Jane M.,Rosenthal Regina,Beck Anna C.,Buys Saundra S.,Vaklavas Christos,Ward John H.,Jensen Randy L.,Jones Kevin B.ORCID,Li Zheqi,Oesterreich SteffiORCID,Dobrolecki Lacey E.,Pathi Satya S.,Woo Xing Yi,Berrett Kristofer C.,Wadsworth Mark E.,Chuang Jeffrey H.ORCID,Lewis Michael T.,Marth Gabor T.,Gertz Jason,Varley Katherine E.,Welm Bryan E.ORCID,Welm Alana L.ORCID

Abstract

AbstractModels that recapitulate the complexity of human tumors are urgently needed to develop more effective cancer therapies. We report a bank of human patient-derived xenografts (PDXs) and matched organoid cultures from tumors that represent the greatest unmet need: endocrine-resistant, treatment-refractory and metastatic breast cancers. We leverage matched PDXs and PDX-derived organoids (PDxO) for drug screening that is feasible and cost-effective with in vivo validation. Moreover, we demonstrate the feasibility of using these models for precision oncology in real time with clinical care in a case of triple-negative breast cancer (TNBC) with early metastatic recurrence. Our results uncovered a Food and Drug Administration (FDA)-approved drug with high efficacy against the models. Treatment with this therapy resulted in a complete response for the individual and a progression-free survival (PFS) period more than three times longer than their previous therapies. This work provides valuable methods and resources for functional precision medicine and drug development for human breast cancer.

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Oncology

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