| Literature DB >> 33498451 |
Joline Roze1, Elena Sendino Garví2, Ellen Stelloo2, Christina Stangl2, Ferdinando Sereno2, Karen Duran2, Jolijn Groeneweg1, Sterre Paijens3, Hans Nijman3, Hannah van Meurs4, Luc van Lonkhuijzen4, Jurgen Piek5, Christianne Lok6, Geertruida Jonges7, Petronella Witteveen8, René Verheijen1, Gijs van Haaften2, Ronald Zweemer1, Glen Monroe1.
Abstract
Adult granulosa cell tumors (AGCTs) arise from the estrogen-producing granulosa cells. Treatment of recurrence remains a clinical challenge, as systemic anti-hormonal treatment or chemotherapy is only effective in selected patients. We established a method to rapidly screen for drug responses in vitro using direct patient-derived cell lines in order to optimize treatment selection. The response to 11 monotherapies and 12 combination therapies, including chemotherapeutic, anti-hormonal, and targeted agents, were tested in 12 AGCT-patient-derived cell lines and an AGCT cell line (KGN). Drug screens were performed within 3 weeks after tissue collection by measurement of cell viability 72 h after drug application. The potential synergy of drug combinations was assessed. The human maximum drug plasma concentration (Cmax) and steady state (Css) thresholds obtained from available phase I/II clinical trials were used to predict potential toxicity in patients. Patient-derived AGCT cell lines demonstrated resistance to all monotherapies. All cell lines showed synergistic growth inhibition by combination treatment with carboplatin, paclitaxel, and alpelisib at a concentration needed to obtain 50% cell death (IC50) that are below the maximum achievable concentration in patients (IC50 < Cmax). We show that AGCT cell lines can be rapidly established and used for patient-specific in vitro drug testing, which may guide treatment decisions. Combination treatment with carboplatin, paclitaxel, and alpelisib was consistently effective in AGCT cell lines and should be further studied as a potential effective combination for AGCT treatment in patients.Entities:
Keywords: alpelisib; drug screens; granulosa cell tumors; ovarian cancer; targeted treatment
Year: 2021 PMID: 33498451 PMCID: PMC7864192 DOI: 10.3390/cancers13030368
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639