PI3Kα Inhibitor and Degrader Inavolisib Can Co-opt FGFR2 to Enhance Responses in Patients with <i>PIK3CA</i> -Mutated Solid Tumors and in Preclinical Models

These findings highlight a novel cooperativity between FGFR2 and p110α that boosts the effectiveness of inavolisib. The data support advancing precision oncology beyond single biomarkers to complex algorithms utilizing co-occurring alterations, suggesting that combining inavolisib with FGFR2 inhibitors may offer enhanced and more durable responses in PIK3CA/FGFR2-altered tumors.

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Publication Details

Journal
Clinical Cancer Research
Published
2025-10-27
DOI
https://doi.org/10.1158/1078-0432.ccr-25-1459
Citations
3
Primary Topic
Fibroblast Growth Factor Research
Type
article
Field-Weighted Citation Impact
2.42
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article

PI3Kα Inhibitor and Degrader Inavolisib Can Co-opt FGFR2 to Enhance Responses in Patients with PIK3CA -Mutated Solid Tumors and in Preclinical Models

Erika Hamilton, Melissa M. Ronan, Trang Pham, Danilo Maddalo et al.
3 citations
Clinical Cancer Research
Fibroblast Growth Factor Research
2.42
article

PI3Kα Inhibitor and Degrader Inavolisib Can Co-opt FGFR2 to Enhance Responses in Patients with PIK3CA -Mutated Solid Tumors and in Preclinical Models

Erika Hamilton, Melissa M. Ronan, Trang Pham, Danilo Maddalo, Zheng Kuang, Sravanthi Cheeti, Marc Hafner, Ethan Sokol, Zachary J. Whitfield, Daniel Zingg, Ian E. Krop, Jennifer L. Schutzman, Andréa Varga, Nicole M. Sodir, Anwesha Dey, Philippe Lucien Bedard, Komal L. Jhaveri, Valentina Gambardella, Jill Fredrickson, Alice R. Wong, Jennifer A. Roth, Mafalda Oliveira, Stephanie Hilz, Kevin Kalinsky, Melissa Accordino, Noopur Shankar, Radia Marie Johnson, Nicholas C. Turner, Peter Schmid, Antoîne Italiano, Ubong Peters, Scott E. Martin, Matthew G. Rees, Robert L. Yauch, Eva Lin, Stephanie Royer‐Joo, Cristina Saura, Steven Gendreau, Dejan Juric, Katherine E. Hutchinson, Jeffrey Lau, Andrés Cervantes, Yanling Jin, Michael S. Hwang, Junko Aimi, Kyung Soon Song
article en
3 citations

Abstract

These findings highlight a novel cooperativity between FGFR2 and p110α that boosts the effectiveness of inavolisib. The data support advancing precision oncology beyond single biomarkers to complex algorithms utilizing co-occurring alterations, suggesting that combining inavolisib with FGFR2 inhibitors may offer enhanced and more durable responses in PIK3CA/FGFR2-altered tumors.

Clinical Cancer ResearchVol. 32(1)
AstraZeneca (United Kingdom) (GB), Broad Institute (US), Hebron University (PS), Royal Marsden NHS Foundation Trust (GB), University Health Network (CA), Memorial Sloan Kettering Cancer Center (US), Harvard University (US), Sciences Po Bordeaux (FR), Emory University (US), Université de Bordeaux (FR), Queen Mary University of London (GB), BioClinica (United States) (US), Columbia University Irving Medical Center (US), Discovery Centre (CA), Institut Gustave Roussy (FR), Boston Foundation (US), Princess Margaret Cancer Centre (CA), Yale Cancer Center (US), GlobalFoundries (United States) (US), Kettering University (US), Massachusetts General Hospital (US), Roche (Canada) (CA), Gene Therapy Laboratory (FR), Hospital Clínico Universitario de Valencia (ES), Rancho BioSciences (United States) (US), Revolution Medicines (United States) (US), Sarah Cannon (US), GenØk (NO), NeuroDevelopment Center (US), Tempus Labs (United States) (US), Dana-Farber Cancer Institute (US), Royal Marsden Hospital (GB), Vietnamese Voluntary Foundation (US), Vall d'Hebron Hospital Universitari (ES), Institut Bergonié (FR), Tennessee Oncology (US), Bioinformatics Institute (SG), Center for Cancer Research (US), INCLIVA Health Research Institute (ES), Vall d'Hebron Institute of Oncology (ES), Foundation Medicine (United States), Sunesis (United States) (US), Columbia University (US)
Openalex Percentile: Top 10%
Fibroblast Growth Factor Research
2.42
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