| Autor: |
David M. Hyman, Deborah Schrag, Alexia Iasonos, Philippe L. Bedard, Funda Meric-Bernstam, Mia Levy, Fabrice André, Charles L. Sawyers, Ben H. Park, Seth Sheffler-Collins, Jocelyn Lee, Stuart M. Gardos, Andrew Zarski, Nikolaus Schultz, JianJiong Gao, Shawn M. Sweeney, Ritika Kundra, Benjamin E. Gross, Jan Hudecek, Hugo Horlings, Chetna Wathoo, Christine M. Micheel, Semih Dogan, Natalie Blauvelt, Michele L. Lenoue-Newton, Michael J. Hasset, Monica Arnedos, Eva M. Lepisto, Celeste Yu, Bastien Nguyen, Qin Zhou, Lillian M. Smyth |
| Rok vydání: |
2023 |
| DOI: |
10.1158/2159-8290.c.6547928.v1 |
| Popis: |
AKT inhibitors have promising activity in AKT1E17K-mutant estrogen receptor (ER)–positive metastatic breast cancer, but the natural history of this rare genomic subtype remains unknown. Utilizing AACR Project GENIE, an international clinicogenomic data-sharing consortium, we conducted a comparative analysis of clinical outcomes of patients with matched AKT1E17K-mutant (n = 153) and AKT1–wild-type (n = 302) metastatic breast cancer. AKT1-mutant cases had similar adjusted overall survival (OS) compared with AKT1–wild-type controls (median OS, 24.1 vs. 29.9, respectively; P = 0.98). AKT1-mutant cases enjoyed longer durations on mTOR inhibitor therapy, an observation previously unrecognized in pivotal clinical trials due to the rarity of this alteration. Other baseline clinicopathologic features, as well as durations on other classes of therapy, were broadly similar. In summary, we demonstrate the feasibility of using a novel and publicly accessible clincogenomic registry to define outcomes in a rare genomically defined cancer subtype, an approach with broad applicability to precision oncology.Significance:We delineate the natural history of a rare genomically distinct cancer, AKT1E17K-mutant ER-positive breast cancer, using a publicly accessible registry of real-world patient data, thereby illustrating the potential to inform drug registration through synthetic control data.See related commentary by Castellanos and Baxi, p. 490. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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