Authors:
Sourat Darabi, David R. Braxton, Joanne Xiu, Benedito A. Carneiro, Jeffrey Swensen, Emmanuel S. Antonarakis, Stephen V. Liu, Rana R. McKay, David Spetzler, Wafik S. El-Deiry, Michael J. Demeure
Key Finding:
The rate of reversion mutations following PARP inhibitor or platinum-based therapy is low among BRCA1/2 mutated tumors (1.0- 2.5%), possibly due to the lack of profiling post-treatment. Repeating tumor profiling at times of treatment resistance can help inform therapy selection in the refractory disease setting.
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