Genotyping with a digital polymerase-chain-reaction test had 70% sensitivity for detecting the T790M mutation in plasma.
Osimertinib, a third-generation epidermal growth factor receptor (EGFR) tyrosine-kinase inhibitor (TKI), is FDA-approved for patients with refractory non–small-cell lung cancer (NSCLC) whose tumors carry the EGFR-resistant T790M mutation. Given the difficulty of repeat tumor biopsy, plasma genotyping to detect resistant mutations is under development. Researchers (some with a pending patent on a plasma genotyping method) retrospectively compared plasma genotyping with tumor genotyping in 216 osimertinib-pretreated patients with EGFR-mutant NSCLC who had been enrolled in the AURA trial (NEJM JW Oncol Hematol Jul 2015 and N Engl J Med 2015; 372:1689).
Plasma genotyping by BEAMing (a digital polymerase-chain-reaction test) had a sensitivity of …
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DisclosuresConsultant/Advisory BoardGenentech; AstraZeneca; Boehringer-Ingelheim; Bristol-Myers Squibb; Clinical Care Options; Heron; Takeda; Ariad; MedIQ; Targeted Healthcare Communications; Novartis; OncLive; Roche; TRM Oncology
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Grant/Research SupportMedimmune; NIH/National Cancer Institute; Millennium; Genentech; Polaris Pharmaceuticals; Seattle Genetics; Boehringer-Ingelheim Pharmaceuticals; SWOG–Hope Foundation; American Cancer Society; Department of Defense; GlaxoSmithKline Pharmaceuticals; Merck; Eli Lilly; Takeda; Bristol-Myers Squibb
DisclosuresConsultant/Advisory BoardGenentech; AstraZeneca; Boehringer-Ingelheim; Bristol-Myers Squibb; Clinical Care Options; Heron; Takeda; Ariad; MedIQ; Targeted Healthcare Communications; Novartis; OncLive; Roche; TRM Oncology
RoyaltiesUpToDate
Grant/Research SupportMedimmune; NIH/National Cancer Institute; Millennium; Genentech; Polaris Pharmaceuticals; Seattle Genetics; Boehringer-Ingelheim Pharmaceuticals; SWOG–Hope Foundation; American Cancer Society; Department of Defense; GlaxoSmithKline Pharmaceuticals; Merck; Eli Lilly; Takeda; Bristol-Myers Squibb