Personalized medicine by molecular profiling in the neoadjuvant setting for stage II and III NSCLC may be feasible.
For early-stage non–small-cell lung cancer (NSCLC), multimodality therapy is standard practice, but 5-year survival rates for stage II and III disease remain low (20%–40%). Molecular profiling has reshaped therapy in stage IV disease with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors for EGFR-mutation patients. In addition, prior studies, specifically the 2006 IALT trial (N Engl J Med 2006; 355:983), demonstrated that high tumor levels of excision repair cross-complementation group 1 (ERCC1) immunohistochemistry (IHC) are predictive of cisplatin resistance.
To assess the feasibility of using EGFR mutation status and ERCC1 expression level to customize adjuvant NSCLC therapy, investigators conducted a phase II, multicente…
Reviewing Author
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