Combination Epigenetic Therapy Has Efficacy in Patients with Refractory Advanced Non–Small Cell Lung Cancer

Rosalyn A. Juergens(Lovelace Respiratory Research Institute), John Wrangle(Lovelace Respiratory Research Institute), Frank P. Vendetti(Lovelace Respiratory Research Institute), Sara C. Murphy(Lovelace Respiratory Research Institute), Ming Zhao(Lovelace Respiratory Research Institute), Barbara Coleman(Lovelace Respiratory Research Institute), Rosa Sebree(Lovelace Respiratory Research Institute), Kristen Rodgers(Lovelace Respiratory Research Institute), Craig M. Hooker(Lovelace Respiratory Research Institute), Noreli Franco(Lovelace Respiratory Research Institute), Beverly Lee(Lovelace Respiratory Research Institute), Salina Tsai(Lovelace Respiratory Research Institute), Igor Espinoza Delgado(Lovelace Respiratory Research Institute), Michelle A. Rudek(Lovelace Respiratory Research Institute), Steven A. Belinsky(Lovelace Respiratory Research Institute), James G. Herman(Lovelace Respiratory Research Institute), Stephen B. Baylin(Lovelace Respiratory Research Institute), Malcolm V. Brock(Lovelace Respiratory Research Institute), Charles M. Rudin(Lovelace Respiratory Research Institute)
Cancer Discovery
November 9, 2011
Cited by 675Open Access
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Abstract

UNLABELLED: Epigenetic alterations are strongly associated with the development of cancer. We conducted a phase I/II trial of combined epigenetic therapy with azacitidine and entinostat, inhibitors of DNA methylation and histone deacetylation, respectively, in extensively pretreated patients with recurrent metastatic non-small cell lung cancer. This therapy is well tolerated, and objective responses were observed, including a complete response and a partial response in a patient who remains alive and without disease progression approximately 2 years after completing protocol therapy. Median survival in the entire cohort was 6.4 months (95% CI 3.8-9.2), comparing favorably with existing therapeutic options. Demethylation of a set of 4 epigenetically silenced genes known to be associated with lung cancer was detectable in serial blood samples in these patients and was associated with improved progression-free (P = 0.034) and overall survival (P = 0.035). Four of 19 patients had major objective responses to subsequent anticancer therapies given immediately after epigenetic therapy. SIGNIFICANCE: This study demonstrates that combined epigenetic therapy with low-dose azacitidine and entinostat results in objective, durable responses in patients with solid tumors and defines a blood-based biomarker that correlates with clinical benefit.


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