4.7 Article

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

Journal

CANCER DISCOVERY
Volume 1, Issue 7, Pages 598-607

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/2159-8290.CD-11-0214

Keywords

-

Categories

Funding

  1. Cancer Therapy Evaluation Program
  2. National Institutes of Health [R21 CA126265, UO1 CA70095, P50 CA058184, P30 CA006973, S10RR026824, UL1 RR 025005]
  3. Flight Attendant Medical Research Institute
  4. American Association for Cancer Research/Stand Up to Cancer Dream Team Translational Cancer Research [SU2C-AACR-DT0109]

Ask authors/readers for more resources

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. Cancer Discovery; 1(7); 598-607. (C) 2011 AACR.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available