CALGARY, Oct. 28, 2013 /PRNewswire/ – Oncolytics Biotech Inc. (“Oncolytics”)
 (TSX:ONC) (NASDAQ:ONCY) today announced a poster presentation
 containing updated efficacy data from a Phase 2 study examining the use
 of REOLYSIN® in combination with carboplatin and paclitaxel in patients with stage
 IV non-small cell lung cancer (NSCLC) with Kras or EGFR-activated tumors (REO 016) was made at International
 Association for the Study of Lung Cancer (IASLC). The conference is
 being held from October 27th to 30th, 2013 in Sydney, Australia.
The poster presentation included new efficacy data that correlated a
 number of molecular abnormalities with best response, progression free
 survival (PFS) and one-year survival. Current data in these patients
 demonstrates that 20 of 36 evaluable patients (56%) survived a year or
 more. There were 13 patients with only EGFR mutations or
 amplifications, of whom nine (69.2%) survived a year or longer. Four of
 four (100%) patients with BRAF and EGFR amplification survived a year
 or longer.
“This is the first time we have reported data correlating the presence
 of specific biomarkers with efficacy, which covers both best response
 and survival in patient tumours with a Ras-activated pathway,” said Dr.
 Brad Thompson, President and CEO of Oncolytics. “Although the study
 examined a relatively small number of patients, this data is
 encouraging, especially in light of a growing focus among healthcare
 professionals on personalizing cancer treatment based on tumour type.
 We are taking a closer look at the specific role biomarkers play in a
 number of our ongoing studies and, based on this data, intend to
 conduct a randomized trial in this indication.”
The chart below summarizes key findings for the 36 evaluable patients:
| Molecular Abnormality | Number of patients | Best Response | Number progression free at six months | Number surviving one year | 
| BRAF mutation, EGFR amplification | 4 | 2 PR, 1 SD, 1 PD | 2 | 4 | 
| EGFR amplification | 10 | 5 PR, 5 SD | 4 | 7 | 
| EGFR mutation, EGFR amplification | 3 | 1 PR, 1 SD, 1 PD | 1 | 2 | 
| KRAS | 12 | 3 PR, 8 SD | 6 | 4 | 
| KRAS, EGFR amplification | 7 | 6 SD, 1 PD | 1 | 3 | 
| Total | 36 | 11 PR, 11 SD (30% response rate) | 14 (38%) | 20 (56%) | 
Partial response (PR), stable disease (SD), progressive disease (PD)
Patients received REOLYSIN (3 x 1010 TCID50) intravenously daily on days one to five, in combination with paclitaxel
 at initial doses of paclitaxel 175 mg/m2 and carboplatin AUC 5, on day one of each 21-day cycle. Overall, 37
 patients received 209 cycles (per patient median four, range one to
 18). The study treatment was found to be well tolerated.
The Company’s collaborators also presented a poster on results from the
 Company’s U.S. Phase 2 single arm clinical trial in patients with
 squamous cell carcinoma of the lung (SCCLC) using intravenous
 administration of REOLYSIN in combination with carboplatin and
 paclitaxel (REO 021). This is the same poster that was previously
 presented on October 22, 2013 at the AACR-NCI-EORTC International
 Conference on Molecular Targets and Cancer Therapeutics conference held
 in Boston, MA.
Conference Call Details
Dr. Brad Thompson, President and CEO of Oncolytics, will host a
 conference call and webcast on Monday, October 28, 2013 at 6:00 a.m. MT
 (8:00 a.m. ET) to discuss in more depth the Company’s lung cancer
 program. To access the conference call by telephone, dial
 1-888-231-8191 or 1-647-427-7450. A live audio webcast will also be
 available at the following link: http://www.newswire.ca/en/webcast/detail/1248341/1375429 or through the Company’s website at www.oncolyticsbiotech.com/presentations. Please connect at least 10 minutes prior to the webcast to ensure
 adequate time for any software download that may be needed. A replay of
 the webcast will be available at www.oncolyticsbiotech.com/presentations and will also be available by telephone through November 4, 2013. To
 access the telephone replay, dial 1-416-849-0833 or 1-855-859-2056 and
 enter reservation number 92453959 followed by the number sign.
About Lung Cancer
The American Cancer Society estimates that in 2013, approximately
 228,190 new cases of lung cancer will be diagnosed. Between 85% and 90%
 of all lung cancers are classified as non-small cell lung cancer
 (NSCLC); squamous cell carcinomas account for 25-30% of all lung
 cancers. Lung cancer is by far the leading cause of cancer death among
 both men and women. There will be an estimated 159,480 deaths from lung
 cancer in the United States in 2013, accounting for around 27% of all
 cancer deaths. Lung cancer is the leading cause of cancer death, with
 more people dying each year of lung cancer than from colon, breast, and
 prostate cancers combined. For more information about SCC lung cancer,
 please go to www.cancer.org.
About Oncolytics Biotech Inc.
Oncolytics is a Calgary-based biotechnology company focused on the
 development of oncolytic viruses as potential cancer therapeutics. 
 Oncolytics’ clinical program includes a variety of human trials
 including a Phase III trial in head and neck cancers using REOLYSIN®, its proprietary formulation of the human reovirus. For further
 information about Oncolytics, please visit: www.oncolyticsbiotech.com.
This press release contains forward-looking statements, within the
 meaning of Section 27A of the Securities Act of 1933, as amended, and
 Section 21E of the Securities Exchange Act of 1934, as amended.
 Forward-looking statements, including the Company’s expectations
 related to the U.S. Phase II non-small cell lung cancer trial, the U.S.
 Phase II squamous cell carcinoma lung cancer trial, future trials in
 these indications, and the Company’s belief as to the potential of
 REOLYSIN as a cancer therapeutic, involve known and unknown risks and
 uncertainties, which could cause the Company’s actual results to differ
 materially from those in the forward-looking statements. Such risks and
 uncertainties include, among others, the availability of funds and
 resources to pursue research and development projects, the efficacy of
 REOLYSIN as a cancer treatment, the tolerability of REOLYSIN outside a
 controlled test, the success and timely completion of clinical studies
 and trials, the Company’s ability to successfully commercialize
 REOLYSIN, uncertainties related to the research, development and
 manufacturing of pharmaceuticals, changes in technology, general
 changes to the economic environment and uncertainties related to the
 regulatory process. Investors should consult the Company’s quarterly
 and annual filings with the Canadian and U.S. securities commissions
 for additional information on risks and uncertainties relating to the
 forward-looking statements. Investors should consider statements that
 include the words “believes”, “expects”, “anticipates”, “intends”,
 “estimates”, “plans”, “projects”, “should”, or other expressions that
 are predictions of or indicate future events or trends, to be uncertain
 and forward-looking. Investors are cautioned against placing undue
 reliance on forward-looking statements. The Company does not undertake
 to update these forward-looking statements, except as required by
 applicable laws.
SOURCE Oncolytics Biotech Inc.
Released October 28, 2013
