Oncolytics Biotech Inc. Collaborators to Present Positive Clinical Trial Data at the 15th Annual World Conference on Lung Cancer
CALGARY, Oct. 1, 2013 /PRNewswire/ – Oncolytics Biotech Inc. (“Oncolytics”)
(TSX:ONC) (NASDAQ:ONCY) today announced that abstracts detailing
results from two Phase II studies examining the use of REOLYSIN(®) in combination with carboplatin and paclitaxel in patients with
non-small cell lung cancer (NSCLC) with Kras or EGFR-activated tumors (REO 016) and in patients with squamous cell
carcinoma of the lung (REO 021), are now available on the International
Association for the Study of Lung Cancer (IASLC) World Conference on
Lung Cancer website at http://wclc.iaslc.org. The conference is being held from October 27(th) to 30(th), 2013 in Sydney, Australia.
The first abstract, titled “Final Results of a Phase 2 Trial of the
Oncolytic Virus REOLYSIN in Metastatic NSCLC Patients with a
Ras-activated Pathway,” indicated that patients received reovirus (3 x
10(10 )TCID(50))( )intravenously daily on days one to five, in combination with paclitaxel
at initial doses of paclitaxel 175 mg/m(2) 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). Grade 3-4 toxicities included febrile neutropenia (two patients),
grade 3 diarrhea (two patients), grade 3 anemia (seven patients),
fatigue in 6 patients (five grade 3, one grade 4), nausea/vomiting (two
patients), electrolyte abnormalities, and single grade 3 episodes of
arthralgia and thrombocytopenia. Molecular tumor demographics included:
20 Kras, 3 EGFR and 4 BRAF mutations, and 10 with EGFR amplifications only.
Response evaluation for 36 evaluable patients showed 11 partial
responses (PR) (30%) (EGFR amplified, five; BRAF two; Kras, three; EGFR mutated, one), 21 stable disease (SD), and four
progressive disease (PD). Of the 36 evaluable patients with sufficient
follow up to date, profession free survival (PFS) at six months is 36%
and one-year survival, 53%.
“The response and clinical benefit rates reported are consistent with
the interim data our collaborators reported in late 2012,” said Dr.
Brad Thompson, President and CEO of Oncolytics. “The six-month
progression-free survival and one-year survival data is very
encouraging. In the literature, it has been reported that treatment
with various chemotherapy combinations alone averaged one-year survival
rates of 33% in patients with advanced non-small cell lung cancer(1). Stage IV patients similar to the ones we treated in this study see
overall one-year survival rates of approximately 16%(2).”
The second abstract, titled “A Phase 2 Study of Intravenous
Administration of REOLYSIN( )(Reovirus Type 3 Dearing) in Combination with Paclitaxel (P) and
Carboplatin (C) in Patients with Squamous Cell Carcinoma of the Lung,”
reflects information submitted to the IASLC conference in June 2013,
prior to the Company’s subsequent announcement of updated data from the
REO 021 study in the press release dated September 9, 2013.
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.
(1 )As reported in The New England Journal of Medicine (N Engl J Med, Vol.
346, No. 2, January 10, 2002) by Schiller, et al, a total of 1,207 patients with advanced non-small-cell lung cancer
were randomly assigned to a reference regimen of cisplatin and
paclitaxel or to one of three experimental regimens: cisplatin and
gemcitabine, cisplatin and docetaxel, or carboplatin and paclitaxel.
The response rate for all 1,155 eligible patients was 19 percent, with
a median survival of 7.9 months (95 percent confidence interval, 7.3 to
8.5), a 1-year survival rate of 33 percent (95 percent confidence
interval, 30 to 36 percent).
(2 )As reported in Clinical Epidemiology (2011:3 139-148), Cetin, et al, using data from the Surveillance, Epidemiology and End Results (SEER)
Program, stratified 51,749 incident stage IV NSCLC patients (1988-2003
with follow-up through 2006) by major histologic subtype. Overall
one-year survival (95% confidence interval) in stage IV non-small cell
lung cancer patients who survived at least 31 days (n=44,172) was
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
SOURCE Oncolytics Biotech Inc.