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BC Cancer Agency Adds PERJETA®-HERCEPTIN® Combo Pack for Treatment of HER2-Positive Metastatic Breast Cancer to the Provincial

BC Cancer Agency Adds PERJETA®-HERCEPTIN® Combo Pack for Treatment of 
HER2-Positive Metastatic Breast Cancer to the Provincial Formulary 
MISSISSAUGA, ON, Dec. 2, 2013 /CNW/ - People with HER2-positive metastatic 
breast cancer in British Columbia will now be able to access a new treatment 
option through the BC Cancer Agency. The BC Cancer Systemic Therapy Program 
has approved the addition of PERJETA to the BCCA Drug Benefit Listing. The 
regimen of pertuzumab (PERJETA) and trastuzumab (HERCEPTIN) in combination 
with docetaxel is given every three weeks for the first‐line treatment of 
metastatic HER2‐positive breast cancer continuing until disease progression 
or toxicity after docetaxel completion.(1) 
"We're pleased the BC Cancer Agency has added the PERJETA-HERCEPTIN Combo Pack 
to the provincial formulary, giving patients with HER2-positive metastatic 
breast cancer in BC access to a new treatment option in the fight against the 
disease," said Mr. Ronnie Miller, president and CEO, Roche Canada. "For more 
than a decade, Roche has been committed to improving breast cancer treatment 
through innovative research and development and we are very proud to be 
expanding our offering and to continue to provide more treatment options." 
In Canada, breast cancer is the most commonly diagnosed cancer in women.(2) 
It accounts for 26 per cent of all cancer cases, making it the second leading 
cause of death in women.(1 )On average, 3,100 women in BC are diagnosed with 
breast cancer every year.(3) 
Metastatic (also known as advanced, secondary or stage IV) breast cancer, the 
spread of cancer cells from the original site where the cancer first formed to 
other parts of the body, is associated with increased severity and is largely 
incurable.(4,5 )The median survival for a woman with this form of breast 
cancer is two years.(4) 
Women with HER2-positive breast cancer test positive for a protein called 
human epidermal growth factor receptor (HER2).(6) This protein is found in 
high quantities on the outside of HER2-positive breast cancer cells. 
HER2-positive breast cancer represents approximately 10 to 20 per cent of 
human cancers, and without treatment, it is associated with aggressive tumour 
growth and poor clinical outcomes. (5,7,8) Approximately 5,000 women in Canada 
are living with this disease.(9) 
British Columbia was the first province to fund the PERJETA-HERCEPTIN Combo 
Pack. 
About PERJETA
PERJETA (pertuzumab), in combination with the current standard of care, 
HERCEPTIN® (trastuzumab) and docetaxel chemotherapy, is approved by Health 
Canada for the treatment of patients with HER2-positive metastatic breast 
cancer who have not received prior anti-HER2 therapy or chemotherapy for 
metastatic disease.(10) 
The Health Canada approval of PERJETA is largely based on the phase III 
CLEOPATRA trial. In the trial, people who received a combination of PERJETA, 
HERCEPTIN and docetaxel chemotherapy, lived a median 6.1 months longer without 
their cancer getting worse (progression-free survival) compared with the 
standard of care, HERCEPTIN plus docetaxel chemotherapy, alone (median PFS 
18.5 versus 12.4 months ; HR=0.62; p<0.0001).(9,11 )Further, the combination 
of PERJETA, HERCEPTIN and docetaxel chemotherapy significantly extended the 
lives of people with previously untreated HER2-positive metastatic breast 
cancer (overall survival) compared to HERCEPTIN, docetaxel chemotherapy and 
placebo. The risk of death was reduced by 34 per cent for people on the 
PERJETA arm of the study, compared to those who received HERCEPTIN and 
docetaxel chemotherapy alone (HR=0.66; p=0.0008).(12) At the time of the 
data analysis, median overall survival had not yet been reached because more 
than half of the patients receiving the PERJETA combination were still 
alive.(11) The combination of PERJETA, HERCEPTIN and chemotherapy is thought 
to provide a more comprehensive blockade of HER signaling pathways. 
About Roche
Headquartered in Basel, Switzerland, Roche is a leader in research-focused 
healthcare with combined strengths in pharmaceuticals and diagnostics. Roche 
is the world's largest biotech company, with truly differentiated medicines in 
oncology, infectious diseases, inflammation, metabolism and neuroscience. 
Roche is also the world leader in in vitro diagnostics and tissue-based cancer 
diagnostics, and a frontrunner in diabetes management. Roche's personalized 
healthcare strategy aims at providing medicines and diagnostic tools that 
enable tangible improvements in the health, quality of life and survival of 
patients. In 2012 Roche had over 82,000 employees worldwide and invested over 
8 billion Swiss francs in R&D. The Group posted sales of 45.5 billion Swiss 
francs. Genentech, in the United States, is a wholly owned member of the Roche 
Group. Roche is the majority shareholder in Chugai Pharmaceutical, Japan. For 
more information, please visit www.roche.com. 
All trademarks used or mentioned in this release are protected by law. 
Disclaimer: Cautionary statement regarding forward-looking statements

This document may contain certain forward-looking statements. These 
forward-looking statements may be identified by words such as 'believes', 
'expects', 'anticipates', 'projects', 'intends', 'should', 'seeks', 
'estimates', 'future' or similar expressions or by discussion of, among other 
things, strategy, goals, plans or intentions. Various factors may cause actual 
results to differ materially in the future from those reflected in 
forward-looking statements contained in this document, among others: (1) 
pricing and product initiatives of competitors; (2) legislative and regulatory 
developments and economic conditions; (3) delay or inability in obtaining 
regulatory approvals or bringing products to market; (4) fluctuations in 
currency exchange rates and general financial market conditions; (5) 
uncertainties in the discovery, development or marketing of new products or 
new uses of existing products, including without limitation negative results 
of clinical trials or research projects, unexpected side effects of pipeline 
or marketed products; (6) increased government pricing pressures; (7) 
interruptions in production; (8) loss of or inability to obtain adequate 
protection for intellectual property rights; (9) litigation; (10) loss of key 
executives or other employees; and (11) adverse publicity and news coverage. 
The statement regarding earnings per share growth is not a profit forecast and 
should not be interpreted to mean that Roche's earnings or earnings per share 
for any current or future period will necessarily match or exceed the 
historical published earnings or earnings per share of Roche. 
References 
(_________________________________ )
(1) BC Cancer Agency. 
http://www.bccancer.bc.ca/HPI/ChemotherapyProtocols/stupdate.htm (Accessed 
November 13, 2013)
(2) Canadian Cancer Society. 
http://www.cancer.ca/en/cancer-information/cancer-type/breast/statistics/?regio
n=on (Accessed October 29, 2013)
(3) Canadian Breast Cancer Foundation. 
http://www.cbcf.org/central/AboutBreastCancerMain/AboutBreastCancer/Pages/Breas
tCancerinCanada.aspx (Accessed November 4, 2013)
(4) Canadian Breast Cancer Network. 
http://www.cbcn.ca/index.php?pageaction=content.page&id=125&lang=en (Accessed 
March 19, 2013)
(5) BC Cancer Agency. 
http://www.bccancer.bc.ca/HPI/CancerManagementGuidelines/Breast/Management/Meta
staticBreastCancer.hm (Accessed March 19, 2013)
(6) Chia et al. Human Epidermal Growth Factor Receptor 2 Overexpression As a 
Prognostic Factor in a Large Tissue Microarray Series of Node-Negative Breast 
Cancers, Journal Of Clinical Oncology. 2008;26:5697-5700
(7) Ross et al. The HER-2 Receptor and Breast Cancer: Ten Years of Targeted 
Anti-HER-2 Therapy and Personalized Medicine, The Oncologist. 2009;14:320-368
(8) Wolff et al. American Society of Clinical Oncology/College of American 
Pathologists Guideline, Recommendations for Human Epidermal Growth Factor 
Receptor 2 Testing in Breast Cancer, Arch Patho Lab Med 2007;101:18-43
(9) Tell Her 2 http://tellher2.ca/her2/ (Accessed October 29, 2013)
(10) PERJETA™ Product Monograph. April 12, 2013. Hoffmann-La Roche 
Limited.
(11) Baselga J, Cortes J, Sung-Bae K, et al. Pertuzumab plus trastuzumab plus 
docetaxel for metastatic breast cancer. N Engl J Med. 2012; 366:109-110.
(12) Swain S, et al. Confirmatory overall survival analysis of CLEOPATRA: A 
randomized, double-blind, placebo-controlled Phase III study with pertuzumab, 
trastuzumab, and docetaxel in patients with HER2-positive first-line 
metastatic breast cancer. Poster presented at the 2012 CTRC-AARC San Antonio 
Breast Cancer Symposium. Abstract # P5-18-26.
 

SOURCE  Roche Canada 
 Jane McCoubrey Director, Corporate Relations Roche Canada 905-542-5535 
jane.mccoubrey@roche.com 
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CO: Roche Canada
ST: Ontario
NI: MTC  
-0- Dec/02/2013 15:00 GMT
 
 
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