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Roche Pharmaceuticals

New Study Suggests Combining Breakthrough Therapies Tarceva(R) and Avastin(R) May Provide More Hope for Lung Cancer Patients

Basel, Switzerland (ots/PRNewswire)

A new study(1) suggests that
treatment with the combination of the innovative cancer drugs Avastin
(bevacizumab) and Tarceva (erlotinib) or Avastin with chemotherapy,
improves progression-free survival in patients with recurrent or
refractory non-small cell lung cancer (NSCLC), the most common form
of lung cancer, when compared with standard chemotherapy alone.
Progression-free survival is the time patients live without their
cancer advancing. These data were presented today at the 42nd Annual
Meeting of the American Society of Clinical Oncology (ASCO), Atlanta.
"These findings signal the potential for combining novel therapies
that target different cancer growth pathways, to achieve better
overall patient outcomes, with a low incidence of serious side
effects," said Willem Verhoofstad, Global Business Director for Roche
Oncology. "We are continuing to invest and explore the safety and
efficacy of the Avastin and Tarceva combination and are currently
conducting Phase III trials with both products in first-line and
relapsed NSCLC settings."
The randomised, Phase II exploratory study evaluated three
treatment regimens in patients with recurrent or refractory NSCLC:
  • Avastin in addition to Tarceva
  • Avastin in addition to chemotherapy (either pemetrexed or docetaxel)
  • Chemotherapy alone (either pemetrexed or docetaxel) as control arm
The study suggests that Avastin in combination with Tarceva or
chemotherapy improves progression-free survival, the primary study
endpoint, compared to chemotherapy alone. Median progression-free
survival in the Avastin plus chemotherapy arm was 4.8 months, and was
4.4 months in the Avastin plus Tarceva arm, compared to just 3.0
months in the chemotherapy alone arm. The study results also showed
that the toxicity profile of the Avastin plus Tarceva combination was
favourable, resulting in fewer serious adverse events, when compared
to either chemotherapy-containing arm. Due to the exploratory nature
of this randomised Phase II study, these data do not provide
definitive conclusions with respect to differences between the three
treatment arms.
About the Phase II Exploratory Study
120 patients with recurrent or refractory NSCLC, who had not
received previous treatment with Avastin or Tarceva, were enrolled
into this study. Patients in the study had histologically or
cytologically confirmed non-squamous NSCLC and had experienced
clinical or radiographic disease progression during or following one
platinum-based chemotherapy regimen for advanced stage disease (IIIb
or IV).
The key study results showed:
  • Treatment with Avastin plus Tarceva reduced the risk of cancer progression or death by 28 per cent compared to chemotherapy alone (based on a hazard ratio of 0.72).
  • Treatment with Avastin plus chemotherapy reduced the risk of cancer progression or death by 34 per cent compared to chemotherapy alone (based on a hazard ratio of 0.66),
  • Treatment with Avastin plus Tarceva saw 78% of patients alive at six months (median progression-free survival 4.4 months)
  • Treatment with Avastin plus chemotherapy saw 72% of patients alive at six months (median progression-free survival 4.8 months)
  • Treatment with chemotherapy alone saw 62% of patients alive at six months (median progression-free survival 3.0 months)
  • The toxicity profile of the Avastin plus Tarceva combination was favourable, resulting in fewer serious adverse events, when compared to either chemotherapy-containing arm
  • Adverse events in the Avastin plus Tarceva arm were similar to those observed in previous clinical trials of Avastin in combination with Tarceva, and included diarrhoea and rash
  • Adverse events in the Avastin plus chemotherapy arm were similar to those observed in previous clinical trials of Avastin in combination with chemotherapy, and included hypertension and bleeding
About Tarceva
Tarceva is an investigational small molecule that targets the
human epidermal growth factor receptor (HER1) pathway. HER1, also
known as EGFR, is a key component of this signalling pathway, which
plays a role in the formation and growth of numerous cancers. Tarceva
blocks tumour cell growth by inhibiting the tyrosine kinase activity
of the HER1 signalling pathway inside the cell.
Taken as an oral, once-daily therapy, Tarceva is the only
EGFR-inhibitor to have demonstrated a survival benefit in lung
cancer. Currently most lung cancer patients are treated with
chemotherapy which can be very debilitating due to its toxic nature.
Tarceva works differently to chemotherapy by specifically targeting
tumour cells, and avoids the typical side-effects of chemotherapy.
Tarceva is approved in the US and across the European Union for
patients with locally advanced or metastatic non-small cell lung
cancer (NSCLC) after failure of at least one prior chemotherapy
regimen. Tarceva is approved in the US in combination with
gemcitabine chemotherapy for the treatment of patients with locally
advanced, inoperable or metastatic pancreatic cancer. A Marketing
Authorisation Application was submitted to the European health
authorities in November 2005.
Tarceva is currently being evaluated in an extensive clinical
development programme by a global alliance among OSI Pharmaceuticals,
Genentech, and Roche, focussing on earlier stages of NSCLC.
Additionally, Tarceva is being studied in combination with Avastin in
NSCLC. Trials are also being conducted with Tarceva in other solid
tumours, such as ovarian, bronchioloalveolar (BAC), colorectal,
pancreatic, head and neck and glioma (brain).
About Avastin
Avastin is the first treatment that inhibits angiogenesis - the
growth of a network of blood vessels that supplies nutrients and
oxygen to cancerous tissues. Avastin targets a naturally occurring
protein called VEGF (Vascular Endothelial Growth Factor), a key
mediator of angiogenesis, thus choking off the blood supply that is
essential for the growth of the tumour and its spread throughout the
body (metastasis).
Avastin is the first and only anti-angiogenic agent to have
demonstrated improved overall and/or progression-free survival in the
three major types of cancer leading to death: colorectal cancer,
non-small cell lung cancer and breast cancer. In Europe, Avastin was
approved in early 2005 for first-line treatment of patients with
metastatic carcinoma of the colon or rectum in combination with the
chemotherapy regimens of intravenous 5-fluorouracil/folinic acid or
intravenous 5-fluorouracil/folinic acid/irinotecan. Avastin received
approval by the US Food and Drug Administration (FDA) in February
2004. In addition, filing occurred in the US on April 10, 2006, for
use of Avastin in previously untreated advanced non-squamous,
non-small cell lung cancer, on May 26 for treatment of women with
advanced breast cancer and in Japan on April 21, 2006 for use of
Avastin in patients with advanced or recurrent colorectal cancer.
Roche and Genentech are pursuing a comprehensive clinical
programme investigating the use of Avastin in various tumour types
(including colorectal, breast, lung, pancreatic cancer, ovarian
cancer, renal cell carcinoma and others) and different settings
(advanced and adjuvant i.e. post-operative). The total development
programme is expected to include over 25,000 patients worldwide.
Roche in Oncology
The Roche Group, including its members Genentech in the United
States and Chugai in Japan, is the world's leading provider of cancer
care products, including anti-cancer treatments, supportive care
products and diagnostics. Its oncology business includes an
unprecedented five products proven to provide survival benefit in
different major tumour indications: Avastin, Herceptin, and Xeloda in
advanced-stage breast cancer, Herceptin in early-stage HER2-positive
breast cancer, MabThera in non-Hodgkin's lymphoma, Avastin and Xeloda
in colorectal cancer, Avastin and Tarceva in non-small cell lung
cancer and Tarceva in pancreatic cancer.
In addition to these anti-cancer agents, the Roche oncology
portfolio includes a comprehensive collection of medicines that can
help improve the quality of life of cancer patients: Bondronat (for
prevention of skeletal events in patients with breast cancer and bone
metastases, hypercalcaemia of malignancy), Kytril (for chemotherapy
and radiotherapy-induced nausea and vomiting), Neupogen (for
cancer-related neutropenia), and NeoRecormon (for anaemia in various
cancer settings). CERA is the most recent demonstration of Roche's
commitment to anaemia management. Other oncology products include
Furtulon (for colorectal cancer) and Roferon-A (for hairy cell and
chronic myeloid leukaemia, Kaposi's sarcoma, malignant melanoma,
renal cell carcinoma).
In addition to the medicines, Roche is developing new diagnostic
tests that will have a significant impact on disease management for
cancer patients in the future. With a broad portfolio of tumour
markers for prostate, colorectal, liver, ovarian, breast, stomach,
pancreas and lung cancer, as well as a range of molecular oncology
tests, Roche will continue to be the leader in providing
cancer-focused treatments and diagnostics.
The unmatched Roche oncology portfolio as well as an extensive
external innovation base through collaborations with companies and
academia is what makes it possible for Roche to provide more
effective cancer therapies.
In the United States Herceptin, MabThera (Rituxan), Avastin and
Tarceva are marketed either by Genentech alone or together with its
partners Biogen Idec Inc. (MabThera) and OSI (Tarceva). Outside of
the United States, Roche and its Japanese partner Chugai are
responsible for the marketing of these medicines.
About Roche
Headquartered in Basel, Switzerland, Roche is one of the world's
leading research-focused healthcare groups in the fields of
pharmaceuticals and diagnostics. As a supplier of innovative products
and services for the early detection, prevention, diagnosis and
treatment of disease, the Group contributes on a broad range of
fronts to improve people's health and quality of life. Roche is a
world leader in diagnostics, the leading supplier of medicines for
cancer and transplantation and a market leader in virology. In 2005
sales by the Pharmaceuticals Division totalled 27.3 billion Swiss
francs, and the Diagnostics Division posted sales of 8.2 billion
Swiss francs. Roche employs roughly 70,000 people in 150 countries
and has R&D agreements and strategic alliances with numerous
partners, including majority ownership interests in Genentech and
Chugai. Additional information about the Roche Group is available on
the Internet (www.roche.com).
All trademarks used or mentioned in this release are legally
protected.
Reference:
1) Fehrenbacher, C et al, A phase II, multicenter, randomized
clinical trial to evaluate the efficacy and safety of Avastin
(bevacizumab) in combination with either chemotherapy (docetaxel or
pemetrexed) or Tarceva (erlotinib hydrochloride) compared with
chemotherapy alone for treatment of recurrent or refractory non-small
cell lung cancer, Abstract #7062, presented at the 42nd Annual
Meeting of the American Society of Clinical Oncology (ASCO) 2006.

Contact:

Christine Hill, International Communications Manager, Avastin, Roche
Pharmaceuticals, Telephone: +41-616-888-995, Mobile: +41-797-888-245,
Email: Christine.mage-hill@roche.com. Martin McInally, International
Communications Manager, Tarceva, Roche Pharmaceuticals, Telephone:
+41-797-888-208, Mobile: +41-797-888-208, Email:
martin.mcinally@roche.com

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