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Roche Pharmaceuticals

Avastin(R) Demonstrates Impressive Survival Benefit in Lung Cancer Study

Basel, Switzerland (ots/PRNewswire)

- Addition of Avastin Boosts Efficacy of First-Line Chemotherapy
for Advanced Non-Small Cell Lung Cancer
A new study, presented for the first time today, reveals that
Avastin(R) (bevacizumab rhuMAb-VEGF) significantly extends survival
for patients with previously untreated, advanced non-small cell lung
cancer (NSCLC), the most common form of lung cancer.(1) The data were
presented at the 2005 American Society of Clinical Oncology (ASCO)
Annual Meeting, Orlando, USA.
The addition of Avastin to platinum-based chemotherapy (paclitaxel
and carboplatin) significantly improved overall survival by 30%. The
median survival was 12.5 months with Avastin compared to 10.2 months
in patients treated with the standard chemotherapy alone. The study
also demonstrated a 61% improvement in progression-free survival. The
median progression-free survival was 6.4 months with Avastin compared
to 4.5 months for those treated with chemotherapy alone. There was
also a significant increase in response rates in the Avastin group
(27% versus 10%) compared to those receiving chemotherapy alone.(1)
This is the first study in years to show an increase in survival for
the first-line treatment of patients with advanced NSCLC.
"The significance of Avastin being able to prolong the life of
patients with advanced, non-squamous NSCLC is truly groundbreaking,
as we have not seen this with any other targeted therapy in the
first-line setting," said Dr Sandler, lead investigator, Vanderbilt
University Medical Centre, Nashville, Tennessee, USA. "The addition
of Avastin to platinum-based chemotherapy may well become the new
standard of care for patients with non-squamous NSCLC."
Avastin has now shown benefits in three of the most common types
of cancer. Lung cancer is the most common cancer worldwide with 1.3
million new cases annually and over 1 million deaths occurring each
year.(2) For colorectal cancer there are over one million new cases
worldwide and over half a million people dying from the disease each
year.(2) In women, breast cancer accounts for one fifth of all cancer
cases and each year more than one million new cases are diagnosed
worldwide, with a death rate of approximately 410,000 people per
year.(2)
About the Study
The randomised, controlled, multi-centre study, sponsored by the
National Cancer Institute (NCI) and conducted by a network of
researchers led by the Eastern Cooperative Oncology Group (ECOG),
enrolled 878 patients with advanced NSCLC. Patients were randomised
to receive treatment with platinum-based chemotherapy (paclitaxel and
carboplatin) with or without Avastin, administered every three weeks
for up to six courses. It was reported that the addition of Avastin
to chemotherapy was well tolerated.
About Avastin
Avastin is the first treatment that inhibits angiogenesis - the
growth of a network of blood vessels that supply 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).
In Europe, Avastin is approved 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 fast-track approval by the US Food
and Drug Administration (FDA) and was launched in the US in February
2004.(i)
In the pivotal Phase III study, the addition of Avastin to
chemotherapy (irinotecan/5-fluorouracil/leucovorin) significantly
extended survival by, on average, five months (20.3 months versus
15.6 months) for people with previously untreated metastatic
colorectal cancer.(3) In a Phase III study with patients who had
previously failed one chemotherapy regimen for their advanced
disease, Avastin was also shown to significantly improve survival, by
an average of approximately two months (12.5 months versus 10.7
months), when added to a widely prescribed oxaliplatin-containing
chemotherapy regimen (oxaliplatin/5-fluorouracil/leucovorin).(4)
People with very advanced colorectal cancer who are too unwell to
tolerate traditional aggressive chemotherapy also benefit from
Avastin. The addition of Avastin to a less aggressive form of
chemotherapy increased the length of time the cancer was not growing,
by four months, compared to chemotherapy alone (a 67% increase in
progression-free survival).(5)
A Phase III trial with Avastin in patients with metastatic breast
cancer has shown that adding Avastin to first-line paclitaxel
chemotherapy resulted in a significant improvement in
progression-free survival compared to chemotherapy alone.(6)
Roche and Genentech are pursuing a comprehensive clinical
programme investigating the use of Avastin in advanced colorectal
cancer with other chemotherapies and also expanding into the adjuvant
setting (post operation). As its mechanism may be relevant in a
number of malignant tumours, Roche and Genentech are also
investigating the potential clinical benefit of Avastin in pancreatic
cancer, ovarian cancer, renal cell carcinoma and others.
Approximately 15,000 patients are expected to be enrolled into
clinical trials over the next years worldwide.
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 improving 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 2004
sales by the Pharmaceuticals Division totalled 21.7 billion Swiss
francs, while the Diagnostics Division posted sales of 7.8 billion
Swiss francs. Roche employs roughly 65,000 people in 150 countries
and has R&D agreements and strategic alliances with numerous
partners, including majority ownership interests in Genentech and
Chugai.
All trademarks used or mentioned in this release are legally
protected.
About Roche: www.roche.com
About Genentech: www.gene.com
About cancer: www.health-kiosk.ch
Roche in Oncology:
http://www.roche.com/pages/downloads/company/pdf/mboncology05e.pdf
To access video clips, in broadcast standard, free of charge,
please go to:
www.thenewsmarket.com
Note for editors
(i) In the US, Avastin is approved for use in combination with
intravenous 5-fluorouracil-based chemotherapy, for first-line
treatment of patients with metastatic carcinoma of the colon or
rectum.
References:
1. Sandler AB, Gray R, Bhramer J, et al. Randomized phase II/III
Trial of paclitaxel (P) plus carboplatin (C) with or without
bevacizumab (NSC # 704865) in patients with advanced non-squamous
non-small cell lung cancer (NSCLC): An Eastern Cooperative Oncology
Group (ECOG) Trial - E4599. ASCO 2005, Abstract LBA4.
2. J. Ferlay, F. Bray, P. Pisani and D.M. Parkin. GLOBOCAN 2002:
Cancer Incidence, Mortality and Prevalence Worldwide IARC CancerBase
No. 5. version 2.0, IARCPress, Lyon, 2004.
3. Hurwitz H, Fehrenbacher L, Novotny W, et al. Bevacizumab plus
Irinotecan, Fluorouracil, and Leucovorin for Metastatic Colorectal
Cancer. New England Journal of Medicine 2004; 350(23): 2335-2342.
4. Mitchell EP, Alberts SR, Schwartz BJ, et al. High-dose
bevacizumab in combination with FOLFOX4 improves survival in patients
with previously treated advanced colorectal cancer: Results from the
Eastern Cooperative Oncology Group (ECOG) study E3200. ASCO
Gastrointestinal 2005 Cancer Symposium, January 2005 (abstract 169a).
5. Kabbinavar FF, Joseph Schulz J, McCleod M, et al. Addition of
Bevacizumab to Bolus 5-FU/Leucovorin in First-Line Metastatic
Colorectal Cancer: Results of a Randomized Phase II Trial. J Clin
Oncol 23:10.1200/JCO.2005.05.112, 2005.
6. Kathy D Miller et al. ECOG E2100 study. Presented at 2005 ASCO
Annual Meeting.

Contact:

Emma Robinson, Resolute Communications, +44-207-357-8187

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