Strand-Triesta
Centre for Cancer Genomics to transform prevention, diagnostics & prescribe
targeted therapy
HealthCare Global
Enterprises’ molecular science lab Triesta Sciences has partnered with Strand
Life Sciences to make a paradigm shift in cancer prevention, diagnostics and
targeted therapy protocols. The new
standard of cancer care is seen to bring in higher affordability and better
decision making for oncology physicians.
The newly formed
Strand-Triesta Centre for Cancer Genomics is now offering three tests. These
are the Strand Somatic 48 gene test, Strand Germline test which is a
saliva-based scan to assess cancer risk factors and the Strand Somatic &
Germline test to guide the course of treatment.
HCG has now led the way by
adopting the Strand-Triesta advanced cancer
diagnostics which defines the future of cancer care. The partnership of
the two companies is also seen to have pioneered a new generation in clinical
diagnostics globally.
At least 33 per cent of
the cancer patients in India do not
respond to any form treatment and therefore the genomics tests would be far
more cost-effective as it allows oncologists to pick patients for chemotherapy
and radiation, said Dr. BS Ajai Kumar, founder and chairman, HCG.
“We will incorporate
genomic testing at all our hospitals and this could be accessed by other
onco-care centres too as it diagnosis and prognosis of cancer. The partnership
will enhance the work done by the multidisciplinary teams of oncologist and
researchers,” he added.
The cost of genomic
diagnostics is estimated to be between Rs. 15,000 and 45,000. But the big advantage is the early detection and
assessment of whether expensive treatment needs to be pursued. However, it is
seen that at least one-third of the one million patients can benefit from genomic
tests, said Dr. Ajai Kumar.
Through genomic testing,
we are looking to build a solution for
India which revolves around affordability and scalability which is
unprecedented even in the West, stated Dr. Vijay Chandru, chairman and chief
executive officer, Strand Life Sciences.
HCG has a cancer registry
and with genomics it will dramatically accelerate diagnostic precision in
cancer, added Dr. Chandru.
Indian annual cancer
incidence is around one million cancer with a
mortality of five lakh patients. By 2015, cancer cases would see a
five-fold rise and increase the healthcare burden. The advanced standard of
care is designed to achieve new frontiers in medicine through a
bench-to-bedside vision.
“Cancer tumour sequencing
is the next generation sequencing (NGS) technologies and thorough analysis of
patient DNA variations will help physicians go beyond one- drug for all and
provide personalised medicine approach. It would significantly enhance not just
the chemo-radiation outcomes but also detect hereditary risks in family members
of cancer patients allowing faster, early stage diagnosis,” said Dr. Chandru.
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