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EMBARGOED
FOR
RELEASE: June
1, 2004 at 6 p.m.
(ET)
CONTACT: Carrie
Housman(703)
519-1423
Elizabeth Milbank (212)
584-5014
Study
Points to the Prospect of “Individualized” Cancer
Treatment
Alexandria, VA -
Genetic variations in an individual’s ability to
repair DNA damage may help predict survival in lung
cancer patients treated with the common chemotherapy
drugs cisplatin or carboplatin, a new study shows. The
findings, if verified in larger studies, may help
oncologists tailor chemotherapy to patients based on
their genetic make-up. The study and an accompanying
editorial will be published online June 1 in the Journal of
Clinical Oncology (JCO).
“The concept of
selecting a chemotherapy drug based on a patient’s
genetic make-up is relatively new and very exciting,”
said lead investigator Sarada Gurubhagavatula, MD, of
Massachusetts General Hospital. “We hope that this type
of research will one day enable doctors and patients to
make more informed decisions about chemotherapy
treatments.”
Study investigators evaluated
genetic variations (also called polymorphisms) in two
DNA repair genes – XPD and XRCC1 – in 103
patients diagnosed with stage III or IV non-small cell
lung cancer who were treated with cisplatin or
carboplatin.
The XPD and XRCC1
genes are involved in correcting mistakes that sometimes
occur when DNA is copied in preparation for cell
division. Researchers suspected that the inability to
repair DNA damage may lead to more aggressive lung
tumors that spread more rapidly to other organs, thereby
decreasing survival.
By comparing combinations of
variations in both genes, researchers found that more
variations were associated with decreased median
survival. Patients with a total of three variations in
the XPD and XRCC1 genes survived a median
of 6.8 months, while those with no variations survived a
median of 20.4 months. Patients with two variations
survived a median of 11 months, and those with one
variation survived 16.6 months.
The presence of
genetic variations independently predicted survival even
after researchers took into account patients’ ability to
carry out daily activities, their stage of disease, and
the type of chemotherapy they received.
While
other researchers have investigated the link between
XPD and XRCC1 gene variations in patients
with other cancers, particularly those with colorectal
cancer, this is the first study to look at variations in
these genes in patients with lung
cancer.
Researchers noted that the retrospective
nature of the study presented certain limitations.
Because evaluation of clinical response and time to
disease progression is often imprecise in the
retrospective setting, the study focused on overall
survival, the most objective outcome. However, they
noted that future studies measuring clinical outcome and
time to disease progression may be critical to further
understand the mechanism by which DNA repair affects
patient outcome.
An accompanying editorial by
Heinz-Josef Lenz, MD, Associate Professor of Medicine
and Preventive Medicine at the USC Norris Comprehensive
Cancer Center discusses the application of polymorphisms
in clinical oncology and the potential for including
analyses of germline (inherited) polymorphisms known to
have an effect on the efficacy and toxicity of certain
common chemotherapeutic agents into clinical trials, and
eventually into clinical practice.
“This paper is
a good example of the potential future using these
polymorphisms in the clinic but at the same time of the
limitations and the need for a better functional
understanding in our quest to elucidate the role of
germline polymorphisms in clinical oncology,” said Dr.
Lenz.
"XPD and XRCC1 Genetic Polymorphisms are
Prognostic Factors in Advanced Non-Small Cell Lung
Cancer Patients Treated with Platinum Chemotherapy.”
Sarada Gurubhagavatula et al, Massachusetts General
Hospital Cancer Center, Boston, MA.
The Journal of
Clinical Oncology is the semi-monthly
peer-reviewed journal of the American Society of
Clinical Oncology (ASCO), the world’s leading
professional society representing physicians who treat
people with cancer.
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