NIH State-of-the-Science Conference: Diagnosis and Management of Ductal Carcinoma In Situ (DCIS); Notice, 25568 [E9-12376]
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Federal Register / Vol. 74, No. 101 / Thursday, May 28, 2009 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
NIH State-of-the-Science Conference:
Diagnosis and Management of Ductal
Carcinoma In Situ (DCIS); Notice
Notice is hereby given of the National
Institutes of Health (NIH) State-of-theScience Conference: Diagnosis and
Management of Ductal Carcinoma in
Situ (DCIS) to be held September 22–24,
2009, in the NIH Natcher Conference
Center, 45 Center Drive, Bethesda,
Maryland 20892. The conference will
begin at 8:30 a.m. on September 22 and
23, and at 9 a.m. on September 24, and
will be open to the public.
Ductal carcinoma in situ (DCIS) is a
condition in which abnormal cells are
found in the lining of a breast duct. As
‘‘in situ’’ means ‘‘in place,’’ this means
the abnormal cells have not spread
outside the duct to other tissues in the
breast. Also referred to as intraductal
carcinoma and stage zero breast cancer,
DCIS is the most common noninvasive
tumor of the breast.
DCIS is most often discovered during
routine mammograms, presenting as
very small specks of calcium known as
microcalcifications. However, not all
microcalcifications indicate the
presence of DCIS, and the diagnosis
must be confirmed by biopsy. Magnetic
Resonance Imaging (MRI) has also been
used more recently as a diagnostic tool,
but questions remain about the impact
of the test on patient outcomes. Since
the implementation of screening
mammography, the rate of new DCIS
cases has increased dramatically.
DCIS currently accounts for
approximately twenty percent of
screening-detected breast cancer, but its
true prevalence is challenging to
measure because nearly all affected
individuals are asymptomatic. By most
reports, the risk factors associated with
the development of DCIS are similar to
those for invasive breast cancer:
increased age, family history of breast
cancer, previous biopsies, history of
hormone replacement therapy, and
older age at first childbirth. Tamoxifen,
a hormonal drug, has demonstrated a
reduction in the incidence of DCIS
among high-risk women.
Although the natural course of the
disease is not well understood, DCIS
can become invasive cancer and spread
to other tissues. It is also a marker of
increased risk for developing cancer
elsewhere in the same or opposite
breast. However, not all DCIS will
progress to invasive disease, and it is
thought that DCIS can be present in
VerDate Nov<24>2008
17:11 May 27, 2009
Jkt 217001
some individuals without causing
problems over a long period of time.
Recent research suggests that DCIS is a
spectrum of disease and that certain
tumor characteristics may be strong or
weak risk factors for subsequent
invasive breast cancer. Unfortunately, it
is currently not clear which lesion types
are more likely to become invasive,
leading to difficult treatment decisions
for patients and providers.
Because of this uncertainty, DCIS
patients are typically treated promptly
following diagnosis and have a
generally good prognosis. Standard
DCIS therapies include breast
conservation, with or without radiation
or mastectomy, depending on patient
and tumor characteristics. Sentinel
lymph node biopsy may also be
recommended to high-risk patients
since this is the area where cancer
spread is often first detected. Hormonal
therapy may also be used in an effort to
prevent DCIS recurrence and to lower
the risk of developing invasive breast
cancer. However, these drugs’ potential
side effects must be weighed carefully.
Since the natural course of DCIS is
not well understood and treatment
benefit may depend on specific tumor
and patient characteristics, the
treatment of DCIS remains controversial.
To examine these important issues, the
NIH National Cancer Institute and
Office of Medical Applications of
Research will convene a State-of-theScience Conference from September 22–
24, 2009. The questions to consider
include:
• What are the incidence and
prevalence of DCIS and its specific
pathologic subtypes, and how are
incidence and prevalence influenced by
mode of detection, population
characteristics, and other risk factors?
• How does the use of MRI or sentinel
lymph node biopsy impact important
outcomes in patients diagnosed with
DCIS?
• How do local control and systemic
outcomes vary in DCIS based on tumor
and patient characteristics?
• In patients with DCIS, what is the
impact of surgery, radiation, and
systemic treatment on outcomes?
• What are the most critical research
questions for the diagnosis and
management of DCIS?
An impartial, independent panel will
be charged with reviewing the available
published literature in advance of the
conference, including a systematic
literature review commissioned through
the Agency for Healthcare Research and
Quality. The first day and a half of the
conference will consist of presentations
by expert researchers and practitioners
and open public discussions. On
PO 00000
Frm 00090
Fmt 4703
Sfmt 4703
Thursday, September 24, the panel will
present a statement of its collective
assessment of the evidence to answer
each of the questions above. The panel
will also hold a press conference to
address questions from the media. The
draft statement will be published online
later that day, and the final version will
be released approximately six weeks
later. The primary sponsors of this
meeting are the NIH National Cancer
Institute and the NIH Office of Medical
Applications of Research.
Advance information about the
conference and conference registration
materials may be obtained from
American Institutes for Research of
Silver Spring, Maryland, by calling 888–
644–2667 or by sending e-mail to
consensus@mail.nih.gov. The American
Institutes for Research’s mailing address
is 10720 Columbia Pike, Silver Spring,
MD 20901. Registration information is
also available on the NIH Consensus
Development Program Web site at
https://consensus.nih.gov.
Please Note: The NIH has instituted
security measures to ensure the safety of NIH
employees, guests, and property. All visitors
must be prepared to show a photo ID upon
request. Visitors may be required to pass
through a metal detector and have bags,
backpacks, or purses inspected or x-rayed as
they enter NIH buildings. For more
information about the security measures at
NIH, please visit the Web site at https://
www.nih.gov/about/visitorsecurity.htm.
Dated: May 20, 2009.
Lawrence A. Tabak,
Acting Deputy Director, National Institutes
of Health.
[FR Doc. E9–12376 Filed 5–27–09; 8:45 am]
BILLING CODE 4140–01–P
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HUMAN SERVICES
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AGENCY: Health Resources and Services
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Agencies
[Federal Register Volume 74, Number 101 (Thursday, May 28, 2009)]
[Notices]
[Page 25568]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-12376]
[[Page 25568]]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
NIH State-of-the-Science Conference: Diagnosis and Management of
Ductal Carcinoma In Situ (DCIS); Notice
Notice is hereby given of the National Institutes of Health (NIH)
State-of-the-Science Conference: Diagnosis and Management of Ductal
Carcinoma in Situ (DCIS) to be held September 22-24, 2009, in the NIH
Natcher Conference Center, 45 Center Drive, Bethesda, Maryland 20892.
The conference will begin at 8:30 a.m. on September 22 and 23, and at 9
a.m. on September 24, and will be open to the public.
Ductal carcinoma in situ (DCIS) is a condition in which abnormal
cells are found in the lining of a breast duct. As ``in situ'' means
``in place,'' this means the abnormal cells have not spread outside the
duct to other tissues in the breast. Also referred to as intraductal
carcinoma and stage zero breast cancer, DCIS is the most common
noninvasive tumor of the breast.
DCIS is most often discovered during routine mammograms, presenting
as very small specks of calcium known as microcalcifications. However,
not all microcalcifications indicate the presence of DCIS, and the
diagnosis must be confirmed by biopsy. Magnetic Resonance Imaging (MRI)
has also been used more recently as a diagnostic tool, but questions
remain about the impact of the test on patient outcomes. Since the
implementation of screening mammography, the rate of new DCIS cases has
increased dramatically.
DCIS currently accounts for approximately twenty percent of
screening-detected breast cancer, but its true prevalence is
challenging to measure because nearly all affected individuals are
asymptomatic. By most reports, the risk factors associated with the
development of DCIS are similar to those for invasive breast cancer:
increased age, family history of breast cancer, previous biopsies,
history of hormone replacement therapy, and older age at first
childbirth. Tamoxifen, a hormonal drug, has demonstrated a reduction in
the incidence of DCIS among high-risk women.
Although the natural course of the disease is not well understood,
DCIS can become invasive cancer and spread to other tissues. It is also
a marker of increased risk for developing cancer elsewhere in the same
or opposite breast. However, not all DCIS will progress to invasive
disease, and it is thought that DCIS can be present in some individuals
without causing problems over a long period of time. Recent research
suggests that DCIS is a spectrum of disease and that certain tumor
characteristics may be strong or weak risk factors for subsequent
invasive breast cancer. Unfortunately, it is currently not clear which
lesion types are more likely to become invasive, leading to difficult
treatment decisions for patients and providers.
Because of this uncertainty, DCIS patients are typically treated
promptly following diagnosis and have a generally good prognosis.
Standard DCIS therapies include breast conservation, with or without
radiation or mastectomy, depending on patient and tumor
characteristics. Sentinel lymph node biopsy may also be recommended to
high-risk patients since this is the area where cancer spread is often
first detected. Hormonal therapy may also be used in an effort to
prevent DCIS recurrence and to lower the risk of developing invasive
breast cancer. However, these drugs' potential side effects must be
weighed carefully.
Since the natural course of DCIS is not well understood and
treatment benefit may depend on specific tumor and patient
characteristics, the treatment of DCIS remains controversial. To
examine these important issues, the NIH National Cancer Institute and
Office of Medical Applications of Research will convene a State-of-the-
Science Conference from September 22-24, 2009. The questions to
consider include:
What are the incidence and prevalence of DCIS and its
specific pathologic subtypes, and how are incidence and prevalence
influenced by mode of detection, population characteristics, and other
risk factors?
How does the use of MRI or sentinel lymph node biopsy
impact important outcomes in patients diagnosed with DCIS?
How do local control and systemic outcomes vary in DCIS
based on tumor and patient characteristics?
In patients with DCIS, what is the impact of surgery,
radiation, and systemic treatment on outcomes?
What are the most critical research questions for the
diagnosis and management of DCIS?
An impartial, independent panel will be charged with reviewing the
available published literature in advance of the conference, including
a systematic literature review commissioned through the Agency for
Healthcare Research and Quality. The first day and a half of the
conference will consist of presentations by expert researchers and
practitioners and open public discussions. On Thursday, September 24,
the panel will present a statement of its collective assessment of the
evidence to answer each of the questions above. The panel will also
hold a press conference to address questions from the media. The draft
statement will be published online later that day, and the final
version will be released approximately six weeks later. The primary
sponsors of this meeting are the NIH National Cancer Institute and the
NIH Office of Medical Applications of Research.
Advance information about the conference and conference
registration materials may be obtained from American Institutes for
Research of Silver Spring, Maryland, by calling 888-644-2667 or by
sending e-mail to consensus@mail.nih.gov. The American Institutes for
Research's mailing address is 10720 Columbia Pike, Silver Spring, MD
20901. Registration information is also available on the NIH Consensus
Development Program Web site at https://consensus.nih.gov.
Please Note: The NIH has instituted security measures to ensure
the safety of NIH employees, guests, and property. All visitors must
be prepared to show a photo ID upon request. Visitors may be
required to pass through a metal detector and have bags, backpacks,
or purses inspected or x-rayed as they enter NIH buildings. For more
information about the security measures at NIH, please visit the Web
site at https://www.nih.gov/about/visitorsecurity.htm.
Dated: May 20, 2009.
Lawrence A. Tabak,
Acting Deputy Director, National Institutes of Health.
[FR Doc. E9-12376 Filed 5-27-09; 8:45 am]
BILLING CODE 4140-01-P