News and Events: Congressional
SENSE
OF CONGRESS REGARDING OVARIAN CANCER
-- (House of Representatives - July 22, 2002)
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Mr. BILIRAKIS. Mr. Speaker, I move to suspend the rules and agree to the
concurrent resolution (H. Con. Res. 385) expressing the sense of the Congress
that the Secretary of Health and Human Services should conduct or support
research on certain tests to screen for ovarian cancer, and Federal health
care programs and groups and individual health plans should cover the
tests if demonstrated to be effective, and for other purposes.
The Clerk read as follows:
H. Con. Res. 385
Resolved by the House of Representatives (the Senate concurring), That
it is the sense of the Congress that--
(1) the Secretary of Health and Human Services, acting through the Director
of the National Institutes of Health--
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(A) should conduct or support research on the effectiveness of the medical
screening technique of using proteomic patterns in blood serum to identify
ovarian cancer, including the effectiveness of using the technique in
combination with other screening methods for ovarian cancer; and
(B) should continue to conduct or support other promising ovarian cancer
research that may lead to breakthroughs in screening techniques;
(2) the Secretary should submit to the Congress a report on the research
described in paragraph (1)(A), including an analysis of the effectiveness
of the medical screening technique for identifying ovarian cancer; and
(3) if the research demonstrates that the medical screening technique
is effective for identifying ovarian cancer, Federal health care programs
and group and individual health plans should cover the technique.
The SPEAKER pro tempore (Mr. Grucci). Pursuant to the rule, the gentleman
from Florida (Mr. Bilirakis) and the gentleman from Ohio (Mr. Brown) each
will control 20 minutes.
The Chair recognizes the gentleman from Florida (Mr. Bilirakis).
GENERAL LEAVE
Mr. BILIRAKIS. Mr. Speaker, I ask unanimous consent that all Members may
have 5 legislative days within which to revise and extend their remarks
on H. Con. Res. 385 and to include extraneous material.
The SPEAKER pro tempore. Is there objection to the request of the gentleman
from Florida?
There was no objection.
Mr. BILIRAKIS. Mr. Speaker, I yield myself such time as I may consume.
Mr. Speaker, I rise today in support of H. Con. Res. 385, which expresses
the support of the Congress for research on tests to screen for ovarian
cancer.
Ovarian cancer ranks fifth in cancer deaths among women. Approximately
50 percent of the women in the United States diagnosed with ovarian cancer
die as a result of the cancer within 5 years. The sooner ovarian cancer
is diagnosed and treated, the better a woman's chance for recovery, since
ovarian cancer is readily treatable when it is detectable before it has
spread beyond the ovaries.
If diagnosed and treated while the cancer is still limited to the ovary,
the 5-year survival rate is 95 percent. However, only 25 percent of all
ovarian cancers are found at this early stage, primarily because ovarian
cancer is hard to detect early. Women with ovarian cancer often do not
display symptoms until the disease is in an advanced stage. Without a
reliable, easy-to-administer screening tool, we will continue to lose
the battle to detect and treat this cancer in its early stages.
This resolution expresses the sense of the Congress that the National
Institutes of Health should conduct or support research on the effectiveness
of screening technologies to detect ovarian cancer. The resolution also
requests that the Secretary of Health and Human Services submit to Congress
a report on this research, including an analysis on the effectiveness
of these screening techniques.
Finally, the resolution states that if the research demonstrates that
the screening technique is effective for identifying ovarian cancer, Federal
health programs and health plans should cover this new diagnostic test.
It is important for women to get tested yearly for ovarian cancer. Effective
screening techniques coupled with yearly exams will ultimately save lives.
Mr. Speaker, I urge my colleagues to support this resolution.
Mr. Speaker, I reserve the balance of my time.
Mr. BROWN of Ohio. Mr. Speaker, I yield myself 2 minutes.
Mr. Speaker, I want to thank the gentlewoman from Connecticut (Ms. DeLauro)
and the gentleman from New York (Mr. Israel) for their efforts to address
the need for continued research in ovarian health screening and subsequent
coverage of proven testing methods by insurers.
Ovarian cancer, the deadliest of the gynecologic cancers, is the fourth
leading cause of cancer deaths among American women. It is estimated there
will be over 23,000 new cases that get diagnosed, approximately 14,000
deaths from ovarian cancer just in this year alone in the U.S. There is
no sound screening test to accurately detect ovarian cancer in its early
stages like a pap smear for the detection of cervical cancer or a mammogram
to detect breast cancer. While the 5-year survival rate for women in the
advanced stages of ovarian cancer is only 15 to 20 percent, for women
in stage I of the disease, the 5-year survival rate approaches 90 percent.
This resolution encourages the development of an effective screening tool
for ovarian cancer and promotes insurance coverage of effective screening
tests. The Subcommittee on Health under the Committee on Energy and Commerce
marked up this bill last week in committee. We passed it unanimously by
voice vote. I urge my colleagues to support the resolution.
Mr. BILIRAKIS. Mr. Speaker, I have no further request for time, and I
yield back the balance of my time.
Mr. BROWN of Ohio. Mr. Speaker, I yield 5 minutes to the gentleman from
New York (Mr. Israel).
Mr. ISRAEL. Mr. Speaker, I thank the gentleman for yielding me this time.
Mr. Speaker, there are times when we can make a difference and sometimes
it is the difference between life and death, and today is one of those
days. We are considering a resolution that could begin a process that
will save the lives of thousands of American women with ovarian cancer
and women all over the world over the next several years.
The resolution before us, which I introduced with the gentlewoman from
Connecticut (Ms. DeLauro), distinguished colleague, calls on the National
Institutes of Health to conduct a complete multi-institutional trial of
a potentially huge breakthrough in the early detection of ovarian cancer.
My colleagues have heard the statistics. About 75 percent of women diagnosed
with ovarian cancer receive that diagnosis in the advanced stages of the
disease when survival rates are only 20 percent. Ovarian cancer is the
deadliest of gynecologic cancers. It is the fifth leading cause of cancer
deaths among American women. One out of every 57 women are diagnosed with
ovarian cancer. Last year nearly 14,000 women in America died from ovarian
cancer.
The statistics are alarming, but we can do something about them tonight.
Thanks to Peter Levine and Dr. Ben Hitt, a reliable method of early detection
may be near and that early detection takes the survival rate from 20 percent
to 95 percent. This is something that saves lives. These are statistics
that we can improve.
The resolution calls for a full field test of the new ovarian cancer early
detection process, and if that full trial of the simple blood test for
ovarian cancer proves effective, I am going to fight to require that the
blood test be given to all women as part of their annual gynecological
exam and that Medicare/Medicaid and private insurance fully cover the
procedure. It is a tough approach, but the time to act is now. In this
case we can do something about the statistics. We can do something to
save thousands of lives. We can make a difference.
Our Nation has found the resolve and the resources to tackle the most
difficult problems on earth, to produce the most advanced technology,
to produce the most sophisticated weapons we need to protect our national
security, and now we have an opportunity, using a simple stick upon a
finger, to protect the health security of nearly 14,000 women. Now is
the time for us to find the resolve and the resources to protect our people
and our women from the ravages of ovarian cancer.
Mr. Speaker, I want to thank the leadership of the Committee on Commerce
for their bipartisan support. I want to thank the leadership of the entire
Congress for their bipartisan support for this legislation that does put
women ahead of politics. I urge my colleagues to support this important
resolution.
Mr. BROWN of Ohio. Mr. Speaker, I yield 3 minutes to the gentlewoman from
Connecticut (Ms. DeLauro), who has been one of the sponsors of this bill
and has been a leader in all kinds of issues regarding women's health.
Ms. DeLAURO. Mr. Speaker, I thank the gentleman from Ohio for yielding
me this time.
I stand here today in thanks to the gentleman from New York (Mr. Israel),
and I want to express how proud I am to join with him on this resolution.
I will explain why to my colleagues.
So many people here know about my own set of health circumstances. Sixteen
years ago, I was diagnosed with ovarian cancer. There is a moment
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when they tell you that you have cancer in which you go blank. You are
not quite listening to anything that the doctor is telling you; you are
only trying to figure out whether or not you are going to live or you
are going to die.
Ovarian cancer is a stealth disease. It does not know a political party;
it does not know age; it does not know religious background; it just strikes.
What is often the case is that women do not know they have ovarian cancer
until the late stages, and that is often too late. By some, I say random
luck, but I always view that someone was watching over me; I was diagnosed
with ovarian cancer in the first stage so that it was treatable, though
16 years ago we did not have all of the new technology and this wonderful
opportunity that we have to see expanded research by looking at blood
samples and determining from the protein in those blood samples whether
or not you have ovarian cancer. But it was random, and no one should live
or die by randomness.
We have an opportunity with this resolution to move forward in that early
detection of ovarian cancer, and in these last 16 years, we have been
unable to come forward with a screen, something like a mammogram which
has been so helpful in determining the early stages of breast cancer so
that we can save lives. That is what this resolution is about. It is about
saving women's lives, because almost 14,000 women will die this year with
ovarian cancer. If we had that screen, we could save 90 percent of them.
They could go and be with their families, with their husbands, with their
children, and have good lives.
I know my colleagues will do the right thing on this resolution. Let us
take advantage of modern technology, of biomedical research, and let us
bring hope to the women of this country and their survival. I say ``thank
you'' from the bottom of my heart to STEVE ISRAEL, who asked me to join
him on this resolution, and I say ``thank you'' to God every day for giving
me my life back and my opportunity to serve in this institution, because
this is the institution that can make things happen. We can save lives
with this resolution.
• [Begin Insert]
Ms. JACKSON-LEE of Texas. Mr. Speaker, I rise to support H. Con. Res.
385 which expresses the sense of Congress that the Secretary of Health
and Human Services should conduct or support research on certain tests
to screen for ovarian cancer, and Federal health care programs and group
and individual health plans should cover the tests if demonstrated to
be effective.
Experts estimate that more than 23,000 cases of ovarian cancer will be
diagnosed this year with an estimated 13,900 women dying this year alone.
While this is a sad reality, it is even more disturbing when we consider
that ovarian cancer is a very treatable disease when it is detected early,
but only 25 percent of ovarian cancer cases in the United States are diagnosed
in the early stages. The vast majorities of cases are not diagnosed until
the cancer has spread beyond the ovaries, often because symptoms are easily
confused with other diseases and because reliable easily administered
screening tools do not exist. Ovarian cancer is the deadliest of all gynecologic
cancers, and is the fourth leading cause of cancer death among women in
the United States.
We all know about the remarkable scientific advances that are made each
day. Today, people worried about certain illnesses may soon know for certain
if they are at risk. Diseases that were once considered incurable are
not preventable. Every day we are exploring new frontiers of the landscape
of life and claiming new scientific victory. We are able to operate on
infants still in the womb, extend the lives of heart patients with artificial
hearts, and predict the development of disease through genetic coding.
But there is a sad side of this story. There are diseases that do not
receive the research attention that is necessary for advancement in treating
and curing them. Ovarian cancer is one of those diseases.
That is why we must actively support all promising new developments in
research. Scientists from the Food and Drug Administration and the National
Cancer Institute reported in the February edition of The Lancet that patterns
of protein found in patients' blood serum may reflect the presence of
ovarian cancer. In the study, scientists used serum proteins to detect
ovarian cancer, even at its earliest stages. Using a test that can be
completed in 30 minutes with blood from a finger prick researchers were
able to differentiate between serum samples taken from patients with ovarian
cancer and those from unaffected patients. This test was one step in a
long journey. Additional, multi-institutional trials must be completed
before the scientific community can agree that this is a reliable tool.
That is why this resolution is so critical. We must push to make this
test available to women. Saving at least one of the 13,900 who will die
has to be our motivation.
Currently, 50 percent of women diagnosed with ovarian cancer die from
it within five years. When the disease is diagnosed in advanced stages,
the chance of five-year survival is only 25 percent. Sadly, the situation
for African American women is even more dismal. Among African American
women, only 48 percent survive five years or more. Overcoming such persistent
and perplexing health disparities and promoting health for all Americans
must be a priority. That is why supporting research on medical screening
techniques to identify ovarian cancer must rank as a priority for the
Department of Health and Human Services.
Early detection of this disease is the best way to save women's lives.
The Department of Health and Human Service has done remarkable work researching
deadly disease like cancer, Alzheimer's, diabetes and AIDS and giving
hope to so many patients through this research. This resolution asks the
Secretary of Health and Human Services to focus research on this unrecognized
threat to the lives of women. Specifically, the Secretary should focus
research on the effectiveness of the medical screening technique of using
proteomic patterns in blood serum to identify ovarian cancer.
Our scientists have tackled some of the most difficult problems known
to man and have the potential to solve some of the most challenging health
problems in the world. We must resolve to put all our resources behind
their efforts particularly for diseases that affect populations that persistently
experience health disparities.
I support this legislation and thank the sponsor Mr. ISRAEL and Ms. ROSA
DELAURO who is a living testimony to how we can get results from good
health care--because she is a survivor of ovarian cancer.
Mr. DINGELL. Mr. Speaker, I commend the House for taking up this resolution
raising the importance of ovarian cancer research and screening.
Despite the severe consequences it poses to women's health, ovarian cancer
is still under-recognized and under-researched. According to the American
Cancer Society, more than 23,000 new cases of ovarian cancer will be diagnosed
this year alone. An estimated 13,900 women will die of ovarian cancer
in 2002, accounting for more deaths than any other cancer of the female
reproductive system, and ranking as the fifth leading cause of cancer
deaths in women.
Ovarian cancer is highly treatable when discovered in its earliest, most
treatable stages. Unfortunately, it is seldom discovered until it has
spread. Only 78 percent of ovarian cancer patients survive one year and
just over 50 percent survive five years after diagnosis.
Currently, no simple standardized tests exist to detect ovarian cancer
the way mammography can reliably check for breast cancer. This is why
it is essential that Congress commit itself to research in the early detection
of ovarian cancer.
The good news is that since 1991, the ovarian cancer incidence rate has
been on the decline. The best way to ensure the continuation of these
waning numbers is to invest in improved testing and research. With multiple
means of early detection on the horizon, it is essential that we address
this important issue as soon as possible. I urge my colleagues to join
me in support of this resolution.
Mrs. MINK of Hawaii. Mr. Speaker, I rise today to ask all of my colleagues
to vote for H. Con. Res. 385, which calls upon the Secretary of Health
and Human Services to conduct or support research on certain tests to
screen for ovarian cancer and to ensure that Federal health care plans
and group and individual health plans cover the tests if they are demonstrated
to be effective. I am a proud co-sponsor of this important legislation.
As many of my colleague know, increasing research funding for ovarian
cancer, especially for development of an early detection test, has been
among my top legislative priorities for the past decade. My bill, H.R.
326, the Ovarian Cancer Research and Information Amendments Act, has 142
co-sponsors. I have introduced a similar bill in each Congress, beginning
in 1991.
I was thrilled to learn in February of this year of a blood test developed
by Correlogic Systems Inc. of Bethesda, Maryland which has been studied
by researchers at the National Cancer Institute and the Food and Drug
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Administration. In the study, scientists used a protein pattern they developed
to classify 116 blood samples that were known to include 50 cancerous
samples and 66 noncancerous samples. The test correctly identified the
50 cancerous samples and correctly identified 95 percent of the control
sample as noncancerous.
It is urgent that large-scale testing of this technology be begun as soon
as possible. As this test only requires a blood test, it will at last
enable the widespread screening needed to identify this disease in its
earliest and most curable stage. In particular, we should make the test
available as soon as possible to those with increased risk factors for
ovarian cancer.
Approximately 23,000 women in the United States are expected to be diagnosed
with ovarian cancer this year and some 14,000 women will die from the
disease. Ovarian cancer is the most lethal cancer of the female reproductive
system, primarily because it is so difficult to detect in its early stages.
While survival rates are quite high if the disease is found before it
spreads beyond the ovaries, the five-year survival rate drops to 28 percent
for women who are diagnosed and treated in the later stages of the disease.
Only 25 percent of ovarian cancer cases are caught in the earliest stage.
This test could change these frightening statistics and lead to the declines
in mortality we've seen since widespread use of early detection tests
for cervical and breast cancer.
I commend Representatives ISRAEL and DELAURO for introducing this bill
and urge all of my colleagues to support it.
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Mr. BROWN of Ohio. Mr. Speaker, I yield back the balance of my time.
The SPEAKER pro tempore. The question is on the motion offered by the
gentleman from Florida (Mr. Bilirakis) that the House suspend the rules
and agree to the concurrent resolution, H. Con. Res. 385.
The question was taken; and (two-thirds having voted in favor thereof)
the rules were suspended and the concurrent resolution was agreed to.
A motion to reconsider was laid on the table.
END