Ovarian
Cancer
by Marian Segal
She crowned herself "the Queen of
Neurosis," but this time, it was not simply an overactive imagination that
made her fear for her health.
It was symptoms of the ovarian cancer
that eventually claimed her life.
Gilda Radner, one of the original
Not Ready for Prime Time Players of television's "Saturday Night Live,"
claimed in her book
It's Always Something that she could
get neurotic over any health problem. "I hated to be sick and I had an
imagination that could turn a stomachache into the plague."
So, she wrote, when a complete physical
examination in January 1986 failed to explain the overwhelming fatigue
and general malaise she was feeling, she agreed with the doctor that her
symptoms might just be from depression; she had, after all, been going
through a rough period in both her personal and professional life.
It was not until October--10 months
and several symptoms, diagnoses, and failed therapies later--that cancer
of the ovaries was confirmed.
Delay in diagnosing ovarian
cancer is not unusual. Early detection is difficult because disease confined
to the ovary seldom produces symptoms. When symptoms do surface, they are
often vague and easily mistaken for other, often minor, ailments.
Radner's cancer was not discovered
until it had spread to her bowel and liver.
She suffered from fatigue, low-grade
fever, pelvic cramping, abdominal bloating, gas, and aches and pains in
her upper thighs and legs. Loss of appetite and a feeling of fullness,
indigestion, nausea, weight loss, and, less often, vaginal bleeding and
low back pain are other symptoms.
As the tumor grows, it may press
on the bowel and bladder, causing constipation and frequent urination.
Malignant cells can break away from
the tumor and spread directly to other organs in the abdomen, such as the
stomach, colon and diaphragm (muscle separating the chest cavity from the
abdomen), causing a fluid buildup that results in swelling and discomfort.
The cells can also enter the bloodstream
or lymph system and spread to other parts of the body.
Radner wrote that her complaints
had been variously attributed to Epstein-Barr virus infection, depression,
stress, and anxiety. She had undergone blood tests, a barium enema, and
ultrasound (pelvic sonogram).
According to Radner, the sonogram,
done in the summer of 1986, showed "congestion" and the "ovaries weren't
exactly in the place they were supposed to be, but that wasn't serious."
There was no sign of tumor or bowel obstruction.
Aspirin
to Acupuncture
Attempting to combat her ills through
both mainstream and holistic medicine, Radner tried remedies that ran the
gamut from aspirin, anti-inflammatories and antidepressants to health foods,
vitamins, acupuncture, and colonics (unconventional type enemas).
"Suddenly, I began to wonder how
to please so many people," she wrote. "Do I take the magnesium citrate?
What about the coffee enema? Do I do both? Do I do the abdominal massage
or the colonic? Do I tell the doctors about each other?"
Then, late in October, an abnormal
liver function test prompted more exams. A CAT scan and analysis of fluid
from the abdomen confirmed ovarian cancer.
Diagnosed at age 40, Radner was younger
than most women with the disease. The chance of developing ovarian cancer
increases with age; most cases are found in women who have gone through
natural menopause, with the average age at diagnosis being 61.
As was true with Radner, however,
women with a family history of the disease generally are diagnosed at a
younger age.
Each year in the United States, ovarian
cancer is diagnosed in about 26,000 women and claims more than 14,000 lives.
It is most common in women living
in Europe and North America; Asian women have a relatively low incidence.
Although Chinese and Japanese women
living in the United States have higher rates of ovarian cancer than their
counterparts in Asia, the disease is still less common among this group
than among the native white population in the United States. Rates among
black women in all parts of the world are low.
Certain factors are associated with
an increased risk of getting ovarian cancer. Although the lifetime risk
for most women is 1 in 70, it doubles for women who have never been pregnant.
Also at increased risk are women
who have had breast, intestinal, or rectal cancer. Under investigation
as possible risk factors are: high-fat diet, early onset and late cessation
of menstruation, being of Eastern European Jewish descent, and use of talcum
powder in the genital area.
Women with close relatives who have
had ovarian cancer are also at greater risk, reaching perhaps a 50 percent
chance if they have at least two first-degree relatives (mother, sister
or daughter) with the disease.
This compares with a 1.4 percent
chance in women without a family history. Women who have a first-degree
relative and one or more second-degree relatives (aunt, grandmother) who
had ovarian cancer have a somewhat lesser risk than those with two first-degree
relatives, but are still considered to be at high risk.
Radner wrote that her mother had
breast cancer and a cousin had both breast and ovarian cancer. Later, it
was learned that other of her relatives had ovarian cancer as well.
About 5 to 7 percent of all ovarian
cancer is thought to be inherited. In 1994, scientists identified a gene,
which they named BRCA1, that related to the development of inherited breast
cancer.
Changes or abnormalities in this
gene are now also considered responsible for about 80 percent of inherited
ovarian cancer. The abnormal gene can be inherited from either parent.
The Gilda Radner Familial Ovarian
Cancer Registry, established in 1981 at Roswell Park Cancer Institute in
Buffalo, N.Y., and named for Gilda Radner after her death in 1989, included
2,946 cases of ovarian cancer in 1,346 families as of January 1997.
Reduced
Risk
Factors associated with a reduced
risk of ovarian cancer include: giving birth to more than one child, breast-feeding,
tubal ligation (female sterilization), and use of birth control pills.
Evidence suggests that hormones may
influence development of the disease. The risk of ovarian cancer is reduced
in women who have had multiple pregnancies and in those who used birth
control pills.
The Cancer and Steroid Hormone Study
by the national Centers for Disease Control and Prevention and the National
Institute of Child Health and Human Services found that use of oral contraceptives
for even a few months reduced the risk of ovarian cancer by 40 percent
in women 20 to 54 years old.
The study, published in the March
12, 1987, New England Journal of Medicine, also found that the longer a
woman used birth control pills, the lower her risk of ovarian cancer, and
that the protective effect persisted long after stopping the pill.
Based on these data, since 1989,
the labeling for oral contraceptives has included decreased incidence of
ovarian cancer among the noncontraceptive health benefits of the pill.
On the reverse side of the coin,
in January 1993, FDA requested that drug firms revise fertility drug labels
to include ovarian cancer as a potential adverse drug reaction.
The action was in response to a report
in the November 1992 issue of the American Journal of Epidemiology suggesting
a possible relationship between use of fertility-enhancing drugs and ovarian
cancer. The analysis was based on data from 12 studies comparing women
with ovarian cancer to those without the disease.
Only three of the studies, however,
contained data on the use of fertility drugs and risk of ovarian cancer.
(A 1987 article in the same journal reported no association between the
drugs and ovarian cancer.)
FDA urged caution in interpreting
the findings of the 1992 report because the analysis only included small
numbers of women and because the article gave no information about the
fertility drugs prescribed, reasons for the infertility, or tumor size
or stage of disease at diagnosis.
Search
for a Screening Test
According to the registry, if ovarian
cancer is diagnosed while still confined to the ovaries, the chance for
cure is 85 to 90 percent.
According to the American Cancer
Society, only 23 percent of all cases are diagnosed at this early stage.
Among women whose cancer has spread beyond the ovary by the time it's diagnosed,
only 20 to 25 percent survive five years.
However, unlike cervical or breast
cancer (which may be detected early by a Pap test or mammogram, respectively),
ovarian cancer has no approved screening test, though some are under investigation.
"The traditional routine pelvic examination
is largely ineffective for early detection," says Julie Beitz, M.D., a
medical oncologist in FDA's division of oncology and pulmonary drug products.
"Often you can't feel a normal-sized
ovary. And even if you can, it's hard to tell if it's enlarged because
ovaries vary in size from person to person and day to day.
Ovarian cancers start very small,
and by the time they're large enough to feel, the cancer is most likely
already advanced."
The problem with ovarian cancer,
she says, is that "you have to detect very small changes, and these are
hard to detect on a pelvic exam because it's a very indirect examination."
Researchers are working on developing
an accurate test for the BRCA1 gene. The American Society of Human Genetics
has recommended that testing for BRCA1 be limited to research in which
subjects are members of families at high risk for either ovarian or breast
cancer.
Researchers continue looking for
tumor markers--substances that may appear in abnormal amounts in the blood
or urine--that may prove useful in developing a screening test.
One such marker is CA 125, a substance
in the blood that is elevated in patients with advanced ovarian tumors.
Doctors now measure CA 125 levels
in patients treated for advanced disease to determine if the tumor has
shrunk or if disease has recurred. Its value in monitoring treatment prompted
scientists to study its potential for early detection. Its use for screening,
however, is investigational.
Transvaginal ultrasound is also being
studied as a screening tool. With ultrasound, high-frequency sound waves
are projected into the body, and the echoes produced are converted by computer
into a picture.
Unlike abdominal ultrasound, in which
the sound wave-emitting device is placed on the outside of the belly, transvaginal
ultrasound uses a probe placed in the vagina that can reach within millimeters
of the ovaries, producing more detailed images.
"There is uncertainty as to the value
of these tools as screening tests and their ultimate impact on mortality,"
says John Gohagan, Ph.D., chief of the National Cancer Institute's Early
Detection Branch in the Division of Cancer Prevention and Control.
NCI is conducting a clinical trial
including 74,000 women aged 60 to 74 to clarify the issue. The trial is
designed to assess the value of CA 125 and transvaginal ultrasound for
early detection of ovarian cancer and to measure their impact on mortality.
Women in the trial are randomly assigned
to either a screening group or a control group of 37,000 women each. The
screening group will have periodic pelvic examinations along with CA 125
and transvaginal ultrasound tests. The control group will have routine
medical care.
Diagnostic
Procedures
If a woman or her doctor suspects
ovarian cancer, diagnosis begins with a medical history of the patient,
review of her symptoms, and complete physical examination, including a
pelvic exam, in which the physician feels the vagina, ovaries, fallopian
tubes, bladder, and rectum to check for any growths.
A Pap test may also be done because,
even though it cannot reliably detect ovarian cancer, it may detect cancer
cells that have migrated to the uterine cervix from the ovaries.
Blood and urine tests may also
be done, as well other procedures, depending on the woman's symptoms and
results of her physical exam. These procedures include:
-
abdominal or transvaginal ultrasound--helps
distinguish fluid-filled cysts from a solid tumor
-
CAT scan--produces x-ray images
of cross-sections of body tissues
-
lower GI series (barium enema)--visualizes
the bowel on x-ray to detect abnormal areas that may be caused by ovarian
cancer
-
intravenous pyelogram (IVP)--produces
x-ray pictures of the kidneys, bladder and ureters (tubes carrying urine
from the kidneys to the bladder). Often, ovarian cysts or tumors can cause
pressure on these organs, which may show up on an IVP.
The only sure way to diagnose ovarian
cancer, however, is through microscopic examination by a pathologist of
abnormal-looking fluid or tissue.
While fluid can sometimes be obtained
by needle aspiration or other techniques, more commonly a laparatomy or
laparoscopy is done.
Laparotomy is an exploratory operation
in which the surgeon examines the abdomen thoroughly and removes fluid
or tissue for examination.
In laparascopy, a flexible, lighted
tube is passed through a small incision in the abdomen, allowing the surgeon
to examine the area and extract tissue for a biopsy.
If cancer is suspected, the surgeon
usually removes the entire affected ovary to avoid cutting through the
outer layer, which might cause the tumor to spread.
The tissue is sent to the pathologist
for immediate evaluation, and if cancer is confirmed, the surgeon nearly
always removes the second ovary, the uterus, and the fallopian tubes.
Samples are taken of nearby lymph
nodes, the diaphragm, the omentum (a fold of membranous lining in the abdominal
cavity), and fluid from the abdomen to see whether the cancer has spread.
If no fluid is found, several "washings"
are taken: A saline solution is put into the abdomen and then removed to
be examined for cancer cells.
If there are suspicious lesions,
tissue samples are also taken from the liver, small intestine, and large
intestine.
Early
Treatment Crucial
Trusting her instincts may have saved
Jessica Marsh's life. Due in part to her own vigilance and persistence,
Marsh (not her real name), a secretary in Rockville, Md., was diagnosed
before her cancer had spread beyond the ovary, affording her a brighter
prognosis.
For three months in the fall of 1985,
Marsh, then 36 years old, had noticed pains in her right side around the
time of her menstrual periods.
Although the pains were brief and
not severe, she decided to have her doctor check it out. A week or so before
her appointment, however, a very sharp pain prompted her to call the doctor
again. Her gynecologist was out of town, but the doctor on call had her
come in.
"He told me that my stomach was distended,
gave me a pelvic exam, and then congratulated me, telling me I was three
months pregnant," Marsh recalls. "I told him I wasn't pregnant, that I
already had two children and knew what it was like to be pregnant, and
this was not a pregnancy."
At Marsh's insistence, the physician
arranged for her to have a pelvic sonogram that day at a local hospital.
"I had the sonogram and the next
thing I knew, the doctor who had examined me at the office came in, repeated
the sonogram, and told me there was a mass and he wanted to do some more
tests. The next morning, I had surgery to remove my ovaries, uterus, and
fallopian tubes."
Although Marsh's experience may not
be typical, it illustrates again the difficulty in correctly diagnosing
the disease early. Yet, early detection and treatment can mean the difference
between life and death.
Treatment
Options
Ovarian cancer is always treated
surgically, removing as much tumor as is feasible. Chemotherapy (drug treatment)
or radiation therapy, or both, may also be given, depending on the extent
of disease.
Ovarian tumors usually grow outward,
with an irregular, cauliflower-like shape. When the cancer spreads, parts
of the tumor break off and attach to nearby organs. Cells may then spread
to lymph nodes and distant organs.
Cancer limited to the ovaries may
be successfully treated with surgery alone, removing the ovaries, fallopian
tubes, omentum (a fold of tissue attached to organs in the abdominal cavity),
and uterus.
Some patients may also receive chemotherapy
or radiation therapy to kill any cancer cells remaining after surgery.
Disease that has spread beyond the
ovaries almost always requires chemotherapy or radiation therapy in addition
to surgery.
Radiation therapy may be given by
placing a radioactive solution into the pelvis and abdomen through a thin
tube, coating the organs and total abdominal contents. Less commonly, external
radiation using high-energy x-rays directed to the pelvis and abdomen may
be prescribed.
The type of drugs used in chemotherapy
depends not only on the extent of disease, but also on the type of cancer.
About 85 to 90 percent of ovarian cancers arise from epithelial cells,
which form the outer layer of the ovary. The rest derive from other cell
types that make up the organ.
FDA has approved several drugs to
treat ovarian cancer. Two of the most commonly used are Platinol (cisplatin)
and Taxol (paclitaxel).
Taxol was approved in April 1998
as a first-line treatment for advanced ovarian cancer. It has been used
since December 1992 to treat advanced ovarian cancer that has not responded
to other therapies or has progressed after treatment (see "Taxol's
Long History"), and is being evaluated for first-line treatment.
National Cancer Institute and FDA
scientists cooperated in studies to evaluate the safety and effectiveness
of Taxol. FDA's research role in drug development is a fairly new concept,
designed to help speed the approval process for drugs for life-threatening
diseases.
"It's a commitment by the agency
to do more than just wait for packages of data to come in [from the drug's
sponsor] and review them for approval," says Jerry M. Collins, Ph.D., director
of the division of clinical pharmacology research in the Center for Drug
Evaluation and Research. "We can't do this for every new drug in every
therapeutic area," he says, "but for AIDS and cancer, we have done similar
research before."
Since Taxol is given in combination
with several other drugs, there was major concern about the potential for
serious drug interaction.
However, according to Collins, this
research demonstrated that "paclitaxel actually had a lower risk of metabolic
interactions than most other drugs."
Other chemotherapeutic agents used
to treat ovarian cancer include Cytoxan and Neosar (cyclophosphamide),
Paraplatin and Adriamycin (doxorubicin), and Hexalen (altretamine).
A recent addition is Hycamtin (topotecon,
approved in 1996 to treat ovarian cancer that recurs after other chemotherapeutic
agents have failed. Hycamtin is the first of a new class of drugs called
topoisomerase I inhibitors. They kill cancer cells by inhibiting an enzyme
essential to the replication of human DNA.
Side
Effects
Surgery, the first-line treatment
for ovarian cancer, requires several days' hospitalization and a recuperative
period of from four to six weeks.
Removing the ovaries, which are the
main source of the female hormones estrogen and progesterone, causes immediate
menopause, and the symptomatic hot flashes are more severe than when menopause
occurs more gradually, as it usually does naturally.
Radiation therapy can cause mild
skin reactions, such as redness and drying in treated areas, urinary discomfort,
diarrhea, and vaginal dryness. (Menopause can also cause vaginal dryness.)
A small percent of patients may develop bowel obstruction, sometimes requiring
surgical correction.
Other possible side effects of radiation
therapy, commonly experienced with chemotherapy as well, include loss of
energy and appetite, nausea, and vomiting.
Chemotherapy may also cause mouth
sores, hair loss, and reduced platelet and blood cell counts that can lead
to infections, anemia or bleeding.
The drugs used to treat ovarian cancer
may also have neurologic effects, causing hearing loss, ringing in the
ears, nerve damage, and numbness or tingling in the face, fingers and toes.
There may also be kidney damage.
Most side effects are temporary,
and sometimes dietary changes or medicines can ease the symptoms.
There are several drugs approved
for countering nausea and vomiting often associated with chemotherapy.
They include Zofran (ondansetron hydrochloride), Reglan (metocloparamide),
and Marinol (dronabinol).
Transfusions can correct red blood
cell and platelet deficiencies. Hematopoietic growth factors such as G-CSF,
approved in 1991, stimulate production of infection-fighting white blood
cells.
GM-CSF, which also received FDA approval
in 1991 to increase white blood cell counts after bone marrow transplantation,
is now being studied for its effectiveness in stimulating white cells after
cancer chemotherapy.
Among other drugs now under study
for their ability to increase white cell counts, and perhaps platelets
as well, are stem cell factor and PIXY 321. PIXY 321 is a genetically engineered
product consisting of GM-CSF and another hematopoietic growth factor, interleukin-3.
When therapy is completed, the woman
continues to have regular checkups that include pelvic examinations and
laboratory tests to measure blood levels of tumor markers such as CA 125.
The doctor may recommend a laparotomy
or laparoscopy after completion of chemotherapy to inspect the abdomen
and pelvis and take multiple tissue biopsies.
This "second-look surgery" helps
evaluate the effectiveness of chemotherapy and determine whether treatment
should be continued or stopped. Often a laparotomy or laparoscopy has been
done previously to diagnose ovarian cancer.
Attempts
at Prevention
The Gilda Radner Familial Ovarian
Cancer Registry advises women with two or more first- or second-degree
relatives who have had the disease to have their ovaries removed via video
laparoscopy as a precautionary measure by age 35, if they have completed
their families.
The registry also advises that there
is a small increased risk (1.8 percent) of developing primary papillary
cancer of the peritoneum for women who have had this prophylactic surgery.
The registry also recommends that
women with a family history of ovarian cancer receive genetic counseling,
beginning in their early 20s, and have pelvic and abdominal examination,
CA 125 testing, and transvaginal ultrasound every six months beginning
in their early 30s.
Jessica Marsh, seven years after
her diagnosis, is today free of cancer and feeling fine. "I've become a
much more positive person since my cancer," she says. "Life is too short
to worry about little things. If life deals me lemons, I'll make lemonade."
Marian Segal is a former member
of FDA's public affairs staff.
The Ovaries--How
They Work
The ovaries are located in the pelvis,
one on each side of the uterus. About the size and shape of almonds, they
are made up of several different cell types.
Some carry out the hormonal functions
of the organ, while others provide physical support. The ovaries have two
main functions:
-
ovulation (the release of an egg each
month)
-
production of estrogen and progesterone,
hormones that regulate the menstrual cycle and pregnancy and control the
development of female physical traits, such as the breasts, pelvic structure,
fat distribution, and body hair.
From birth, the ovaries contain the
cells that eventually become ova (eggs).
Each month, beginning with puberty
and until menopause, hormones produced by the pituitary gland in the brain
stimulate ovulation (release of an egg), which alternates each month between
the two ovaries. (Not all women ovulate every month.)
The egg travels through the fallopian
tube to the uterus. If it is fertilized, it may grow and develop in the
womb. If not, hormone changes cause shedding of the uterine lining, and
menstruation begins about two weeks later.
Benign Ovarian
Cysts
Noncancerous ovarian cysts are a very
common condition among women of reproductive age. But before diagnosing
a condition as a benign ovarian cyst, doctors rule out cancer.
Normally, the follicle (or cyst)
created by the ovaries each month bursts harmlessly when ovulation occurs.
Sometimes, however, this normal physiologic process goes awry.
The follicle, instead of bursting
and releasing its egg, may continue to swell with fluid, or the corpus
luteum (tissue that secretes hormones to prepare for pregnancy) may fail
to dissolve even though the egg has not been fertilized.
In either of these situations, the
result is a "functional," or physiologic, cyst--a fluid-filled sac that
may be as small as a grape or as large as a grapefruit.
Functional cysts are the most common
ovarian cysts. In a premenopausal woman, such a cyst is always benign (noncancerous)
and will frequently disappear spontaneously within a couple of months.
Sometimes a functional cyst ruptures,
spilling ovarian fluid into the abdominal cavity and causing pain. As the
body absorbs the fluid, however, the pain subsides, and surgery is rarely
necessary.
Ovarian cysts may be diagnosed by
pelvic examination or by ultrasound imaging. A woman who has a functional
cyst may have abdominal cramps, nausea, and menstrual irregularity. However,
many women have no symptoms at all.
A gynecologist who diagnoses a cyst
of less than 6 centimeters (2 1/4 inches) in diameter in a premenopausal
woman who is ovulating will usually want to observe the patient for a couple
of menstrual cycles to see if the cyst goes away by itself, says Lisa Rarick,
M.D., director of FDA's division of reproductive and urologic drug products.
If the cyst doesn't disappear spontaneously,
the doctor may recommend that the woman take birth control pills to suppress
ovulation. Most birth control pills are combinations of two female sex
hormones, estrogen and progestin.
In some cases, progestin-only pills
(also called "mini-pills") may be prescribed instead of combination pills.
Both combination birth control pills
and mini-pills work by preventing the release from the brain of other hormones
that stimulate ovulation. Deprived of hormonal stimulation, a functional
ovarian cyst will often shrink and eventually disappear.
An ovarian cyst that doesn't disappear
after a couple of months may be a benign semisolid cyst. This kind of cyst
is usually diagnosed by ultrasound imaging. The most common semisolid cyst
is a dermoid cyst, so-called because it is made up of skin-like tissue;
it can usually be removed by laparoscopic surgery.
Occasionally, an ovary containing
a dermoid cyst becomes twisted on itself, causing severe pain. Surgical
removal of the affected ovary, or oophorectomy, may be necessary if this
happens.
Any cyst that is 6 centimeters in
diameter--about the size of a peach--or larger in a premenopausal woman
should be investigated immediately as a possible malignancy, says Rarick,
as should a cyst of any kind in a woman who has completed menopause.
While some doctors will recommend
surgical examination of a large ovarian cyst, many gynecologists will examine
the mass through a laparoscope, says Rarick. "It's possible to use a needle
to puncture the cyst or aspirate its contents. The cyst can even be removed
through the laparoscopic incision."
Polycystic ovarian disease, also
known as Stein-Leventhal syndrome, is a benign condition characterized
by multiple small cysts on the ovaries.
This disease has a distinct set of
symptoms that may appear as early as adolescence and may include menstrual
irregularity, abnormal growth of body hair, lack of breast development,
obesity, and infertility.
--Eleanor Mayfield
Taxol's Long History
The healing properties of Taxol were
known to at least one community long before Western medicine recognized
the drug's potential.
According to an article in the Sept.
4, 1991, Journal of the American Medical Association, around the turn of
the century, a British official in the Indian subcontinent noted that parts
of the European yew, Taxus baccata, were used in an Indian clarified butter
preparation for treating cancer.
It wasn't until 1962, however, that
the U.S. Forest Service delivered crude bark extracts of the Pacific yew,
Taxus brevifola, to the National Cancer Institute.
A series of NCI experiments showed
the extract was effective against several kinds of cancer in mice.
In 1971, researchers at the Research
Triangle Institute in Durham, N.C., isolated Taxol from the extract, but
interest in the compound waned until the mid-1970s. In 1979, a researcher
at Albert Einstein College of Medicine in New York described how Taxol
works to defeat cancer by inhibiting cell division.
Today, Taxol--alone or in combination
with other drugs--is being studied for a wide variety of adult and childhood
cancers.
In July 1992, FDA authorized use
of the drug for ovarian cancer under a "treatment IND." Treatment INDs
permit earlier and wider access to experimental drugs by patients with
life-threatening conditions for which there is no satisfactory treatment.
Taxol was approved in December 1992
for advanced disease unresponsive to other therapies. The drug was approved
in a record five months.
In April 1998, it was approved as
a first-line therapy for advanced ovarian cancer.
--M.S.
See also:
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