What
Is Thyroid Cancer?
The thyroid gland is located under the Adam's
apple in the front part of the neck. In most people,
it cannot be seen or felt. It is butterfly shaped,
with 2 lobes - the right lobe and the left lobe -
joined by a narrow isthmus (see diagram).
The thyroid gland makes a hormone (called thyroid
hormone), which is important for many body functions.
The production of this hormone depends on iodine,
and the thyroid gland absorbs iodine from the blood.
Thyroid hormone regulates a person's metabolism. Too
much hormone causes a person to be hyperactive, feel
nervous, warm, hungry, and often lose weight. Too
little hormone causes a person to slow down, feel
tired and gain weight. All this is regulated by the
pituitary gland, at the base of the brain, which produces
a substance called thyroid stimulating hormone (TSH)
The thyroid gland contains mainly 2 types of cells:
• Thyroid follicle cells actually make and store
thyroid hormone. They also make a special thyroid
protein called thyroglobulin.
• C cells make another hormone, calcitonin, which
helps regulate the body's calcium metabolism.
Different cancers develop from each kind of cell.
The differences are important because they determine
the seriousness of the cancer and the type of treatment
needed.
Many types of tumors can develop in the thyroid gland.
Most of these tumors are benign (noncancerous). Others
are malignant (cancerous), which means they can spread
into nearby tissues and to other parts of the body.
Because the thyroid gland is close to the skin, tumors
often appear as bumps in the neck. They are called
thyroid nodules. Thyroid nodules can develop at any
age, but they are most common in adults, occurring
in at least half of all people. Often people find
these bumps themselves by seeing or feeling them.
Most of the time they are never noticed and never
cause a problem. Thyroid nodules can be either benign
or malignant. Fortunately, most are benign.
Benign Thyroid Tumors
A study out of Framingham, Massachusetts found thyroid
nodules in one out of 1000 people undergoing yearly
physical examinations. Almost all (90%-95%) of thyroid
nodules or tumors are benign. They develop from thyroid
follicular cells and can be found in normal-sized
thyroid glands and goiters (enlarged thyroid glands).
Goiters often develop when a person doesn't have enough
iodine in his or her diet. The thyroid may contain
1 nodule or several nodules. A gland with several
benign nodules is called a multinodular goiter. Often
these nodules are cysts filled with fluid, or they
may be "lumps" of stored thyroid hormone called colloid
nodules. Colloid nodules have very few cells in them.
Other nodules may have too many cells, but the cells
are not cancer cells. This type of nodule includes
hyperplastic nodules and adenomas. Sometimes hyperplastic
nodules or adenomas make too much thyroid hormone,
causing a condition called hyperthyroidism. Symptoms
of hyperthyroidism include nervousness, irregular
and rapid beating of the heart, excessive sweating,
and weight loss. But even these nodules are not cancerous.
Malignant Thyroid Tumors
Only 5% to10% of thyroid nodules are cancerous. There
are several types of thyroid cancer. Papillary carcinoma
and follicular carcinoma are the most common. Hürthle
cell carcinoma is a subtype of follicular carcinoma.
Some doctors group these together and call them "differentiated
thyroid cancer" or "well-differentiated thyroid cancer."
Other types of thyroid cancer, including medullary
carcinoma, anaplastic carcinoma, and thyroid lymphoma
occur less often.
Malignant Thyroid Tumors - Differentiated
Thyroid Cancer
Papillary carcinoma:
About 80% of thyroid cancers are papillary carcinomas
(also called papillary cancer or papillary adenocarcinoma).
Papillary carcinomas develop from the thyroid follicle
cells and typically grow very slowly. Usually they
occur in only one lobe of the thyroid gland, but about
10% to 20% of the time both lobes are involved. Several
different variants (subtypes) of papillary carcinoma
can be recognized under the microscope. These include
the follicular variant, tall cell variant, columnar
cell variant, and diffuse sclerosing variant. Of these
variants, the follicular variant of papillary carcinoma
is the most common.
The usual form of papillary adenocarcinoma and the
follicular variant have the same outlook for survival
(prognosis), and treatment is the same for both. The
other variants tend to spread more quickly and have
a worse prognosis. Even though papillary cancer cells
grow slowly, they often spread early to the lymph
nodes in the neck. Most of the time, however, this
can be successfully treated and is rarely fatal.
Follicular carcinoma:
Follicular carcinoma is the next most common type
of thyroid cancer. It is also sometimes called follicular
cancer or follicular adenocarcinoma. Follicular cancer
is much less common than papillary thyroid cancer,
making up about 10% of thyroid cancers. It is more
common in countries where people don't get enough
iodine in their diet. These cancers usually remain
in the thyroid gland but can spread to other parts
of the body, such as lungs and bone. Unlike papillary
carcinoma, follicular carcinomas spread to lymph nodes
less often. The prognosis of follicular carcinoma
is probably the same or slightly worse than that of
papillary carcinoma.
Hürthle cell carcinoma, also known as oxyphil cell
carcinoma, is thought to be a subtype of follicular
cancer. This type accounts for about 4% of thyroid
cancers. It may have a worse prognosis than typical
follicular carcinoma because this subtype of follicular
cancer, unlike the usual subtype, does not concentrate
radioactive iodine well (see below).
Malignant Thyroid Tumors - Other
Types
Medullary thyroid carcinoma:
Medullary thyroid carcinoma (MTC- about 3% of thyroid
cancers ) is the only thyroid cancer that develops
from the C cells of the thyroid gland. Sometimes this
cancer can spread to lymph nodes, the lungs, or liver
even before a thyroid nodule is discovered or a screening
test is done. These cancers usually make calcitonin
and carcinoembryonic antigen (CEA). Calcitonin, a
hormone also produced by normal C cells, helps control
the amount of calcium in blood. CEA is a protein produced
by certain cancers, such as colorectal cancer and
MTC. Both calcitonin and CEA are released into the
blood and can be found by blood tests. About 5% of
thyroid cancers are medullary. Medullary cancer does
not concentrate radioactive iodine and has a worse
prognosis.
There are 2 types of MTC. The first type, occurring
in 85% of cases, is called sporadic MTC. Sporadic
MTC is not inherited; that is, it does not run in
families. It occurs mostly in older adults and in
only 1 thyroid lobe.
The other type of MTC is inherited and can occur in
each generation of a family. When MTC is the only
type of cancer found in the family, it is called isolated
familial medullary thyroid carcinoma (FMTC). The combination
of FMTC and tumors of certain other organs is called
type 2 multiple endocrine neoplasia (MEN 2). Type
2 MEN has 2 subtypes, MEN 2a and MEN 2b:
• In MEN 2a, MTC occurs with adrenal gland tumors
called pheochromocytomas and with parathyroid gland
tumors that cause high blood calcium levels. The adrenal
glands are found next to the upper part of each kidney.
Most people have 4 parathyroid glands, which are found
next to the thyroid.
• In MEN 2b, MTC is associated with pheochromocytoma
but not parathyroid gland disease. Instead, MEN 2b
includes benign growths of nerve tissues on the tongue
and elsewhere called neuromas. In these familial or
genetic forms of MTC, the cancers often develop during
childhood or early adulthood and can spread early.
MTC is most aggressive in the MEN 2b syndrome.
Anaplastic carcinoma:
Anaplastic carcinoma is an uncommon (about 2% of all
thyroid cancers) form of thyroid cancer. It is believed
to develop from an existing papillary or follicular
cancer. It is an aggressive cancer that rapidly invades
the neck, often spreads to other parts of the body,
and is usually fatal. Anaplastic carcinoma is sometimes
called undifferentiated thyroid cancer. Both of these
names indicate that, under the microscope, they have
very little, if any, similarity to normal thyroid
tissue. In contrast, the similarity of differentiated
thyroid cancer to normal thyroid tissue is easily
seen under the microscope.
Thyroid lymphoma: Lymphoma
can develop in the thyroid gland but is very uncommon
in that location. It does not develop from either
thyroid follicular cells or C cells. Rather, lymphomas
develop from lymphocytes, the main cell type of the
immune system. Most lymphocytes are found in pea-sized
collections scattered throughout the body called lymph
nodes, and that is where most lymphomas begin. These
types of lymphomas are discussed in the American Cancer
Society document, "Non-Hodgkin Lymphoma."
Parathyroid cancer:
The thyroid gland contains 4 tiny glands, called parathyroid
glands, which are separate from the thyroid gland.
The parathyroid gland regulates the body's calcium.
Cancers of the gland are very rare - probably less
than100 per year in the U.S. When they occur they
almost always cause the blood calcium level to be
elevated. This causes a person to become fatigued,
weak and drowsy. It also blocks the ability of the
kidneys to regulate the body's water content and excess
water is lost through high volumes of urine. This
further complicates the weakness and drowsiness by
causing dehydration.
The cancer may also be detected as a thyroid nodule
if it grows to large. No matter how large, the only
treatment is surgical removal. Unfortunately, parathyroid
cancer is more deadly than thyroid cancer and much
harder to cure. This document only discusses thyroid
cancer.
What Are the Key Statistics About
Thyroid Cancer?
The American Cancer Society estimates that in the
year 2006 about 30,180 new cases of thyroid cancer
will be diagnosed in the United States. It is much
more common in women. Of the new cases, about 22,590
will occur in women, and 7,590 in men. This is one
of the least deadly cancers. The 5-year survival for
all cases is nearly 97% (see below for more specific
information). An estimated 870 women and 630 men (1,500
total) will die of thyroid cancer during the year
2006.
Thyroid cancer is also different in that it mainly
affects younger people. Nearly two-thirds of people
are diagnosed between the ages of 20 and 55.
The number of new cases of thyroid cancer is increasing.
This is due to a 2% a year increase in the actual
rate per 100,000 people.
What Are the Risk Factors for
Thyroid Cancer?
A risk factor is anything that increases a person's
chance of getting a disease such as cancer. Different
cancers have different risk factors. For example,
exposing skin to strong sunlight is a risk factor
for skin cancer. Smoking is a risk factor for cancers
of the lung, mouth, larynx, bladder, kidney, and several
other organs. But having a risk factor, or even several,
does not mean that a person will get the disease.
Scientists have found a few risk factors that make
a person more likely to develop thyroid cancer. Most
people with thyroid cancer, however, have no apparent
risk factors, and other people with 1 or more risk
factors never develop this disease. Even if a patient
with thyroid cancer has 1 or more risk factors, it
is impossible to know exactly how much that risk factor
may have contributed to causing the cancer.
Diet Low in Iodine
Follicular thyroid cancers are more common in areas
of the world where people's diets are low in iodine.
In the United States, dietary iodine is plentiful
because iodine is added to table salt and other foods.
A diet low in iodine may also increase the rate of
papillary cancer if there is exposure to radioactivity.
Radiation
One proven risk factor for papillary thyroid cancer
is a history of head or neck radiation treatments
in childhood. In the past, children were sometimes
treated with radiation for acne, fungus infections
of the scalp, an enlarged thymus gland, or to shrink
tonsils or adenoids. Years later, studies linked these
treatments to an increased risk of thyroid cancer.
Radiation exposure as an adult carries little risk
of thyroid cancer.
Therapeutic radiation for a cancer such as Hodgkin
disease is another risk factor in children. This may
be increasing as doses of radiation have been lowered.
Although this avoids many of the side effects of radiation
therapy, lower radiation doses can increase the risk
for thyroid cancer.
Several studies have pointed to an increased risk
of thyroid cancer in children, due to radioactive
fallout from nuclear weapons or power plant accidents.
Recently, the risk of thyroid cancer associated with
exposure to nuclear fallout has received more attention
in the press. For instance, there appears to be 5
to 8 times more cases of thyroid cancer than expected
in children living near the Ukrainian city of Chernobyl,
the site of a 1986 nuclear plant accident that exposed
millions of people to fallout. People involved with
the cleanup after the accident and those who lived
near the plant in Ukraine and Belarus have also had
a higher rate of thyroid cancer, even though they
were adults. One factor that may make a difference
was whether the children had adequate iodine in their
diet. Children with more iodine in their diet appeared
to have a lower risk. Recent information shows that
some radioactive iodine fallout occurred over certain
regions of the United States after nuclear weapons
testing in western states during the 1950s. This exposure
was much, much lower than around Chernobyl. At such
low exposures, a heightened risk of thyroid cancer
has not been proven. If you are concerned about possible
exposure to radioactive fallout, make an appointment
to discuss it with your doctor.
Hereditary Conditions
About 20% of medullary thyroid carcinomas (MTCs) result
from inheriting an abnormal gene. These cases are
known as familial medullary thyroid carcinoma (FMTC).
The combination of FMTC and tumors of other endocrine
glands is called type 2 multiple endocrine neoplasia
(MEN 2). If MEN 2a, MEN 2b, or FMTC runs in your family,
then you may be at very high risk of developing MTC.
Ask your doctor for information about blood chemistry
tests and genetic testing. There are no known risk
factors for sporadic MTC.
People with certain inherited medical conditions are
also at higher risk of thyroid cancer. Higher rates
of the disease occur among people with conditions
called Gardner syndrome and familial polyposis. These
conditions cause a very high risk of colorectal cancer
and a slightly increased risk of cancers in some other
organs. Also linked to an increased risk of thyroid
cancer is CowdenÂ's disease, a rare genetic condition.
Certain families have been found with an excess number
of papillary thyroid cancers. The genetic basis for
this is unknown.
Gender and Age
For unclear reasons, benign thyroid nodules and thyroid
cancers occur almost 3 times more often in women than
in men. Most cases of papillary and follicular thyroid
cancer are found in people between the ages of 20
and 60 years. Benign thyroid nodules and thyroid cancers
can occur in people of all ages.
Lifestyle Risk Factors
Although tobacco and alcohol use are the main risk
factors for most types of head and neck cancer (including
cancers of the mouth, throat, and esophagus). Neither
of these behaviors, however, has been shown to be
risk factors for thyroid cancer.
Do We Know What Causes Thyroid
Cancer?
Although scientists have found that thyroid cancer
is associated with a number of other conditions (described
in the section, "What Are the Risk Factors for Thyroid
Cancer?"), the exact cause of most thyroid cancers
is not yet known.
Researchers have made great progress in understanding
how certain changes in a person's DNA can cause cells
of the thyroid to become cancerous. DNA is the molecule
that carries the instructions for nearly everything
our cells do. We usually resemble our parents because
they are the source of our DNA. However, DNA affects
more than our outward appearance. It also can influence
our risk for developing certain diseases, such as
some kinds of cancer.
Some genes (parts of our DNA) contain instructions
for controlling when our cells grow and divide. Genes
that can be involved in cancer are called oncogenes.
Such genes are often involved in DNA maintenance or
repair. Others that slow down cell division or cause
cells to die at the appropriate time are called tumor
suppressor genes. Cancers can be caused by DNA mutations
(defects) that influence the function of these genes.
People inherit 2 copies of each gene - one from each
parent. People can inherit damaged DNA from one or
both parents, which accounts for inherited cancers.
Many times, though, a personÂ's DNA becomes damaged
by exposure to something in the environment, like
smoking or exposure to radiation. Sometimes DNA mutations
occur for no apparent reason.
The DNA mutations that cause some forms of papillary
thyroid cancer are known to involve over-activation
or specific parts of the RET oncogene. These mutations
usually are acquired during life rather than being
inherited. They are present only in the cancer cell
and are not passed on to the patient's children. Acquired
changes in other oncogenes and tumor suppressor genes
(such as ras, trk, gsp, and p53) also have a role
in causing papillary and follicular thyroid cancers.
Recently scientists have discovered that many papillary
thyroid cancers contain a mutation of the BRAF gene.
The BRAF mutation is less common in cancers thought
to arise from exposure to radioactive iodine -- such
as around Chernobyl. This mutation is thought to cause
cells to grow and divide. Researchers still do not
know exactly why or how these mutations happen to
some people but not to others.
Single point mutations in people who have medullary
thyroid carcinoma (MTC) involve different parts of
the RET gene compared to papillary carcinoma patients.
Nearly all patients with the inherited form of MTC
and about 1 of every 5 with the sporadic form of MTC
have a mutation in the RET gene. Most patients with
sporadic MTC have acquired mutations present only
in their cancer cells. Those with familial MTC and
MEN 2 inherit the RET mutation from a parent. These
mutations are present in every cell of the patient's
body and can be detected by testing the DNA of blood
cells.
Because every person has 2 RET genes but passes only
1 to a child (the child's other RET gene comes from
the other parent), the odds that a patient with familial
MTC will pass a mutated gene to a child are 1 of 2
(or a 50% chance). RET gene mutations do not occur
in follicular cancer. These cancers sometimes have
changes to other oncogenes and/or tumor suppressor
genes. Undifferentiated thyroid cancers often have
acquired (not inherited) mutations of the p53 tumor
suppressor gene.
Can Thyroid Cancer Be Prevented?
Most people with thyroid cancer have no known risk
factors; therefore, it is not possible to reliably
prevent most cases of this disease. Some doctors have
suggested that the increase in thyroid cancers may
be due to x-ray testing of young children. This has
not been proven, but it is a good idea for children
to avoid x-rays that arenÂ't necessary.
Because of the genetic blood tests now available,
most of the familial cases of medullary thyroid carcinoma
(MTC) can be treated early or prevented. Once the
disease is discovered in a family, the rest of the
family can be tested.
If you have a family history of MTC, it is important
that you see a doctor who is familiar with the latest
advances in genetic counseling and genetic testing
for this disease. Removing the thyroid gland in children
who carry the abnormal gene will prevent a cancer
that might otherwise be fatal.
Can Thyroid Cancer Be Found Early?
Many cases of thyroid cancer can be found early. In
fact, most thyroid cancers are now found much earlier
than in the past and can be treated successfully.
Although it's unusual, some thyroid cancers may not
cause symptoms until after reaching an advanced stage.
Most early thyroid cancers are found when patients
ask their doctors about lumps or nodules they have
noticed. Others are found by health care professionals
during a routine checkup. No blood tests are regularly
recommended for early detection of sporadic (not familial)
thyroid cancers.
If you have unusual symptoms such as a lump or your
neck looks swollen, you should make an appointment
to see your doctor right away. During routine physical
examinations, be sure your doctor does a cancer-related
checkup that, depending on your age, might include
examinations for cancers of the thyroid, mouth, skin,
lymph nodes, and other cancers. Some doctors recommend
that people examine their own necks twice a year to
look for any growths or lumps.
People with a family history of medullary thyroid
carcinoma (MTC) with or without type 2 multiple endocrine
neoplasia (MEN 2) may be at very high risk for developing
this cancer. Most doctors recommend genetic testing
for these people when they are young to see if they
carry the gene for MTC. If a person refuses genetic
testing and surgery to prevent MTC, other tests are
available that can help find MTC at an early stage
when it may still be curable.
How is Thyroid Cancer Diagnosed?
Signs and Symptoms of Thyroid
Cancer
Prompt attention to signs and symptoms is the best
approach to early diagnosis of most thyroid cancers.
Thyroid cancer can cause any of the following local
signs or symptoms:
• a lump in the neck, sometimes growing rapidly
• a pain in the front of the neck, sometimes
going up to the ears
• hoarseness or voice change which does not go
away
• trouble swallowing
• breathing problems (feeling as if one were
•breathing through a straw•)
• a cough that continues and is not due to a
cold
If you have any of these signs or symptoms, talk to
your doctor right away. Other cancers of the neck
area and many noncancerous conditions can cause some
of the same symptoms. Thyroid nodules are common,
and they are usually benign. But the only way to find
out if these symptoms are due to a thyroid cancer,
some other cancer, or a benign condition is to have
a medical evaluation. The sooner you receive a correct
diagnosis, the sooner you can start treatment and
the more effective your treatment will be.
History and Physical Examination
If you have any signs or symptoms that suggest you
might have thyroid cancer, the first step toward arriving
at a diagnosis is for your health care professional
to take a complete medical history. This is an interview
in which you will be asked questions about your risk
factors, symptoms, and any other health problems or
concerns. If someone in your family has had thyroid
cancer (especially medullary thyroid cancer) or adrenal
gland tumors called pheochromocytomas, it is important
to tell your doctor.
A physical exam will provide other information about
signs of thyroid cancer and other health problems.
During your physical exam, your doctor will pay special
attention to the size and firmness of your thyroid
and any enlarged lymph nodes in your neck.
Fine Needle Aspiration Biopsy
The simplest way to test whether a thyroid lump or
nodule is cancerous is with a fine needle aspiration
(FNA) of the thyroid nodule. This type of biopsy can
usually be done in your doctor's office or clinic.
Local anesthesia (numbing medication) may be injected
into the skin over the nodule, but in some cases an
anesthetic may not be needed at all. The major complication
is bleeding, but this is rare except in people with
bleeding disorders. Be sure to tell your doctor is
you have a bleeding disorder.
Your doctor will place a thin needle directly into
the nodule for about 10 seconds and withdraws cells
and a few drops of fluid. The doctor usually repeats
this procedure 2 or 3 times during the same appointment
to take samples from several areas of the nodule.
The cells can then be viewed under a microscope to
see if they appear cancerous or benign.
This test is generally done on all thyroid nodules
that are large enough to be felt. Sometimes FNA tests
are done with ultrasound machines to help guide the
needle into nodules that are otherwise too small to
be felt. FNA can help your doctor decide if surgery
or other tests are needed.
About 1 test in every 10 will need to be repeated
on another day. Of every 10 FNA tests, up to 8 clearly
show that the nodule is benign. Cancer is clearly
shown in only 1 of every 20 FNA tests. Some test results
are classified as "suspicious" or "atypical" because
the FNA findings do not clearly show whether the nodule
is benign or malignant. In these cases, additional
tests such as a diagnostic surgical lobectomy (i.e.
removal of the gland on one side of the windpipe)
may be needed, particularly if the doctor thinks the
nodule is cancerous.
A new way of testing the thyroid cells is by examining
their genetic profile. This is too new to be used
in most situations, but may play a role in the future.
Imaging Tests
Thyroid scan: For this
test, a small amount of radioactive iodine is taken
by mouth or injected into a vein. The body concentrates
these radioactive chemicals in the thyroid gland,
and a special camera placed in front of your neck
then measures the amount of radiation in the gland.
Abnormal areas of the thyroid that contain less radioactivity
than the surrounding tissue are called cold nodules,
and nodules that take up more radiation are called
hot nodules.
Most thyroid nodules appear as cold nodules on thyroid
scans. Because both benign and cancerous nodules can
appear cold, this test is usually not very helpful
in diagnosing thyroid cancer. However, once a biopsy
has determined that a thyroid cancer is present, scans
are very useful in follow-up for potential spread.
Scans following initial surgical treatment can also
help assess how far a thyroid cancer has initially
spread, if at all.
If the entire thyroid gland is removed for cancer,
repeated thyroid scans will be done. The test becomes
more sensitive in this instance because more of the
injected radioactive iodine enters thyroid cancer
cells. Radioiodine scans are frequently used in the
care and management of
patients with differentiated (papillary and follicular
and Hurthle cell) thyroid cancer. Because MTC cells
do not take up iodine, radioiodine scans are not used
in this cancer.
Radioiodine thyroid scans are most accurate if patients
have high blood levels of thyroid-stimulating hormone
(TSH, or thyrotropin). In the past, the only way to
increase TSH levels in patients whose thyroid glands
had been surgically removed was to stop thyroid hormone
pills 2 to 6 weeks before treatment. This lowers thyroid
hormone levels (a condition known as hypothyroidism)
and causes the pituitary gland to release more TSH,
which in turn stimulates the cancer cells to take
up the radioactive iodine. Although this intentional
hypothyroidism is temporary, it is sometimes uncomfortable
for the patient. Symptoms include tiredness, depression,
some weight gain, sleepiness, constipation, muscle
aches, and reduced concentration, in addition to other
conditions. An injectable form of thyrotropin is now
available that can increase patients' TSH levels before
radioiodine scanning so that withholding thyroid hormone
replacement is not necessary.
Ultrasound: Ultrasound,
or ultrasonography, uses sound waves to create images
of your body. A transducer held near your thyroid
gland gives off high-frequency sound waves and detects
echoes that bounce off thyroid tissue. Normal thyroid
tissue and most thyroid nodules make different echo
patterns. These echo patterns are processed by a computer
to create a picture of the thyroid gland. This test
can be used to check the number and size of thyroid
nodules. However, thyroid cancers and most benign
nodules look the same on ultrasound studies, so this
test is not done routinely.
Computed tomography (CT or CT
scan): The CT scan is an x-ray procedure
that produces detailed cross-sectional images of your
body. Instead of taking one picture, as does a normal
x-ray, a CT scanner takes many pictures of the part
of your body being studied as it rotates around you.
A computer then combines these pictures into an image
of a slice of your body. A CT scan isnÂ't usually
used to diagnose thyroid cancer, but might be used
to see if a known thyroid cancer has spread.
Magnetic resonance imaging (MRI
or MRI scan): MRI scans use radio waves and
strong magnets instead of x-rays. The energy from
the radio waves is absorbed and then released in a
pattern formed by the type of tissue and by certain
diseases. A computer translates the pattern of radio
waves given off by the tissues into a very detailed
image of parts of the body. A contrast material might
be injected just as with CT scans. MRI scans are very
helpful in looking at cancers. Sometimes they can
tell a benign tumor from a malignant one.
MRI scans take longer than CT scans - often up to
an hour. Also, you have to lie inside a narrow tube,
which is confining and can upset people with a fear
of enclosed spaces. The machine makes a thumping noise,
and some facilities provide headphones with music
to block out the noise. However the benefits of the
test outweigh any discomfort.
MRI and CT scans can reveal tumors within a thyroid
gland but may also determine the size of the tumor,
whether it is growing into nearby tissues, and if
it has spread to lymph nodes in the neck or distant
structures.
Octreotide scan: Sometimes
an octreotide scan, which uses a radioactively tagged
hormone, may be done to evaluate the spread of medullary
thyroid cancer.
Positron emission tomography
(PET): Positron emission tomography (PET)
uses glucose (a form of sugar) that contains a radioactive
atom. Cancer cells in the body absorb large amounts
of the radioactive sugar and a special camera can
detect the radioactivity. This can be a very important
test if your thyroid cancer is one that doesnÂ't take
up radioactive iodine. In this
situation, the PET scan may be able to tell if the
cancer has spread. Newer techniques and devices can
combine a CT scan and a PET scan to even better pinpoint
tumor spread
Blood Tests
No blood test can tell whether a thyroid nodule is
cancerous. However, testing your blood levels of thyroid-stimulating
hormone (TSH) may be useful in checking the overall
activity of your thyroid gland. If medullary thyroid
carcinoma (MTC) is suspected, a blood calcitonin test
will be done. This test can help tell if MTC is present.
Thyroglobulin is a protein manufactured by the thyroid
gland. Its measurement cannot be used to diagnose
thyroid cancer. However, after the removal of most
of the thyroid by surgery and ablation of residual
normal cells by radioactive iodine, its level in the
blood should be very low. If it is not low, this might
mean that thyroid cancer is still present. If the
level rises, it is a sign that the cancer may be coming
back.
How Is Thyroid Cancer Treated?
After thyroid cancer is found, your doctor will discuss
treatment options or choices with you. It is important
to take the time to consider each of them. In choosing
a treatment plan, factors to consider include the
type and stage of the cancer and your overall physical
health. Sometimes it is a good idea to seek a second
opinion, and many experienced physicians encourage
this. Some insurance companies even require a second
opinion before they will agree to pay for certain
treatments. A second opinion can provide more information
and help you feel confident about the treatment plan
you choose.
The methods of treatment for thyroid cancer include
surgery, radioactive iodine treatment, thyroid hormone
therapy, external beam radiation therapy, and chemotherapy.
The best approach to treatment usually uses 2 or more
of these methods, and most patients are cured of their
thyroid cancer in this way.
If a cure is not possible, the goal may be to remove
or destroy as much of the cancer as possible and to
prevent the tumor from growing, spreading, or returning
for as long as possible. Sometimes treatment is aimed
at palliation (relieving symptoms, such as pain or
problems with breathing and swallowing), even if a
cure will not result.
Clinical Trials
The purpose of clinical trials: Studies of promising
new or experimental treatments in patients are known
as clinical trials. A clinical trial is only done
when there is some reason to believe that the treatment
being studied may be valuable to the patient. Treatments
used in clinical trials are often found to have real
benefits. Researchers conduct studies of new treatments
to answer the following questions:
• Is the treatment helpful?
• How does this new type of treatment work?
• Does it work better than other treatments already
available?
• What side effects does the treatment cause?
• Are the side effects greater or less than the
standard treatment?
• Do the benefits outweigh the side effects?
• In which patients is the treatment most likely
to be helpful?
Types of clinical trials: There are 3 phases of clinical
trials in which a treatment is studied before it is
eligible for approval by the FDA (Food and Drug Administration).
Phase I clinical trials:
The purpose of a phase I study is to find the best
way to give a new treatment and how much of it can
be given safely. The cancer care team watches patients
carefully for any harmful side effects. The treatment
has been well tested in lab and animal studies, but
the side effects in patients are not completely known.
Doctors conducting the clinical trial start by giving
very low doses of the drug to the first patients and
increasing the dose for later groups of patients until
side effects appear. Although doctors are hoping to
help patients, the main purpose of a phase I study
is to test the safety of the drug.
Phase II clinical trials:
These studies are designed to see if the drug works.
Patients are given the highest dose that doesnÂ’t
cause severe side effects (determined from the phase
I study) and closely observed for an effect on the
cancer. The cancer care team also looks for side effects.
Phase III clinical trials: Phase III studies
involve large numbers of patient - often several hundred.
One group (the control group) receives the standard
(most accepted) treatment. The other group receives
the new treatment. All patients in phase III studies
are closely watched. The study will be stopped if
the side effects of the new treatment are too severe
or if one group has had much better results than the
others.
If you are in a clinical trial, you will have a team
of experts watching your progress very carefully.
The study is especially designed to pay close attention
to you.
However, there are some risks. No one involved in
the study knows in advance whether the treatment will
work or exactly what side effects will occur. That
is what the study is designed to find out. While most
side effects disappear in time, some can be permanent
or even life threatening. Keep in mind, though, that
even standard treatments have side effects. Depending
on many factors, you may decide to enroll in a clinical
trial.
Deciding to enter a clinical
trial: Enrollment in any clinical trial is
completely up to you. Your doctors and nurses will
explain the study to you in detail and will give you
a form to read and sign indicating your desire to
take part. This process is known as giving your informed
consent. Even after signing the form and after the
clinical trial begins, you are free to leave the study
at any time, for any reason. Taking part in the study
does not prevent you from getting other medical care
you may need.
Courtesy: www.cancer.org,
Please visit the website for further information
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