Dictionary Definition
actinotherapy n : (medicine) the treatment of
disease (especially cancer) by exposure to radiation from a
radioactive substance [syn: radiotherapy, radiation
therapy, radiation, irradiation]
Extensive Definition
Radiation therapy (or radiotherapy) is the
medical use of ionizing
radiation as part of cancer treatment to control malignant cells (not
to be confused with radiology, the use of
radiation in medical
imaging and diagnosis). Radiotherapy may
be used for curative or
adjuvant
cancer treatment. It is used as palliative
treatment (where cure is not possible and the aim is for local
disease control or symptomatic relief) or as therapeutic treatment
(where the therapy has survival benefit and it can be curative).
Total
body irradiation (TBI) is a radiotherapy technique used to
prepare the body to receive a bone
marrow transplant. Radiotherapy has several applications in
non-malignant conditions, such as the treatment of trigeminal
neuralgia, severe thyroid
eye disease, pterygium,
pigmented villonodular synovitis, prevention of keloid scar growth, and
prevention of heterotopic
ossification. The use of radiotherapy in non-malignant
conditions is limited partly by worries about the risk of
radiation-induced cancers.
Radiotherapy is used for the treatment of
malignant tumors (cancer), and may be used as the
primary therapy. It is also common to combine radiotherapy with
surgery, chemotherapy,
hormone therapy or some mixture of the three. Most common
cancer types can be treated with radiotherapy in some way. The
precise treatment intent (curative, adjuvant, neoadjuvant, therapeutic, or
palliative) will
depend on the tumour type, location, and stage, as well as the
general health of the patient.
Radiation therapy is commonly applied to the
cancerous tumour. The radiation fields may also include the
draining lymph nodes if they are clinically or radiologically
involved with tumour, or if there is thought to be a risk of
subclinical malignant spread. It is necessary to include a margin
of normal tissue around the tumour to allow for uncertainties in
daily set-up and internal tumor motion. These uncertainties can be
caused by internal movement (for example, respiration and bladder
filling) and movement of external skin marks relative to the tumour
position.
To spare normal tissues (such as skin or organs
which radiation must pass through in order to treat the tumour),
shaped radiation beams are aimed from several angles of exposure to
intersect at the tumour, providing a much larger absorbed
dose there than in the surrounding, healthy tissue.
Side effects
Radiation therapy is in itself painless. Many low-dose palliative treatments (for example, radiotherapy to bony metastases) cause minimal or no side effects. Treatment to higher doses causes varying side effects during treatment (acute side effects), in the months or years following treatment (long-term side effects), or after re-treatment (cumulative side effects). The nature, severity, and longevity of side effects depends on the organs that receive the radiation, the treatment itself (type of radiation, dose, fractionation, concurrent chemotherapy), and the patient.Most side effects are predictable and expected.
Side effects from radiation are usually limited to the area of the
patients body that is under treatment. One of the aims of modern
radiotherapy is to reduce side effects to a minimum, and to help
the patient to understand and to deal with those side effects which
are unavoidable.
Acute side effects
- The rates of onset and of recovery depend on the rate of
turnover of the epithelial
cells. Typically the skin starts to become pink and sore
several weeks into treatment. The reaction may become more severe
during the treatment and for up to about one week following the end
of radiotherapy, and the skin may break down. Although this
moist
desquamation is uncomfortable, recovery is usually quick. Skin
reactions tend to be worse in areas where there are natural folds
in the skin, such as underneath the female breast, behind the ear,
and in the groin.
- The lower bowel may be treated directly with radiation (treatment of rectal or anal cancer) or be exposed by radiotherapy to other pelvic structures (prostate, bladder, female genital tract). Typical symptoms are soreness, diarrhoea, and nausea.
- As part of the general inflammation that occurs, swelling of soft tissues may cause problems during radiotherapy. This is a concern during treatment of brain tumours and brain metastases, especially where there is pre-existing raised intracranial pressure or where the tumour is causing near-total obstruction of a lumen (e.g., trachea or main bronchus). Surgical intervention may be considered prior to treatment with radiation. If surgery is deemed unnecessary or inappropriate, the patient may receive steroids during radiotherapy to reduce swelling.
- The gonads (ovaries and testicles) are very sensitive to radiation. They may be unable to produce gametes following direct exposure to most normal treatment doses of radiation. Treatment planning for all body sites is designed to minimize, if not completely exclude dose to the gonads if they are not the primary area of treatment.
- The lower bowel may be treated directly with radiation (treatment of rectal or anal cancer) or be exposed by radiotherapy to other pelvic structures (prostate, bladder, female genital tract). Typical symptoms are soreness, diarrhoea, and nausea.
Medium and long-term side effects
These depend on the tissue that received the
treatment; they may be minimal.
- Tissues which have been irradiated tend to become less elastic
over time due to a diffuse scarring process.
- This may be most pronounced in patients who have received radiotherapy to the brain. Unlike the hair loss seen with chemotherapy, radiation-induced hair loss is more likely to be permanent, but is also more likely to be limited to the area treated by the radiation.
- The salivary glands and tear glands have a radiation tolerance of about 30 Gy in 2 Gy fractions, a dose which is exceeded by most radical head and neck cancer treatments. Dry mouth (xerostomia) and dry eyes (xerophthalmia) can become irritating long-term problems and severely reduce the patient's quality of life. Similarly, sweat glands in treated skin (such as the armpit) tend to stop working, and the naturally moist vaginal mucosa is often dry following pelvic irradiation.
- Radiation is a potential cause of cancer, and secondary malignancies are seen in a very small minority of patients, generally many years after they have received a course of radiation treatment. In the vast majority of cases, this risk is greatly outweighed by the reduction in risk conferred by treating the primary cancer.
- This may be most pronounced in patients who have received radiotherapy to the brain. Unlike the hair loss seen with chemotherapy, radiation-induced hair loss is more likely to be permanent, but is also more likely to be limited to the area treated by the radiation.
Cumulative side effects
Cumulative effects from this process should not
be confused with long-term effects—when short-term effects have
disappeared and long-term effects are subclinical, reirradiation
can still be problematic.
Dose
The amount of radiation used in radiation therapy is measured in gray (Gy), and varies depending on the type and stage of cancer being treated. For curative (radical) cases, the typical dose for a solid epithelial tumor ranges from 60 to 80 Gy, while lymphoma tumors are treated with 20 to 40 Gy.Preventative (adjuvant) doses are typically
around 45 - 60 Gy in 1.8 - 2 Gy fractions (for Breast, Head and
Neck cancers respectively.) Many other factors are considered by
radiation
oncologists when selecting a dose, including whether the
patient is receiving chemotherapy, whether radiation therapy is
being administered before or after surgery, and the degree of
success of surgery.
Fractionation
The total dose is fractionated (spread out over time) in order to give normal cells time to recover. Fractionation regimes are highly individualised between different radiotherapy centres and even between individual doctors. In the USA, Australia, and Europe, the typical fractionation schedule for adults is 1.8 to 2 Gy per day, five days a week. In the northern United Kingdom, fractions are more commonly 2.67 to 2.75 Gy per day, which eases the burden on thinly spread resources in the National Health Service. For children, a typical fraction is 1.5 to 1.7 Gy per day, reducing the chance and severity of late-onset side effects.In some cases, two fractions per day are used
near the end of a course of treatment. This schedule, known as a
concomitant boost regimen or hyperfractionation, is used on tumors
that regenerate more quickly when they are smaller. In particular,
tumors in the head and neck demonstrate this behavior.
One of the best-known alternative fractionation
schedules is Continuous Hyperfractionated Accelerated Radiotherapy
(CHART). CHART, used to treat lung cancer, consists of three
smaller fractions per day. Although reasonably successful, CHART
can be a strain on radiation therapy departments.
Implants can be fractionated over minutes or
hours, or they can be permanent seeds which slowly deliver
radiation until they become inactive.
Mechanism of action
Radiation therapy works by damaging the DNA of cells. The
damage is caused by a photon, electron, proton, neutron, or ion beam directly or indirectly
ionizing the atoms
which make up the DNA chain. Indirect
ionization happens as
a result of the ionization of water, forming free
radicals, notably hydroxyl radicals, which then
damage the DNA. In the most common forms of radiation therapy, most
of the radiation effect is through free radicals. Because cells
have mechanisms for repairing DNA damage, breaking the DNA on both
strands proves to be the most significant technique in modifying
cell characteristics. Because cancer cells generally are
undifferentiated and stem cell-like,
they reproduce more, and have a diminished ability to repair
sub-lethal damage compared to most healthy differentiated
cells. The DNA damage is inherited through cell division,
accumulating damage to the cancer cells, causing them to die or
reproduce more slowly. Proton radiotherapy works by sending protons
with varying kinetic
energy to precisely stop at the tumor.
One of the major limitations of radiotherapy is
that the cells of solid tumors become deficient in oxygen. This is
because solid tumours usually outgrow their blood supply, causing a
low-oxygen state known as hypoxia.
The more hypoxic the tumours are the more resistant they are to the
effects of radiation because oxygen makes the radiation damage to
DNA permanent. Much research has been devoted to overcoming this
problem including the use of high pressure oxygen tanks, blood
substitutes that carry increased oxygen, hypoxic cell
radiosensitizers such as misonidazole and metronidazole, and hypoxic
cytotoxins, such as tirapazamine. There is also
interest in the fact that high-LET (linear
energy transfer) particles such as carbon or neon ions may have
an antitumour effect which is independent of tumour hypoxia.
History of radiation therapy
Radiation therapy has been in use as a cancer treatment for more than 100 years, with its earliest roots traced from the discovery of x-rays in 1895. The concept of therapeutic radiation was invented by German physicist Wilhelm Conrad Röntgen when he discovered that the x-ray was a powerful and effective tool with which to treat cancer.The field of radiation therapy began to grow in
the early 1900s largely due to the groundbreaking work of Nobel
Prize-winning scientist Marie Curie,
who discovered the radioactive elements polonium and radium. This began a new era in
medical treatment and research. Radium was used in various forms
until the mid-1900s when cobalt and caesium units came into use.
Medical linear accelerators have been developed since the late
1940s.
With Godfrey
Hounsfield’s discovery of computed
tomography (CT), three-dimensional planning became a
possibility and created a shift from 2-D to 3-D radiation delivery;
physicians and physics were no longer limited because CT-based
planning allowed physicians to directly measure the dose delivered
to the patient's anatomy based on axial tomographical images.
Orthovoltage and cobalt units have largely been replaced by
megavoltage linear accelerators, useful for their penetrating
energies and lack of physical radiation source.
In the last few decades, the advent of new
imaging technologies, e.g., magnetic
resonance imaging (MRI) in the 1970s and
positron emission tomography (PET) in the 1980s, as well as new
radiation delivery and visualization products, e.g., digital
linear accelerator, image fusion
has moved radiation therapy from 3-D conformal to IMRT and
eventually to IGRT (4-D) in the near future. These advances have
resulted in better treatment outcomes and less side effects. Now
70% of cancer patients receive radiation therapy as part of their
cancer treatment.
Types of radiation therapy
Historically, the three main divisions of radiotherapy are external beam radiotherapy (EBRT or XBRT) or teletherapy, brachytherapy or sealed source radiotherapy and unsealed source radiotherapy. The differences relate to the position of the radiation source; external is outside the body, while sealed and unsealed source radiotherapy has radioactive material delivered internally. Brachytherapy sealed sources are usually extracted later, while unsealed sources may be administered by injection or ingestion. Proton therapy is a special case of external beam radiotherapy where the particles are protons. Introperative radiotherapy is a special type of radiotherapy that is delivered immediately after surgical removal of the cancer. This method has been employed in breast cancer (TARGeted Introperative radioTherapy), brain tumours and rectal cancers.Conventional external beam radiotherapy
Conventional external beam radiotherapy (2DXRT) is delivered via two-dimensional beams using linear accelerator machines. 2DXRT mainly consists of a single beam of radiation delivered to the patient from several directions: often front or back, and both sides. Conventional refers to the way the treatment is planned or simulated on a specially calibrated diagnostic x-ray machine known as a simulator because it recreates the linear accelerator actions (or sometimes by eye), and to the usually well-established arrangements of the radiation beams to achieve a desired plan. The aim of simulation is to accurately target or localize the volume which is to be treated. This technique is well established and is generally quick and reliable. The worry is that some high-dose treatments may be limited by the radiation toxicity capacity of healthy tissues which lay close to the target tumor volume. An example of this problem is seen in radiation of the prostate gland, where the sensitivity of the adjacent rectum limits the dose which can be safely prescribed to such an extent that tumor control may not be easily achievable. Previous to the invention of the CT, physicians and physicists had limited knowledge about the true radiation dosage delivered to both cancerous and healthy tissue. For this reason, 3-dimensional conformal radiotherapy is becoming the standard treatment for a number of tumor sites.Virtual simulation, 3-dimensional conformal radiotherapy, and intensity-modulated radiotherapy
The planning of radiotherapy treatment has been revolutionized by the ability to delineate tumors and adjacent normal structures in three dimensions using specialized CT and/or MRI scanners and planning software. Virtual simulation, the most basic form of planning, allows more accurate placement of radiation beams than is possible using conventional X-rays, where soft-tissue structures are often difficult to assess and normal tissues difficult to protect.An enhancement of virtual simulation is
3-Dimensional Conformal Radiotherapy (3DCRT), in which the profile
of each radiation beam is shaped to fit the profile of the target
from a beam's eye
view (BEV) using a multileaf
collimator (MLC) and a variable number of beams. When the
treatment volume conforms to the shape of the tumour, the relative
toxicity of radiation to the surrounding normal tissues is reduced,
allowing a higher dose of radiation to be delivered to the tumor
than conventional techniques would allow.
Intensity-Modulated Radiation Therapy (IMRT) is
an advanced type of high-precision radiation that is the next
generation of 3DCRT.IMRT also improves the ability to conform the
treatment volume to concave tumor shapes, for example when the
tumor is wrapped around a vulnerable structure such as the spinal
cord or a major organ or blood vessel. Computer-controlled x-ray
accelerators distribute precise radiation doses to malignant tumors
or specific areas within the tumor. The pattern of radiation
delivery is determined using highly-tailored computing applications
to perform optimization
and treatment simulation (Treatment
Planning). The radiation dose is consistent with the 3-D shape
of the tumor by controlling, or modulating, the radiation beam’s
intensity. The radiation dose intensity is elevated near the gross
tumor volume while radiation among the neighboring normal tissue is
decreased or avoided completely. The customized radiation dose is
intended to maximize tumor dose while simultaneously protecting the
surrounding normal tissue. Because sparing healthy tissue as
compared with conventional radiation therapy techniques (2DXRT and
3DCRT). This in turn results in better tumor targeting, lessened
side effects, and improved treatment outcomes than even
3DCRT.
3DCRT is still used extensively for many body
sites but the use of IMRT is growing in more complicated body sites
such as CNS, head and neck, prostate, breast and lung.
Unfortunately, IMRT is limited by its need for additional time from
experienced medical personnel. This is because physicians must
manually delineate the tumors one CT image at a time through the
entire disease site which can take much longer than 3DCRT
preparation. Then, medical physicists and dosimetrists must be
engaged to create a viable treatment plan. Also, the IMRT
technology has only been used commercially since the late 1990s
even at the most advanced cancer centers, so radiation oncologists
who did not learn it as part of their residency program must find
additional sources of education before implementing IMRT.
Proof of improved survival benefit from either of
these two techniques over conventional radiotherapy (2DXRT) is
growing for many tumor sites, but the ability to reduce toxicity is
generally accepted. Both techniques enable dose escalation,
potentially increasing usefulness. There has been some concern,
particularly with 3DCRT, about increased exposure of normal tissue
to radiation and the consequent potential for secondary malignancy.
Overconfidence in the accuracy of imaging may increase the chance
of missing lesions that are invisible on the planning scans (and
therefore not included in the treatment plan) or that move between
or during a treatment (for example, due to respiration or
inadequate patient immobilization). New techniques are being
developed to better control this uncertainty—for example, real-time
imaging combined with real-time adjustment of the therapeutic
beams. This new technology is called
image-guided radiation therapy (IGRT) or
four-dimensional radiotherapy.
Radioisotope Therapy (RIT)
Radiotherapy can also be delivered through
infusion
(into the bloodstream) or ingestion. Examples are the infusion of
metaiodobenzylguanidine
(MIBG) to treat neuroblastoma, of oral
iodine-131 to
treat thyroid
cancer or thyrotoxicosis, and of
hormone-bound lutetium-177 and yttrium-90 to treat neuroendocrine
tumors (peptide receptor radionuclide therapy). Another example
is the injection of radioactive glass or resin microspheres into
the hepatic
artery to radioembolize liver tumors or liver metastases.
In 2002, the United States Food and Drug
Administration (FDA) approved Ibritumomab
tiuxetan (Zevalin), which is a monoclonal
antibody anti-CD20 conjugated to a
molecule of Yttrium-90.
In 2003, the FDA approved Tositumomab
Iodine-131
(Bexxar), which conjugates a molecule of Iodine-131 to
the monoclonal
antibody anti-CD20.
These medications were the first agents of what
is known as radioimmunotherapy,
and they were approved for the treatment of refractory non-Hodgkins
lymphoma.
References
- Practical Radiotherapy Planning, Dobbs J, Barrett A, Ash D (1999) Arnold ISBN 0-340-70631-7
- ''Williams, J.R. and Thwaites. D.I. (1993). Radiotherapy Physics (1st Edition. Oxford University Press, New York).
- Principles and Practice of Stereotactic Radiosurgery, Lawrence Chin, MD and William Regine, MD, Editors (2008)
Notes
External links
wikibooks Radiation Oncology- PROS (Paediatric Radiation Oncology Society)
- American Society Therapeutic Radiology and Oncology – ASTRO: the official site for radiation oncologists
- RT Answers – ASTRO: patient information site
- PACT: Programme of Action for Cancer Therapy Program to establish cancer care capacity and comprehensive cancer control in developing world with the help of radiation therapy
- Proton Radiation Therapy
- The Radiation Therapy Oncology Group: an organisation for radiation oncology research
- video
- European Society for Therapeutic Radiology and Oncology
- RadiologyInfo -The radiology information resource for patients: Radiation Therapy
- Academic Clinical Oncology and Radiobiology Research Network: A NCRI initiative to revitalise radiotherapy research in the UK
- Who does what in Radiation Oncology? - A Useful breakdown of responsibilities of the various personnel within Radiation Oncology in the United States
- Society of Radiographers (UK)
- Cancer backup. A useful NHS backed site for Cancer professionals and Patients
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actinotherapy in Chinese:
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