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Pleural Mesothelioma
Medical experts have been unable to definitively
assess the prognosis of pleural mesothelioma partly because there
are relatively few cases and it is so difficult to diagnose that
patients don't get treatment for a long time after the disease strikes.
Studies of pleural mesothelioma patients show that
important prognostic factors include stage of cancer, age, and histology.
Surgery improves the lifespan of the patient, even though it does
not cure the disease. For patients treated with surgery, factors
associated with improved long-term survival include epithelial histology,
negative lymph nodes, and negative surgical margins. Nodal status
is an important prognostic factor. Studies have shown the median
survival of patients with malignant pleural disease is 16 months.
Pleural effusions and peritoneal effusions
are experienced by two-thirds of patients. Hemothorax - the collection
of blood in the pleural cavity - also is a symptom. To
get a diagnosis, doctors use imaging technologies as well as histological
analysis and molecular biologic analyses. A pleural smear examines
a sample of pleural fluid under the microscope to detect for abnormal
organisms. The test is performed when infection of the pleural space
is suspected or when an abnormal collection of pleural fluid is
noticed by chest X-ray. Sometimes the tumor grows through the diaphragm,
making the site of origin difficult to assess.
Pleural Mesothelioma Treatment Options
Extrapleural pneumonectomy is surgery to remove a diseased lung,
part of the pericardium (membrane covering the heart), part of the
diaphragm (muscle between the lungs and the abdomen), and part of
the parietal pleura (membrane lining the chest). Extrapleural pneumonectomy
may improve survival, but its impact on long-term survival is unknown.
Aggressive treatment approaches help some people, but remains unclear
if overall survival has been significantly altered by the different
treatment modalities or by combinations of modalities.
Pleurectomy and decortication (removal of part or all of the external
surface of the lung or mesothelium) can provide palliative relief
from symptomatic effusions, discomfort, and pain caused by invasive
tumor. There is always a risk with surgery, and statistics show
that operative mortality from pleurectomy/decortication is <2%,
while mortality from extrapleural pneumonectomy has ranged from
6% to 30%.
Radiation therapy and chemotherapy are usually done after surgery
but they have not been effective in improving survival. Radiation
therapy has been shown to alleviate pain in most patients although
the duration of symptom control is short-lived.
Single-agent and combination chemotherapy have been evaluated in
single and combined modality studies. Some combination chemotherapy
regimens have been reported to have higher response rates in small
phase II trials; however, the toxic effects reported are also higher,
and there is no evidence that combination regimens result in longer
survival or longer control of symptoms than single-agent regiments.
Recurrent pleural effusions may be treated with pleural sclerosing
procedures; however, failure rates are usually secondary to the
bulk of the tumor, which precludes pleural adhesion due to the inability
of the lung to fully expand.
Prognosis for those with pleural mesothelioma
Age and morphology (epithelial, biphasic, or sarcomatoid) are the
main prognostic factors. Scientists have attempted to find a more
rigorous way (histology and hematologic parameters) of predicting
the course of the disease, and studies have found noval biomarkers
for pleural mesothelioma, but these have
not proved effective in clinical use. Advanced imaging (PET-CT)
can be used in diagnosis and helps doctors establish a prognosis.
Oncologists generally
use either the Cancer and Leukemia Group B or the European Organization
for Research and Treatment of Cancer scoring system to predict outcomes
of treatment.
More on malignant
mesothelioma and on benign
mesothelioma.
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