what us the treatment for
mesothelioma?
Treatment of MM using conventional
therapies has not proved successful and
patients have a median survival time of
6 - 12 months after presentation.
The clinical behaviour of the
malignancy is affected by several
factors including the continuous
mesothelial surface of the pleural
cavity which favours local metastasis
via exfoliated cells, invasion to
underlying tissue and other organs
within the pleural cavity, and the
extremely long latency period between
asbestos exposure and development of
the disease.
Surgery
Surgery, either by
itself or used in combination with pre-
and post-operative adjuvant therapies
has proved disappointing with a 5 year
survival rate of less than 10%. A
pleurectomy/decortication is the most
common surgery, in which the lining of
the chest is removed. Less common is an
extrapleural pneumonectomy (EPP), in
which the lung, lining of the inside of
the chest, the hemi-diaphragm and the
pericardium are removed.
Radiation
Although the tumor is
highly resistant to radiotherapy, these
regimens are sometimes used to relieve
symptoms arising from tumor growth,
such as obstruction of a major blood
vessel.
Radiotherapy is commonly applied to the
sites of chest drain insertion, in
order to prevent growth of the tumor
along the track in the chest
wall.
Chemotherapy
In February 2004,
the Food and Drug Administration
approved pemetrexed (brand name Alimta)
for treatment of malignant pleural
mesothelioma.
Immunotherapy
Treatment
regimens involving immunotherapy have
yielded variable results. For example,
intrapleural inoculation of Bacillus
Calmette-Guérin (BCG) in an
attempt to boost the immune response,
was found to be of no benefit to the
patient (while it may benefit patients
with bladder cancer).
Mesothelioma cells proved susceptible
to in vitro lysis by LAK cells
following activation by interleukin-2
(IL-2), but patients undergoing this
particular therapy experienced major
side effects. Indeed, this trial was
suspended in view of the unacceptably
high levels of IL-2 toxicity and the
severity of side effects such as fever
and cachexia. Nonetheless, other trials
involving interferon alpha have proved
more encouraging with 20% of patients
experiencing a greater than 50%
reduction in tumor mass combined with
minimal side effects.
Heated Intraoperative
Intraperitoneal Chemotherapy
A
procedure known as heated
intraoperative intraperitoneal
chemotherapy was developed by Paul
Sugarbaker at the Washington Cancer
Institute[7]. The surgeon removes as
much of the tumor as possible followed
by the direct administration of a
chemotherapy agent, heated to between
40 and 48°C, in the abdomen.
The fluid is perfused for 60 to 120
minutes and then drained.
This technique permits the
administration of high concentrations
of selected drugs into the abdominal
and pelvic surfaces. Heating the
chemotherapy treatment increases the
penetration of the drugs into tissues.
Also, heating itself damages the
malignant cells more than the normal
cells.