Bronchology Past, Present and Future Diagnostic Procedures
15
The general observation and agreement was:
Within the trials there was no advantage in terms of mortality reduction to
the groups offered intensive screening in the Mayo Clinic Study (MLP) with
sputum cytology and chest radiology every four months, while in the JHLP
and MSKLP studies there was no advantage to the group with sputum
cytology in addition to annual chest radiography examination. The
Czechoslovak Trial patients underwent radiology and sputum cytology
every six months.
This led to the adoption of policies discouraging routine X-ray and sputum
screening for early detection of lung cancer. The search for other avenues for
early detection continues.
Molecular Markers in Screening
An intensive search for genetic markers is in progress. The markers should be
detectable at a very early stage of the carcinogenic process and be specific for
malignancy. Other criteria include reproducible detectability, inexpensive, auto-
mated or semi-automated techniques. The Ras (Rous avian sarcoma) oncogene
meets some of these criteria. Both healthy individuals and cancer patients show
small amounts of soluble DNA fragments in the blood stream permitting the
development of a PCR (polymerase chain reaction) assay to look for Ras muta-
tions (in codon 12). The methodology is under study for high-risk individuals.
With respect to circulating tumor markers, blood levels of carcinoembryonic
antigen and neurospecific enolase are commonly elevated in histologic lung
cancer and SCLC, respectively. However early stages of disease and relapse
after treatment are not clearly detected. Bronchial lavage levels are high,
whereas serum levels are not.
Immunostaining of Sputum Specimens
In the John Hopkins Lung Project, Tockman reported 20 months early detection
of lung cancer prior to the development of invasive carcinoma. This result was
obtained by analysis of immunostained, cytologically atypical sputum speci-
mens from exfoliated cells. The process is under study for evaluation.
A new quantitative, solid-state microscopy system has been developed at
Columbia Cancer Research Center. The system features different DNA distribu-
tion patterns which permit to differentiate between cancerous and normal cells.
The location of the site of malignancy has to be determined by bronchoscopy
even when the system has proved efficacious. There is a misconception that
radiologically occult lung cancer detected by sputum cytology with negative
chest film represents an early stage of the disease. The number of in-situ carci-
nomas in such cases is reported to be very low. The tumors detected by cyto-
logy are not small.
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