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PET
–CLINICAL APPLICATIONS IN ONCOLOGY
Dr.
Lalatendu Sarangi,MS.
Surgical
Oncologist
Indian
Railways Cancer Institue,
VARANASI
–221 002
Positron
emission tomography (PET) is an imaging technology that delivers high
resolution images using biologically active compounds, substrates or
drugs labelled with positron emitters. Most physiological molecules
are made up of carbon, nitrogen and oxygen which enable them to be labelled
with 11G, 13N, 150, (and 18F) that are positron emitters. This provides
the clinicians and researchers with an unique tool to study and quantify
physiological and pathological functions of human tissues and organs.
Diagnosticians have traditionally been trained to analyse informations
provided by structural and anatomically based techniques. Biochemical
processes are, however, altered virtually in all disease states and
these alterations usually precede gross anatomical changes. With the
advent of molecular biology based medicine, a transition must be made
to incorporate information based on biochemical pertuberations into
diagnostic informations, without waiting for structural changes. PET
provides such information. PET is also very useful adjunct to anatomical
imaging techniques, providing unique informations and an additional
dimensions to the characterization of disease.
Application
of PET initially focussed on brain and heart. Now it is being primarily
used in oncological indications. This development has resulted from
successful application of Flourine-18-Fluro- deoxyglucose (FOG) to a
growing number of clinical indications at varying stages of diagnosis.
staging and follow up. Using FOG in vivo cancer imaging is based on
the observation of enhanced glycolysis in tumour cells. A high rate
of aerobic glycolysis (degradation of glucose to lactic acid in the
presence of oxygen) in several types of cancer cells was first described
by Warburg. This phenomenon has been linked to both increase in the
amount of glucoase membrane transporters and an increase in the activity
of the principal enzyms controlling the glycolytic pathways. It is important
to stress that FOG uptake by neoplastic tumours in vivo remains under
the dependance of other physiological factors, such as, tissue oxygenation,
regional blood flow and peritumoural inflammatory reactions.
DIFFERENTIAL
DIAGNOSIS
Solitary
pulmonary nodule:- Predictive accuracy for both benign and malignant
nodule is 94% in addition to reducing the complications encountered
by other methods of investigations like transthoracic needle aspiration.
Pancreatic
Mass:-
Several
studies from Germany and Japan have evaluated the role of FDG PET in
differentiations of pancreatic adeno carcinoma from benign chronic prancreatitis
and mass forming pancreatitis. Sensivity for carcinoma has been reported
to be 94% with a specificity ranging from 78% to 90%.
STAGING
Initial
staging by FOG PET has been useful in lung cancer, melaoma, sarcoma
and Lymphoma. It is probabaly indicated in other tumour types
like ovarian, head & neck and pancreatic carcinoma, especially when
the tumour is in an advanced stage or when metastatic lesions are suspected
by conventional Imaging or by raised tumour markers. Indeed, in these
cases, FDG PET can provide sensitive whole body screening.
DIFFERENTIATION
OF SCAR AND RESIDUAL DISEASE:-
Differentiation
of scar and residual or recurrent disease is a frequent indication of
PET and one of the first to be documented. It is used for lung, head
and neck, colorectal carcinomas. FDG has also proven useful in the evaluation
of residual masses after therapy for lymphoma.
DEMONSTRATIQN
OF SUSPECTED RECURRENCES:-
In
a suspected case of recurrence (by raised marker or other clinical signs)
where conventional imaging fails to detect because of small size of
recurrence PET may have immense value for its high sensitivity and whole
body capability. It not only can confirm but can delineate the extent
of recurrent disease. The impact of PET on management, avoiding unnecessary
surgery, allowing more complete surgery forms the basis of cost effectiveness.
FOLLOW-UP
THERAPY
FOG
PET can be helpful in evaluation of therapeutic response well before
morphologral decrease of tumour mass can be demonstrated by conventional
imaging. Early determination ()f therapeutic resistance is also important
to avoid the toxicity of an ineffective therapy and to allow selection
of a new therapeutic regimes.
Thus
PET has a tremendous potential for diagnosis and decision making in
a complex oncological problem. Extensive clinical research are bring
undertaken to find out the sensitivity and specificity in various situations
and define its precise role.
SUGGESTED
READINGS
- P.
Rigo, P. Paulus et el: Oncological applications of positron emission
tomography with fluorine-18-fluoro- deoxyglucose. European journal
of Nuclear Medicine, Voi 23; No.12 Dec.'96: 1641- 74.
- Wagner
HN Jr. Clinical PET: its time has come. J Nucl. Med. 1991 ;32:561-564.
- Wahl
RL: Positron emission tomography: application in oncology. In: Murray
ICP, Ell PJ, eds. Nuclear Medicine in clinical diagnosis and treatment.
London. Churchill Livingstone 1995;801-820
- Strauss
LG, Conli PS: The applications of PET in clinical oncology. J. Nucl.
Med. 1991 ;32:623-648.
- Warburg
0: The metabolism of tumors. New York: Smith RR, 1931; 129-169.
- Warburg
0: On the origin of cancer cells. Scrence 1956; 1323:309-314.
-
Bares R, Klever P, Hauptmann S et al. F-18 Flourodeoxyglucose PET
in vivo evaluation of pancreatic glucose metabolism for detection
of pancreatic cancer. Radiology 1994; 192:79-86.
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