|
Select Language:
Richard Wolf GmbH |
DAFE - Diagnostic Auto Fluorescence EndoscopyBronchial carcinoma has become one of the most common cancers. DAFE -Autofouresence System to detect early stage cancer and precancerous tissue in the lungs.Operating Procedure and OR PreparationWith the DAFE system from R. WOLF, the basic procedure is identical to that for conventional white-light endoscopy in the bronchial region. No additional preparation is necessary. In contrast to PDD (photodynamic diagnosis), no photosensitisers are necessary to generate the fluorescence.The fluorescence is produced in the body's own molecules, such as riboflavin and is therefore known as autofluorescence. IndicationsDespite great efforts in recent decades, it has not been possible to significantly improve the 5-year survival rate of patients with bronchial carcinoma which remains poor at between 10% and 15%. One reason for this is that with conventional forms of diagnosis (including white light endoscopy), preinvasive (in other words, intraepithelial) lesions cannot be adequately detected and localised [Ken01]. However, it can be assumed that a more or less high proportion of these precancerous lesions will develop into invasive carcinomas. This proportion is considerable with carcinoma in situ [Ven00] but cannot be ignored in cases of medium to severe dysplasia [Ris88]. Especially with the preinvasive lesions (stage 0 according to ISS) the chances of healing with a 5-year survival rate of over 90% must be considered good but diminish dramatically as the disease develops [Tho02]. The reason for the low sensitivity of conventional forms of diagnosis for intraepithelial lesions, on the one hand, is the small size of these lesions which are usually only a few millimetres in diameter (at times even less) and often extend over only a few cell layers [Lam00]. As a result, they cannot always be distinguished from surrounding healthy tissue by their form; in other words by their size and elevation. On the other hand, differentiation between preinvasive lesions and healthy tissue based on colour is very restricted or even impossible. Autofluorescence endoscopy is a great help in dealing with this problem. It leads to a significant improvement in the detection and localisation of intraepithelial lesions [Gou], [Ren01], [Hor99]. By exciting bronchial tissue by exposing it to violet and blue light at a defined wavelength, autofluorescence light is induced in the endogenous fluorophors of the bronchial walls. This radiation is in a waveband lower than that of the applied excitation light. The fluorescent response depends greatly on the state of the tissue (healthy tissue fluoresces strongly, whereas the fluorescence of pathological tissue is weaker) so that it is possible to distinguish early stage cancer and precancerous tissue clearly from healthy tissue, in contrast to conventional white light endoscopy [Zel]. Even tissue with only slight pathological changes stands out clearly from healthy tissue in the fluorescence image. All patients with suspected preinvasive lesions or microinvasive carcinoma should therefore be examined by fluorescence bronchoscopy. These include:
When collecting the anamnesis, the following aspects should be taken into account:
For autofluorescence endoscopy, the endoscopically accessible bronchial regions and therefore central carcinomas and early forms are of significance. Contraindications Patients who should be excluded from fluorescence bronchoscopic examination are primarily those barred from conventional white light endoscopy. Also patients
Advantages of the Indications The decisive advantage of autofluorescence endoscopy is that it allows bronchial carcinoma to be visualised and treated at a stage at which the chances of healing are still very good. Change from white light to autofluorescence with Cursor It is also possible to detect lesions about which there is still controversy as to whether they should be resected or not (for example slight dysplasia) and to monitor their development during follow up (carcinogenesis). These lesions can, when necessary, be treated early with medication or surgically if malignant growth continues. In some situations, the detection and localisation of preinvasive lesions (stage 0 according to ISS) also allows the option of employing endobronchial therapeutic methods such as PDT (photodynamic therapy) [Mon90], [McC97], [Fre96], [Fre99] laser therapy [Cav94], cryotherapy [Oze90], therapy with electrocautery [Box98], APC (argon plasma coagulation), brachytherapy [Per97] etc. In contrast to surgical tumour resection (for example, lobectomy, bilobectomy or even pneumonectomy), which is recommended from ISS stage I onwards [Dom00], firstly most of these procedures can generally be repeated, for example, with recurrences or new occurrences and secondly due to their less invasive character they involve no or comparatively little reduction in quality of life of the patient at least in the medium to long term in many cases. In addition to this, classical surgical resection
If the therapy is intended to be curative, postoperative lung function must also be guaranteed. In surgical resection, a not insignificant risk of mortality must be accepted in the order of several percent for a lobectomy [Lod98] and increasing with the extent of the resection. A further advantage of autofluorescence endoscopy is that the margins of the tumour can be visualised clearly. Change from white light to autofluorescence with Cursor The extent of a tumour is much easier to recognise than under white light allowing more accurate staging. This is also true when a high-resolution video bronchoscope is used instead of a conventional fibre bronchoscope in white light bronchoscopy [Fuj00]. Especially with intraepithelial lesions, this can be decisive in the choice of therapy (see above) [Ren01]. It is a great advantage of autofluorescence endoscopy – in contrast to PDD (photodynamic diagnosis) – that no medication is required to produce the fluorescence. This avoids a number of potential problems such as the approvals for the medication (known as photosensitisers), the method of administering the medication and the dose, toxicity, fading of the tumour marker, etc.
Further information about human medicine |
• News |