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Photodynamic diagnosis of pleural malignant lesions with a combination of 5-aminolevulinic acid and intrinsic fluorescence observation systems
© Kitada et al.; licensee BioMed Central. 2015
- Received: 3 November 2014
- Accepted: 19 February 2015
- Published: 25 March 2015
We have developed a new diagnostic method using the photosensitizer 5-aminolevulinic acid (5ALA) for diagnosing intrathoracic malignant lesions. When ingested exogenously, 5ALA is metabolized to a heme precursor, protoporphyrin IX, which stays in malignant cells and emits red to pink luminescence of about 630 nm.
We enrolled 40 patients who underwent respiratory surgery and consented to participate in this study. Twenty-eight patients had primary lung cancer, 8 metastatic lung tumors, 2 malignant pleural tumors, and 2 benign tumors. Localization of malignant lesions was attempted by observing such lesions with an autofluorescence imaging system and by comparing the color tone of the autofluorescence between malignant lesions and normal tissues after oral administration of 5ALA. Malignant lesions on the pleural surface emitted pink autofluorescence in contrast to the green autofluorescence of the surrounding normal tissues.
When 28 patients with primary lung cancer were examined according to the degree of pleural infiltration (pl), red fluorescence was confirmed in 10 of 10 patients (100%) with p11-p13 and 5 of 18 patients (27.7%) with p10. The latter 5 patients had been diagnosed with PL1 preoperatively or intraoperatively.
This system achieved accurate localization of malignant lesions, suggesting that it may also be applicable to photodynamic therapy.
- 5-aminolevulinic acid (5ALA)
- Photodynamic diagnosis
- Autofluorescence imaging system
Diagnostic imaging techniques such as computed tomography, magnetic resonance imaging, and positron emission tomography (PET), as well as visual diagnosis during surgery, are of limited value for diagnosing early malignant pleural mesothelioma or minute intrathoracic dissemination that may contribute to intrathoracic recurrence after surgery for lung cancer. Thus, a highly accurate method of evaluation and diagnosis is awaited. Focusing attention on autofluorescence, we endeavored to develop a new method of photodynamic diagnosis (PDD) using an autofluorescence imaging system. However, the initial system had drawbacks such as limitations in the visualization of lesions and unclear borders between normal tissues and malignant lesions . We thus made efforts to improve the accuracy of this system. Five-aminolevulinic acid (5ALA), a photosensitizer, thereby came to our attention. Exogenous 5ALA is ingested and then metabolized to the heme precursor protoporphyrin IX, which stays in malignant cells and shows photogenesis, emitting red to pink fluorescence of about 630 nm . At present, this issue is studied in the fields of neurosurgery involving brain tumors  and urology involving bladder and prostate cancers [4,5], but there are no reports describing the use of this technique for intrathoracic malignant lesions. In this study, we gave 5ALA orally to lung cancer patients prior to surgery, and then viewed malignant lesions using the autofluorescence imaging system. By comparing the color tone of autofluorescence between normal tissues and malignant lesions, we were able to devise a highly accurate method of localizing malignant lesions.
Autofluorescence imaging system
PL category: pleural invasion of lung cancer
Tumor within the subpleural parenchyma, or, invading superficially into the pleural connective tissue below the elastic layer.
Tumor invades beyond the elastic layer.
Tumor invades to visceral pleural surface.
Tumor invades the parietal pleura.
Patients baseline characteristics and pathology of primary lung cancer (n=28)
baseline characteristics and pathology
Men: Women: 15:13
Adenocarcinoma :21 , Squamous cell carcinoma 5
Large cell carcinoma: 1; Pleomorphic carcinoma: 1
There were no adverse events attributable to oral administration of 5ALA.
Visualization of red fluorescence
All metastatic lung tumors present on the pleural surface were visualized even when they were very small. Two pleural malignant mesotheliomas were also successfully visualized. Benign tumors (leiomyoma of the trachea and neurinoma of the mediastinum) were also observed at the time of surgery, and there were no changes in color tone in any of these cases.
Red fluorescence was confirmed in 15 of 28 patients (53.5%) with primary lung cancer. In terms of the degree of pleural invasion, the tumor was visualized in 10/10 (100%) cases with p11-p13. Although visualization was confirmed in 5/18 (27.7%) p10 cases, all 5 cases had been diagnosed as suspected PL1 (the degree of pleural infiltration of gross appearance or image diagnosis preoperatively). Thus, we were able to localize the lesions when there was suspected or definitive contact or infiltration of the tumor lesions into the pleura.
A possible causative factor in the early recurrence of lung cancer is the presence of minute disseminated lesions. Accurate diagnosis of such lesions is a very important issue in formulating optimal therapeutic strategies. Considerable attention has been given to early diagnosis of malignant pleural mesothelioma, which has a poor prognosis and has as yet no established standard treatment. It is true that there are limitations in visual diagnosis with preoperative diagnostic imaging or thoracoscopic visualization, and a diagnostic method with high accuracy is therefore desired. We have been carrying out studies focused on autofluorescence of normal tissues emitted in response to an excitation wavelength of light. We have also been striving to improve our diagnostic system, by correcting its drawbacks such as unfavorable visualization of lesions and unclear borders between normal tissues and malignant lesions .
Although studies on PDD using 5ALA have been reported for brain tumors, and so on, in the field of neurosurgery , and for bladder and prostate cancers in the field of urology [4,5], there are no reports describing such a study for thoracic malignant lesions. We have assessed PDD based on the observation of green intrinsic fluorescence emitted by normal tissue and changes in tone due to decreased fluorescent substances in malignant tumor tissue, employing our own observation system. The results showed that this system allowed us to depict actual lesions. However, because the lesion borders were blurred in some cases, the accuracy of our system required improvement. We consider the current study to demonstrate that PDD combined with 5ALA administration allows more accurate diagnosis of malignant lesions exposed on the pleural surface and that our system is effective for the detection and localization of small disseminated lesions and small metastatic tumors in lung cancer.
This technique yielded favorable results for lesions exposed on the pleura but had limitations in terms of localizing lesions without pleural invasion (pl0). In cases pathologically diagnosed as pl1 to pl3, localization was achieved with certainty. In pl0 cases, although some lesions macroscopically classified as PL1 or above could be depicted, depiction of PL0 lesions was difficult. The pleural invasion (pl) factor is emphasized in lung cancer tissue classification, and the differentiation between pl0 and pl1 lesions has important implications for lung cancer treatment guidelines and for therapeutic strategies including surgical procedures . Taking these points into consideration, we have found our technique to be effective. Differentiation between benign and malignant lesions is also an important issue. In this study, there were distinct differences between malignant and benign lesions including fibrous thickening and neurogenic tumors, suggesting that our technique is applicable, to some extent, to differential diagnosis, i.e., distinguishing malignant from benign lesions. However, high standardized uptake values on PET have been reported in cases with inflammatory masses such as those of IgG4-related disease , underscoring the importance of further investigations in this area.
Although this study addressed the diagnosis of intrathoracic malignant disease, using 5ALA, we believe that the application of this technique is necessary not only to diagnosis but also to photodynamic therapy (PDT). In combination with heat therapy, the inhibitory effect of PDT on tumor growth was reported to be markedly enhanced by accumulation of protoporphyrin IX in tumor tissue after administration of 5ALA  and PDT with 5ALA achieved decreases in epidermal growth factor receptor expression and the degree of infiltration of cancer cells . At present, two oncotropic photosensitizers, i.e., Photofrin (porfimer sodium)  and Laserphyrin (talaporfin sodium) , are approved for use in PDT. The principle of PDT is as follows: the photosensitizer is activated by laser light to produce active oxygen in the cellular recovery phase, resulting in attacks on malignant cells. To date, laser irradiation covering a wide area has been used to treat the malignant tumor site because oncotropic photosensitizers characteristically accumulate in malignant tumors rather than in normal tissues. However, selective localization using 5ALA may allow more selective laser irradiation, improving its therapeutic effect. This technique may also be useful as a new treatment for malignant pleural mesothelioma for which no current consensus on effective therapy exists. Studies of this issue are also underway.
Photodynamic diagnosis using 5ALA for malignant intrathoracic lesions was carried out. In comparison with diagnosis using the autofluorescence observation system alone, it was possible to localize lesions based on the difference in color tone. In the future, localization of malignant intrathoracic lesions using 5ALA may allow PDT of high accuracy.
Informed consent was obtained from each patient for publication. A copy of the written consent is available for review by the Editor-in Chief of this journal.
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