Cargando…
Photodynamic therapy as adjuvant therapy in surgically treated pleural malignancies.
Five patients with a pleural malignancy (four malignant mesotheliomas and one localized low grade carcinoid) were treated with maximal surgical resection of the tumour followed by intraoperative adjuvant photodynamic therapy (PDT). The additional photodynamic treatment was performed with light of 65...
Autores principales: | , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1997
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2228043/ https://www.ncbi.nlm.nih.gov/pubmed/9310252 |
_version_ | 1782149823382683648 |
---|---|
author | Baas, P. Murrer, L. Zoetmulder, F. A. Stewart, F. A. Ris, H. B. van Zandwijk, N. Peterse, J. L. Rutgers, E. J. |
author_facet | Baas, P. Murrer, L. Zoetmulder, F. A. Stewart, F. A. Ris, H. B. van Zandwijk, N. Peterse, J. L. Rutgers, E. J. |
author_sort | Baas, P. |
collection | PubMed |
description | Five patients with a pleural malignancy (four malignant mesotheliomas and one localized low grade carcinoid) were treated with maximal surgical resection of the tumour followed by intraoperative adjuvant photodynamic therapy (PDT). The additional photodynamic treatment was performed with light of 652 nm from a high power diode laser, and meta-tetrahydroxy phenylchlorin as the photosensitizer. The light delivery to the thoracic cavity was monitored by in situ isotropic light detectors. The position of the light delivery fibre was adjusted to achieve optimal light distribution, taking account of reflected and scattered light in this hollow cavity. There was no 30-day post-operative mortality and only one patient suffered from a major complication (diaphragmatic rupture and haematopericardium). The operation time was increased by a maximum of 1 h to illuminate the total hemithoracic surface with 10 J cm(-2) (incident and scattered light). The effect of the adjuvant PDT was monitored by examination of biopsies taken 24 h after surgery under thoracoscopic guidance. Significant damage, including necrosis, was observed in the marker lesions with remaining malignancy compared with normal tissue samples, which showed only an infiltration with PMN cells and oedema of the striated muscles cells. Of the five patients treated, four are alive with no signs of recurrent tumour with a follow-up of 9-11 months. One patient was diagnosed as having a tumour dissemination in the skin around the thoracoscopy scar and died of abdominal tumour spread. Light delivery to large surfaces for adjuvant PDT is feasible in a relatively short period of time (< 1 h). In situ dosimetry ensures optimal light distribution and allows total doses (incident plus scattered light) to be monitored at different positions within the cavity. This combination of light delivery and dosimetry is well suited for adjuvant treatment with PDT in malignant pleural tumours. IMAGES: |
format | Text |
id | pubmed-2228043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22280432009-09-10 Photodynamic therapy as adjuvant therapy in surgically treated pleural malignancies. Baas, P. Murrer, L. Zoetmulder, F. A. Stewart, F. A. Ris, H. B. van Zandwijk, N. Peterse, J. L. Rutgers, E. J. Br J Cancer Research Article Five patients with a pleural malignancy (four malignant mesotheliomas and one localized low grade carcinoid) were treated with maximal surgical resection of the tumour followed by intraoperative adjuvant photodynamic therapy (PDT). The additional photodynamic treatment was performed with light of 652 nm from a high power diode laser, and meta-tetrahydroxy phenylchlorin as the photosensitizer. The light delivery to the thoracic cavity was monitored by in situ isotropic light detectors. The position of the light delivery fibre was adjusted to achieve optimal light distribution, taking account of reflected and scattered light in this hollow cavity. There was no 30-day post-operative mortality and only one patient suffered from a major complication (diaphragmatic rupture and haematopericardium). The operation time was increased by a maximum of 1 h to illuminate the total hemithoracic surface with 10 J cm(-2) (incident and scattered light). The effect of the adjuvant PDT was monitored by examination of biopsies taken 24 h after surgery under thoracoscopic guidance. Significant damage, including necrosis, was observed in the marker lesions with remaining malignancy compared with normal tissue samples, which showed only an infiltration with PMN cells and oedema of the striated muscles cells. Of the five patients treated, four are alive with no signs of recurrent tumour with a follow-up of 9-11 months. One patient was diagnosed as having a tumour dissemination in the skin around the thoracoscopy scar and died of abdominal tumour spread. Light delivery to large surfaces for adjuvant PDT is feasible in a relatively short period of time (< 1 h). In situ dosimetry ensures optimal light distribution and allows total doses (incident plus scattered light) to be monitored at different positions within the cavity. This combination of light delivery and dosimetry is well suited for adjuvant treatment with PDT in malignant pleural tumours. IMAGES: Nature Publishing Group 1997 /pmc/articles/PMC2228043/ /pubmed/9310252 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Baas, P. Murrer, L. Zoetmulder, F. A. Stewart, F. A. Ris, H. B. van Zandwijk, N. Peterse, J. L. Rutgers, E. J. Photodynamic therapy as adjuvant therapy in surgically treated pleural malignancies. |
title | Photodynamic therapy as adjuvant therapy in surgically treated pleural malignancies. |
title_full | Photodynamic therapy as adjuvant therapy in surgically treated pleural malignancies. |
title_fullStr | Photodynamic therapy as adjuvant therapy in surgically treated pleural malignancies. |
title_full_unstemmed | Photodynamic therapy as adjuvant therapy in surgically treated pleural malignancies. |
title_short | Photodynamic therapy as adjuvant therapy in surgically treated pleural malignancies. |
title_sort | photodynamic therapy as adjuvant therapy in surgically treated pleural malignancies. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2228043/ https://www.ncbi.nlm.nih.gov/pubmed/9310252 |
work_keys_str_mv | AT baasp photodynamictherapyasadjuvanttherapyinsurgicallytreatedpleuralmalignancies AT murrerl photodynamictherapyasadjuvanttherapyinsurgicallytreatedpleuralmalignancies AT zoetmulderfa photodynamictherapyasadjuvanttherapyinsurgicallytreatedpleuralmalignancies AT stewartfa photodynamictherapyasadjuvanttherapyinsurgicallytreatedpleuralmalignancies AT rishb photodynamictherapyasadjuvanttherapyinsurgicallytreatedpleuralmalignancies AT vanzandwijkn photodynamictherapyasadjuvanttherapyinsurgicallytreatedpleuralmalignancies AT petersejl photodynamictherapyasadjuvanttherapyinsurgicallytreatedpleuralmalignancies AT rutgersej photodynamictherapyasadjuvanttherapyinsurgicallytreatedpleuralmalignancies |