First autopsy analysis of the efficacy of intra-operative additional photodynamic therapy for patients with glioblastoma.


Journal

Brain tumor pathology
ISSN: 1861-387X
Titre abrégé: Brain Tumor Pathol
Pays: Japan
ID NLM: 9716507

Informations de publication

Date de publication:
Oct 2019
Historique:
received: 23 03 2019
accepted: 26 08 2019
pubmed: 6 9 2019
medline: 11 2 2020
entrez: 6 9 2019
Statut: ppublish

Résumé

The study aim to demonstrate the therapeutic tissue depth of photodynamic therapy (PDT) using the photosensitizer talaporfin sodium and semiconductor laser for malignant glioma from an autopsy finding. Three patients diagnosed with glioblastoma by pre-operative imaging (1 newly diagnosed patient and 2 patients with recurrence) were treated with intra-operative additional PDT and adjuvant therapy such as post-operative radiotherapy or chemotherapy. All three patients died of brain stem dysfunction owing to cerebrospinal fluid dissemination or direct invasion of the tumor cells from 13, 18, or 20 months after PDT. Antemortem magnetic resonance images demonstrated no tumor recurrence in the site of PDT, and autopsy was performed for the pathological analysis. Macroscopic observation demonstrated no tumor recurrence in two patients, but one patient demonstrated tumor recurrence in the therapeutic depth of PDT. Microscopic analysis demonstrated histopathological changes reaching depths of 9, 11, and 18 mm (mean: 12.7 mm) from the surface of the cavity of tumor resection, suggesting the therapeutic tissue depth of PDT to be in this range. This region demonstrated glial scarring with infiltration of T lymphocytes and macrophages, with slight degeneration of small vessel walls. However, viable tumor tissues were observed beyond or around the therapeutic tissue depth of PDT in two patients. PDT for glioblastoma prevented early local recurrence, which suggests the possibility that activation of the immune mechanisms was involved. The therapeutic tissue depth was suggested to be 9-18 mm from the surface of the cavity of tumor resection; however, the viable tumor tissues were demonstrated beyond this therapeutic range.

Identifiants

pubmed: 31487014
doi: 10.1007/s10014-019-00351-0
pii: 10.1007/s10014-019-00351-0
doi:

Substances chimiques

Photosensitizing Agents 0
Porphyrins 0
Talaporfin P4ROX5ELT2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

144-151

Auteurs

Jiro Akimoto (J)

Department of Neurosurgery, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan. jiroaki@gmail.com.
Department of Neurosurgery, Kohsei Chuo General Hospital, Tokyo, Japan. jiroaki@gmail.com.

Shinjiro Fukami (S)

Department of Neurosurgery, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan.

Tomohiro Suda (T)

Department of Neurosurgery, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan.

Megumi Ichikawa (M)

Department of Neurosurgery, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan.

Rei Haraoka (R)

Department of Neurosurgery, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan.

Michihiro Kohno (M)

Department of Neurosurgery, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan.

Yukiko Shishido-Hara (Y)

Department of Human Pathology, Tokyo Medical University, Tokyo, Japan.

Toshitaka Nagao (T)

Department of Human Pathology, Tokyo Medical University, Tokyo, Japan.

Masahiko Kuroda (M)

Department of Molecular Pathology, Tokyo Medical University, Tokyo, Japan.

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Classifications MeSH