» Articles » PMID: 33425438

Photodynamic Diagnosis and Therapy for Peritoneal Carcinomatosis from Gastrointestinal Cancers: Status, Opportunities, and Challenges

Overview
Date 2021 Jan 11
PMID 33425438
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Selective accumulation of a photosensitizer and the subsequent response in only the light-irradiated target are advantages of photodynamic diagnosis and therapy. The limited depth of the therapeutic effect is a positive characteristic when treating surface malignancies, such as peritoneal carcinomatosis. For photodynamic diagnosis (PDD), adjunctive use of aminolevulinic acid- protoporphyrin IX-guided fluorescence imaging detects cancer nodules, which would have been missed during assessment using white light visualization only. Furthermore, since few side effects have been reported, this has the potential to become a vital component of diagnostic laparoscopy. A variety of photosensitizers have been examined for photodynamic therapy (PDT), and treatment protocols are heterogeneous in terms of photosensitizer type and dose, photosensitizer-light time interval, and light source wavelength, dose, and dose rate. Although several studies have suggested that PDT has favorable effects in peritoneal carcinomatosis, clinical trials in more homogenous patient groups are required to identify the true benefits. In addition, major complications, such as bowel perforation and capillary leak syndrome, need to be reduced. In the long term, PDD and PDT are likely to be successful therapeutic options for patients with peritoneal carcinomatosis, with several options to optimize the photosensitizer and light delivery parameters to improve safety and efficacy.

Citing Articles

Prognostic value of hyperthermic intraperitoneal chemotherapy in gastric cancer with synchronous peritoneal metastases: a real-world retrospective study.

Guo J, Deng Z, Jin L, Yin S, Xiong Z, Wang C J Cancer Res Clin Oncol. 2023; 149(20):17881-17896.

PMID: 37947869 DOI: 10.1007/s00432-023-05481-9.


A Recap of Heme Metabolism towards Understanding Protoporphyrin IX Selectivity in Cancer Cells.

Kiening M, Lange N Int J Mol Sci. 2022; 23(14).

PMID: 35887311 PMC: 9324066. DOI: 10.3390/ijms23147974.


Current Status of Photodynamic Diagnosis for Gastric Tumors.

Kurumi H, Kanda T, Ikebuchi Y, Yoshida A, Kawaguchi K, Yashima K Diagnostics (Basel). 2021; 11(11).

PMID: 34829314 PMC: 8618298. DOI: 10.3390/diagnostics11111967.


Alectinib treatment improves photodynamic therapy in cancer cell lines of different origin.

Gillissen B, Richter A, Essmann F, Kemmner W BMC Cancer. 2021; 21(1):971.

PMID: 34461853 PMC: 8404354. DOI: 10.1186/s12885-021-08667-x.


Photodynamic Therapy for the Treatment and Diagnosis of -A Review of the Current Clinical Status.

Gunaydin G, Gedik M, Ayan S Front Chem. 2021; 9:686303.

PMID: 34409014 PMC: 8365093. DOI: 10.3389/fchem.2021.686303.

References
1.
Kwon I, Son T, Kim H, Hyung W . Fluorescent Lymphography-Guided Lymphadenectomy During Robotic Radical Gastrectomy for Gastric Cancer. JAMA Surg. 2018; 154(2):150-158. PMC: 6439673. DOI: 10.1001/jamasurg.2018.4267. View

2.
Mlkvy P, Messmann H, Regula J, Conio M, Pauer M, Millson C . Sensitization and photodynamic therapy (PDT) of gastrointestinal tumors with 5-aminolaevulinic acid (ALA) induced protoporphyrin IX (PPIX). A pilot study. Neoplasma. 1995; 42(3):109-13. View

3.
Garza O, Abati A, Sindelar W, Pass H, Hijazi Y . Cytologic effects of photodynamic therapy in body fluids. Diagn Cytopathol. 1996; 14(4):356-61. DOI: 10.1002/(SICI)1097-0339(199605)14:4<356::AID-DC14>3.0.CO;2-J. View

4.
Perry R, Evans S, Matthews W, Rizzoni W, Russo A, Pass H . Potentiation of phototherapy cytotoxicity with light scattering media. J Surg Res. 1989; 46(4):386-90. DOI: 10.1016/0022-4804(89)90207-2. View

5.
Wong Kee Song L, Wilson B . Endoscopic detection of early upper GI cancers. Best Pract Res Clin Gastroenterol. 2005; 19(6):833-56. DOI: 10.1016/j.bpg.2005.04.006. View