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     INNOSC Theranostics and
            Pharmacological Sciences                           The biochemical and biophysical guide for photodynamic therapy
                                        Figure 2. The mechanistic presentation of photodynamic therapy
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                       Abbreviations:  O : Singlet oxygen;  O : Triplet oxygen; O : Oxygen; O : Superoxide anion; R: Radical; R : Free radical.
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            Table 1. Efficacy of photodynamic therapy in the treatment   adenomas  located near  the head  of  the  pancreas  that
            of various cancers                                 were not amenable to surgery. Patients were administered
                                                               an oral dose of 0.15  mg/kg mesotetrahydroxyphenyl
            Type of cancer             Photodynamic therapy (%)  chlorite, followed by light delivery to the tumor through
            Skin                              85 – 95          percutaneous fiber insertion under CT guidance 3  days
            Head and neck                     70 – 90          later. Three patients subsequently received chemotherapy.
            Lung                              50 – 70          Significant tumor necrosis was observed in all patients,
            Esophageal                        70 – 80          as evidenced by imaging studies. Fourteen of the 16 were
            Bladder                           70 – 85          discharged after 10 days. Several adverse events, including
            Pancreatic                        60 – 75          gastrointestinal bleeding and duodenal obstruction, were
                                                               recorded, which may have been related to the treatment.
            Prostate                          60 – 80
                                                               The median survival after PDT was 9.5 months, with seven
                                                               out of 16 patients surviving for 1 year. This study highlighted
            clinical study involved 15 patients with unresectable, high-  that,  while  pancreatic  tumor  necrosis  was  achieved  as
            stage tumors.  All patients were allergic to verteporfin at   expected, caution should be exercised, particularly in cases
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            a dose of 0.4 mg/kg, whereas 13 received treatment using   of tumors infiltrating the duodenal wall.
            single fiber lasers and two with multiple fibers, each 690 nm
            in length, placed transdermally. The light dose was gradually   In another study, the feasibility and safety of endoscopic
            increased until constant necrosis was achieved, and all   PDT in the treatment of unresectable ampullary cancer
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            procedures were monitored using a computed tomography   were evaluated.  Sixteen patients received an intravenous
            (CT) scan. Necrotic changes of 12 nm in size were observed   dose of 4 mg/kg of a HDP derivative, followed by red light
            in all patients, though the volumes varied. No side effects   (630 nm wavelength) administered during duodenoscopy
            were reported in patients who underwent chemotherapy.   two days later. A constant light energy density of either 50 J
            This  study  concluded  that  PDT  with verteporfin  for the   or 200 J/cm² was used, with three or four exposures during
            treatment of malignant pancreatic cancer (PCa) is safe, and   each session. Treatment was repeated up to 5  times at
                                                               intervals of 3 – 6 months. Skin hypersensitivity was the only
            the compound is flexible in terms of administration.
                                                               complication observed, affecting three patients. Tumor
              The next study aimed to evaluate PDT in PCa through   size was assessed every 4 – 8 weeks, and biopsy specimens
            a similar phase 1 trial.  It involved 16  patients with   were taken if the tumor was not visible macroscopically.
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             Volume 8 Issue 2 (2025)                        19                               doi: 10.36922/itps.4559
     	
