Literature DB >> 16788928

A dose ranging study of photodynamic therapy with porfimer sodium (Photofrin) for treatment of basal cell carcinoma.

Allan R Oseroff1, Leslie R Blumenson, B Dale Wilson, Thomas S Mang, David A Bellnier, John C Parsons, Noreen Frawley, Michele Cooper, Nathalie Zeitouni, Thomas J Dougherty.   

Abstract

BACKGROUND AND OBJECTIVES: While basal cell carcinoma (BCC) is effectively treated by several methods, many patients with numerous or frequently occurring lesions seek alternatives that can treat multiple cancers, with improved cosmetic outcome. PDT for esophageal and lung carcinomas is approved at a porfimer sodium (Photofrin) dose of 2 mg/kg, but lower doses increase selectivity and decrease both cutaneous phototoxicity and cost. We evaluated low doses of porfimer sodium PDT for treatment of multiple BCC.
MATERIALS AND METHODS: Seventy-seven patients with 2,041 BCC were injected with 0.75, 0.875, or 1.0 mg/kg porfimer sodium and treated 2 days later with 630-nm light. Clinical responses were determined at 6 months, then periodically to 5 years.
RESULTS: Increasing porfimer sodium dose increased complete responses (CR), with initial CR rates of 72.7% (66-78%, 95% CI), 79.9% (73-86%, 95% CI), and 92.2% (91-93%, 95% CI), albeit with some lower selectivity at the highest dose. At 1 mg/kg, 5-year recurrence rates were 28% (21-35%, 95% CI) and 15% (11-18%, 95% CI) for sporadic and nevoid basal cell carcinoma syndrome (NBCCS) lesions, respectively.
CONCLUSIONS: This is the largest dose-ranging study of porfimer sodium, and the largest number of lesions treated in a single study. We found that with 1 mg/kg porfimer sodium, PDT can be a selective and durable treatment for sporadic and NBCCS-associated BCC. Copyright 2006 Wiley-Liss, Inc.

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Year:  2006        PMID: 16788928     DOI: 10.1002/lsm.20363

Source DB:  PubMed          Journal:  Lasers Surg Med        ISSN: 0196-8092            Impact factor:   4.025


  8 in total

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3.  Enhanced systemic immune reactivity to a Basal cell carcinoma associated antigen following photodynamic therapy.

Authors:  Edith Kabingu; Allan R Oseroff; Gregory E Wilding; Sandra O Gollnick
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4.  Preliminary clinical and pharmacologic investigation of photodynamic therapy with the silicon phthalocyanine photosensitizer pc 4 for primary or metastatic cutaneous cancers.

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Authors:  Marilyn T Wan; Jennifer Y Lin
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6.  Assessing Photosensitizer Targeting Using Meso-Tetra(Carboxyphenyl) Porphyrin.

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7.  A Novel Role of Connexin 40-Formed Channels in the Enhanced Efficacy of Photodynamic Therapy.

Authors:  Deng-Pan Wu; Li-Ru Bai; Yan-Fang Lv; Yan Zhou; Chun-Hui Ding; Si-Man Yang; Fan Zhang; Yuan-Yuan Wang; Jin-Lan Huang; Xiao-Xing Yin
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Review 8.  Role of Photoactive Phytocompounds in Photodynamic Therapy of Cancer.

Authors:  Kasipandi Muniyandi; Blassan George; Thangaraj Parimelazhagan; Heidi Abrahamse
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  8 in total

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