Aditi Sahu1, Jose Cordero1,2, Xiancheng Wu1,3, Susanne Kossatz4,5,6, Ucalene Harris1, Paula Demetrio Desouza Franca4, Nicholas R Kurtansky1, Niasia Everett1, Stephen Dusza1, Jilliana Monnier1,7, Piyush Kumar8, Christi Fox9, Christian Brand10, Sheryl Roberts4, Kivanc Kose1, William Phillips1, Erica Lee1, Chih-Shan Jason Chen1, Anthony Rossi1, Kishwer Nehal1, Melissa Pulitzer1, Caterina Longo11,12, Allan Halpern1, Thomas Reiner4,13,14, Milind Rajadhyaksha1, Manu Jain15. 1. Dermatology Service, MSKCC, New York, New York. 2. Medical Sciences Campus, University of Puerto Rico, San Juan, Puerto Rico. 3. SUNY Upstate Medical University, Syracuse, New York. 4. Department of Radiology, MSKCC, New York, New York. 5. Department of Nuclear Medicine, University Hospital Klinikum Rechts der Isar and Central Institute for Translational Cancer Research, Technical University Munich, Munich, Germany. 6. Department of Chemistry, Technical University Munich, Munich, Germany. 7. Dermatology Department and Skin Cancer Department, La Timone Hospital, AP-HM, Aix-Marseille University, Marseille, France. 8. Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mt. Sinai, New York, New York. 9. Caliber Imaging and Diagnostics, Rochester, New York. 10. Summit Biomedical Imaging, New York, New York. 11. Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy. 12. Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Centro Oncologico ad Alta Tecnologia Diagnostica-Dermatologia, Reggio Emilia, Italy. 13. Department of Radiology, Weill Cornell Medical College, New York, New York; and. 14. Chemical Biology Program, MSKCC, New York, New York. 15. Dermatology Service, MSKCC, New York, New York; jainm@mskcc.org.
Abstract
Reflectance confocal microscopy (RCM) with endogenous backscattered contrast can noninvasively image basal cell carcinomas (BCCs) in skin. However, BCCs present with high nuclear density, and the relatively weak backscattering from nuclei imposes a fundamental limit on contrast, detectability, and diagnostic accuracy. We investigated PARPi-FL, an exogenous nuclear poly(adenosine diphosphate ribose) polymerase (PARP1)-targeted fluorescent contrast agent, and fluorescence confocal microscopy toward improving BCC diagnosis. Methods: We tested PARP1 expression in 95 BCC tissues using immunohistochemistry, followed by PARPi-FL staining in 32 fresh surgical BCC specimens. The diagnostic accuracy of PARPi-FL contrast was evaluated in 83 surgical specimens. The optimal parameters for permeability of PARPi-FL through intact skin was tested ex vivo on 5 human skin specimens and in vivo in 3 adult Yorkshire pigs. Results: We found significantly higher PARP1 expression and PARPi-FL binding in BCCs than in normal skin structures. Blinded reading of RCM-and-fluorescence confocal microscopy images by 2 experts demonstrated a higher diagnostic accuracy for BCCs with combined fluorescence and reflectance contrast than for RCM alone. Optimal parameters (time and concentration) for PARPi-FL transepidermal permeation through intact skin were successfully determined. Conclusion: Combined fluorescence and reflectance contrast may improve noninvasive BCC diagnosis with confocal microscopy.
Reflectance confocal microscopy (RCM) with endogenous backscattered contrast can noninvasively image basal cell carcinomas (BCCs) in skin. However, BCCs present with high nuclear density, and the relatively weak backscattering from nuclei imposes a fundamental limit on contrast, detectability, and diagnostic accuracy. We investigated PARPi-FL, an exogenous nuclear poly(adenosine diphosphate ribose) polymerase (PARP1)-targeted fluorescent contrast agent, and fluorescence confocal microscopy toward improving BCC diagnosis. Methods: We tested PARP1 expression in 95 BCC tissues using immunohistochemistry, followed by PARPi-FL staining in 32 fresh surgical BCC specimens. The diagnostic accuracy of PARPi-FL contrast was evaluated in 83 surgical specimens. The optimal parameters for permeability of PARPi-FL through intact skin was tested ex vivo on 5 human skin specimens and in vivo in 3 adult Yorkshire pigs. Results: We found significantly higher PARP1 expression and PARPi-FL binding in BCCs than in normal skin structures. Blinded reading of RCM-and-fluorescence confocal microscopy images by 2 experts demonstrated a higher diagnostic accuracy for BCCs with combined fluorescence and reflectance contrast than for RCM alone. Optimal parameters (time and concentration) for PARPi-FL transepidermal permeation through intact skin were successfully determined. Conclusion: Combined fluorescence and reflectance contrast may improve noninvasive BCC diagnosis with confocal microscopy.
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