TY - JOUR
T1 - Imaging Tumor Variation in Response to Photodynamic Therapy in Pancreatic Cancer Xenograft Models
AU - Samkoe, Kimberley S.
AU - Chen, Alina
AU - Rizvi, Imran
AU - O'Hara, Julia A.
AU - Hoopes, P. Jack
AU - Pereira, Stephen P.
AU - Hasan, Tayyaba
AU - Pogue, Brian W.
N1 - Funding Information:
Support was provided by National Institutes of Health grant PO1CA84203 . The verteporfin was a gift from QLT Inc (Vancouver, BC, Canada).
PY - 2010/1
Y1 - 2010/1
N2 - Purpose: A treatment monitoring study investigated the differential effects of orthotopic pancreatic cancer models in response to interstitial photodynamic therapy (PDT), and the validity of using magnetic resonance imaging as a surrogate measure of response was assessed. Methods and Materials: Different orthotopic pancreatic cancer xenograft models (AsPC-1 and Panc-1) were used to represent the range of pathophysiology observed in human beings. Identical dose escalation studies (10, 20, and 40J/cm) using interstitial verteporfin PDT were performed, and magnetic resonance imaging with T2-weighted and T1-weighted contrast were used to monitor the total tumor volume and the vascular perfusion volume, respectively. Results: There was a significant amount of necrosis in the slower-growing Panc-1 tumor using high light dose, although complete necrosis was not observed. Lower doses were required for the same level of tumor kill in the faster-growing AsPC-1 cell line. Conclusions: The tumor growth rate and vascular pattern of the tumor affect the optimal PDT treatment regimen, with faster-growing tumors being relatively easier to treat. This highlights the fact that therapy in human beings shows a heterogeneous range of outcomes, and suggests a need for careful individualized treatment outcomes assessment in clinical work.
AB - Purpose: A treatment monitoring study investigated the differential effects of orthotopic pancreatic cancer models in response to interstitial photodynamic therapy (PDT), and the validity of using magnetic resonance imaging as a surrogate measure of response was assessed. Methods and Materials: Different orthotopic pancreatic cancer xenograft models (AsPC-1 and Panc-1) were used to represent the range of pathophysiology observed in human beings. Identical dose escalation studies (10, 20, and 40J/cm) using interstitial verteporfin PDT were performed, and magnetic resonance imaging with T2-weighted and T1-weighted contrast were used to monitor the total tumor volume and the vascular perfusion volume, respectively. Results: There was a significant amount of necrosis in the slower-growing Panc-1 tumor using high light dose, although complete necrosis was not observed. Lower doses were required for the same level of tumor kill in the faster-growing AsPC-1 cell line. Conclusions: The tumor growth rate and vascular pattern of the tumor affect the optimal PDT treatment regimen, with faster-growing tumors being relatively easier to treat. This highlights the fact that therapy in human beings shows a heterogeneous range of outcomes, and suggests a need for careful individualized treatment outcomes assessment in clinical work.
KW - Magnetic resonance imaging
KW - Orthotopic tumor
KW - Pancreatic cancer
KW - Photodynamic therapy
KW - Tumor aggressiveness
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U2 - 10.1016/j.ijrobp.2009.08.041
DO - 10.1016/j.ijrobp.2009.08.041
M3 - Article
C2 - 20005458
AN - SCOPUS:72049132603
SN - 0360-3016
VL - 76
SP - 251
EP - 259
JO - International Journal of Radiation Oncology Biology Physics
JF - International Journal of Radiation Oncology Biology Physics
IS - 1
ER -