TY - JOUR
T1 - Therapy for regionally unresectable pancreatic cancer
AU - Kozuch, Peter
AU - Petryk, Magdalena
AU - Evans, Andrew
AU - Bruckner, Howard W.
PY - 2001
Y1 - 2001
N2 - Chemoradiotherapy for unresectable LAPA is associated with a median survival time of 9 months or more and manageable toxic side effects. Experience with RT-FSP provides evidence that chemoradiotherapy may extend survival time with or without resection. Chemoradiotherapy or entry into clinical trials is the standard for LAPA. The next generation of clinical trials for LAPA will incorporate newer agents, such as gemcitabine and irinotecan into chemoradiotherapy regimens. Novel agents, such as matrix-metaloproteinase inhibitors, transcription factor inhibitors, antiangiogenic factors, cyclooxegenase-2 inhibitors, and agents that target the K-ras point mutations associated with 90% of pancreatic cancers, are in early phases of clinical development and may have activity for micrometastatic or minimal residual disease. Lower toxicity makes these drugs attractive agents for maintenance therapies. The multitude of new agents provides hope to patients and a welcome challenge for further investigation.
AB - Chemoradiotherapy for unresectable LAPA is associated with a median survival time of 9 months or more and manageable toxic side effects. Experience with RT-FSP provides evidence that chemoradiotherapy may extend survival time with or without resection. Chemoradiotherapy or entry into clinical trials is the standard for LAPA. The next generation of clinical trials for LAPA will incorporate newer agents, such as gemcitabine and irinotecan into chemoradiotherapy regimens. Novel agents, such as matrix-metaloproteinase inhibitors, transcription factor inhibitors, antiangiogenic factors, cyclooxegenase-2 inhibitors, and agents that target the K-ras point mutations associated with 90% of pancreatic cancers, are in early phases of clinical development and may have activity for micrometastatic or minimal residual disease. Lower toxicity makes these drugs attractive agents for maintenance therapies. The multitude of new agents provides hope to patients and a welcome challenge for further investigation.
UR - http://www.scopus.com/inward/record.url?scp=0034972566&partnerID=8YFLogxK
U2 - 10.1016/S0039-6109(05)70154-7
DO - 10.1016/S0039-6109(05)70154-7
M3 - Article
AN - SCOPUS:0034972566
SN - 0039-6109
VL - 81
SP - 691
EP - 697
JO - Surgical Clinics of North America
JF - Surgical Clinics of North America
IS - 3
ER -