TY - JOUR
T1 - Proteomic and metabolic prediction of response to therapy in gastrointestinal cancers
AU - Herrmann, Ken
AU - Walch, Axel
AU - Balluff, Benjamin
AU - Tänzer, Marc
AU - Höfler, Heinz
AU - Krause, Bernd J.
AU - Schwaiger, Markus
AU - Friess, Helmut
AU - Schmid, Roland M.
AU - Ebert, Matthias P.A.
N1 - Funding Information:
MPA Ebert and A Walch are supported by a grant from the Deutsche Forschungsgemeinschaft (SFB 824/TP B1), the Deutsche Krebshilfe (107885) and the MolBioMed Program (EndoMed 01EZ0802) of the Federal Ministry of Education and Research (BMBF), Germany.
PY - 2009
Y1 - 2009
N2 - Despite substantial improvements in the diagnosis and treatment of many gastrointestinal cancers, particularly colorectal cancer, numerous patients are only diagnosed in advanced stages of disease, which can preclude curative treatment. Screening and early diagnosis of high-risk individuals might be the most promising approach to improve prognosis; however, molecular biomarkers for early diagnosis of most gastrointestinal cancers are not yet available. The prognosis of patients with advanced gastrointestinal cancers has improved through the development of multimodal treatments and the introduction of targeted therapies. Nonetheless, not all patients benefit equally from these treatment approaches, and toxicity can be substantial. The ability to predict whether a patient will respond to therapy early in their treatment for gastrointestinal cancer may be of particular value to stratify and individualize patient treatment strategies. Despite improvement in the understanding of cancer pathogenesis and progression at the molecular level, the molecular changes that underlie treatment response and/or drug resistance are still largely unknown. PET is the first technique to show promise in prediction of response to therapy, and has resulted in promising advancements, particularly in esophageal and gastric cancers. Tissue-based and blood-based molecular biomarkers are still subject to validation. Prediction of response to treatment could ultimately lead to an overall improvement in prognosis.
AB - Despite substantial improvements in the diagnosis and treatment of many gastrointestinal cancers, particularly colorectal cancer, numerous patients are only diagnosed in advanced stages of disease, which can preclude curative treatment. Screening and early diagnosis of high-risk individuals might be the most promising approach to improve prognosis; however, molecular biomarkers for early diagnosis of most gastrointestinal cancers are not yet available. The prognosis of patients with advanced gastrointestinal cancers has improved through the development of multimodal treatments and the introduction of targeted therapies. Nonetheless, not all patients benefit equally from these treatment approaches, and toxicity can be substantial. The ability to predict whether a patient will respond to therapy early in their treatment for gastrointestinal cancer may be of particular value to stratify and individualize patient treatment strategies. Despite improvement in the understanding of cancer pathogenesis and progression at the molecular level, the molecular changes that underlie treatment response and/or drug resistance are still largely unknown. PET is the first technique to show promise in prediction of response to therapy, and has resulted in promising advancements, particularly in esophageal and gastric cancers. Tissue-based and blood-based molecular biomarkers are still subject to validation. Prediction of response to treatment could ultimately lead to an overall improvement in prognosis.
UR - http://www.scopus.com/inward/record.url?scp=62549139738&partnerID=8YFLogxK
U2 - 10.1038/ncpgasthep1366
DO - 10.1038/ncpgasthep1366
M3 - Review article
C2 - 19259108
AN - SCOPUS:62549139738
SN - 1743-4378
VL - 6
SP - 170
EP - 183
JO - Nature Clinical Practice Gastroenterology and Hepatology
JF - Nature Clinical Practice Gastroenterology and Hepatology
IS - 3
ER -