TY - JOUR
T1 - Identification of a novel metabolic-related mutation (IDH1) in metastatic pancreatic cancer
AU - Brody, Jonathan R.
AU - Yabar, Cinthya S.
AU - Zarei, Mahsa
AU - Bender, Joseph
AU - Matrisian, Lynn M.
AU - Rahib, Lola
AU - Heartwell, Craig
AU - Mason, Kimberly
AU - Yeo, Charles J.
AU - Peiper, Stephen C.
AU - Jiang, Wei
AU - Varieur, Katelyn
AU - Madhavan, Subha
AU - Petricoin, Emanuel
AU - Fortuna, Danielle
AU - Curtis, Mark
AU - Wang, Zi Xuan
AU - Pishvaian, Michael J.
AU - Winter, Jordan M.
N1 - Publisher Copyright:
© 2018 Taylor & Francis Group, LLC.
PY - 2018/4/3
Y1 - 2018/4/3
N2 - Isocitrate dehydrogenase 1 (IDH1) is a metabolic enzyme implicated in cancer cell metabolic reprogramming. This is underscored by the detection of functional, somatic IDH1 mutations frequently found in secondary glioblastoma. To our knowledge, there has never been a reported, validated case of an IDH1 mutation in a pancreatic ductal adenocarcinoma (PDA). Herein, we present a case of a patient with metastatic PDA that harbored a potentially actionable, albeit rare, IDH1 mutation. As part of the Know Your Tumor project (Pancreatic Cancer Action Network), a 48-year-old female was diagnosed with metastatic PDA and subsequently started on standard of care chemotherapy, during which her hepatic lesions progressed. Detailed molecular profiling was performed on a biopsy from a liver lesion that demonstrated an IDH1 mutation, R132H. This mutation was confirmed by an independent sequencing reaction from the tumor sample, and by immunohistochemistry using an antibody specific for the IDH1 R132H mutation. The patient subsequently received a mutant IDH1 inhibitor (AG-120, Agios Pharmaceuticals, Cambridge, MA), but with no response. IDH1 mutations are common in certain cancer types, but have not been reported in PDA. We report the first case of an IDH1 mutation in this tumor type, perhaps providing a rare opportunity for a targeted therapy as a treatment option for PDA.
AB - Isocitrate dehydrogenase 1 (IDH1) is a metabolic enzyme implicated in cancer cell metabolic reprogramming. This is underscored by the detection of functional, somatic IDH1 mutations frequently found in secondary glioblastoma. To our knowledge, there has never been a reported, validated case of an IDH1 mutation in a pancreatic ductal adenocarcinoma (PDA). Herein, we present a case of a patient with metastatic PDA that harbored a potentially actionable, albeit rare, IDH1 mutation. As part of the Know Your Tumor project (Pancreatic Cancer Action Network), a 48-year-old female was diagnosed with metastatic PDA and subsequently started on standard of care chemotherapy, during which her hepatic lesions progressed. Detailed molecular profiling was performed on a biopsy from a liver lesion that demonstrated an IDH1 mutation, R132H. This mutation was confirmed by an independent sequencing reaction from the tumor sample, and by immunohistochemistry using an antibody specific for the IDH1 R132H mutation. The patient subsequently received a mutant IDH1 inhibitor (AG-120, Agios Pharmaceuticals, Cambridge, MA), but with no response. IDH1 mutations are common in certain cancer types, but have not been reported in PDA. We report the first case of an IDH1 mutation in this tumor type, perhaps providing a rare opportunity for a targeted therapy as a treatment option for PDA.
KW - IDH1
KW - IDH1 mutation
KW - multimodal treatment
KW - pancreatic cancer
KW - pancreatic ductal adenocarcinoma
KW - personalized medicine
KW - targeted therapy
UR - http://www.scopus.com/inward/record.url?scp=85028057298&partnerID=8YFLogxK
U2 - 10.1080/15384047.2016.1210743
DO - 10.1080/15384047.2016.1210743
M3 - Article
C2 - 27466707
AN - SCOPUS:85028057298
SN - 1538-4047
VL - 19
SP - 249
EP - 253
JO - Cancer Biology and Therapy
JF - Cancer Biology and Therapy
IS - 4
ER -