TY - JOUR
T1 - Current status of gastrointestinal tract cancer brain metastasis and the use of blood-based cancer biomarker biopsy
AU - Shoji, Yoshiaki
AU - Furuhashi, Satoru
AU - Kelly, Daniel F.
AU - Bilchik, Anton J.
AU - Hoon, Dave S.B.
AU - Bustos, Matias A.
N1 - Funding Information:
The authors acknowledge the support of Dr. Miriam and Sheldon G. Adelson Medical Research Foundation (DSBH) in brain metastasis studies. The authors would also like to thank Rebecca R. Gross, from the Department of Translational Molecular Medicine, John Wayne Cancer Institute, for proofreading.
Funding Information:
The authors acknowledge the support of Dr. Miriam and Sheldon G. Adelson Medical Research Foundation (DSBH) in brain metastasis studies. The authors would also like to thank Rebecca R. Gross, from the Department of Translational Molecular Medicine, John Wayne Cancer Institute, for proofreading.
Publisher Copyright:
© 2021, Springer Nature B.V.
PY - 2022/2
Y1 - 2022/2
N2 - Brain metastasis (BM) frequently occurs in patients with cutaneous melanoma, lung, and breast cancer; although, BM rarely arises from cancers of the gastrointestinal tract (GIT). The reported incidence of GIT cancer BM is less than 4%. In the last few years, effective systemic therapy has prolonged the survival of GIT patients and consequently, the incidence of developing BM is rising. Therefore, the epidemiology and biology of BM arising from GIT cancer requires a more comprehensive understanding. In spite of the development of new therapeutic agents for patients with metastatic GIT cancers, survival for patients with BM still remains poor, with a median survival after diagnosis of less than 4 months. Limited evidence suggests that early detection of isolated intra-cranial lesions will enable surgical resection plus systemic and/or radiation therapy, which may lead to an increase in overall survival. Novel diagnostic methods such as blood-based biomarker biopsies may play a crucial role in the early detection of BM. Circulating tumor cells and circulating cell-free nucleic acids are known to serve as blood biomarkers for early detection and treatment response monitoring of multiple cancers. Blood biopsy may improve early diagnosis and treatment monitoring of GIT cancers BM, thus prolonging patients’ survivals.
AB - Brain metastasis (BM) frequently occurs in patients with cutaneous melanoma, lung, and breast cancer; although, BM rarely arises from cancers of the gastrointestinal tract (GIT). The reported incidence of GIT cancer BM is less than 4%. In the last few years, effective systemic therapy has prolonged the survival of GIT patients and consequently, the incidence of developing BM is rising. Therefore, the epidemiology and biology of BM arising from GIT cancer requires a more comprehensive understanding. In spite of the development of new therapeutic agents for patients with metastatic GIT cancers, survival for patients with BM still remains poor, with a median survival after diagnosis of less than 4 months. Limited evidence suggests that early detection of isolated intra-cranial lesions will enable surgical resection plus systemic and/or radiation therapy, which may lead to an increase in overall survival. Novel diagnostic methods such as blood-based biomarker biopsies may play a crucial role in the early detection of BM. Circulating tumor cells and circulating cell-free nucleic acids are known to serve as blood biomarkers for early detection and treatment response monitoring of multiple cancers. Blood biopsy may improve early diagnosis and treatment monitoring of GIT cancers BM, thus prolonging patients’ survivals.
KW - Blood biomarker biopsy
KW - Brain metastasis
KW - Circulating cell-free nucleic acid
KW - Circulating tumor cells
KW - Colorectal cancer
KW - Gastrointestinal tract cancer
UR - http://www.scopus.com/inward/record.url?scp=85105481134&partnerID=8YFLogxK
U2 - 10.1007/s10585-021-10094-y
DO - 10.1007/s10585-021-10094-y
M3 - Review article
C2 - 33950411
AN - SCOPUS:85105481134
SN - 0262-0898
VL - 39
SP - 61
EP - 69
JO - Clinical and Experimental Metastasis
JF - Clinical and Experimental Metastasis
IS - 1
ER -