TY - JOUR
T1 - Heterogeneous Tumor-Immune Microenvironments among Differentially Growing Metastases in an Ovarian Cancer Patient
AU - Jiménez-Sánchez, Alejandro
AU - Memon, Danish
AU - Pourpe, Stephane
AU - Veeraraghavan, Harini
AU - Li, Yanyun
AU - Vargas, Hebert Alberto
AU - Gill, Michael B.
AU - Park, Kay J.
AU - Zivanovic, Oliver
AU - Konner, Jason
AU - Ricca, Jacob
AU - Zamarin, Dmitriy
AU - Walther, Tyler
AU - Aghajanian, Carol
AU - Wolchok, Jedd D.
AU - Sala, Evis
AU - Merghoub, Taha
AU - Snyder, Alexandra
AU - Miller, Martin L.
N1 - Publisher Copyright:
© 2017 The Authors
PY - 2017/8/24
Y1 - 2017/8/24
N2 - We present an exceptional case of a patient with high-grade serous ovarian cancer, treated with multiple chemotherapy regimens, who exhibited regression of some metastatic lesions with concomitant progression of other lesions during a treatment-free period. Using immunogenomic approaches, we found that progressing metastases were characterized by immune cell exclusion, whereas regressing and stable metastases were infiltrated by CD8+ and CD4+ T cells and exhibited oligoclonal expansion of specific T cell subsets. We also detected CD8+ T cell reactivity against predicted neoepitopes after isolation of cells from a blood sample taken almost 3 years after the tumors were resected. These findings suggest that multiple distinct tumor immune microenvironments co-exist within a single individual and may explain in part the heterogeneous fates of metastatic lesions often observed in the clinic post-therapy.
AB - We present an exceptional case of a patient with high-grade serous ovarian cancer, treated with multiple chemotherapy regimens, who exhibited regression of some metastatic lesions with concomitant progression of other lesions during a treatment-free period. Using immunogenomic approaches, we found that progressing metastases were characterized by immune cell exclusion, whereas regressing and stable metastases were infiltrated by CD8+ and CD4+ T cells and exhibited oligoclonal expansion of specific T cell subsets. We also detected CD8+ T cell reactivity against predicted neoepitopes after isolation of cells from a blood sample taken almost 3 years after the tumors were resected. These findings suggest that multiple distinct tumor immune microenvironments co-exist within a single individual and may explain in part the heterogeneous fates of metastatic lesions often observed in the clinic post-therapy.
UR - http://www.scopus.com/inward/record.url?scp=85028377618&partnerID=8YFLogxK
U2 - 10.1016/j.cell.2017.07.025
DO - 10.1016/j.cell.2017.07.025
M3 - Article
C2 - 28841418
AN - SCOPUS:85028377618
SN - 0092-8674
VL - 170
SP - 927-938.e20
JO - Cell
JF - Cell
IS - 5
ER -