TY - JOUR
T1 - Immune checkpoint inhibitors plus debulking surgery for patients with metastatic renal cell carcinoma
T2 - clinical outcomes and immunological correlates of a prospective pilot trial
AU - Goswami, Sangeeta
AU - Gao, Jianjun
AU - Basu, Sreyashi
AU - Shapiro, Daniel D.
AU - Karam, Jose A.
AU - Tidwell, Rebecca Slack
AU - Ahrar, Kamran
AU - Campbell, Matthew T.
AU - Shen, Yu
AU - Trevino, Alexandro E.
AU - Mayer, Aaron T.
AU - Espejo, Alexsandra B.
AU - Seua, Christian
AU - Macaluso, Marc D.
AU - Chen, Yulong
AU - Liu, Wenbin
AU - He, Zhong
AU - Yadav, Shalini S.
AU - Wang, Ying
AU - Rao, Priya
AU - Zhao, Li
AU - Zhang, Jianhua
AU - Jindal, Sonali
AU - Tannir, Nizar M.
AU - Futreal, Andrew
AU - Wang, Linghua
AU - Sharma, Padmanee
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12
Y1 - 2025/12
N2 - Surgical removal of primary tumors reverses tumor-mediated immune suppression in pre-clinical models with metastatic disease. However, how cytoreductive surgery in the metastatic setting modulates the immune responses in patients, especially in the context of immune checkpoint therapy (ICT), is not understood. We report the first prospective, pilot, non-comparative clinical trial (NCT02210117) to evaluate the feasibility, clinical benefits, and immunologic changes of combining three different ICT-containing strategies with cytoreductive surgery or biopsy for patients with metastatic clear cell renal cell carcinoma. Primary safety endpoint of this trial has been met, with 43 patients completing cytoreductive surgery, 36 patients undergoing post-ICT biopsy, and 25 patients without either procedure due to progressive disease or toxicities or withdrawal of consent (total N = 104). Patients receiving ICT with cytoreductive surgery or biopsy, did not experience additional ICT- or procedure-related toxicities. The median overall survival was 54.7 months for patients who received ICT plus cytoreductive surgery. Immune-monitoring studies demonstrated that cytoreductive surgery increased antigen-presenting dendritic cell population and decreased KDM6B-expressing immune-suppressive myeloid cells in the peripheral blood. This study highlighted the feasibility of combining ICT with cytoreductive surgery in a metastatic setting and demonstrated the potential enhancement of immune responses following ICT plus cytoreductive surgery.
AB - Surgical removal of primary tumors reverses tumor-mediated immune suppression in pre-clinical models with metastatic disease. However, how cytoreductive surgery in the metastatic setting modulates the immune responses in patients, especially in the context of immune checkpoint therapy (ICT), is not understood. We report the first prospective, pilot, non-comparative clinical trial (NCT02210117) to evaluate the feasibility, clinical benefits, and immunologic changes of combining three different ICT-containing strategies with cytoreductive surgery or biopsy for patients with metastatic clear cell renal cell carcinoma. Primary safety endpoint of this trial has been met, with 43 patients completing cytoreductive surgery, 36 patients undergoing post-ICT biopsy, and 25 patients without either procedure due to progressive disease or toxicities or withdrawal of consent (total N = 104). Patients receiving ICT with cytoreductive surgery or biopsy, did not experience additional ICT- or procedure-related toxicities. The median overall survival was 54.7 months for patients who received ICT plus cytoreductive surgery. Immune-monitoring studies demonstrated that cytoreductive surgery increased antigen-presenting dendritic cell population and decreased KDM6B-expressing immune-suppressive myeloid cells in the peripheral blood. This study highlighted the feasibility of combining ICT with cytoreductive surgery in a metastatic setting and demonstrated the potential enhancement of immune responses following ICT plus cytoreductive surgery.
UR - https://www.scopus.com/pages/publications/85218503765
UR - https://www.scopus.com/inward/citedby.url?scp=85218503765&partnerID=8YFLogxK
U2 - 10.1038/s41467-025-57009-z
DO - 10.1038/s41467-025-57009-z
M3 - Article
C2 - 39984485
AN - SCOPUS:85218503765
SN - 2041-1723
VL - 16
JO - Nature communications
JF - Nature communications
IS - 1
M1 - 1846
ER -