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Pilot study of Tremelimumab with and without cryoablation in patients with metastatic renal cell carcinoma.

Authors :
Campbell MT
Matin SF
Tam AL
Sheth RA
Ahrar K
Tidwell RS
Rao P
Karam JA
Wood CG
Tannir NM
Jonasch E
Gao J
Zurita AJ
Shah AY
Jindal S
Duan F
Basu S
Chen H
Espejo AB
Allison JP
Yadav SS
Sharma P
Source :
Nature communications [Nat Commun] 2021 Nov 04; Vol. 12 (1), pp. 6375. Date of Electronic Publication: 2021 Nov 04.
Publication Year :
2021

Abstract

Cryoablation in combination with immune checkpoint therapy was previously reported to improve anti-tumor immune responses in pre-clinical studies. Here we report a pilot study of anti-CTLA-4 (tremelimumab) with (n = 15) or without (n = 14) cryoablation in patients with metastatic renal cell carcinoma (NCT02626130), 18 patients with clear cell and 11 patients with non-clear cell histologies. The primary endpoint is safety, secondary endpoints include objective response rate, progression-free survival, and immune monitoring studies. Safety data indicate ≥ grade 3 treatment-related adverse events in 16 of 29 patients (55%) including 6 diarrhea/colitis, 3 hepatitis, 1 pneumonitis, and 1 glomerulonephritis. Toxicity leading to treatment discontinuation occurs in 5 patients in each arm. 3 patients with clear cell histology experience durable responses. One patient in the tremelimumab arm experiences an objective response, the median progression-free survival for all patients is 3.3 months (95% CI: 2.0, 5.3 months). Exploratory immune monitoring analysis of baseline and post-treatment tumor tissue samples shows that treatment increases immune cell infiltration and tertiary lymphoid structures in clear cell but not in non-clear cell. In clear cell, cryoablation plus tremelimumab leads to a significant increase in immune cell infiltration. These data highlight that treatment with tremelimumab plus cryotherapy is feasible and modulates the immune microenvironment in patients with metastatic clear cell histology.<br /> (© 2021. The Author(s).)

Details

Language :
English
ISSN :
2041-1723
Volume :
12
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
34737281
Full Text :
https://doi.org/10.1038/s41467-021-26415-4