TY - JOUR
T1 - Treatment Outcomes in Patients with Metastatic Renal Cell Carcinoma with Sarcomatoid and/or Rhabdoid Dedifferentiation after Progression on Immune Checkpoint Therapy
AU - Hahn, Andrew W.
AU - Surasi, Devaki Shilpa
AU - Viscuse, Paul V.
AU - Bathala, Tharakeswara K.
AU - Wiele, Andrew J.
AU - Campbell, Matthew T.
AU - Zurita, Amado J.
AU - Shah, Amishi Y.
AU - Jonasch, Eric
AU - Gao, Jianjun
AU - Goswami, Sangeeta
AU - Alhalabi, Omar
AU - Rao, Priya
AU - Sircar, Kanishka
AU - Tannir, Nizar M.
AU - Msaouel, Pavlos
N1 - Publisher Copyright:
© 2023 The Author(s). Published by Oxford University Press.
PY - 2024/5
Y1 - 2024/5
N2 - Background: Metastatic RCC with sarcomatoid and/or rhabdoid (S/R) dedifferentiation is an aggressive disease associated with improved response to immune checkpoint therapy (ICT). The outcomes of patients treated with VEGFR-targeted therapies (TT) following ICT progression have not been investigated. Patients and Methods: Retrospective review of 57 patients with sarcomatoid (S), rhabdoid (R), or sarcomatoid plus rhabdoid (S+R) dedifferentiation who received any TT after progression on ICT at an academic cancer center. Clinical endpoints of interest included time on TT, overall survival (OS) from initiation of TT, and objective response rate (ORR) by RECIST version 1.1. Multivariable models adjusted for epithelial histology, IMDC risk, prior VEGFR TT, and inclusion of cabozantinib in the post-ICT TT regimen. Results: 29/57 patients had S dedifferentiation and 19 had R dedifferentiation. The most frequently used TT was cabozantinib (43.9%) followed by selective VEGFR TT (22.8%). The median time on TT was 6.4 months for all, 6.1 months for those with S dedifferentiation, 15.6 months for R dedifferentiation, and 6.1 months for S+R dedifferentiation. Median OS from initiation of TT was 24.9 months for the entire cohort, and the ORR was 20.0%. Patients with R dedifferentiation had significantly longer time on TT than those with S dedifferentiation (HR 0.44, 95% CI, 0.21-0.94). IMDC risk was associated with OS. Conclusions: A subset of patients with S/R dedifferentiation derive clinical benefit from TT after they have progressive disease on ICT. Patients with R dedifferentiation appeared to derive more benefit from TT than those with S dedifferentiation.
AB - Background: Metastatic RCC with sarcomatoid and/or rhabdoid (S/R) dedifferentiation is an aggressive disease associated with improved response to immune checkpoint therapy (ICT). The outcomes of patients treated with VEGFR-targeted therapies (TT) following ICT progression have not been investigated. Patients and Methods: Retrospective review of 57 patients with sarcomatoid (S), rhabdoid (R), or sarcomatoid plus rhabdoid (S+R) dedifferentiation who received any TT after progression on ICT at an academic cancer center. Clinical endpoints of interest included time on TT, overall survival (OS) from initiation of TT, and objective response rate (ORR) by RECIST version 1.1. Multivariable models adjusted for epithelial histology, IMDC risk, prior VEGFR TT, and inclusion of cabozantinib in the post-ICT TT regimen. Results: 29/57 patients had S dedifferentiation and 19 had R dedifferentiation. The most frequently used TT was cabozantinib (43.9%) followed by selective VEGFR TT (22.8%). The median time on TT was 6.4 months for all, 6.1 months for those with S dedifferentiation, 15.6 months for R dedifferentiation, and 6.1 months for S+R dedifferentiation. Median OS from initiation of TT was 24.9 months for the entire cohort, and the ORR was 20.0%. Patients with R dedifferentiation had significantly longer time on TT than those with S dedifferentiation (HR 0.44, 95% CI, 0.21-0.94). IMDC risk was associated with OS. Conclusions: A subset of patients with S/R dedifferentiation derive clinical benefit from TT after they have progressive disease on ICT. Patients with R dedifferentiation appeared to derive more benefit from TT than those with S dedifferentiation.
KW - cabozantinib
KW - immune checkpoint therapy
KW - renal cell carcinoma
KW - rhabdoid
KW - sarcomatoid
KW - somatic DNA
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U2 - 10.1093/oncolo/oyad302
DO - 10.1093/oncolo/oyad302
M3 - Article
C2 - 38035767
AN - SCOPUS:85188930339
SN - 1083-7159
VL - 29
SP - 392
EP - 399
JO - Oncologist
JF - Oncologist
IS - 5
ER -