TY - JOUR
T1 - Efficacy of Cabozantinib in Metastatic MiT Family Translocation Renal Cell Carcinomas
AU - Thouvenin, Jonathan
AU - Alhalabi, Omar
AU - Carlo, Maria
AU - Carril-Ajuria, Lucia
AU - Hirsch, Laure
AU - Martinez-Chanza, Nieves
AU - NCrossed D Sign©grier, Sylvie
AU - Campedel, Luca
AU - Martini, Dylan
AU - Borchiellini, Delphine
AU - Chahoud, Jad
AU - Lodi, Massimo
AU - Barthélémy, Philippe
AU - Hasanov, Elshad
AU - Hahn, Andrew W.
AU - Gil, Thierry
AU - Viswanathan, Srinivas R.
AU - Bakouny, Ziad
AU - Msaouel, Pavlos
AU - Asim Bilen, Mehmet
AU - Choueiri, Toni K.
AU - Albiges, Laurence
AU - Tannir, Nizar M.
N1 - Publisher Copyright:
© 2022 The Author(s). Published by Oxford University Press.
PY - 2022/12/1
Y1 - 2022/12/1
N2 - Background: MiT family translocation renal cell carcinoma (TRCC) is a rare and aggressive subgroup of renal cell carcinoma harboring high expression of c-MET. While TRCC response rates to VEGF receptor tyrosine kinase inhibitors (TKIs) and immune checkpoint inhibitors are limited, efficacy of cabozantinib (a VEGFR, MET, and AXL inhibitor) in this subgroup is unclear. Methods: We performed a multicenter, retrospective, international cohort study of patients with TRCC treated with cabozantinib. The main objectives were to estimate response rate according to RECIST 1.1 and to analyze progression-free survival (PFS) and overall survival (OS). Results: Fifty-two patients with metastatic TRCC treated in the participating centers and evaluable for response were included. Median age at metastatic diagnosis was 40 years (IQR 28.5-53). Patients' IMDC risk groups at diagnosis were favorable (9/52), intermediate (35/52), and poor (8/52). Eleven (21.2%) patients received cabozantinib as frontline therapy, 15 (28.8%) at second line, and 26 (50%) at third line and beyond. The proportion of patients who achieved an objective response was 17.3%, including 2 complete responses and 7 partial responses. For 26 (50%) patients, stable disease was the best response. With a median follow-up of 25.1 months (IQR 12.6-39), median PFS was 6.8 months (95%CI 4.6-16.3) and median OS was 18.3 months (95%CI 17.0-30.6). No difference of response was identified according to fusion transcript features. Conclusion: This real-world study provides evidence of the activity of cabozantinib in TRCC, with more durable responses than those observed historically with other VEGFR-TKIs or ICIs.
AB - Background: MiT family translocation renal cell carcinoma (TRCC) is a rare and aggressive subgroup of renal cell carcinoma harboring high expression of c-MET. While TRCC response rates to VEGF receptor tyrosine kinase inhibitors (TKIs) and immune checkpoint inhibitors are limited, efficacy of cabozantinib (a VEGFR, MET, and AXL inhibitor) in this subgroup is unclear. Methods: We performed a multicenter, retrospective, international cohort study of patients with TRCC treated with cabozantinib. The main objectives were to estimate response rate according to RECIST 1.1 and to analyze progression-free survival (PFS) and overall survival (OS). Results: Fifty-two patients with metastatic TRCC treated in the participating centers and evaluable for response were included. Median age at metastatic diagnosis was 40 years (IQR 28.5-53). Patients' IMDC risk groups at diagnosis were favorable (9/52), intermediate (35/52), and poor (8/52). Eleven (21.2%) patients received cabozantinib as frontline therapy, 15 (28.8%) at second line, and 26 (50%) at third line and beyond. The proportion of patients who achieved an objective response was 17.3%, including 2 complete responses and 7 partial responses. For 26 (50%) patients, stable disease was the best response. With a median follow-up of 25.1 months (IQR 12.6-39), median PFS was 6.8 months (95%CI 4.6-16.3) and median OS was 18.3 months (95%CI 17.0-30.6). No difference of response was identified according to fusion transcript features. Conclusion: This real-world study provides evidence of the activity of cabozantinib in TRCC, with more durable responses than those observed historically with other VEGFR-TKIs or ICIs.
KW - MiT family translocation renal cell carcinoma
KW - cabozantinib
KW - non-clear cell renal cell carcinoma
UR - http://www.scopus.com/inward/record.url?scp=85141161247&partnerID=8YFLogxK
U2 - 10.1093/oncolo/oyac158
DO - 10.1093/oncolo/oyac158
M3 - Article
C2 - 35979929
AN - SCOPUS:85141161247
SN - 1083-7159
VL - 27
SP - 1041
EP - 1047
JO - Oncologist
JF - Oncologist
IS - 12
ER -