TY - JOUR
T1 - Long-term efficacy of crizotinib in a metastatic papillary renal carcinoma with MET amplification
T2 - A case report and literature review
AU - Rochigneux, Philippe
AU - Thomassin-Piana, Jeanne
AU - Laibe, Sophy
AU - Brunelle, Serge
AU - Salem, Naji
AU - Escudier, Bernard
AU - Vassal, Gilles
AU - Gravis, Gwenaelle
N1 - Publisher Copyright:
© 2018 The Author(s).
PY - 2018/11/22
Y1 - 2018/11/22
N2 - Background: Papillary renal cell carcinoma (pRCC) is the 2nd most frequent histological type of kidney cancer and accounts for approximately 15% of all renal cell carcinoma. It has a poorer prognosis than clear cell RCC (ccRCC) with a lack of standard treatments. Case presentation: We report the case of a 51 year old man with a metastatic pRCC (hepatic dome and left colonic peritoneal carcinomatosis) progressive after sunitinib, with a MET amplification. The patient was enrolled in the UNICANCER-sponsored AcSé crizotinib trial (NCT02034981), designed to give an access to crizotinib for patients with tumors harboring a genomic alteration on one of the biological targets of the drug. With 2nd line crizotinib (250 mg twice/day), the patient had a very good tolerance, a partial response in the target lesions using RECIST 1.1, and a 19 months' clinical efficacy. Conclusions: In metastatic pRCC with a MET amplification, crizotinib maybe a potential met-inhibitory therapeutic option.
AB - Background: Papillary renal cell carcinoma (pRCC) is the 2nd most frequent histological type of kidney cancer and accounts for approximately 15% of all renal cell carcinoma. It has a poorer prognosis than clear cell RCC (ccRCC) with a lack of standard treatments. Case presentation: We report the case of a 51 year old man with a metastatic pRCC (hepatic dome and left colonic peritoneal carcinomatosis) progressive after sunitinib, with a MET amplification. The patient was enrolled in the UNICANCER-sponsored AcSé crizotinib trial (NCT02034981), designed to give an access to crizotinib for patients with tumors harboring a genomic alteration on one of the biological targets of the drug. With 2nd line crizotinib (250 mg twice/day), the patient had a very good tolerance, a partial response in the target lesions using RECIST 1.1, and a 19 months' clinical efficacy. Conclusions: In metastatic pRCC with a MET amplification, crizotinib maybe a potential met-inhibitory therapeutic option.
KW - Crizotinib
KW - MET
KW - MET inhibitor
KW - Papillary renal cell carcinoma
KW - Radiotherapy
UR - http://www.scopus.com/inward/record.url?scp=85057107930&partnerID=8YFLogxK
U2 - 10.1186/s12885-018-5049-3
DO - 10.1186/s12885-018-5049-3
M3 - Article
C2 - 30466410
AN - SCOPUS:85057107930
SN - 1471-2407
VL - 18
JO - BMC Cancer
JF - BMC Cancer
IS - 1
M1 - 1159
ER -