TY - JOUR
T1 - Lenvatinib Plus Pembrolizumab Versus Standard of Care for Previously Treated Metastatic Colorectal Cancer
T2 - Final Analysis of the Randomized, Open-Label, Phase III LEAP-017 Study
AU - the LEAP-017 Investigators
AU - Kawazoe, Akihito
AU - Xu, Rui Hua
AU - García-Alfonso, Pilar
AU - Passhak, Maria
AU - Teng, Hao Wei
AU - Shergill, Ardaman
AU - Gumus, Mahmut
AU - Qvortrup, Camilla
AU - Stintzing, Sebastian
AU - Towns, Kathryn
AU - Kim, Tae Won
AU - Shiu, Kai Keen
AU - Cundom, Juan
AU - Ananda, Sumitra
AU - Lebedinets, Andrey
AU - Fu, Rong
AU - Jain, Rishi
AU - Adelberg, David
AU - Heinemann, Volker
AU - Yoshino, Takayuki
AU - Elez, Elena
AU - Cundom, Juan
AU - Slutsky, Ezequiel
AU - Grasselli, Julieta
AU - Fein, Luis
AU - Bella Quero, Luciana
AU - Joubert, Warren
AU - Gibbs, Peter
AU - Price, Timothy
AU - Burge, Matthew
AU - Ananda, Sumitra
AU - Khattak, Muhammad
AU - Colwell, Bruce
AU - Couture, Felix
AU - Meyers, Brandon
AU - Towns, Kathryn
AU - Sawyer, Michael
AU - Sideris, Lucas
AU - Xu, Ruihua
AU - Wang, Wei
AU - Pan, Hongming
AU - Pfeiffer, Per
AU - Jensen, Lars Henrik
AU - Qvortrup, Camilla
AU - Stintzing, Sebastian
AU - Arnold, Dirk
AU - Lorenzen, Sylvie
AU - Kubicka, Stefan
AU - Depenbusch, Reinhard
AU - Lee, Myung Ah
N1 - Publisher Copyright:
© American Society of Clinical Oncology.
PY - 2024/8/20
Y1 - 2024/8/20
N2 - PURPOSETreatment options are limited for patients with previously treated metastatic colorectal cancer (mCRC). In the LEAP-017 study, we evaluate whether lenvatinib in combination with pembrolizumab improves outcomes compared with standard of care (SOC) in previously treated mismatch repair proficient or not microsatellite instability high (pMMR or not MSI-H) mCRC.METHODSIn this international, multicenter, randomized, controlled, open-label, phase III study, eligible patients age 18 years and older with unresectable, pMMR or not MSI-H mCRC, that had progressed on or after, or could not tolerate, standard treatment, were randomly assigned 1:1 to lenvatinib 20 mg orally once daily plus pembrolizumab 400 mg intravenously once every 6 weeks or investigator's choice of regorafenib or trifluridine/tipiracil (SOC). Randomization was stratified by presence or absence of liver metastases. The primary end point was overall survival (OS). LEAP-017 is registered at ClinicalTrials.gov (NCT04776148), and has completed recruitment.RESULTSBetween April 8, 2021, and December 21, 2021, 480 patients were randomly assigned to lenvatinib plus pembrolizumab (n = 241) or SOC (n = 239). At final analysis (median follow-up of 18.6 months [IQR, 3.9]), median OS with lenvatinib plus pembrolizumab versus SOC was 9.8 versus 9.3 months (hazard ratio [HR], 0.83 [95% CI, 0.68 to 1.02]; P =.0379; prespecified threshold P =.0214). Grade ≥3 treatment-related adverse events occurred in 58.4% (lenvatinib plus pembrolizumab) versus 42.1% (SOC) of patients. Two participants died due to treatment-related adverse events, both in the lenvatinib plus pembrolizumab arm.CONCLUSIONIn patients with pMMR or not MSI-H mCRC that had progressed on previous therapy, there was no statistically significant improvement in OS after lenvatinib plus pembrolizumab treatment versus SOC. No new safety signals were observed.
AB - PURPOSETreatment options are limited for patients with previously treated metastatic colorectal cancer (mCRC). In the LEAP-017 study, we evaluate whether lenvatinib in combination with pembrolizumab improves outcomes compared with standard of care (SOC) in previously treated mismatch repair proficient or not microsatellite instability high (pMMR or not MSI-H) mCRC.METHODSIn this international, multicenter, randomized, controlled, open-label, phase III study, eligible patients age 18 years and older with unresectable, pMMR or not MSI-H mCRC, that had progressed on or after, or could not tolerate, standard treatment, were randomly assigned 1:1 to lenvatinib 20 mg orally once daily plus pembrolizumab 400 mg intravenously once every 6 weeks or investigator's choice of regorafenib or trifluridine/tipiracil (SOC). Randomization was stratified by presence or absence of liver metastases. The primary end point was overall survival (OS). LEAP-017 is registered at ClinicalTrials.gov (NCT04776148), and has completed recruitment.RESULTSBetween April 8, 2021, and December 21, 2021, 480 patients were randomly assigned to lenvatinib plus pembrolizumab (n = 241) or SOC (n = 239). At final analysis (median follow-up of 18.6 months [IQR, 3.9]), median OS with lenvatinib plus pembrolizumab versus SOC was 9.8 versus 9.3 months (hazard ratio [HR], 0.83 [95% CI, 0.68 to 1.02]; P =.0379; prespecified threshold P =.0214). Grade ≥3 treatment-related adverse events occurred in 58.4% (lenvatinib plus pembrolizumab) versus 42.1% (SOC) of patients. Two participants died due to treatment-related adverse events, both in the lenvatinib plus pembrolizumab arm.CONCLUSIONIn patients with pMMR or not MSI-H mCRC that had progressed on previous therapy, there was no statistically significant improvement in OS after lenvatinib plus pembrolizumab treatment versus SOC. No new safety signals were observed.
UR - http://www.scopus.com/inward/record.url?scp=85200057000&partnerID=8YFLogxK
U2 - 10.1200/JCO.23.02736
DO - 10.1200/JCO.23.02736
M3 - Article
C2 - 38833658
AN - SCOPUS:85200057000
SN - 0732-183X
VL - 42
SP - 2918
EP - 2927
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 24
ER -