Lenvima (lenvatinib) / Eisai, Merck (MSD) 
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 53 Diseases   490 Trials   490 Trials   8927 News 


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  • ||||||||||  Avastin (bevacizumab) / Roche, Lenvima (lenvatinib) / Eisai, Merck (MSD), Tecentriq (atezolizumab) / Roche
    Clinical, Retrospective data, Journal, Real-world evidence, Real-world:  Atezolizumab/bevacizumab and lenvatinib for hepatocellular carcinoma: A comparative analysis in a European real-world cohort. (Pubmed Central) -  Nov 4, 2024   
    The increased risk of hepatic decompensation in patients treated with AZ/BV who have impaired baseline liver function underscores the need for careful monitoring. Future trials should aim to distinguish more clearly between metabolic dysfunction-associated steatotic liver disease and alcohol-associated liver disease.
  • ||||||||||  Keytruda (pembrolizumab) / Merck (MSD), Lenvima (lenvatinib) / Eisai, Merck (MSD)
    Outcome of metastatic, radioactive-iodine refractory differentiated, medullary and anaplastic thyroid carcinoma  (Halls 1 & 2) -  Nov 3, 2024 - Abstract #COSA2024COSA_344;    
    Our research revealed one mechanism by which hepatoma cells can survive the combination therapy, providing a theoretical basis for the refined treatment of HCC. Our study showed real world data of patients with RAIR DTC, metastatic medullary TC, and anaplastic TC with promising real-world response rate to lenvatinib, redifferentiation therapy, RET inhibitors, long-term response to BRAF & MEK inhibitor combination and immunotherapy with lenvatinib combination.
  • ||||||||||  Jemperli (dostarlimab-gxly) / GSK
    Post-Progression Survival Outcomes in Patients with Primary Advanced or Recurrent Endometrial Cancer (pA/rEC) in the ENGOT-EN6-NSGO/GOG-3031/RUBY Trial Who Received Follow-up Immunotherapy (Halls 1 & 2) -  Nov 3, 2024 - Abstract #COSA2024COSA_80;    
    P3
    Aims: In Part 1 of the phase 3 ENGOT-EN6-NSGO/GOG-3031/RUBY trial (NCT03981796; funding: GSK), dostarlimab+carboplatin-paclitaxel (CP) significantly improved PFS (HR 0.64) and OS (HR 0.69) vs placebo+CP in the overall population of patients with pA/rEC...At interim analysis 2 (37.2 mo of follow-up), updated post hoc analyses of OS adjusted for treatment switching via rank-preserving structural failure time (RPSFT) were performed in the overall and MMRp/MSS populations of pts who received FUACT of IO and for patients receiving pembrolizumab-lenvatinib (PEM-LEN) in the MMRp/MSS population... Adjusted OS using RPSFT for subsequent use of IO in the overall and MMRp/MSS populations, including PEM-LEN in the MMRp/MSS population, showed limited impact on survival benefits, supporting frontline use of dostarlimab+CP as standard of care in all patients with pA/rEC.
  • ||||||||||  Tyvyt (sintilimab) / Eli Lilly, Lenvima (lenvatinib) / Eisai, Merck (MSD)
    Journal, Metastases:  Multidisciplinary approaches in the management of advanced hepatocellular carcinoma: Exploring future directions. (Pubmed Central) -  Oct 30, 2024   
    This case report demonstrated the efficacy of the combination therapy of transcatheter arterial chemoembolization, hepatic arterial infusion chemotherapy, epclusa, lenvatinib and sintilimab for a patient with advanced HCC, and the report can serve as a reference for clinical practice. We would also like to share some of our views.
  • ||||||||||  Lenvima (lenvatinib) / Eisai, Merck (MSD), Cabometyx (cabozantinib tablet) / Exelixis
    Review, Journal, IO biomarker:  Systemic treatments for radioiodine-refractory thyroid cancers. (Pubmed Central) -  Oct 30, 2024   
    Due to DTCs' distinctive radioiodine (RAI) uptake mechanism, standard treatment involving surgery, with or without adjunctive therapy using RAI and levothyroxine inhibition, typically yields favorable prognoses for the majority of patients with DTCs...Lenvatinib and sorafenib, multi-kinase inhibitors, represent the standard first-line systemic treatment options, while cabozantinib is the standard second-line treatment option, for this purpose...However, further validation through multicenter, large-sample, double-blinded randomized controlled trials are essential. Enhanced treatment strategies and innovative therapies are expected to benefit a broader spectrum of patients as these advancements progress.
  • ||||||||||  Loqtorzi (toripalimab-tpzi) / Shanghai Junshi Biosci, Coherus Biosci, Lenvima (lenvatinib) / Eisai, Merck (MSD)
    Biomarker, Enrollment change, Trial primary completion date, IO biomarker, Metastases:  GEMOX Combined With Targeted Therapy and Immunotherapy for Patients With Advanced Cholangiocarcinoma (clinicaltrials.gov) -  Oct 27, 2024   
    P=N/A,  N=80, Recruiting, 
    This study highlights that TBC1D31 at 8q24.13 is a new critical oncogene, uncovers a novel mechanism of EGFR activation in HCC, and proposes the potential strategies for treating HCC patients with TBC1D31 amplification or overexpression. N=120 --> 80 | Trial primary completion date: Jan 2024 --> May 2024
  • ||||||||||  Fotivda (tivozanib) / Kyowa Kirin, LG Chem, Lenvima (lenvatinib) / Eisai, Merck (MSD)
    Retrospective data, Journal, Adverse events, Metastases:  Estimated cost of VEGFR TKI associated adverse events in metastatic renal cell carcinoma patients. (Pubmed Central) -  Oct 26, 2024   
    The estimated costs of managing VEGFR TKI class-effect AEs were lowest with tivozanib, and highest with lenvatinib and everolimus, indicating potentially differential healthcare resource burden by TKI regimen. The use of tivozanib in the 3
  • ||||||||||  Lenvima (lenvatinib) / Eisai, Merck (MSD)
    Journal, PD(L)-1 Biomarker, IO biomarker, Surgery:  Prognostic Value of Pathological Response for Patients with Unresectable Hepatocellular Carcinoma Undergoing Conversion Surgery. (Pubmed Central) -  Oct 22, 2024   
    Transarterial chemoembolization combined with lenvatinib and PD-1 inhibitor (triple therapy) has displayed encouraging clinical outcomes for unresectable hepatocellular carcinoma (uHCC)...The presence of MPR or pCR could improve prognosis in patients with initially uHCC who underwent conversion surgery following triple therapy. The PR may become a surrogate marker for predicting the prognosis of these patients.
  • ||||||||||  Lenvima (lenvatinib) / Eisai, Merck (MSD)
    Biomarker, Journal, PD(L)-1 Biomarker, IO biomarker:  Gut microbiota as a prognostic biomarker for unresectable hepatocellular carcinoma treated with anti-PD-1 therapy. (Pubmed Central) -  Oct 18, 2024   
    The multivariate analysis showed that the abundance of Bacteroides_AF20_13LB and Ruminococcus_ AF25_28AC was independent related factors for PFS, and the abundance of Bacteroides_AF20_13LB was an independent related factor of OS. The enrichment of specific gut microbiota affected clinical efficacy and survival benefits in HCC treated with anti-PD-1 therapy and may be a promising non-invasive gut microbial biomarker and a new strategy for modulating immunotherapy in HCC.
  • ||||||||||  Lenvima (lenvatinib) / Eisai, Merck (MSD)
    Review, Journal, Metastases:  Roles of clinical application of lenvatinib and its resistance mechanism in advanced hepatocellular carcinoma (Review). (Pubmed Central) -  Oct 17, 2024   
    In addition, the superiority of LEN combination therapy has been shown to potentially overcome the limitations of LEN monotherapy in a series of research, and a range of promising indicators for predicting treatment response and prognosis have been discovered in recent years. In this review, we summarize the latest developments in LEN resistance, the efficacy and safety of LEN combination therapy as well as associated indicators, which may provide new insight into its resistance as well as ideas in the treatment of advanced HCC.
  • ||||||||||  Tevimbra (tislelizumab-jsgr) / BeiGene, Lenvima (lenvatinib) / Eisai, Merck (MSD)
    Retrospective data, Journal:  Transarterial chemoembolization combined with lenvatinib plus tislelizumab for unresectable hepatocellular carcinoma: a multicenter cohort study. (Pubmed Central) -  Oct 16, 2024   
    Subgroup analysis showed that for patients with a maximum tumor diameter greater than 7 cm, AFP > 400 ng/ml and accompanied by portal vein tumor thrombus, and Child-Pugh class A, there was a statistically significant difference in OS between TLT and TL groups. OS and PFS were significantly improved in patients who received TLT compared to those who received TL, patients with a largest tumor diameter greater than 7 cm, AFP > 400 ng/ml, Child-Pugh class A and PVTT appeared to derive more benefit.
  • ||||||||||  Puyouheng (pucotenlimab) / Taizhou Hanzhong Biopharma, Lepu Med, Lenvima (lenvatinib) / Eisai, Merck (MSD)
    Trial completion date, Trial primary completion date:  CCGLC-013: Combined HAIC, Lenvatinib and Pucotenlimab As Conversion Therapy for Unresectable Intrahepatic Cholangiocarcinoma (clinicaltrials.gov) -  Oct 16, 2024   
    P2,  N=36, Recruiting, 
    OS and PFS were significantly improved in patients who received TLT compared to those who received TL, patients with a largest tumor diameter greater than 7 cm, AFP > 400 ng/ml, Child-Pugh class A and PVTT appeared to derive more benefit. Trial completion date: Jun 2026 --> Jun 2028 | Trial primary completion date: Dec 2025 --> Dec 2026