Erbitux (cetuximab) / Eli Lilly 
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 245 Diseases   389 Trials   389 Trials   11400 News 


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  • ||||||||||  Avastin (bevacizumab) / Roche, Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Biomarker, Journal:  Molecular prognostic factors in colorectal cancer: 5-year follow-up. (Pubmed Central) -  May 6, 2023   
    Using the Kaplan-Meier test, we calculated the correlation coefficient between survival time and immunohistochemical prognostic factors. The patients were followed for 60 months postoperatively.
  • ||||||||||  PF-07284892 / Pfizer
    Trial completion date, Combination therapy, Metastases:  PF-07284892 in Participants With Advanced Solid Tumors (clinicaltrials.gov) -  May 6, 2023   
    P1,  N=196, Recruiting, 
    The patients were followed for 60 months postoperatively. Trial completion date: Apr 2026 --> Sep 2026
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    The promising role of TGF-?RII mutations and EGFR immunostaining in response to anti-EGFR therapies (Poster HALL LEVEL 0) -  May 6, 2023 - Abstract #ESMOGI2023ESMO_GI_646;    
    The approach we propose through these research results has the potential to adapt current targeted therapies (anti-EGFR) to the biological characteristics of sporadic CRC through TGF? pathway and could thus decrease the risk of administering expensive and potentially toxic treatments to patients unnecessarily.
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono, Opdivo (nivolumab) / Ono Pharma, BMS
    The contribution of circulating tumor cells' gene expression in treatment response (Poster HALL LEVEL 0) -  May 6, 2023 - Abstract #ESMOGI2023ESMO_GI_593;    
    These preliminary data indicate that not all cases exhibit the same behavior, as it was expected. There are overexpressed genes, whose expression associated with response to chemotherapeutic drugs, like fluorouracil, oxaliplatin, irinotecan, monoclonal antibodies, such as nivolumab, cetuximab etc. However, these genes are not upregulated in all cases, since there is a percentage of approximately 30% with different expression profile.
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    BRAF mutant metastatic colon cancer expect the unexpected: A single centre study (Poster HALL LEVEL 0) -  May 6, 2023 - Abstract #ESMOGI2023ESMO_GI_428;    
    Despite the availability of cetuximab/ encorafinib from early 2020 in second line indication only 9 patients (19%) received second-line BRAF inhibitor therapy. In conclusion there should be a low threshold to investigate any reported symptoms with possibility of metastases in mind in patients with BRAF mutated colon cancer as they can exhibit an atypical pattern of metastatic spread.
  • ||||||||||  Avastin (bevacizumab) / Roche, Erbitux (cetuximab) / Eli Lilly, EMD Serono, Braftovi (encorafenib) / Ono Pharma, Pierre Fabre, Pfizer
    Retrospective analysis of management of BRAF V600E mutated colorectal cancer in a single institution (Poster HALL LEVEL 0) -  May 6, 2023 - Abstract #ESMOGI2023ESMO_GI_383;    
    Our study emphasizes the poor prognosis of BRAF V600E-mutated metastasic colorrectal cancer, In our population, similar as the one in the BEACON study, the combination of encorafenib-cetuximab stands out as a well-tolerated option in second line, with a PFS of 9,9 months. Of note, in our experience encorafenib-cetuximab could also be a remarkable option in third-line setting, with a PFS of 10,4 months.
  • ||||||||||  FT536 / Fate Therap
    Enrollment closed, Enrollment change, Combination therapy, Monotherapy, Metastases:  FT536 Monotherapy and in Combination With Monoclonal Antibodies in Advanced Solid Tumors (clinicaltrials.gov) -  May 1, 2023   
    P1,  N=5, Active, not recruiting, 
    It is suggested that FPE therapy is an alternative ICT regimen to TPF therapy, but further long-term follow-up is needed. Recruiting --> Active, not recruiting | N=322 --> 5
  • ||||||||||  FT538 / Fate Therap
    Enrollment closed, Enrollment change, Combination therapy, Metastases:  FT538 in Combination With Monoclonal Antibodies in Advanced Solid Tumors (clinicaltrials.gov) -  May 1, 2023   
    P1,  N=16, Active, not recruiting, 
    Recruiting --> Active, not recruiting | N=322 --> 5 Recruiting --> Active, not recruiting | N=189 --> 16
  • ||||||||||  MEN1611 / Menarini
    Enrollment closed, Trial completion date, Trial primary completion date, Metastases:  MEN1611 With Cetuximab in Metastatic Colorectal Cancer (C-PRECISE-01) (clinicaltrials.gov) -  Apr 28, 2023   
    P1/2,  N=42, Active, not recruiting, 
    The results suggest that our device may be a valuable tool for evaluating the success of less intensive treatment regimens. Recruiting --> Active, not recruiting | Trial completion date: Jul 2023 --> Oct 2023 | Trial primary completion date: Jul 2023 --> Oct 2023
  • ||||||||||  MK-1084 / Merck (MSD), Otsuka
    Enrollment change, Trial completion date, Trial primary completion date, Combination therapy, Monotherapy, Metastases:  A Study of MK-1084 in KRAS Mutant Advanced Solid Tumors (MK-1084-001) (clinicaltrials.gov) -  Apr 27, 2023   
    P1,  N=450, Recruiting, 
    Trial completion date: Oct 2022 --> Oct 2023 N=264 --> 450 | Trial completion date: Feb 2026 --> Aug 2026 | Trial primary completion date: Feb 2026 --> Aug 2026
  • ||||||||||  Avastin (bevacizumab) / Roche, Erbitux (cetuximab) / Eli Lilly, EMD Serono
    The smart options of induction therapy for locally advanced betel-nuts related HNSCC in Taiwan. () -  Apr 26, 2023 - Abstract #ASCO2023ASCO_5705;    
    Flexible chemotherapy backbones, such as TP/DP-HDFL(weekly docetaxel or paclitaxel with cisplatin and 24-hr high dose 5-fluorouracil/leucovorin infusion), might produce acceptable response rates with less toxicity. Bio(EGFR or VEGFR-targeting)-chemotherapy or Bio-chemoimmunotherapy has brought encouraging induction response with favorable toxicity profiles to conversion surgery or definite CCRT.
  • ||||||||||  Erbitux (cetuximab) / Eli Lilly, EMD Serono
    Real-world survival of older adults with LA SCCHN using SEER-Medicare. () -  Apr 26, 2023 - Abstract #ASCO2023ASCO_5696;    
    mOS was lower in patients who received non-DT vs DT. Despite available treatment options, there remains a need for novel therapies that can improve outcomes in LA SCCHN.