Torisel (temsirolimus) / Pfizer 
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 366 Diseases   40 Trials   40 Trials   1659 News 


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  • ||||||||||  perifosine (D21266) / AEterna Zentaris, Torisel (temsirolimus) / Pfizer
    Trial completion, Trial completion date:  Temsirolimus and Perifosine in Treating Patients With Recurrent or Progressive Malignant Glioma (clinicaltrials.gov) -  Jul 19, 2021   
    P1/2,  N=36, Completed, 
    The combination demonstrated promising evidence of disease control in this highly refractory population and could be considered for testing in disease-specific phase II trials. Terminated --> Completed | Trial completion date: Oct 2015 --> Sep 2020
  • ||||||||||  Torisel (temsirolimus) / Pfizer
    Clinical, P1 data, Journal:  A phase I trial of temsirolimus and erlotinib in patients with refractory solid tumors. (Pubmed Central) -  Jun 24, 2021   
    P1
    Furthermore, the ARCC risk model performed better than the other risk models in predicting survival. The combination of temsirolimus and erlotinib at the RP2D was well tolerated, and the regimen resulted in prolonged disease stabilization in selected patients (NCT00770263).
  • ||||||||||  sirolimus / Generic mfg.
    [VIRTUAL] Evidence for a nucleolar involvement in the effect of mTOR inhibitors on cell viability () -  May 30, 2021 - Abstract #EACR2021EACR_2023;    
    Conclusion These results indicate that mTORC2 inhibition must be considered therapeutically, in agreement with the ongoing effort to translate those drugs into clinical practice. Importantly, these results agree with the notion that inhibition of nucleolar function is therapeutically useful and that the mTOR pathways offer possible targets to achieve such inhibition.
  • ||||||||||  sirolimus / Generic mfg.
    [VIRTUAL] Evidence for a nucleolar involvement in the effect of mTOR inhibitors on cell viability () -  May 30, 2021 - Abstract #EACR2021EACR_2022;    
    Conclusion These results indicate that mTORC2 inhibition must be considered therapeutically, in agreement with the ongoing effort to translate those drugs into clinical practice. Importantly, these results agree with the notion that inhibition of nucleolar function is therapeutically useful and that the mTOR pathways offer possible targets to achieve such inhibition.
  • ||||||||||  sirolimus / Generic mfg.
    [VIRTUAL] Evidence for a nucleolar involvement in the effect of mTOR inhibitors on cell viability () -  May 30, 2021 - Abstract #EACR2021EACR_2021;    
    Conclusion These results indicate that mTORC2 inhibition must be considered therapeutically, in agreement with the ongoing effort to translate those drugs into clinical practice. Importantly, these results agree with the notion that inhibition of nucleolar function is therapeutically useful and that the mTOR pathways offer possible targets to achieve such inhibition.
  • ||||||||||  sirolimus / Generic mfg.
    [VIRTUAL] Evidence for a nucleolar involvement in the effect of mTOR inhibitors on cell viability () -  May 30, 2021 - Abstract #EACR2021EACR_2020;    
    Conclusion These results indicate that mTORC2 inhibition must be considered therapeutically, in agreement with the ongoing effort to translate those drugs into clinical practice. Importantly, these results agree with the notion that inhibition of nucleolar function is therapeutically useful and that the mTOR pathways offer possible targets to achieve such inhibition.
  • ||||||||||  Cabometyx (cabozantinib tablet) / Takeda, Exelixis, Ipsen
    [VIRTUAL] B7 immune checkpoint proteins as mediators of resistance to targeted therapy in renal cancer cells () -  May 30, 2021 - Abstract #EACR2021EACR_1651;    
    Material and Methods In this study, we have analyzed the global expression of B7-family members (including PD-L1, PD-L2, B7-H2, B7-H3, B7-H4, B7-H5, B7-H6 and B7-H7) in renal cancer cells upon treatment with clinically relevant targeted therapies, including VEGF inhibitors (Axitinib, Cabozantinib, and Lenvatinib) and mTOR inhibitors (Everolimus and Temsirolimus)...Cell functional assays revealed the potential of specific B7 proteins to mediate intrinsic resistance to targeted therapy in renal cancer cells. Conclusion Our findings highlight novel B7 proteins as actionable immune checkpoint proteins in advanced and metastatic renal cancer cases resistant to current treatments.
  • ||||||||||  Cabometyx (cabozantinib tablet) / Takeda, Exelixis, Ipsen
    [VIRTUAL] B7 immune checkpoint proteins as mediators of resistance to targeted therapy in renal cancer cells () -  May 30, 2021 - Abstract #EACR2021EACR_1650;    
    Material and Methods In this study, we have analyzed the global expression of B7-family members (including PD-L1, PD-L2, B7-H2, B7-H3, B7-H4, B7-H5, B7-H6 and B7-H7) in renal cancer cells upon treatment with clinically relevant targeted therapies, including VEGF inhibitors (Axitinib, Cabozantinib, and Lenvatinib) and mTOR inhibitors (Everolimus and Temsirolimus)...Cell functional assays revealed the potential of specific B7 proteins to mediate intrinsic resistance to targeted therapy in renal cancer cells. Conclusion Our findings highlight novel B7 proteins as actionable immune checkpoint proteins in advanced and metastatic renal cancer cases resistant to current treatments.
  • ||||||||||  Cabometyx (cabozantinib tablet) / Takeda, Exelixis, Ipsen
    [VIRTUAL] B7 immune checkpoint proteins as mediators of resistance to targeted therapy in renal cancer cells () -  May 30, 2021 - Abstract #EACR2021EACR_1649;    
    Material and Methods In this study, we have analyzed the global expression of B7-family members (including PD-L1, PD-L2, B7-H2, B7-H3, B7-H4, B7-H5, B7-H6 and B7-H7) in renal cancer cells upon treatment with clinically relevant targeted therapies, including VEGF inhibitors (Axitinib, Cabozantinib, and Lenvatinib) and mTOR inhibitors (Everolimus and Temsirolimus)...Cell functional assays revealed the potential of specific B7 proteins to mediate intrinsic resistance to targeted therapy in renal cancer cells. Conclusion Our findings highlight novel B7 proteins as actionable immune checkpoint proteins in advanced and metastatic renal cancer cases resistant to current treatments.
  • ||||||||||  Cabometyx (cabozantinib tablet) / Takeda, Exelixis, Ipsen
    [VIRTUAL] B7 immune checkpoint proteins as mediators of resistance to targeted therapy in renal cancer cells () -  May 30, 2021 - Abstract #EACR2021EACR_1648;    
    Material and Methods In this study, we have analyzed the global expression of B7-family members (including PD-L1, PD-L2, B7-H2, B7-H3, B7-H4, B7-H5, B7-H6 and B7-H7) in renal cancer cells upon treatment with clinically relevant targeted therapies, including VEGF inhibitors (Axitinib, Cabozantinib, and Lenvatinib) and mTOR inhibitors (Everolimus and Temsirolimus)...Cell functional assays revealed the potential of specific B7 proteins to mediate intrinsic resistance to targeted therapy in renal cancer cells. Conclusion Our findings highlight novel B7 proteins as actionable immune checkpoint proteins in advanced and metastatic renal cancer cases resistant to current treatments.
  • ||||||||||  Revlimid (lenalidomide) / BMS
    [VIRTUAL] High-risk Mantle Cell Lymphoma in the LyMa Trial: a LYSA Study. () -  May 22, 2021 - Abstract #ICML2021ICML_376;    
    Known risk factors do not perfectly identify high-risk MCL patients at baseline. High-risk patients with early disease progression had an extremely dismal prognosis and should receive innovative strategies combined with systematic CNS prophylaxis as salvage therapy.
  • ||||||||||  Avastin (bevacizumab) / Roche, Opdivo (nivolumab) / Ono Pharma, BMS, Cabometyx (cabozantinib tablet) / Takeda, Exelixis, Ipsen
    Journal:  Interdisciplinary recommendations for the treatment of advanced metastatic renal cell carcinoma (Pubmed Central) -  May 15, 2021   
    The use of both the combination of nivolumab + ipilimumab and cabozantinib is restricted to intermediate and high-risk patients...Temsirolimus is only approved for high-risk patients.Sunitinib and pazopanib can also be applied as second-line options - for pazopanib the use is restricted to the event of cytokine failure...Furthermore, the combination of lenvatinib + everolimus and axitinib are approved treatment options in the second-line and further settings...As in previous years, the experts intended to provide recommendations for clinical practice. The results are presented in this publication.
  • ||||||||||  Revlimid (lenalidomide) / BMS
    [VIRTUAL] HIGH-RISK MANTLE CELL LYMPHOMA IN THE LYMA TRIAL: A LYSA STUDY. () -  May 13, 2021 - Abstract #EHA2021EHA_1439;    
    P3
    Salvage therapies consisted of chemotherapy in 26 patients (CHOP, MTX-AraC, bendamustine, VR-CAP), rituximab in 26, temsirolimus in five, lenalidomide and combination of ibrutinib and lenalidomide in two other patients, as second line therapy...Conclusion Known risk factors do not perfectly identify high-risk MCL patients at baseline. High-risk patients with early disease progression had an extremely dismal prognosis and should receive innovative strategies combined with systematic CNS prophylaxis as salvage therapy.
  • ||||||||||  Torisel (temsirolimus) / Pfizer, Sutent (sunitinib) / Pfizer
    Trial completion date, Trial primary completion date, Metastases:  Phase II Study of Alternating Sunitinib and Temsirolimus (clinicaltrials.gov) -  Apr 29, 2021   
    P2,  N=37, Active, not recruiting, 
    The progression free and overall survival rates of patients were similar to literature . Trial completion date: Jun 2021 --> Dec 2021 | Trial primary completion date: Feb 2021 --> Dec 2021
  • ||||||||||  cisplatin / Generic mfg., sirolimus / Generic mfg.
    Journal, Cancer stem cells:  mTOR Inhibition Ablates Cisplatin-Resistant Salivary Gland Cancer Stem Cells. (Pubmed Central) -  Apr 24, 2021   
    Viability assays determined the effect of several inhibitors of PI3k/mTOR signaling (e.g., temsirolimus, BKM120, AZD8055, PF4708671) and/or cisplatin on survival of human MEC cells...Remarkably, temsirolimus slowed down tumor growth and decreased the fraction of CSCs (P < 0.05) even in presence of cisplatin in a short-term in vivo experiment. Collectively, these results demonstrate that therapeutic inhibition of mTOR ablates cytotoxic-resistant CSCs, and they suggest that a combination of an mTOR inhibitor and platinum-based chemotherapy might be beneficial to patients with salivary gland mucoepidermoid carcinoma.
  • ||||||||||  Recentin (cediranib) / AstraZeneca, Torisel (temsirolimus) / Pfizer
    Trial completion, Enrollment change, Trial completion date, Metastases:  AZD2171 and Temsirolimus in Patients With Advanced Gynecological Malignancies (clinicaltrials.gov) -  Apr 21, 2021   
    P1,  N=11, Completed, 
    Collectively, these results demonstrate that therapeutic inhibition of mTOR ablates cytotoxic-resistant CSCs, and they suggest that a combination of an mTOR inhibitor and platinum-based chemotherapy might be beneficial to patients with salivary gland mucoepidermoid carcinoma. Active, not recruiting --> Completed | N=50 --> 11 | Trial completion date: Apr 2020 --> Mar 2021
  • ||||||||||  perifosine (D21266) / AEterna Zentaris, Torisel (temsirolimus) / Pfizer
    Clinical, P1 data, Journal:  Phase I clinical trial of temsirolimus and perifosine for recurrent glioblastoma. (Pubmed Central) -  Apr 20, 2021   
    Active, not recruiting --> Completed | N=50 --> 11 | Trial completion date: Apr 2020 --> Mar 2021 Combining the mTOR inhibitor temsirolimus dosed at 115 mg weekly and the AKT inhibitor perifosine dosed at 100 mg daily (following 600 mg load) is tolerable in heavily pretreated adults with recurrent MGs.
  • ||||||||||  Avastin (bevacizumab) / Roche, Erbitux (cetuximab) / Eli Lilly, EMD Serono
    [VIRTUAL] Falcon-X 3D in vitro tumor model platform for screening patient-derived NSCLC, CRC, and RCC tumors with targeted therapy and immunotherapy () -  Mar 13, 2021 - Abstract #AACR2021AACR_4204;    
    For CRC PDX tumors, Oxaliplatin, Cetuximab, 5-FU, Bevacizumab (anti-VEGF), and Pembrolizumab (anti-PD1) were assayed; for RCC: Sunitinib, Pazopanib, Temsirolimus, Bevacizumab, and Pembrolizumab; for NSCLC: Docetaxel, Cisplatin, Afatinib, Atezolizumab (anti-PDL1), and Pembrolizumab...Such a platform is potentially suitable for cancer drug discovery and clinical decision making for screening cancer therapeutic efficacy. Further studies include identifying cytokines that modulate the immune response to fibroblast co-culture, expanding the approach to other solid tumor types such as breast, brain, sarcoma, and melanoma, as well as screening novel immunotherapy agents.
  • ||||||||||  Torisel (temsirolimus) / Pfizer
    [VIRTUAL] mTOR inhibitor induces non-apoptotic, autophagy dependent cell death (ADCD) in TP53 mutant HNSCC () -  Mar 11, 2021 - Abstract #AACR2021AACR_2878;    
    We investigated the mechanism by which the mTOR inhibitor CCI-779 inhibits cell growth of TP53 mutant HNSCC in vitro...This is a novel mechanism of how rapalogues induce ADCD through the stabilization/ activation of ULK1 in HPV-negative TP53 mutant HNSCC cells. Together these data highlight the importance of how mTORi can be used to accelerate tumor cell death in HPV-negative TP53 mutant HNSCC.