Search Results - "González Manzano, Ramón"

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  1. 1

    RB1 and TP53 co-mutations correlate strongly with genomic biomarkers of response to immunity checkpoint inhibitors in urothelial bladder cancer by Manzano, Ramon Gonzalez, Catalan-Latorre, Ana, Brugarolas, Antonio

    Published in BMC cancer (20-04-2021)
    “…Muscle invasive urothelial bladder carcinoma (MIBC) present RB1 and TP53 somatic alterations in a variable percentage of tumors throughout all molecular…”
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    Journal Article
  2. 2

    Relevance of Fc Gamma Receptor Polymorphisms in Cancer Therapy With Monoclonal Antibodies by Mata-Molanes, Juan J., Rebollo-Liceaga, Joseba, Martínez-Navarro, Elena Mª, Manzano, Ramón González, Brugarolas, Antonio, Juan, Manel, Sureda, Manuel

    Published in Frontiers in oncology (24-06-2022)
    “…Therapeutic monoclonal antibodies (mAbs), including immune checkpoint inhibitors (ICIs), are an important breakthrough for the treatment of cancer and have…”
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  3. 3

    Immunological profile could be responsible of the unusual long-lasting cutaneous-only breast cancer recurrence: An observational study by Rebollo, Joseba, González-Manzano, Ramón, Sureda, Manuel, Martínez, Elena Ma, Monedero, Elena, Bretcha, Pedro, Brugarolas, Antonio

    Published in Journal of clinical oncology (01-06-2022)
    “…e13000 Background: A small number of breast cancer patients develops long-lasting loco-regional cutaneous recurrent disease with a delayed appearance of…”
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    Journal Article
  4. 4

    Transcriptome (RNA next generation sequencing) for personalizing of cancer treatment: A correlation with previous clinical resistance by Sureda, Manuel, Rebollo, Joseba, González-Manzano, Ramón, Martínez, Elena Ma, Rostagno, Roman, Mata, Juan José, Monedero, Elena, Ortega, Jose, Brugarolas, Antonio

    Published in Journal of clinical oncology (20-05-2021)
    “…Abstract only e15046 Background: RNA Next Generation Sequencing (transcriptome) is a potential useful tool to predict chemoresistance to available anticancer…”
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  5. 5

    DNA and RNA next generation sequencing for personalizing cancer treatment: A single-center experience by Rebollo, Joseba, Sureda, Manuel, González-Manzano, Ramón, Martínez, Elena Ma, Rostagno, Roman, Mata, Juan José, Monedero, Elena, Ortega, Jose, Brugarolas, Antonio

    Published in Journal of clinical oncology (20-05-2020)
    “…Abstract only e13509 Background: Personalized multidrug therapies improve outcomes in patients with drug resistant cancer. For 8 years we have been using…”
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  6. 6

    A Patient With Metastatic Sarcoma was Successfully Treated With Radiolabeled Somatostatin Analogs by Crespo-Jara, Aurora, González Manzano, Ramón, Lopera Sierra, Maribel, Redal Peña, María Carmen, Brugarolas Masllorens, Antonio

    Published in Clinical nuclear medicine (01-09-2016)
    “…ABSTRACTWe present a sarcoma patient with a tumor reduction of more than 50% in lung metastasis after 2 single courses of the investigational medical product…”
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  7. 7

    A novel genomic signature predicting FDG uptake in diverse metastatic tumors by Crespo-Jara, Aurora, Redal-Peña, Maria Carmen, Martinez-Navarro, Elena Maria, Sureda, Manuel, Fernandez-Morejon, Francisco Jose, Garcia-Cases, Francisco J., Manzano, Ramon Gonzalez, Brugarolas, Antonio

    Published in EJNMMI research (18-01-2018)
    “…Background Building a universal genomic signature predicting the intensity of FDG uptake in diverse metastatic tumors may allow us to understand better the…”
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    Abstract 2213: Influence of genetic polymorphism in UGT1A1, UGT1A7 and UGT1A9 on irinotecan, SN-38 and SN-38G pharmacokinetics by Valenzuela, Belen, González-Sales, Mario, Escudero, Vanessa, Navarro, Elena, Perez-Ruixo, Carlos, Rebollo, Joseba, González-Manzano, Ramon, Pérez-Ruixo, Juan José

    Published in Cancer research (Chicago, Ill.) (15-04-2013)
    “…Background and objective: SN-38 is the active metabolite of irinotecan (CPT-11) and mainly responsible of hematological and intestinal toxicity after CPT-11…”
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    Chemotherapy selection by gene expression profiling (MAGE) in resistant/refractory (R/R) patients with solid tumors: A feasibility study by Rebollo, Joseba, Gonzalez-Manzano, Ramon, Fernandez-Morejon, Francisco J., Rey, Severino, Farre, Jose, Sureda, Manuel, Brugarolas, Antonio

    Published in Journal of clinical oncology (20-05-2013)
    “…Abstract only e22120 Background: Genomic-based profiling of tumors is a promising approach that allows the selection of the optimal chemotherapy regimen…”
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  16. 16

    Abstract 4677: Irinotecan plus anthracycline - based combination chemotherapy in advanced solid tumors by Rebollo, Joseba, Sureda, Manuel, Gonzalez-Manzano, Ramon, Balenzuela, Belen, Brugarolas, Antonio

    Published in Cancer research (Chicago, Ill.) (15-04-2010)
    “…Irinotecan and Anthracyclines (Topoisomerase I and II inhibitors, respectively) are widely used as antitumoral agents in cancer treatment. However, no data…”
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  17. 17

    Phase II evaluation of doxorubicin, ifosfamide, and dacarbazine plus amphotericin B in the treatment of metastatic soft tissue sarcomas. A pilot study by González-Manzano, R, Vieitez, J M, Tangco, E, Fernandez de Alava, E, Herranz, P, Garcia-Foncillas, J

    Published in American journal of clinical oncology (01-08-1993)
    “…Amphotericin B enhances the cytotoxicity of certain antineoplastic agents in vitro and in vivo. A phase II study was designed to evaluate whether this effect…”
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  18. 18

    Modulation by acrolein and chloroacetaldehyde of multidrug resistance mediated by the multidrug resistance-associated protein (MRP) by GONZALEZ MANZANO, R, WRIGHT, K. A, TWENTYMAN, P. R

    Published in Clinical cancer research (01-08-1996)
    “…Acrolein (AC) and chloroacetaldehyde (CHA) are metabolites of the non-multidrug resistance cytotoxic drugs cyclophosphamide and ifosfamide. It has previously…”
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    Evolution of plasminogen-related growth factors (HGF/SF and HGF1/MSP) by Gherardi, E, Gonzalez Manzano, R, Cottage, A, Hawker, K, Aparicio, S

    Published in Ciba Foundation symposium (1997)
    “…HGF/SF and HGF1/MSP define a novel growth factor family whose members share the domain structure and the proteolytic process of activation of the blood…”
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