Search Results - "Balmañà, J."

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    Risk reduction and screening of cancer in hereditary breast-ovarian cancer syndromes: ESMO Clinical Practice Guideline by Sessa, C., Balmaña, J., Bober, S.L., Cardoso, M.J., Colombo, N., Curigliano, G., Domchek, S.M., Evans, D.G., Fischerova, D., Harbeck, N., Kuhl, C., Lemley, B., Levy-Lahad, E., Lambertini, M., Ledermann, J.A., Loibl, S., Phillips, K.-A., Paluch-Shimon, S.

    Published in Annals of oncology (01-01-2023)
    “…•It provides recommendations for risk reduction and screening in hereditary breast and ovarian cancer syndrome.•It focuses on risk reduction and screening…”
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    Phase I trial of olaparib in combination with cisplatin for the treatment of patients with advanced breast, ovarian and other solid tumors by Balmaña, J., Tung, N.M., Isakoff, S.J., Graña, B., Ryan, P.D., Saura, C., Lowe, E.S., Frewer, P., Winer, E., Baselga, J., Garber, J.E.

    Published in Annals of oncology (01-08-2014)
    “…To establish the maximum tolerated dose, determine safety/tolerability and evaluate the pharmacokinetics and preliminary efficacy of olaparib in combination…”
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    A decade of clinical development of PARP inhibitors in perspective by Mateo, J., Lord, C.J., Serra, V., Tutt, A., Balmaña, J., Castroviejo-Bermejo, M., Cruz, C., Oaknin, A., Kaye, S.B., de Bono, J.S.

    Published in Annals of oncology (01-09-2019)
    “…Genomic instability is a hallmark of cancer, and often is the result of altered DNA repair capacities in tumour cells. DNA damage repair defects are common in…”
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    Olaparib monotherapy as primary treatment in unselected triple negative breast cancer by Eikesdal, H.P., Yndestad, S., Elzawahry, A., Llop-Guevara, A., Gilje, B., Blix, E.S., Espelid, H., Lundgren, S., Geisler, J., Vagstad, G., Venizelos, A., Minsaas, L., Leirvaag, B., Gudlaugsson, E.G., Vintermyr, O.K., Aase, H.S., Aas, T., Balmaña, J., Serra, V., Janssen, E.A.M., Knappskog, S., Lønning, P.E.

    Published in Annals of oncology (01-02-2021)
    “…The antitumor efficacy of PARP inhibitors (PARPi) for breast cancer patients harboring germline BRCA1/2 (gBRCA1/2) mutations is well established. While PARPi…”
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    SEOM clinical guidelines in hereditary breast and ovarian cancer (2019) by González-Santiago, S., Ramón y Cajal, T., Aguirre, E., Alés-Martínez, J. E., Andrés, R., Balmaña, J., Graña, B., Herrero, A., Llort, G., González-del-Alba, A.

    Published in Clinical & translational oncology (01-02-2020)
    “…Mutations in BRCA1 and BRCA2 high penetrance genes account for most hereditary breast and ovarian cancer, although other new high-moderate penetrance genes…”
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    A narrative overview of the patients’ outcomes after multigene cancer panel testing, and a thorough evaluation of its implications for genetic counselling by Esteban, I., Lopez-Fernandez, A., Balmaña, J.

    Published in European journal of medical genetics (01-05-2019)
    “…Massively parallel sequencing is being implemented in clinical practice through the use of multigene panel testing, whole exome sequencing and whole genome…”
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    SEOM clinical guidelines in Hereditary Breast and ovarian cancer by Llort, G., Chirivella, I., Morales, R., Serrano, R., Sanchez, A. Beatriz, Teulé, A., Lastra, E., Brunet, J., Balmaña, J., Graña, B.

    Published in Clinical & translational oncology (01-12-2015)
    “…Approximately, 7 % of all breast cancers (BC) and 11–15 % of ovarian cancers (OC) are associated with inherited predisposition, mainly related to germline…”
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    Post-hematopoietic stem cell transplant squamous cell carcinoma in patients with Fanconi anemia: a dreadful enemy by Murillo-Sanjuán, L., Balmaña, J., de Pablo García-Cuenca, A., Lorente Guerrero, J., Uria Oficialdegui, M. L., Carrasco, E., Diaz-de-Heredia, C.

    Published in Clinical & translational oncology (01-02-2022)
    “…Introduction Hematopoietic stem cell transplantation (HSCT) is a curative option for patients with Fanconi anemia (FA) and hematological manifestations but it…”
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