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  1. Article: An Emollient PLUS Balm Is Useful for the Management of Xerosis in Patients Treated for Cancer: A Real-World, Prospective, Observational, Multicenter Study.

    Vendrely, Véronique / Mayor-Ibarguren, Ander / Stennevin, Aline / Ortiz-Brugués, Ariadna

    Dermatology and therapy

    2022  Volume 12, Issue 3, Page(s) 683–699

    Abstract: ... chemotherapy, targeted therapy, radiotherapy, and hormonotherapy. We evaluated the effectiveness ... of their physician. The practitioner assessed xerosis severity and objective clinical signs, and the patients ... assessed subjective clinical signs and the impact of their skin condition on their quality of life ...

    Abstract Introduction: Xerosis is a common skin side effect of current anticancer therapies, including chemotherapy, targeted therapy, radiotherapy, and hormonotherapy. We evaluated the effectiveness of an emollient PLUS containing an Aquaphilus dolomiae extract (ADE-G1) for the management of xerosis in adult patients treated for cancer.
    Methods: This real-world, prospective, observational, multicenter study involved 319 xerotic cancer patients, who were prescribed the study product according to the usual practice of their physician. The practitioner assessed xerosis severity and objective clinical signs, and the patients assessed subjective clinical signs and the impact of their skin condition on their quality of life, at inclusion and after around 4 weeks of use. Overall effectiveness and tolerance were assessed at the end of the study. Clinical success was defined by the combination of several of these effectiveness outcomes.
    Results: Daily application of the emollient PLUS reduced xerosis severity in 62.7% of patients (p < 0.0001). The mean total severity scores for objective and subjective clinical signs were reduced by 67.7% and 57.4% (p < 0.0001), respectively, compared with baseline. The mean Dermatology Life Quality Index (DLQI) score also significantly improved at the end of follow-up (-56.6%, p < 0.0001). The product was rated as "effective" or "very effective" by the physician for over 80% of patients, regardless of the initial severity grade of xerosis. Overall clinical success was achieved in 73.7% of patients. A trend toward higher effectiveness and clinical success was observed in patients under hormonotherapy. The study product was well tolerated, regardless of the anticancer therapy being received.
    Conclusion: This study shows that the emollient PLUS containing ADE-G1 is an effective treatment for xerosis in cancer patients, regardless of the initial grade of xerosis and the anticancer treatment received.
    Language English
    Publishing date 2022-02-02
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2680284-3
    ISSN 2190-9172 ; 2193-8210
    ISSN (online) 2190-9172
    ISSN 2193-8210
    DOI 10.1007/s13555-022-00685-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: A Hypothesis for the Possible Role of Zinc in the Immunological Pathways Related to COVID-19 Infection.

    Mayor-Ibarguren, Ander / Busca-Arenzana, Carmen / Robles-Marhuenda, Ángel

    Frontiers in immunology

    2020  Volume 11, Page(s) 1736

    MeSH term(s) Adjuvants, Pharmaceutic ; Antimalarials/therapeutic use ; Betacoronavirus/enzymology ; Betacoronavirus/immunology ; COVID-19 ; Coronavirus Infections/drug therapy ; Coronavirus Infections/immunology ; Coronavirus Infections/mortality ; Coronavirus Infections/virology ; DNA-Directed RNA Polymerases/antagonists & inhibitors ; Dietary Supplements ; Drug Synergism ; Homeostasis/immunology ; Humans ; Interferon Type I/immunology ; Interleukin-6/genetics ; Interleukin-6/immunology ; Pandemics ; Pneumonia, Viral/drug therapy ; Pneumonia, Viral/immunology ; Pneumonia, Viral/mortality ; Pneumonia, Viral/virology ; Polymorphism, Genetic ; SARS-CoV-2 ; Virus Replication/drug effects ; Zinc/deficiency ; Zinc/immunology ; Zinc/pharmacology ; Zinc/therapeutic use
    Chemical Substances Adjuvants, Pharmaceutic ; Antimalarials ; IL6 protein, human ; Interferon Type I ; Interleukin-6 ; DNA-Directed RNA Polymerases (EC 2.7.7.6) ; Zinc (J41CSQ7QDS)
    Keywords covid19
    Language English
    Publishing date 2020-07-10
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2020.01736
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Ibrutinib-induced leg ulcer successfully treated with platelet-rich plasma.

    Quintana-Castanedo, Lucía / Mayor-Ibarguren, Ander / Tarín-Vicente, Eloy / Herranz-Pinto, Pedro

    Dermatologic therapy

    2021  Volume 34, Issue 2, Page(s) e14874

    MeSH term(s) Adenine/analogs & derivatives ; Humans ; Leg Ulcer/chemically induced ; Leg Ulcer/diagnosis ; Leg Ulcer/drug therapy ; Piperidines ; Platelet-Rich Plasma ; Pyrazoles/adverse effects ; Pyrimidines/adverse effects
    Chemical Substances Piperidines ; Pyrazoles ; Pyrimidines ; ibrutinib (1X70OSD4VX) ; Adenine (JAC85A2161)
    Language English
    Publishing date 2021-02-19
    Publishing country United States
    Document type Letter
    ZDB-ID 1354801-3
    ISSN 1529-8019 ; 1396-0296
    ISSN (online) 1529-8019
    ISSN 1396-0296
    DOI 10.1111/dth.14874
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Real-world Performance of a New Strategy for Off-Label Use of Guselkumab in Moderate to Severe Psoriasis: Super-Responder Patients as the Epitome of Efficacy and Optimisation.

    Herranz-Pinto, Pedro / Alonso-Pacheco, Maria Luisa / Feltes-Ochoa, Rosa / Mayor-Ibarguren, Ander / Servera-Negre, Guillermo / Busto-Leis, Jose Manuel / Gonzalez-Fernández, Maria Angeles / Herrero-Ambrosio, Alicia

    Clinical drug investigation

    2023  Volume 43, Issue 7, Page(s) 517–527

    Abstract: ... practice. The study also aimed to evaluate the drug's efficacy, safety, and survival, as well ... patients who started treatment with guselkumab between March 2019 and July 2021. Patients were followed up ... until April 2022, during which time their efficacy, safety, persistence, and use of guselkumab were recorded ...

    Abstract Background: Guselkumab is a drug used to treat moderate to severe plaque psoriasis. However, real-life clinical data on its off-label use are limited, especially regarding the optimal drug dosage regimen for different patient profiles.
    Objective: The main objective of this real-world, single-centre, retrospective study was to identify the off-label guselkumab dosing regimen used in clinical practice. The study also aimed to evaluate the drug's efficacy, safety, and survival, as well as the proportion of super-responders (SR) based on a newly proposed definition.
    Methods: The study included 69 patients who started treatment with guselkumab between March 2019 and July 2021. Patients were followed up until April 2022, during which time their efficacy, safety, persistence, and use of guselkumab were recorded. Patients were aged ≥  18 years and had moderate to severe plaque psoriasis.
    Results: The mean disease duration was 18.6 years, and 59% of patients had received at least one biologic treatment before guselkumab with a mean of 1.3 biologics per patient. The initial absolute Psoriasis Area and Severity Index (PASI) was 10.1 and decreased to 2.1 between Week 11-20 without significant changes in the PASI value throughout the 90 weeks of follow-up. The cumulative probability of drug survival was 93.5% at Week 52. No differences were found in terms of efficacy and survival associated with the off-label drug dosage regimens compared to the doses described in the Summary of Product Characteristics (SmPC). The greatest adjustments in the drug administration regimen were achieved in the subgroups of bio-naïve and SR patients, with a reduction in the number of administrations by 40% and 47% compared to the regimen described in the SmPC. Super-response to guselkumab was mainly associated with patients naïve to previous biologic treatment.
    Conclusion: The study demonstrated that off-label use of guselkumab was safe and effective in real-life clinical practice. The findings suggest that adjustments to the drug administration regimen may be necessary to optimise its use in different patient profiles, especially in SR and bio-naïve patients. Further studies are needed to confirm these findings.
    MeSH term(s) Humans ; Antibodies, Monoclonal ; Off-Label Use ; Retrospective Studies ; Treatment Outcome ; Severity of Illness Index ; Double-Blind Method ; Psoriasis/diagnosis ; Psoriasis/drug therapy
    Chemical Substances guselkumab (089658A12D) ; Antibodies, Monoclonal
    Language English
    Publishing date 2023-07-04
    Publishing country New Zealand
    Document type Journal Article
    ZDB-ID 1220136-4
    ISSN 1179-1918 ; 0114-2402 ; 1173-2563
    ISSN (online) 1179-1918
    ISSN 0114-2402 ; 1173-2563
    DOI 10.1007/s40261-023-01280-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: A Hypothesis for the Possible Role of Zinc in the Immunological Pathways Related to COVID-19 Infection

    Ander Mayor-Ibarguren / Carmen Busca-Arenzana / Ángel Robles-Marhuenda

    Frontiers in Immunology, Vol

    2020  Volume 11

    Keywords COVID-19 ; SARS-CoV-2 ; treatment ; zinc ; IL-6 ; Immunologic diseases. Allergy ; RC581-607 ; covid19
    Language English
    Publishing date 2020-07-01T00:00:00Z
    Publisher Frontiers Media S.A.
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article ; Online: A Hypothesis for the Possible Role of Zinc in the Immunological Pathways Related to COVID-19 Infection

    Mayor-Ibarguren, Ander / Busca-Arenzana, Carmen / Robles-Marhuenda, Ángel

    Frontiers in Immunology

    2020  Volume 11

    Keywords covid19
    Publisher Frontiers Media SA
    Publishing country ch
    Document type Article ; Online
    ZDB-ID 2606827-8
    ISSN 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2020.01736
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article: A Hypothesis for the Possible Role of Zinc in the Immunological Pathways Related to COVID-19 Infection

    Mayor-Ibarguren, Ander / Busca-Arenzana, Carmen / Robles-Marhuenda, Ángel

    Front Immunol

    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #689807
    Database COVID19

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  8. Article ; Online: Response of Darier Disease Following Treatment With Baricitinib.

    Busto Leis, José Manuel / Negre, Guillermo Servera / Mayor Ibarguren, Ander Paulo / Pinto, Pedro Herranz

    JAMA dermatology

    2022  Volume 158, Issue 6, Page(s) 699–701

    MeSH term(s) Azetidines/adverse effects ; Darier Disease/diagnosis ; Darier Disease/drug therapy ; Humans ; Purines/therapeutic use ; Pyrazoles/adverse effects ; Sulfonamides
    Chemical Substances Azetidines ; Purines ; Pyrazoles ; Sulfonamides ; baricitinib (ISP4442I3Y)
    Language English
    Publishing date 2022-04-27
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2701761-8
    ISSN 2168-6084 ; 2168-6068
    ISSN (online) 2168-6084
    ISSN 2168-6068
    DOI 10.1001/jamadermatol.2022.1021
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Apremilast for immune checkpoint inhibitor-induced psoriasis: A case series.

    Mayor Ibarguren, Ander / Enrique, Espinosa Arranz / Diana, Peiteado Lopez / Ana, Custodio / Pedro, Herranz Pinto

    JAAD case reports

    2021  Volume 11, Page(s) 84–89

    Language English
    Publishing date 2021-03-13
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2834220-3
    ISSN 2352-5126
    ISSN 2352-5126
    DOI 10.1016/j.jdcr.2021.03.015
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  10. Article ; Online: Identifying biomarkers of treatment response to ciclosporin in atopic dermatitis through multiomic predictive modelling: DERMATOMICS study protocol.

    Marín-Candón, Alicia / García-García, Irene / Arias, Pedro / Carcas, Antonio J / Díaz-García, Lucía / Feltes Ochoa, Rosa / Hernández Cano, Natalia / Herranz Pinto, Pedro / Jiménez González, María / López-Granados, Eduardo / Martínez-Feito, Ana / Mayor-Ibarguren, Ander / Rosas-Alonso, Rocío / Seco-Meseguer, Enrique / Borobia, Alberto M

    BMJ open

    2023  Volume 13, Issue 7, Page(s) e072350

    Abstract: ... the efficacy of treatments and reducing the toxicity associated with them. Although the efficacy of ciclosporine (CsA ... Methods and analysis: The study is a low-intervention phase 4 trial to optimise the treatment of patients ... that could allow for the selection of responders and non-responders to first-line treatment with CsA and to develop ...

    Abstract Introduction: There is a need to optimise the management of atopic dermatitis (AD), improving the efficacy of treatments and reducing the toxicity associated with them. Although the efficacy of ciclosporine (CsA) in the treatment of AD has been thoroughly documented in the literature, the optimal dose has not been yet established. The use of multiomic predictive models of treatment response could optimise CsA therapy in AD.
    Methods and analysis: The study is a low-intervention phase 4 trial to optimise the treatment of patients with moderate-severe AD requiring systemic treatment. The primary objectives are to identify biomarkers that could allow for the selection of responders and non-responders to first-line treatment with CsA and to develop a response prediction model to optimise the CsA dose and treatment regimen in responding patients based on these biomarkers. The study is divided into two cohorts: the first comprised of patients starting treatment with CsA (cohort 1), and the second, of patients already receiving or who have received CsA therapy (cohort 2).
    Ethics and dissemination: The study activities began following authorisation by the Spanish Regulatory Agency (AEMPS) and the Clinical Research Ethics Committee of La Paz University Hospital approval. Trial results will be submitted for publication in an open access peer-reviewed medical speciality-specific publication.Trial registration of this study can be located at the EU Clinical Trials Register, available from https://euclinicaltrials.eu/search-for-clinical-trials/?lang=en. Our clinical trial was registered in the website before the enrolment of the first patient complying with European regulations. EU Clinical Trials Register is a primary registry according the WHO. Once our trial was included in a primary and official registry, in order to extend the accessibility to our research, we also registered it retrospectively in clinicaltrials.gov; however, this is not mandatory as per our regulation.
    Trial registration number: NCT05692843.
    MeSH term(s) Humans ; Biomarkers ; Cyclosporine/therapeutic use ; Dermatitis, Atopic/drug therapy ; Multiomics ; Retrospective Studies ; Clinical Trials, Phase IV as Topic
    Chemical Substances Biomarkers ; Cyclosporine (83HN0GTJ6D)
    Language English
    Publishing date 2023-07-10
    Publishing country England
    Document type Clinical Trial Protocol ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2599832-8
    ISSN 2044-6055 ; 2044-6055
    ISSN (online) 2044-6055
    ISSN 2044-6055
    DOI 10.1136/bmjopen-2023-072350
    Database MEDical Literature Analysis and Retrieval System OnLINE

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