LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 3 of total 3

Search options

  1. Article ; Online: VOTRAGE study: Phase I dose-escalation study of pazopanib in unfit older patients.

    Mourey, Loïc / Le Louedec, Félicien / Ravaud, Alain / Paludetto, Marie-Noëlle / Digue, Laurence / Gomez-Roca, Carlos Alberto / Valentin, Thibaud / Balardy, Laurent / Olivier, Pascale / Cabarrou, Bastien / Filleron, Thomas / Chatelut, Etienne

    Journal of geriatric oncology

    2021  Volume 12, Issue 5, Page(s) 759–764

    Abstract: Background: Pazopanib is a tyrosine kinase inhibitor given at the approved dose of 800 mg orally once daily (OD), but often requiring individual dose adjustment due to toxicity. Limited data is available to guide prescription in older patients ... ...

    Abstract Background: Pazopanib is a tyrosine kinase inhibitor given at the approved dose of 800 mg orally once daily (OD), but often requiring individual dose adjustment due to toxicity. Limited data is available to guide prescription in older patients especially the unfit according to geriatric assessment.
    Patients and methods: VOTRAGE is a 3 + 3 dose-escalation, open-label phase I trial of continuous OD oral administration of pazopanib to evaluate safety, PK and PD data in unfit older patients with advanced solid tumors. The primary objective was to determine the maximum tolerated dose (MTD). PK data were compared with those obtained in younger adult patients in a population PK analysis.
    Results: Eighteen patients with a median age of 82.5 years (range 75-91) were included in three dosing cohorts (400, 600, and 800 mg daily). Three dose-limiting toxicities (DLT) were observed in five patients at 800 mg and one DLT at 600 mg in six evaluable patients. MTD was defined as level 2 dose (600 mg). Individual oral clearance was not correlated with age. A relationship was observed between the occurrence of DLT and pazopanib plasma exposure. Decreased oral bioavailability of pazopanib when given with proton-pump inhibitors was confirmed in this group of patients.
    Conclusion: We recommend performing geriatric assessment in patients older than 75 and starting pazopanib at 600 mg per day in unfit older patients. Therapeutic drug monitoring appears very helpful in this population.
    MeSH term(s) Aged ; Aged, 80 and over ; Antineoplastic Combined Chemotherapy Protocols ; Dose-Response Relationship, Drug ; Humans ; Indazoles ; Neoplasms/drug therapy ; Pyrimidines/adverse effects ; Sulfonamides/adverse effects ; Treatment Outcome
    Chemical Substances Indazoles ; Pyrimidines ; Sulfonamides ; pazopanib (7RN5DR86CK)
    Language English
    Publishing date 2021-03-11
    Publishing country Netherlands
    Document type Clinical Trial, Phase I ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2556813-9
    ISSN 1879-4076 ; 1879-4068
    ISSN (online) 1879-4076
    ISSN 1879-4068
    DOI 10.1016/j.jgo.2021.02.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Nivolumab and Relatlimab in Patients With Advanced Melanoma That Had Progressed on Anti-Programmed Death-1/Programmed Death Ligand 1 Therapy: Results From the Phase I/IIa RELATIVITY-020 Trial.

    Ascierto, Paolo Antonio / Lipson, Evan J / Dummer, Reinhard / Larkin, James / Long, Georgina V / Sanborn, Rachel E / Chiarion-Sileni, Vanna / Dréno, Brigitte / Dalle, Stéphane / Schadendorf, Dirk / Callahan, Margaret K / Nyakas, Marta / Atkinson, Victoria / Gomez-Roca, Carlos Alberto / Yamazaki, Naoya / Tawbi, Hussein A / Sarkis, Naomey / Warad, Deepti / Dolfi, Sonia /
    Mitra, Priyam / Suryawanshi, Satyendra / Grob, Jean-Jacques

    Journal of clinical oncology : official journal of the American Society of Clinical Oncology

    2023  Volume 41, Issue 15, Page(s) 2724–2735

    Abstract: Purpose: Nivolumab and relatlimab activity in advanced melanoma with prior progression on anti-programmed death-1/programmed death ligand 1 (PD-(L)1)-containing regimens is under investigation. RELATIVITY-047 demonstrated significantly improved ... ...

    Abstract Purpose: Nivolumab and relatlimab activity in advanced melanoma with prior progression on anti-programmed death-1/programmed death ligand 1 (PD-(L)1)-containing regimens is under investigation. RELATIVITY-047 demonstrated significantly improved progression-free survival (PFS) for nivolumab and relatlimab over nivolumab in previously untreated advanced melanoma.
    Methods: The phase I/IIa, open-label RELATIVITY-020 trial part D assessed efficacy and safety of nivolumab and relatlimab in advanced melanoma with progression during, or within 3 months of, 1 (D1) or ≥ 1 (D2) anti-PD-(L)1-containing regimens. Safety was a primary end point. Objective response rate (coprimary end point) and PFS by blinded independent central review (BICR) were assessed.
    Results: Five hundred eighteen patients (D1 = 354; D2 = 164) received nivolumab and relatlimab. Among evaluable patients, the objective response rate by BICR was 12.0% (95% CI, 8.8 to 15.8) in D1 (n = 351) and 9.2% (95% CI, 5.2 to 14.7) in D2 (n = 163). Responses appeared to be enriched among patients with tumors expressing programmed death ligand 1 or lymphocyte activation gene 3; however, responses were observed regardless of programmed death ligand 1 and lymphocyte activation gene 3 expression (1%). The median duration of response was not reached (95% CI, 12.9 to not reached) in D1 and 12.8 months (95% CI, 6.9 to 12.9) in D2. The median PFS by BICR was 2.1 months (95% CI, 1.9 to 3.5) in D1 and 3.2 months (95% CI, 1.9 to 3.6) in D2; the 6-month PFS rate was 29.1% (95% CI, 24.2 to 34.1) and 27.7% (95% CI, 20.5 to 35.4), respectively. The grade 3-4 treatment-related adverse event incidence was 15.0% in D1 and 12.8% in D2. One case of grade 3 myocarditis and no treatment-related deaths occurred across part D.
    Conclusion: Nivolumab and relatlimab had a manageable safety profile and demonstrated durable clinical activity in a proportion of patients with heavily pretreated advanced melanoma with prior progression on anti-PD-(L)1-containing regimens.
    [Media: see text].
    MeSH term(s) Humans ; Nivolumab/adverse effects ; Melanoma ; Antibodies, Monoclonal, Humanized/therapeutic use ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use
    Chemical Substances Nivolumab (31YO63LBSN) ; relatlimab ; CD274 protein, human ; Antibodies, Monoclonal, Humanized
    Language English
    Publishing date 2023-02-13
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 604914-x
    ISSN 1527-7755 ; 0732-183X
    ISSN (online) 1527-7755
    ISSN 0732-183X
    DOI 10.1200/JCO.22.02072
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: The ATR inhibitor ceralasertib potentiates cancer checkpoint immunotherapy by regulating the tumor microenvironment.

    Hardaker, Elizabeth L / Sanseviero, Emilio / Karmokar, Ankur / Taylor, Devon / Milo, Marta / Michaloglou, Chrysis / Hughes, Adina / Mai, Mimi / King, Matthew / Solanki, Anisha / Magiera, Lukasz / Miragaia, Ricardo / Kar, Gozde / Standifer, Nathan / Surace, Michael / Gill, Shaan / Peter, Alison / Talbot, Sara / Tohumeken, Sehmus /
    Fryer, Henderson / Mostafa, Ali / Mulgrew, Kathy / Lam, Carolyn / Hoffmann, Scott / Sutton, Daniel / Carnevalli, Larissa / Calero-Nieto, Fernando J / Jones, Gemma N / Pierce, Andrew J / Wilson, Zena / Campbell, David / Nyoni, Lynet / Martins, Carla P / Baker, Tamara / Serrano de Almeida, Gilberto / Ramlaoui, Zainab / Bidar, Abdel / Phillips, Benjamin / Boland, Joseph / Iyer, Sonia / Barrett, J Carl / Loembé, Arsene-Bienvenu / Fuchs, Serge Y / Duvvuri, Umamaheswar / Lou, Pei-Jen / Nance, Melonie A / Gomez Roca, Carlos Alberto / Cadogan, Elaine / Critichlow, Susan E / Fawell, Steven / Cobbold, Mark / Dean, Emma / Valge-Archer, Viia / Lau, Alan / Gabrilovich, Dmitry I / Barry, Simon T

    Nature communications

    2024  Volume 15, Issue 1, Page(s) 1700

    Abstract: The Ataxia telangiectasia and Rad3-related (ATR) inhibitor ceralasertib in combination with the PD-L1 antibody durvalumab demonstrated encouraging clinical benefit in melanoma and lung cancer patients who progressed on immunotherapy. Here we show that ... ...

    Abstract The Ataxia telangiectasia and Rad3-related (ATR) inhibitor ceralasertib in combination with the PD-L1 antibody durvalumab demonstrated encouraging clinical benefit in melanoma and lung cancer patients who progressed on immunotherapy. Here we show that modelling of intermittent ceralasertib treatment in mouse tumor models reveals CD8
    MeSH term(s) Humans ; Animals ; Mice ; CD8-Positive T-Lymphocytes ; B7-H1 Antigen ; Tumor Microenvironment ; Cell Line, Tumor ; Immunotherapy ; Disease Models, Animal ; Neoplasms ; Ataxia Telangiectasia Mutated Proteins ; Indoles ; Morpholines ; Pyrimidines ; Sulfonamides
    Chemical Substances ceralasertib (85RE35306Z) ; B7-H1 Antigen ; ATR protein, human (EC 2.7.11.1) ; Ataxia Telangiectasia Mutated Proteins (EC 2.7.11.1) ; Indoles ; Morpholines ; Pyrimidines ; Sulfonamides
    Language English
    Publishing date 2024-02-24
    Publishing country England
    Document type Journal Article
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-024-45996-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top