Symptomatic and functional outcomes after treatment with paliperidone palmitate 3-month formulation for 52 weeks in patients with clinically stable schizophrenia

被引:26
作者
Garcia-Portilla, Maria Paz [2 ]
Llorca, Pierre-Michel [3 ]
Maina, Giuseppe [4 ]
Bozikas, Vasilis P. [5 ]
Devrimci-Ozguven, Halise [6 ]
Kim, Sung-Wan [7 ]
Bergmans, Paul [8 ]
Usankova, Irina [9 ]
Pungor, Katalin [1 ]
机构
[1] Janssen Cilag GmbH, EMEA Med Affairs, Johnson & Johnson Pl 1, D-41470 Neuss, Germany
[2] Univ Oviedo, CIBERSAM, Dept Psychiat, Oviedo, Spain
[3] Clermont Auvergne Univ, CHU Clermont Ferrand, CMP B, Clermont Ferrand, France
[4] Univ Torino, AOU San Luigi Gonzaga, SCDU Psichiatria, Turin, Piemonte, Italy
[5] Aristotle Univ Thessaloniki, Sch Med, Dept Psychiat 2, Thessaloniki, Greece
[6] Ankara Univ, Sch Med, Dept Psychiat, Ankara, Turkey
[7] Chonnam Natl Univ, Med Sch, Dept Psychiat, Gwangju, South Korea
[8] Janssen Cilag, Biostat, Breda, Netherlands
[9] Johnson & Johnson, EMEA Med Affairs Org, Moscow, Russia
关键词
functional remission; paliperidone palmitate 3-monthly formulation; paliperidone palmitate 1-monthly formulation; schizophrenia; symptomatic remission; QUALITY-OF-LIFE; ANTIPSYCHOTIC MEDICATION; MAINTENANCE TREATMENT; NATIONWIDE COHORT; NEGATIVE SYNDROME; REMISSION; RISPERIDONE; CARE; DISCONTINUATION; PREDICTORS;
D O I
10.1177/2045125320926347
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Paliperidone palmitate 3-monthly (PP3M) formulation is a long-acting, injectable antipsychotic treatment approved in many countries worldwide for the maintenance treatment of adult patients with schizophrenia. This single-arm, open-label, phase IIIb study evaluated the efficacy and safety of converting patients with schizophrenia stabilized with paliperidone palmitate 1-month (PP1M) to PP3M in a naturalistic clinical setting. Methods: After screening (days -7 to 1), patients were converted from PP1M (50-150 mg eq.) to PP3M (175-525 mg eq.), and entered a 52-week, flexible-dose PP3M treatment period. The primary efficacy endpoint was symptomatic remission (SR) (Andreasen criteria) at last observation carried forward (LOCF) endpoint. Results: Patients (n = 305) received PP3M, of whom 291 (95.4%) completed the study. Doses of PP3M remained stable during the 12-month treatment period, and changes in dose were uncommon. Overall, 56.8% of patients [95% confidence interval (CI): 51.0, 62.4] achieved SR, and 31.8% achieved both symptomatic and functional remission (Personal and Social Performance scale total score > 70) at LOCF endpoint. Secondary endpoint results were generally consistent with primary endpoint results. There were improvements in Positive and Negative Syndrome Scale total, subscale and Marder factor scores, and also Clinical Global Impression-Severity and -Change scores from baseline to LOCF endpoint. Carer burden was reduced, and the proportion of patients requiring hospitalization for psychiatric reasons decreased from 13.5% in the 12 months prior to baseline to 4.6% during the treatment period. No new safety signals were identified. Conclusion: Results from this naturalistic study were similar to those observed in previous randomized clinical trials of PP3M and underline the importance of continuous maintenance treatment in patients with schizophrenia.
引用
收藏
页数:20
相关论文
共 41 条
  • [1] Remission in Schizophrenia: Critical and Systematic Review
    AlAqeel, Bandar
    Margolese, Howard C.
    [J]. HARVARD REVIEW OF PSYCHIATRY, 2012, 20 (06) : 281 - 297
  • [2] Treatment response in psychotic patients classified according to social and clinical needs, drug side effects, and previous treatment; a method to identify functional remission
    Alenius, Malin
    Hammarlund-Udenaes, Margareta
    Hartvig, Per
    Sundquist, Staffan
    Lindstrom, Leif
    [J]. COMPREHENSIVE PSYCHIATRY, 2009, 50 (05) : 453 - 462
  • [3] Remission in schizophrenia: Proposed criteria and rationale for consensus
    Andreasen, NC
    Carpenter, WT
    Kane, JM
    Lasser, RA
    Marder, SR
    Weinberger, DR
    [J]. AMERICAN JOURNAL OF PSYCHIATRY, 2005, 162 (03) : 441 - 449
  • [4] Arango C, REV PSIQUIATR SALUD, DOI [10.1016/j.rpsm.2018.03.006., DOI 10.1016/J.RPSM.2018.03.006.]
  • [5] A prospective study of risk factors for nonadherence with antipsychotic medication in the treatment of schizophrenia
    Ascher-Svanum, Haya
    Zhu, Baojin
    Faries, Douglas
    Lacro, Jonathan P.
    Dolder, Christian R.
    [J]. JOURNAL OF CLINICAL PSYCHIATRY, 2006, 67 (07) : 1114 - 1123
  • [6] Bera Rimal, 2013, J Med Econ, V16, P522, DOI 10.3111/13696998.2013.771641
  • [7] Efficacy and Safety of the 3-Month Formulation of Paliperidone Palmitate vs Placebo for Relapse Prevention of Schizophrenia A Randomized Clinical Trial
    Berwaerts, Joris
    Liu, Yanning
    Gopal, Srihari
    Nuamah, Isaac
    Xu, Haiyan
    Savitz, Adam
    Coppola, Danielle
    Schotte, Alain
    Remmerie, Bart
    Maruta, Nataliya
    Hough, David W.
    [J]. JAMA PSYCHIATRY, 2015, 72 (08) : 830 - 839
  • [8] A review of compliance, depot intramuscular antipsychotics and the new long-acting injectable atypical antipsychotic risperidone in schizophrenia
    Bhanji, NH
    Chouinard, G
    Margolese, HC
    [J]. EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2004, 14 (02) : 87 - 92
  • [9] Compliance, persistence, costs and quality of life in young patients treated with antipsychotic drugs: results from the COMETA study
    Cortesi, Paolo A.
    Mencacci, Claudio
    Luigi, Ferrannini
    Pirfo, Elvezio
    Berto, Patrizia
    Sturkenboom, Miriam C. J. M.
    Lopes, Fabiana L.
    Giustra, Maria G.
    Mantovani, Lorenzo G.
    Scalone, Luciana
    [J]. BMC PSYCHIATRY, 2013, 13
  • [10] Targets, attitudes, and goals of psychiatrists treating patients with schizophrenia: key outcome drivers, role of quality of life, and place of long-acting antipsychotics
    de Bartolomeis, Andrea
    Fagiolini, Andrea
    Vaggi, Marco
    Vampini, Claudio
    [J]. NEUROPSYCHIATRIC DISEASE AND TREATMENT, 2016, 12 : 99 - 108