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  1. Article: Hepatobiliary Adverse Reactions during Treatment with Cladribine: Analysis of Data from the European Spontaneous Reporting System.

    Velișcu, Elena Mirabela / Liguori, Valerio / Anatriello, Antonietta / Maniscalco, Giorgia Teresa / Cantone, Andrea / Di Costanzo, Luigi / Stefanelli, Pasquale / Scavone, Cristina / Capuano, Annalisa

    Pharmaceuticals (Basel, Switzerland)

    2023  Volume 16, Issue 8

    Abstract: Background: Cladribine belongs to the group of disease-modifying therapies (DMTs) used to treat multiple sclerosis (MS). According to the highlights of a meeting held by the Pharmacovigilance Risk Assessment Committee (PRAC) on 14 January 2022, ... ...

    Abstract Background: Cladribine belongs to the group of disease-modifying therapies (DMTs) used to treat multiple sclerosis (MS). According to the highlights of a meeting held by the Pharmacovigilance Risk Assessment Committee (PRAC) on 14 January 2022, cladribine may be associated with the occurrence of liver injury, and thus liver function monitoring is recommended.
    Objectives and methods: Using data from the European spontaneous reporting database (EudraVigilance-EV), we aimed to describe the main characteristics of Individual Case Safety Reports (ICSRs) reporting cases of hepatobiliary disorders related to cladribine. The reporting odds ratio (ROR) was calculated to provide the probability of reporting hepatobiliary ICSRs among DMTs used to treat MS.
    Results: Overall, 118 ICSRs described the occurrence of cladribine-induced hepatobiliary ADRs. The majority of the ICSRs reported ADRs that were classified as serious (93%), and the outcome was mostly reported as "unknown" (50.8%). The most reported hepatobiliary disorders were drug-induced liver injury, abnormal hepatic function, ALT increases, liver disorders, hepatic failure, jaundice, lymphocyte count decreases, hepatotoxicity and hypertransaminasemia. The majority of cladribine-induced hepatic ADRs occurred in female patients belonging to the age group of 18-65 years.
    Conclusion: Considering the seriousness of cladribine-induced hepatic ADRs, a close monitoring of patients receiving this drug is highly recommended. In this context, further pharmacovigilance studies evaluating the hepatic safety profile of cladribine are strongly needed.
    Language English
    Publishing date 2023-07-27
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2193542-7
    ISSN 1424-8247
    ISSN 1424-8247
    DOI 10.3390/ph16081071
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Immune-related adverse events and immune checkpoint inhibitors: a focus on neurotoxicity and clinical management.

    Ruggiero, Rosanna / Di Napoli, Raffaella / Balzano, Nunzia / Ruggiero, Donatella / Riccardi, Consiglia / Anatriello, Antonietta / Cantone, Andrea / Sportiello, Liberata / Rossi, Francesco / Capuano, Annalisa

    Expert review of clinical pharmacology

    2023  Volume 16, Issue 5, Page(s) 423–434

    Abstract: Introduction: Immune checkpoint inhibitors (ICIs) represent an innovative therapeutic approach of oncologic diseases. In Europe, this therapeutic class currently includes eight agents: ipilimumab, pembrolizumab, nivolumab, atezolizumab, avelumab, ... ...

    Abstract Introduction: Immune checkpoint inhibitors (ICIs) represent an innovative therapeutic approach of oncologic diseases. In Europe, this therapeutic class currently includes eight agents: ipilimumab, pembrolizumab, nivolumab, atezolizumab, avelumab, cemiplimab, durvalumab and dostarlimab. Despite their proved clinical benefits, they can induce immune-related adverse events (irADRs), that can also involve the nervous system.
    Areas covered: Despite their rarity, neurological irADRs related to ICI-treatments can lead to serious and dangerous complications, highlighting the importance of a strict monitoring of patients. This review aims to summarize the safety profile of ICIs, focusing on their possible neurotoxicity and their management.
    Expert opinion: Considering the clinical relevance of ICIs-induced irADRs and that the underlying mechanisms are still not completely understood, the use of ICIs requires extensive safety monitoring. Before to prescribe immunotherapy, oncologists should identify possible individual risk factors that may favor the onset of irADRs. Oncologists and general practitioners should inform and educate patients about the specific toxicities of immunological checkpoint inhibitors, including nervous ones. They should be carefully monitored at least 6 months after the end of treatment. ICIs-related nervous toxicities require a multidisciplinary management, in which neurologists and clinical pharmacologists should participate.
    MeSH term(s) Humans ; Immune Checkpoint Inhibitors/adverse effects ; Neoplasms/drug therapy ; Antineoplastic Agents, Immunological/adverse effects ; Immunotherapy/adverse effects ; Europe
    Chemical Substances Immune Checkpoint Inhibitors ; Antineoplastic Agents, Immunological
    Language English
    Publishing date 2023-05-11
    Publishing country England
    Document type Journal Article ; Review
    ISSN 1751-2441
    ISSN (online) 1751-2441
    DOI 10.1080/17512433.2023.2211262
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Skin Toxicities Associated with Botulin Toxin Injection for Aesthetic Procedures: Data from the European Spontaneous Reporting System.

    Nicoletti, Maria Maddalena / Anatriello, Antonietta / Liguori, Valerio / Cantone, Andrea / di Mauro, Gabriella / Izzo, Imma / Lettera, Nicoletta / Della Ragione, Joao Marcos / Campitiello, Maria Rosaria / Cosenza, Vincenzo / Scavone, Cristina

    Pharmaceuticals (Basel, Switzerland)

    2023  Volume 16, Issue 11

    Abstract: Botulinum toxin is a protein deriving from the ... ...

    Abstract Botulinum toxin is a protein deriving from the bacteria
    Language English
    Publishing date 2023-11-15
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2193542-7
    ISSN 1424-8247
    ISSN 1424-8247
    DOI 10.3390/ph16111611
    Database MEDical Literature Analysis and Retrieval System OnLINE

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