Expert Narrative Review of the Safety of Cladribine Tablets for the Management of Relapsing Multiple Sclerosis

被引:0
作者
Pierre Clavelou
Giovanni Castelnovo
Valérie Pourcher
Jerome De Sèze
Patrick Vermersch
Ali-Frederic Ben-Amor
Carine Savarin
Gilles Defer
机构
[1] Clermont-Ferrand University Hospital,Department of Neurology
[2] Nîmes University Hospital,Department of Neurology
[3] Hopital Caremeau,Department of Infectious and Tropical Diseases
[4] Pitié-Salpêtrière Hospital,Department of Neurology
[5] APHP,Global Medical Affairs Neurology and Immunology
[6] Sorbonne Université,Neurology Department
[7] INSERM 1136,Department of Neurology
[8] Institut Pierre Louis d’Epidémiologie et de Santé Publique Paris,undefined
[9] Strasbourg University Hospital,undefined
[10] Univ. Lille,undefined
[11] Inserm U1172 LilNCog,undefined
[12] CHU Lille,undefined
[13] FHU Precise,undefined
[14] Ares Trading SA (An affiliate of Merck KGaA,undefined
[15] Darmstadt,undefined
[16] Germany),undefined
[17] Medical Affairs (An affiliate of Merck KGaA,undefined
[18] Darmstadt,undefined
[19] Germany),undefined
[20] Caen University Hospital,undefined
来源
Neurology and Therapy | 2023年 / 12卷
关键词
Multiple sclerosis; Cladribine tablets; Disease-modifying therapy; Immune reconstitution therapy; Drug safety;
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摘要
Cladribine tablets (CladT) is a highly active oral disease-modifying therapy (DMT) for the management of relapsing multiple sclerosis (RMS). CladT acts as an immune reconstitution therapy, in that two short courses of treatment 1 year apart have been shown to suppress disease activity for a prolonged period in most patients, without need for continued DMT. Each course of CladT induces a profound reduction in B lymphocytes that recovers over months, and serious lymphopenia (Grade 3–4) is uncommon. Smaller reductions in levels of T lymphocytes occur slightly later: on average, these remain within the normal range and repopulate progressively. A larger effect occurs on CD8 vs. CD4 cells. Reactivation of latent or opportunistic infections (e.g. varicella zoster, tuberculosis) is mostly associated with very low lymphocyte counts (< 200/mm3). Screening and managing pre-existing infections, vaccinating non-exposed patients and delaying the 2nd year of treatment with CladT to allow lymphocytes to recover to > 800/mm3 (if necessary) are important for avoiding infections and higher-grade lymphopenia. There was no demonstrable or apparent effect of CladT on the efficacy of vaccinations, including against Covid-19. Adverse events consistent with drug-induced liver injury (DILI) represent a rare but potentially serious complication of CladT therapy in spontaneous adverse event reporting; patients should be screened for liver dysfunction before starting treatment. Ongoing hepatic monitoring is not required, but CladT must be withdrawn if signs and symptoms of DILI develop. There was a numerical imbalance for malignancies when comparing cladribine to placebo in the clinical programme, particularly in short-term data, but recent evidence shows that the risk of malignancy with CladT is similar to the background rate in the general population and to that with other DMTs. Overall, CladT is well tolerated with a favorable safety profile appropriate for the management of RMS.
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页码:1457 / 1476
页数:19
相关论文
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