TY - JOUR
T1 - MRI activity and extended interval of Natalizumab dosing regimen: a multicentre Italian study
AU - De Mercanti, Stefania Federica
AU - Signori, Alessio
AU - Cordioli, Cinzia
AU - Signoriello, Elisabetta
AU - Lus, Giacomo
AU - Bonavita, Simona
AU - Abbadessa, Gianmarco
AU - Lavorgna, Luigi
AU - Maniscalco, Giorgia Teresa
AU - Curti, Erica
AU - Lorefice, Lorena
AU - Cocco, Eleonora
AU - Nociti, Viviana
AU - Mirabella, Massimiliano
AU - Baroncini, Damiano
AU - Mataluni, Giorgia
AU - Landi, Doriana
AU - Petruzzo, Martina
AU - Lanzillo, Roberta
AU - Gandoglia, Ilaria
AU - Laroni, Alice
AU - Frangiamore, Rita
AU - Sartori, Arianna
AU - Cavalla, Paola
AU - Costantini, Gianfranco
AU - Capra, Ruggero
AU - Sormani, Maria Pia
AU - Clerico, Marinella
PY - 2021
Y1 - 2021
N2 - Background: To minimize the risk of Progressive Multifocal Leukoencephalopathy and rebound in JCV-positive multiple sclerosis (MS) patients after 24 natalizumab doses, it has been proposed to extend the administrations interval. The objective is to evaluate the EID efficacy on MRI activity compared with the standard interval dosing (SID). Methods: Observational, multicentre, retrospective cohort study, starting from the 24th natalizumab infusion to the loss of follow-up or 2 years after baseline. Three hundred and sixteen patients were enrolled. The median dose interval (MDI) following the 24th infusion was 5 weeks, with a bimodal distribution (modes at 4 and 6 weeks). Patients were grouped into 2 categories according to the mean number of weeks between doses: < 5 weeks, SID; ≥ 5 weeks, EID. Results: One hundred and eighty-seven patients were in the SID group (MDI = 4.5 weeks) and 129 in the EID group (MDI 6.1 weeks). The risk to develop active lesions on MRI is similar in SID and EID groups during the 6 and 12 months after the 24th natalizumab infusion, respectively 4.27% (95% CI:0.84–7.70) vs 4.71% (95% CI:0.16–9.25%) [p = 0.89] and 8.50% (95% CI:4.05–12.95) vs 6.55% (95% CI:2.11–11.00%) [p = 0.56]. The EID regimen does not appear to increase the occurrence of MRI activity during follow-up. Conclusion: There is no evidence of the reduced efficacy of natalizumab in an EID setting regarding the MRI activity. This observation supports the need for a bigger randomized study to assess the need to change the standard of the natalizumab dosing schedule, to better manage JCV-positive patients.
AB - Background: To minimize the risk of Progressive Multifocal Leukoencephalopathy and rebound in JCV-positive multiple sclerosis (MS) patients after 24 natalizumab doses, it has been proposed to extend the administrations interval. The objective is to evaluate the EID efficacy on MRI activity compared with the standard interval dosing (SID). Methods: Observational, multicentre, retrospective cohort study, starting from the 24th natalizumab infusion to the loss of follow-up or 2 years after baseline. Three hundred and sixteen patients were enrolled. The median dose interval (MDI) following the 24th infusion was 5 weeks, with a bimodal distribution (modes at 4 and 6 weeks). Patients were grouped into 2 categories according to the mean number of weeks between doses: < 5 weeks, SID; ≥ 5 weeks, EID. Results: One hundred and eighty-seven patients were in the SID group (MDI = 4.5 weeks) and 129 in the EID group (MDI 6.1 weeks). The risk to develop active lesions on MRI is similar in SID and EID groups during the 6 and 12 months after the 24th natalizumab infusion, respectively 4.27% (95% CI:0.84–7.70) vs 4.71% (95% CI:0.16–9.25%) [p = 0.89] and 8.50% (95% CI:4.05–12.95) vs 6.55% (95% CI:2.11–11.00%) [p = 0.56]. The EID regimen does not appear to increase the occurrence of MRI activity during follow-up. Conclusion: There is no evidence of the reduced efficacy of natalizumab in an EID setting regarding the MRI activity. This observation supports the need for a bigger randomized study to assess the need to change the standard of the natalizumab dosing schedule, to better manage JCV-positive patients.
KW - Efficacy
KW - Extended dose
KW - Magnetic resonance imaging
KW - Multiple sclerosis
KW - Natalizumab
KW - Efficacy
KW - Extended dose
KW - Magnetic resonance imaging
KW - Multiple sclerosis
KW - Natalizumab
UR - http://hdl.handle.net/10807/176938
U2 - 10.1016/j.jns.2021.117385
DO - 10.1016/j.jns.2021.117385
M3 - Article
SN - 0022-510X
VL - 424
SP - 117385-N/A
JO - Journal of the Neurological Sciences
JF - Journal of the Neurological Sciences
ER -