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MS Sequencing: Part 4 – What is the treatment plan?

…arget”, a term borrowed from rheumatology. The three requirements for treat-to-target are: to have a target; have a treatment that can hit the target; and have a way of determining if the target has been hit. Arguably, none of these criteria applies to MS (see Part 1 of this series), leaving the usefulness of this concept in question. A more practical approach to treatment planning is to initiate therapy with the most efficacious agent, with the v…

FDA approves ocrelizumab in RRMS, PPMS

…o ocrelizumab 600 mg by infusion every 24 weeks, or subcutaneous interferon-beta-1a 44 mcg three times per week, for 96 weeks. The annualized relapse rate was 0.16 with ocrelizumab versus 0.29 with the interferon (47% reduction). The mean number of enhancing lesions was 94-95% lower with ocrelizumab. In a pooled analysis, the proportion of patients with 12-week confirmed disability progression was significantly lower with ocrelizumab versus interf…

Adversity, hunger and early-life depression: 2 reports

…ceration, death, disability, psychiatric diagnosis), family disruption, out-of-home care, and childhood abuse. All adverse events were associated with an increased risk of moderate-to-severe depression (hazard ratio 1.30 to 2.72). The timing of adverse events was significant: depression risk was highest for family disruption before age 5 (hazard ratio 1.66); and for out-of-home care for ages 10 to 14 years (hazard ratio 2.45). Researchers at the U…

MS Sequencing: Part 3 – Evaluating treatment response

…87:134-140). Thus, one-third of patients who are seemingly stable – relapse-free and a low number of new lesions – during the first year on treatment would be expected to experience worsening disability over the next few years. A more stringent benchmark of treatment response is no evidence of disease activity (NEDA), defined as no relapses, no MRI activity and no EDSS change. Perhaps the most common objection is that this measure is not sustainab…

NEUROSOUND: CHARCOT 2016 HIGHLIGHTS

…. Virender Bhan, Dalhousie University MS Research clinic, Halifax; Dr. Hyman Rabinovitch, University of Ottawa MS clinic, Ottawa; and Dr. Yves Lapierre, Montreal Neurological Hospital, Montreal. Part 1: The group talks the strengths and limitations of using non-randomized controlled data to guide clinical decisions, and the merits of MEDA (minimal evidence of disease activity) as a benchmark of treatment success. Part 2: The group discusses useful…