Skip to main content
. 2009 Sep;2(5):291–297. doi: 10.1177/1756285609337992

Table 1.

CLinicaL features, outcome and side effects of dacLizumab treatment.

No Age/sex Years with MS CLinicaL course Previous Rx Time Dac Rx (mo) Comb Rx w/Dac Pre RX EDSS During Rx EDSS EDSS Δ Side effects
1 31F 12 RR/A* I,P,S 43 None 3.5 1.5 -2.0 Rash
2 44F 12 RR/A I,P,S 28b None 3.0 1.0 -2.0 None
3 34F 10 RR/A I,P,S 41b None 4.0 1.5 -2.5 Fatigue
7 40M 8 RR/A I,P,S,G 43a None 2.5 1.5 -1.0 Lymphadenopathy, rash, high fever
12 61F 21 RR/A I,P,S 43 None 5.0 2.5 -2.5 Lymphadenopathy, EBV infection, headache, paresthesia
14 46F 12 RR/A I,P,S,G 28b (I) 3.5 3.0 -0.5 None
16 45M 15 RR/A I,P,S 45 None 4.0 1.5 -2.5 None
17 30M 8 RR/A* I,S,G,PP,M 60 (I) 6.5 2.0 -4.5 Constipation, toe infection, fever, sore throat
18 34M 6 RR/A I,S,P,G 51 None 3.5 1.0 -2.5 Transient eLevation LFT, seasonaL rash, chest discomfort
19 39M 12 RR/A I,S,P,G 51 None 2.5 1.0 -1.5 None
20 45M 15 RR/A I,S,P 49 (I) 3.5 2.0 -1.5 None
22 33M 3 RR/A S,P,I 24 None 6.0 2.5 -3.5 Rash, chest discomfort

Clinical characteristics: Five females and seven males ranging from 30 to 61 years of age. The average disease duration for aLL patients was 11.1 years.

DacLizumab treatment: The dose range from 0.85 to 1.5mg/kg IV. The average duration of treatment was 42.1 months. Nine patients received treatment for more that 3 years, two patients for more than two years and one patient for two years.

DacLizumab Rx status: Patients continuing Rx: 1,12,16,17,18,19,20 and 22.

aDiscontinued Rx due to side effects: (patient #7).

bDiscontinued Rx due to insurance issue: (patients #2, #3 and #14).

CLinicaL course: RR: reLapsing—remitting; RR/A: active (one ore two reLapses per year); RR/A*: active (three or more reLapses/year). Previous Rx: I, interferon; S, soLumedroL; P, prednisone; Mtx, methotrexate; G, gLatiramer acetate; PP, pLasmapheresis; Pac, pacLitaxeL. Combined therapy: (I): interferon.