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Property:Results after intervention

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Body weight, BMI, fat (%) significantly lower in intervention arm compared to comparison arm (p<0.001, p<0.001, p=0.03) after 3 months  +
Baseline: average score, placebo: 55.9 points, intervention: 54.3 points, After radiotherapy: placebo: 56.2 points, intervention: 58.6 points, Follow-up after 4 weeks: placebo: 53.8 points, intervention: 61.3 points  +
Volume of cerebral edema: Significantly greater reduction of edema in the boswellia arm (reduction of 75%: 60% of patients) compared to the placebo arm (reduction of 75%: 26% of patients), p=0.023, Baseline: placebo: 188.4 mL (range, 0-617.3 mL), intervention: 159.3 mL (range, 0-506.2 mL) After radiotherapy: placebo: 97.4 mL (range, 0-346.8 mL) intervention: 45.7 (range, 0-264.0 mL) Follow-up after 4 weeks: placebo: 83.3 mL (range, 0-352.7 mL), intervention: 73.9 mL (range, 0-413.1 mL)  +
Tumor volume: Significantly lower tumor volume in the Boswellia arm (2.9cm3) compared to the placebo arm (16.1cm3), p=0.008, Tendentially fewer patients with progressive disease in Boswellia arm (0%) compared to placebo arm (18%) Baseline: placebo: ratio = 0.11, intervention: ratio = 0.15 After radiotherapy: placebo: ratio = 0.15, intervention: ratio = 0.06  +
Baseline: average score, placebo: 28 points, intervention: 29 points, After radiotherapy: placebo: 28 points, intervention: 27 points, Follow-up after 4 weeks: placebo: 26 points, intervention: 29 points  +
In intervention arm significantly lower change in appetite score than in placebo arm for day 22, 43, 64, adjusted with baseline values from day 1: r -1.65, 95% CI -2.64 to -0.67; p=0.001  +
Most common adverse events: anemia, neutropenia, thrombocytopenia, febrile neutropenia, fatigue, myalgia, dyspepsia, headache, increased creatinine, ALT, ALP, AST values. No significant difference between arms (p=0.244-1.000) except for fatigue: significantly lower grade 3 fatigue in intervention arm than in placebo arm (2% vs. 20%, p=0.020)  +
Overall: Median in days (95% CI) intervention arm: 58 (43.0, 97.0); placebo arm: 69 (49.0, 105.0); p = 0.58, ns.  +
Overall: Numer in percentage (95% CI) intervention arm: 34 (25.0, 44.8) placebo arm: 29 (20.1, 39.4); p = 0.43, ns. No significant differences were found in subgroup analyses by gender, age, number of chemotherapy cycles, and types of chemotherapy (p > 0.05 for each). No significant differences in self-reported issues from neuropathic symptoms such as numbness, tingling, etc. (p = 0.11-0.88).  +
Overall: Median in days (95% CI) intervention arm: 36 (28.0, 44.0); placebo arm: could not be calculated as symptom reduction occurred in only 27 patients  +