Safety and efficacy of Vitamin D<sub>3</sub> supplementation with Imatinib in Chronic Phase- Chronic Myeloid Leukaemia: an Exploratory Randomized Controlled Trial.

Bandyopadhyay, Arkapal; Palepu, Sarika; Dhamija, Puneet; Nath, Uttam Kumar; Chetia, Rituparna; Bakliwal, Anamika; Vaniyath, Sudeep; Chattopadhyay, Debranjani et al. · BMJ Open · 2023

rct · Level II

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Abstract

The study aimed to compare early molecular response (EMR) rates at 3 months of imatinib therapy with and without vitamin D<sub>3</sub> supplementation in patients newly diagnosed with chronic-phase chronic myeloid leukaemia (CML-CP). The secondary objective was to assess the effects of vitamin D<sub>3</sub> on complete haematological response (CHR) and its safety. Double-blind, placebo-controlled, exploratory randomised trial. Tertiary care hospital in northern India. Treatment-naive patients with chronic phase chronic myeloid leukaemia (n=62) aged >12 years were recruited from January 2020 to January 2021. Patients with progressive disease, pregnancy and hypercalcaemia were excluded. Oral vitamin D<sub>3</sub> supplementation (60 000 IU) or matched placebo was given once weekly for an initial 8 weeks along with imatinib after randomisation with 1:1 allocation ratio. The primary outcome was to compare EMR (defined as <i>BCR-ABL1</i> transcript level ≤10%, international scale) at 3 months. The secondary outcomes were to compare effect of the intervention on CHR, correlation of 25(OH)2D<sub>3</sub> levels with treatment response and safety according to Common Terminology Criteria for Adverse Events (CTCAE) version 5. At baseline, 14.5% of the patients had normal vitamin D<sub>3</sub> levels. EMR at 3 months was attained in 24 patients (82.7%) of the vitamin D<sub>3</sub> group and 21 (75%) of the placebo group (OR 1.6, 95% CI 0.37 to 7.37, p=0.4). A significant difference in vitamin D<sub>3</sub> levels from baseline to the end of study was observed. Patients with vitamin D<sub>3</sub> supplementation did not achieve higher CHR in comparison with placebo (OR 1.3, 95% CI 0.25 to 7.23, p=1.0). Vitamin D3 levels were not significantly correlated with <i>BCR-ABL1</i> levels. No dose-limiting toxicities were observed. Vitamin D<sub>3</sub> levels were low among patients with CML-CP in this study. Vitamin D<sub>3</sub> supplementation with imatinib therapy did not have significant effect on EMR or CHR. Further clinical trials could be undertaken to assess the effective dosage and duration of vitamin D<sub>3</sub> supplementation in these patients. CTRI/2019/09/021164.

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