Key result
Trastuzumab, in combination with carboplatin and docetaxel, did not prolong the QTcF interval, demonstrating a mean baseline-adjusted QTcF change of -8.4 ms at steady-state.
Why the study?
Does trastuzumab in combination with carboplatin and docetaxel prolong the QT interval in patients with HER2-positive metastatic or locally advanced inoperable solid tumors?
Does trastuzumab in combination with carboplatin and docetaxel prolong the QT interval in patients with HER2-positive metastatic or locally advanced inoperable solid tumors?
Answers are grounded in this paper and cite their sources.
Trastuzumab combined with carboplatin and docetaxel does not cause clinically relevant QT prolongation in patients with HER2-positive solid tumors.
PURPOSE: This study evaluated the potential effect of trastuzumab on the electrocardiogram (ECG) QT interval and assessed the potential pharmacokinetic interaction between trastuzumab and carboplatin. Here, we report the QT and safety results. METHODS: Patients with metastatic or inoperable HER2-positive solid tumors received docetaxel and carboplatin on Day 1 of each 3-week (q3w) cycle. Trastuzumab was administered intravenously, as an accelerated loading dose regimen, on Cycle 1, Day 2 and Cycle 1, Day 8, and then on Day 1 of each subsequent q3w cycle. ECG assessments were performed pre- and posttrastuzumab infusion in the first two cycles. Fridericia's correction was applied to QT intervals (QTcF). Baseline-adjusted QTcF intervals (the change from baseline) and their 90 % confidence intervals (CIs) were calculated. RESULTS: The study enrolled 59 patients. At all time points, the 90 % CI upper bound for the mean baseline-adjusted QTcF was <10 ms. At steady-state serum trastuzumab concentrations, the mean baseline-adjusted QTcF interval was -8.4 ms (90 % CI -11.1, -5.7). No patient exhibited an absolute QTcF interval of >480 ms. No relationship was observed between trastuzumab concentration and baseline-adjusted QTcF interval. At data cutoff, 84.5 % of patients had experienced grade ≥3 adverse events, the most common of which were hematologic and as expected. Left ventricular ejection fraction remained ≥45 % in all patients during the study. CONCLUSIONS: The results suggest that trastuzumab had no clinically relevant effect on QTcF interval. The safety profile of trastuzumab in combination with carboplatin and docetaxel was consistent with the known safety profile of this combination.
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Xu et al. (2014) studied HER2-positive metastatic or locally advanced inoperable solid tumors (n=59). Trastuzumab in combination with carboplatin and docetaxel was evaluated on Change in mean QTcF interval from baseline to steady-state trastuzumab concentration (Mean change -8.4 ms, 95% CI -11.1, -5.7). Trastuzumab, in combination with carboplatin and docetaxel, did not prolong the QTcF interval, demonstrating a mean baseline-adjusted QTcF change of -8.4 ms at steady-state.
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