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One patient prematurely discontinued study drug because of patient/parent/caregiver request and died following discontinuation.
Adherence data included participants who discontinued study product for any reason, including those instructed to discontinue study product by study staff.
All patients discontinued study treatment.
In total, 25 patients discontinued study treatment early.
Patients discontinued study medication immediately before starting RT.
Few subjects discontinued study participation because of an adverse experience.
Most patients in both trials discontinued study therapy because of disease progression or deteriorating performance status.
Patients who have discontinued study treatment for reasons other than progressive disease will enter follow-up.
In our study, 75 treatment-naïve patients (25.4%) discontinued study medication.
Overall, 14 patients (26%) discontinued study medication because of an adverse event or serious adverse event.
Apart from this SAE, no other participant prematurely discontinued study medication.
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