Patients with metastatic melanoma treated with TIL-IMP experienced similar HRQoL compared to IPI monotherapy, with indications of better HRQoL outcomes over time. Ongoing follow-up is essential to assess longer-term HRQoL and its generalizability to a larger patient population to help guide personalized treatments decisions.
Of 168 patients randomized 1:1, n=143 baseline HRQoL scores (85%) were calculated. Of these, 75 (89%) were in the TIL-IMP-group and 73 (87%) in the IPI-group. TIL-IMP-treated patients reported higher global health status scores at week 24 compared to ipilimumab-treated patients (78.2 vs 73.9; p<0.05) and emotional functioning (85.9 vs 77.9; p<0.05). Patients treated with TIL-IMP had significantly lower fatigue (25.0 vs 32.4; p<0.05) and pain (13.7 vs 17.6; p<0.05) scores at week 24, but marginal higher nausea & vomiting (7.5 vs 5.2; p<0.05) symptom scores. EQ-5D scores were also higher in the TIL-IMP-group (0.89 vs. 0.83; p<0.05). These statistically significant differences were not considered clinically meaningful. The hypothesized higher impact of the more intensive TIL-IMP-treatment compared to IPI was not observed, according to IES scores (11.8 vs. 17.4; p<0.05 at 24 weeks). Sensitivity analyses showed similar results.
In a multicenter, randomized phase 3-trial, patients with metastatic melanoma (unresectable stage IIIC-IV) were randomized to TIL-IMP or IPI treatment (NCT02278887). HRQoL was measured using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 15 Palliative Care (EORTC QLQ-C15-PAL), EuroQol 5D-3L (EQ-5D), and the Impact of Event Scale (IES). HRQoL outcomes were evaluated using a generalized estimating equations model. Sensitivity analyses were performed to assess drop-out assumptions. Results were interpreted for statistically and clinically significant differences.
To assess health-related quality of life (HRQoL) in patients with metastatic melanoma treated with a tumor infiltrating lymphocyte investigational medicinal product (TIL-IMP) or ipilimumab (IPI) after failure of first- or second-line treatment.
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