Health-related Quality-of-life in a Randomized Phase III First-line Study of Gefitinib Versus Carboplatin/paclitaxel in Clinically Selected Patients from Asia with Advanced NSCLC (IPASS)
Overview
Pulmonary Medicine
Authors
Affiliations
Introduction: Evaluation of health-related quality-of-life (HRQoL) and symptom improvement were preplanned secondary objectives for the overall population and posthoc analyses for epidermal growth factor receptor (EGFR) mutation-positive/negative subgroups in IPASS.
Methods: HRQoL was assessed using the Functional Assessment of Cancer Therapy-Lung (FACT-L) and Trial Outcome Index (TOI); symptom improvement by the Lung Cancer Subscale (LCS). Improvements defined as: 6 or more (FACT-L; TOI), 2 or more (LCS) points increase maintained for 21 or more days.
Results: Overall (n = 1151/1217 evaluable), HRQoL improvement rates were significantly greater with gefitinib versus carboplatin/paclitaxel; symptom improvement rates were similar for both treatments. Significantly more patients recorded improvements in HRQoL and symptoms with gefitinib in the EGFR mutation-positive subgroup (n = 259; FACT-L 70.2% versus 44.5%; odds ratio, 3.01 [95% confidence interval, 1.79-5.07]; p < 0.001; TOI 70.2% versus 38.3%; 3.96 [2.33-6.71]; p < 0.001; LCS 75.6% versus 53.9%; 2.70 [1.58-4.62]; p < 0.001), and with carboplatin/paclitaxel in the EGFR mutation-negative subgroup (n = 169; FACT-L 14.6% versus 36.3%; odds ratio, 0.31 [0.15-0.65]; p = 0.002; TOI 12.4% versus 28.8%; 0.35 [0.16-0.79]; p = 0.011; LCS 20.2% versus 47.5%; 0.28 [0.14-0.55]; p < 0.001). Median time-to-worsening (months) FACT-L score was longer with gefitinib versus carboplatin/paclitaxel for the overall population (8.3 versus 2.5) and EGFR mutation-positive subgroup (15.6 versus 3.0), and similar for both treatments in the EGFR mutation-negative subgroup (1.4 versus 1.4). Median time-to-improvement with gefitinib was 8 days in patients with EGFR mutation-positive tumors who improved.
Conclusions: HRQoL and symptom endpoints were consistent with efficacy outcomes in IPASS and favored gefitinib in patients with EGFR mutation-positive tumors and carboplatin/paclitaxel in patients with EGFR mutation-negative tumors.
Ulrich C, Himbert C, Barnes C, Boucher K, Daniels B, Bandera V JAMA Surg. 2025; .
PMID: 40072448 PMC: 11904799. DOI: 10.1001/jamasurg.2025.0130.
Yeo S, Sun J, Zibrik K, Shaipanich T, Carolan H, Melosky B BMJ Open Qual. 2025; 14(1).
PMID: 39971592 PMC: 11840910. DOI: 10.1136/bmjoq-2024-003001.
Cheng Y, Chen B, Fang Q, Zang G, Yao J Discov Oncol. 2024; 15(1):274.
PMID: 38980474 PMC: 11233477. DOI: 10.1007/s12672-024-01094-x.
Luo Y, Shen C, Chiang C, Huang H, Chen Y Front Immunol. 2024; 15:1269253.
PMID: 38343550 PMC: 10853389. DOI: 10.3389/fimmu.2024.1269253.
Tournoy K, Adam V, Muylle I, De Rijck H, Everaert E, Eqlimi E Cancers (Basel). 2023; 15(15).
PMID: 37568637 PMC: 10417517. DOI: 10.3390/cancers15153821.