Patient-reported outcomes in immunotherapy for head and neck cancer

被引:1
|
作者
Kirtane, Kedar [1 ,8 ]
Hoogland, Aasha I. [2 ]
Li, Xiaoyin [2 ]
Rodriguez, Yvelise [2 ]
Scheel, Kelsey [2 ]
Small, Brent J. [3 ]
Oswald, Laura B. [2 ]
Muzaffar, Jameel [1 ]
Kish, Julie A. [4 ]
Bonomi, Marcelo [5 ,6 ]
Bhateja, Priyanka [5 ,6 ]
Saba, Nabil F. [7 ]
Steuer, Conor E. [7 ]
Chung, Christine H. [1 ]
Jim, Heather S. L. [2 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Dept Head & Neck Endocrine Oncol, Tampa, FL USA
[2] H Lee Moffitt Canc Ctr & Res Inst, Dept Hlth Outcomes & Behav, Tampa, FL USA
[3] Univ S Florida, Sch Aging Studies, Tampa, FL USA
[4] H Lee Moffitt Canc Ctr & Res Inst, Dept Personalized Med, Tampa, FL USA
[5] Ohio State Univ, Dept Internal Med, Columbus, OH USA
[6] Ohio State Univ, James Comprehens Canc Ctr, Columbus, OH USA
[7] Emory Univ, Winship Canc Inst, Dept Hematol & Med Oncol, Atlanta, GA USA
[8] H Lee Moffitt Canc Ctr & Res Inst, Dept Head & Neck Endocrine Oncol, 12902 USF Magnolia Dr, Tampa, FL 33612 USA
来源
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK | 2023年 / 45卷 / 07期
关键词
clinical trials; head and neck; immunotherapy; patient-reported outcomes; quality of life; SQUAMOUS-CELL CARCINOMA; QUALITY-OF-LIFE; RECURRENT METASTATIC HEAD; FUNCTIONAL ASSESSMENT; CLINICAL-TRIALS; ADVERSE EVENTS; OPEN-LABEL; PEMBROLIZUMAB; TOXICITY; NIVOLUMAB;
D O I
10.1002/hed.27388
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
BackgroundData about patient-reported outcomes (PROs) among patients with head and neck squamous cell carcinoma (HNSCC) treated with immune checkpoint inhibitors are sparse. Our exploratory study evaluated PROs in patients with HNSCC starting treatment with immune checkpoint inhibitor monotherapy or combination therapy with cetuximab. MethodsPatients were recruited prior to receipt of their first checkpoint inhibitor therapy infusion. Participants completed measures of checkpoint inhibitor toxicities and quality of life (QOL) at on-treatment clinic visits. ResultsAmong patients treated with checkpoint inhibitor monotherapy (n = 48) or combination therapy (n = 38) toxicity increased over time (p < 0.05), while overall QOL improved from baseline to 12 weeks, with stable or declining QOL thereafter (p < 0.05). There were no group differences in change in toxicity index or QOL. Toxicity index scores were significantly higher in the combination group at 18-20 weeks and 6 months post-initiation of immune checkpoint inhibitor (p < 0.05). There were no significant group differences at baseline, the 6-8 week (p = 0.13) or 3-month (p = 0.09) evaluations. The combination group reported better emotional well-being at baseline than the monotherapy group (p = 0.04), There were no other group differences QOL at baseline or later timepoints. ConclusionsDespite increasing patient-reported toxicity, checkpoint inhibitor monotherapy and combination therapy were associated with similar transient improvements, then worsening, of QOL in patients with HNSCC.
引用
收藏
页码:1761 / 1771
页数:11
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