Late Toxicity and Health-Related Quality of Life Following Definitive Chemoradiotherapy for Esophageal Cancer: A Systematic Review and Meta-analysis

被引:3
作者
Pape, Marieke [1 ,2 ,3 ]
Veen, Linde M. [2 ,3 ]
Smit, Thom M. [2 ,3 ]
Kuijper, Steven C. [2 ]
Vissers, Pauline A. J. [4 ]
Geijsen, Elisabeth D. [5 ]
Rossum, Peter S. N. van [5 ]
Sprangers, Mirjam A. G. [3 ,6 ]
Derks, Sarah [7 ,8 ,9 ]
Verhoeven, Rob H. A. [1 ,2 ,3 ]
van Laarhoven, Hanneke W. M. [1 ]
机构
[1] Netherlands Comprehens Canc Org, Dept Res & Dev, Utrecht, Netherlands
[2] Univ Amsterdam, Amsterdam UMC Locat, Med Oncol, Amsterdam, Netherlands
[3] Canc Ctr Amsterdam, Canc Treatment & Qual Life, Amsterdam, Netherlands
[4] Radboud Univ Nijmegen, Med Ctr, Dept Surg, Nijmegen, Netherlands
[5] Univ Amsterdam, Amsterdam UMC Locat, Radiat Oncol, Amsterdam, Netherlands
[6] Univ Amsterdam, Amsterdam UMC Locat, Med Psychol, Amsterdam, Netherlands
[7] Vrije Univ Amsterdam, Amsterdam UMC Locat, Med Oncol, Amsterdam, Netherlands
[8] Canc Ctr Amsterdam, Canc Biol & Immunol, Amsterdam, Netherlands
[9] Oncode Inst, Utrecht, Netherlands
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2023年 / 117卷 / 01期
关键词
SQUAMOUS-CELL CARCINOMA; POTENTIALLY CURATIVE TREATMENT; PATIENT-REPORTED OUTCOMES; HIGH-DOSE RADIOTHERAPY; CONCURRENT CHEMORADIOTHERAPY; RANDOMIZED-TRIAL; PHASE-II; RECURRENCE PATTERNS; RADIATION-THERAPY; CISPLATIN;
D O I
10.1016/j.ijrobp.2023.05.025
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Definitive chemoradiotherapy (dCRT) is a treatment option with curative intent for patients with esophageal cancer that could result in late toxicities and affect health-related quality of life (HRQoL). This study aimed to review the literature and perform a meta-analysis to investigate the effect of dCRT on late toxicities and HRQoL in esophageal cancer.Methods and Materials: A systematic search was performed in MEDLINE, EMBASE, and PsychINFO. Prospective phase II and III clinical trials, population-based studies, and retrospective chart reviews investigating late toxicity or HRQoL after dCRT (=50 Gy) were included. The HRQoL outcomes were analyzed using linear mixed-effect models with restricted cubic spline transformation. Any HRQoL changes of =10 points were considered clinically relevant. The risk of toxicities was calculated using the number of events and the total study population.Results: Among 41 included studies, 10 assessed HRQoL and 31 late toxicity. Global health status remained stable over time and improved after 36 months compared with baseline (mean change, +11). Several tumor-specific symptoms, including dysphagia, eating restrictions, and pain, improved after 6 months compared with baseline. Compared with baseline, dyspnea worsened after 6 months (mean change, +16 points). The risk of any late toxicity was 48% (95% CI, 33%-64%). Late toxicity risk ofany grade for the esophagus was 17% (95% CI, 12%-21%), pulmonary 21% (95% CI, 11%-31%), cardiac 12% (95% CI, 6%-17%), and any other organ 24% (95% CI, 2%-45%).Conclusions: Global health status remained stable over time, and tumor-specific symptoms improved within 6 months after dCRT compared with baseline, with the exception of dyspnea. In addition, substantial risks of late toxicity were observed. & DBLBOND; 2023 Elsevier Inc. All rights reserved.
引用
收藏
页码:31 / 44
页数:14
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