Efficacy and safety of photodynamic therapy sequential dose-reduction concurrent chemoradiotherapy in locally advanced obstructive esophageal carcinoma: A propensity score matching analysis

IF 2.6 3区 医学 Q2 ONCOLOGY Photodiagnosis and Photodynamic Therapy Pub Date : 2025-04-01 Epub Date: 2025-01-31 DOI:10.1016/j.pdpdt.2025.104509
Ming Zhang , Zhenhua Sun , Gang Qiu , Hualin Wei , Baoshuan Fang , Ying Wang , Xiaopeng Zhang , Juan Li
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Abstract

Background

Dysphagia is a major symptom in esophageal carcinoma (EC) patients. photodynamic therapy (PDT) was approved for palliative treatment of patients with obstructive EC. Although it can remove the obstruction quickly, PDT may be difficult to achieve eradication alone. Thus, we aimed to assess whether photodynamic therapy sequential Dose-Reduction concurrent chemoradiotherapy (CCRT) can be an effective and safe approach for locally advanced obstructive EC.

Methods

This retrospective study included 121 patients with locally advanced obstructive EC who treated with radical CCRT (conventional treatment) and PDT sequential dose-reduction CCRT (combined treatment). A 1:1 propensity score matching (PSM) was conducted to balance potential bias. The improvement of dysphagia and overall survival (OS) was analyzed as the primary endpoint. Progression-free survival (PFS), local control, nutritional improvement and toxicities were analyzed as secondary endpoints.

Results

After PSM, 15 pairs of patients were selected for final analysis. Although the data failed to identify discrepancy in the remission rate of dysphagia between the two groups (73.3 % VS 93.3 %, P = 0.33), the degree of dysphagia relief deviated significantly (2.13 ± 0.52 VS 2.47 ± 0.52, P = 0.005). The onset of dysphagia remission was earlier in the combined treatment group than in the conventional treatment group (17.29 ± 9.29 days VS 33.73 ± 6.77 days, P < 0.001). The median OS of conventional treatment group and combined treatment group were 21.10 months (95 %CI 10.24∼31.96) and 36.67 months (95 %CI 21.54∼51.80), respectively (P = 0.048). The median PFS were 14.30 months (95 %CI 7.79∼20.81) and 31.23 months (95 %CI 13.68∼47.78), respectively (P = 0.039). The rates of 1-year, 2-year and 3-year OS of conventional treatment and combined treatment group were 60 %, 33.3 %, 20 % and 86.7 %, 66.7 %, 41.5 %, respectively. The rates of 1-year, 2-year, and 3-year PFS of the two groups were 53.3 %, 26.7 %, 13.3 % and 73.3 %, 53.3 %, 38.1 %, respectively. The improvement of nutritional status in combined treatment group was better than that in conventional treatment group. The grade 3 toxicity rate was 46.7 %, and no grade 4 or more toxicity was observed in all patients. The addition of PDT did not increase the risk of toxic reactions compared with concurrent chemoradiotherapy.

Conclusion

Photodynamic therapy sequential dose-reduction concurrent chemoradiotherapy can rapidly relieve dysphagia symptoms in patients with locally advanced obstructive EC. Compared with radical CCRT, it does not increase the incidence of treatment-related adverse reactions.
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光动力疗法序贯减量同步放化疗治疗局部晚期梗阻食管癌的疗效和安全性:倾向评分匹配分析。
背景:吞咽困难是食管癌患者的主要症状。光动力疗法(PDT)被批准用于阻塞性EC患者的姑息性治疗。虽然PDT可以快速清除阻塞,但单靠PDT可能难以实现根除。因此,我们的目的是评估光动力疗法序贯减量同步放化疗(CCRT)是否可以有效和安全的治疗局部晚期阻塞性EC。方法:本回顾性研究纳入121例局部晚期阻塞性EC患者,采用根治性CCRT(常规治疗)和PDT序贯减量CCRT(联合治疗)治疗。采用1:1倾向评分匹配(PSM)来平衡潜在偏倚。吞咽困难的改善和总生存期(OS)作为主要终点进行分析。无进展生存期(PFS)、局部控制、营养改善和毒性作为次要终点进行分析。结果:经PSM后,选取15对患者进行最终分析。虽然数据没有发现两组患者的吞咽困难缓解率差异(73.3% VS 93.3%, P=0.33),但吞咽困难缓解程度差异明显(2.13±0.52 VS 2.47±0.52,P=0.005)。联合治疗组吞咽困难缓解的发病时间早于常规治疗组(17.29±9.29天VS 33.73±6.77天)。结论:光动力治疗序贯减量同步放化疗可快速缓解局部晚期梗阻EC患者的吞咽困难症状。与根治性CCRT相比,它不会增加治疗相关不良反应的发生率。
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来源期刊
CiteScore
5.80
自引率
24.20%
发文量
509
审稿时长
50 days
期刊介绍: Photodiagnosis and Photodynamic Therapy is an international journal for the dissemination of scientific knowledge and clinical developments of Photodiagnosis and Photodynamic Therapy in all medical specialties. The journal publishes original articles, review articles, case presentations, "how-to-do-it" articles, Letters to the Editor, short communications and relevant images with short descriptions. All submitted material is subject to a strict peer-review process.
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