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累及野调强放疗联合S-1单药放疗用于老年食管癌患者的疗效比较

Comparison of involved-field intensity-modulated radiotherapy combined with S-1 radiotherapy alone for elderly patients with esophageal cancer.

作者信息

Liu Li-Hua, Yan Mao-Hui, Di Yu-Peng, Fu Zhi-Guang, Zhang Xiao-Dan, Li Hong-Qi

机构信息

Department of Radiotherapy, Heze Hospital of Traditional Chinese Medicine, Heze 274000, Shandong Province, China.

Department of Radiotherapy, Air Force Medical Center, Chinese People's Liberation Army, Beijing 100142, China.

出版信息

World J Clin Cases. 2022 Jul 26;10(21):7365-7375. doi: 10.12998/wjcc.v10.i21.7365.

DOI:10.12998/wjcc.v10.i21.7365
PMID:36157997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9353918/
Abstract

BACKGROUND

It is estimated that about 30% of esophageal cancer (EC) patients are over 70 years old. Therefore, there is less evidence on the diagnosis and management of elderly EC patients. It is important to explore how elderly EC patients benefit from radical radiochemotherapy regimens, including the target area of radiotherapy (RT), radiation dose and fraction, and choice of chemotherapy drugs.

AIM

To compare the efficacy of involved-field intensity-modulated RT (IF-IMRT) combined with S-1 RT alone in the treatment of elderly EC patients in terms of safety, short-term response, and survival.

METHODS

Thirty-four EC patients aged > 70 years were prospectively enrolled between December 2017 and December 2019. Based on the random number table, they were divided into an IF-IMRT + S-1 group and an IF-IMRT alone group, with 17 patients in each group. All patients were treated with IF-IMRT at a dose of 50.4-56 Gy in 28-30 fractions (1.8-2 Gy/fraction, 5 fractions/wk). Oral S-1 was administered concomitantly in the IF-IMRT + S-1 group for 14 consecutive days, and a second cycle was started 7 d after drug withdrawal. After RT, 4 cycles of S-1 treatment were offered as the consolidation chemotherapy. The safety, short-term response, and survival were observed after the treatment.

RESULTS

As of April 2022, these 34 patients had been followed up for 15.2-32.5 mo, with a median follow-up period of 24.5 mo. Complete efficacy indicators were obtained from all the patients. The objective response rate was 88.2% 76.5%, respectively, in the IF-IMRT + S-1 group and the RT alone group, where as the disease control rate was 100% 82.4%, respectively. The incidence of adverse events including grade 1-2 fatigue, granulocytopenia, thrombocytopenia, anemia, radiation esophagitis, radiation-induced skin injury, and radiation-induced lung injury was not significantly different between these two groups, so was the incidence of the grade 3 radiation esophagitis (0% 5.7%). The rate of progressive disease (PD) was 52.9% ( = 9) in the IF-IMRT + S-1 group and 64.7% ( = 11) in the RT alone group. The median progression-free survival (PFS) was 23.4 mo 16.3 mo, and the 2-year PFS rate was 42% 41.2%. The median overall survival (OS) was 27.0 mo 23.0 mo, and the 2-year OS rate was 58.8% 47.1%. Multivariate analysis showed that age was a significant prognostic factor ( = 0.0019); patients aged < 75 years had a significant survival advantage over patients aged ≥ 75 years. The locations of EC also affected the prognosis. In the IF-IMRT + S-1 group, the number of chemotherapy cycles was a significant prognostic factor ( = 0.0125), and the risk of PD was significantly lower in EC patients who had received 6 cycles of chemotherapy than those who had received 2-5 cycles of chemotherapy.

CONCLUSION

Compared with IF-IMRT alone, IF-IMRT + S-1 shows the benefits of preventing PD and prolonging survival without increasing adverse reactions. Therefore, this concurrent radiochemotherapy deserves clinical application.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce32/9353918/1a8ed54e52de/WJCC-10-7365-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce32/9353918/4827ea5206a2/WJCC-10-7365-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce32/9353918/1a8ed54e52de/WJCC-10-7365-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce32/9353918/4827ea5206a2/WJCC-10-7365-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce32/9353918/1a8ed54e52de/WJCC-10-7365-g002.jpg
摘要

背景

据估计,约30%的食管癌(EC)患者年龄超过70岁。因此,关于老年EC患者诊断和治疗的证据较少。探索老年EC患者如何从根治性放化疗方案中获益很重要,包括放疗(RT)的靶区、放射剂量和分割方式以及化疗药物的选择。

目的

比较累及野调强放疗(IF-IMRT)联合S-1与单纯IF-IMRT在老年EC患者治疗中的安全性、短期反应和生存率。

方法

2017年12月至2019年12月前瞻性纳入34例年龄>70岁的EC患者。根据随机数字表,将他们分为IF-IMRT+S-1组和单纯IF-IMRT组,每组17例。所有患者均接受IF-IMRT治疗,剂量为50.4-56 Gy,分28-30次(1.8-2 Gy/次,每周5次)。IF-IMRT+S-1组口服S-1连续14天,停药7天后开始第二个周期。放疗后,给予4周期S-1治疗作为巩固化疗。治疗后观察安全性、短期反应和生存率。

结果

截至2022年4月,这34例患者随访了15.2-32.5个月,中位随访期为24.5个月。所有患者均获得了完整的疗效指标。IF-IMRT+S-1组和单纯放疗组的客观缓解率分别为88.2%和76.5%,疾病控制率分别为100%和82.4%。两组1-2级疲劳、粒细胞减少、血小板减少、贫血、放射性食管炎、放射性皮肤损伤和放射性肺损伤等不良事件的发生率无显著差异,3级放射性食管炎的发生率也无显著差异(0%和5.7%)。IF-IMRT+S-1组疾病进展(PD)率为52.9%(n=9),单纯放疗组为64.7%(n=11)。中位无进展生存期(PFS)分别为23.4个月和16.3个月,2年PFS率分别为42%和41.2%。中位总生存期(OS)分别为27.0个月和23.0个月,2年OS率分别为58.8%和47.1%。多因素分析显示年龄是一个显著的预后因素(P=0.0019);年龄<75岁的患者比年龄≥75岁的患者有显著的生存优势。EC的部位也影响预后。在IF-IMRT+S-1组,化疗周期数是一个显著的预后因素(P=0.0125),接受6周期化疗的EC患者PD风险显著低于接受2-5周期化疗的患者。

结论

与单纯IF-IMRT相比,IF-IMRT+S-1在不增加不良反应的情况下显示出预防PD和延长生存的益处。因此,这种同步放化疗值得临床应用。

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