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阿帕替尼联合 S-1/卡培他滨用于根治性放化疗后食管鳞癌残留患者的口腔维持治疗。

Oral maintenance therapy using apatinib combined with S-1/capecitabine for esophageal squamous cell carcinoma with residual disease after definitive chemoradiotherapy.

机构信息

Department of Radiation Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center of Cancer Medicine, Guangzhou, Guangdong, P.R. China.

Guangdong Esophageal Cancer Research Institute, Guangzhou, Guangdong, P. R. China.

出版信息

Aging (Albany NY). 2021 Mar 10;13(6):8408-8420. doi: 10.18632/aging.202652.

Abstract

BACKGROUND

A substantial number of patients with esophageal squamous cell carcinoma (ESCC) do not achieve complete remission after definitive concurrent chemoradiotherapy (dCRT). We performed this retrospective study to evaluate the efficacy and safety of apatinib combined with S-1/capecitabine as the oral maintenance therapy for these patients.

METHODS

Thirty-nine ESCC patients with residual disease after dCRT were included. Patients were treated with apatinib combined with S-1 /capecitabine after dCRT. Efficacy, toxicity, and survival were analyzed.

RESULTS

Of the 39 patients, 5 (12.8%) achieved a partial response and 29 (74.4%) achieved stable disease, yielding a disease control rate of 87.2%. The median progression-free survival (PFS) and overall survival (OS) were 27.5 (95%CI: 14.9 - 40.1) and 38.1 (95%CI: 31.3 - 44.8) months. Most frequent adverse events were of grade 1 to 2. Multivariate analysis revealed the occurrence of any adverse events (HR = 0.274, 95%[CI] = 0.119 - 0.630) correlated to better PFS and occurrence of proteinuria (HR = 0.108, 95%[CI] = 0.025 - 0.456) predicted better OS.

CONCLUSION

The oral combination therapy consisting of apatinib and S-1/capecitabine showed a tolerable toxicity profile and achieved satisfactory disease control in ESCC patients with residual disease after dCRT.

摘要

背景

相当数量的食管鳞癌(ESCC)患者在接受根治性同步放化疗(dCRT)后无法达到完全缓解。我们进行了这项回顾性研究,以评估阿帕替尼联合 S-1/卡培他滨作为这些患者的口服维持治疗的疗效和安全性。

方法

纳入 39 例 dCRT 后有残留病灶的 ESCC 患者。患者在 dCRT 后接受阿帕替尼联合 S-1/卡培他滨治疗。分析疗效、毒性和生存情况。

结果

39 例患者中,5 例(12.8%)部分缓解,29 例(74.4%)疾病稳定,疾病控制率为 87.2%。中位无进展生存期(PFS)和总生存期(OS)分别为 27.5(95%CI:14.9-40.1)和 38.1(95%CI:31.3-44.8)个月。最常见的不良反应为 1-2 级。多因素分析显示,任何不良反应的发生(HR=0.274,95%CI=0.119-0.630)与更好的 PFS 相关,蛋白尿的发生(HR=0.108,95%CI=0.025-0.456)与更好的 OS 相关。

结论

阿帕替尼联合 S-1/卡培他滨的口服联合治疗在 dCRT 后有残留病灶的 ESCC 患者中显示出可耐受的毒性特征,并获得了令人满意的疾病控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab28/8034932/0dfac23c68e2/aging-13-202652-g001.jpg

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