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抗血管生成治疗联合免疫治疗期间的急性炎症反应作为治疗效果的可能指标:三例病例报告及文献综述

Acute inflammatory reaction during anti-angiogenesis therapy combined with immunotherapy as a possible indicator of the therapeutic effect: Three case reports and literature review.

作者信息

Lei Yihui, Lin Li, Cheng Shuyu, Shao Qiming, Ding Chenchun, Zuo Renjie, Chen Weiping, Liao Quan, Liu Guoyan

机构信息

The School of Clinical Medical, Fujian Medical University, Fuzhou, Fujian, China.

Department of Gastrointestinal Surgery, Zhongshan Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.

出版信息

Front Oncol. 2023 Apr 14;13:1072480. doi: 10.3389/fonc.2023.1072480. eCollection 2023.

DOI:10.3389/fonc.2023.1072480
PMID:37124541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10140593/
Abstract

The posterior line treatment of unresectable advanced or metastatic gastrointestinal (GI) tumors has always been a challenging point. In particular, for patients with microsatellite stable (MSS)/mismatch repair proficient (pMMR) 0GI tumors, the difficulty of treatment is exacerbated due to their insensitivity to immune drugs. Accordingly, finding a new comprehensive therapy to improve the treatment effect is urgent. In this study, we report the treatment histories of three patients with MSS/pMMR GI tumors who achieved satisfactory effects by using a comprehensive treatment regimen of apatinib combined with camrelizumab and TAS-102 after the failure of first- or second-line regimens. The specific contents of the treatment plan were as follows: apatinib (500 mg/d) was administered orally for 10 days, followed by camrelizumab (200 mg, ivgtt, day 1, 14 days/cycle) and TAS-102 (20 mg, oral, days 1-21, 28 days/cycle). Apatinib (500 mg/d) was maintained during treatment. Subsequently, we discuss the possible mechanism of this combination and review the relevant literature, and introduce clinical trials on anti-angiogenesis therapy combined with immunotherapy.

摘要

不可切除的晚期或转移性胃肠道(GI)肿瘤的二线治疗一直是一个具有挑战性的问题。特别是对于微卫星稳定(MSS)/错配修复功能正常(pMMR)的胃肠道肿瘤患者,由于其对免疫药物不敏感,治疗难度进一步加大。因此,迫切需要找到一种新的综合治疗方法来提高治疗效果。在本研究中,我们报告了3例MSS/pMMR胃肠道肿瘤患者的治疗历程,这些患者在一线或二线治疗方案失败后,采用阿帕替尼联合卡瑞利珠单抗和TAS-102的综合治疗方案取得了满意的效果。治疗方案的具体内容如下:阿帕替尼(500mg/d)口服10天,随后给予卡瑞利珠单抗(200mg,静脉滴注,第1天,每14天为1个周期)和TAS-102(20mg,口服,第1 - 21天,每28天为1个周期)。治疗期间维持阿帕替尼(500mg/d)剂量。随后,我们讨论了这种联合治疗的可能机制并回顾了相关文献,并介绍了抗血管生成治疗联合免疫治疗的临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7341/10140593/1c5724fa4adc/fonc-13-1072480-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7341/10140593/f620ccae15ba/fonc-13-1072480-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7341/10140593/bd2836065bf0/fonc-13-1072480-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7341/10140593/ebe048747e85/fonc-13-1072480-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7341/10140593/1c5724fa4adc/fonc-13-1072480-g010.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7341/10140593/98060a2f00a3/fonc-13-1072480-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7341/10140593/8c6641141174/fonc-13-1072480-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7341/10140593/95acc89682a9/fonc-13-1072480-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7341/10140593/a5825385bb37/fonc-13-1072480-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7341/10140593/bd2836065bf0/fonc-13-1072480-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7341/10140593/ebe048747e85/fonc-13-1072480-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7341/10140593/1c5724fa4adc/fonc-13-1072480-g010.jpg

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