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

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 ins...

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Autores principales: Lei, Yihui, Lin, Li, Cheng, Shuyu, Shao, Qiming, Ding, Chenchun, Zuo, Renjie, Chen, Weiping, Liao, Quan, Liu, Guoyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10140593/
https://www.ncbi.nlm.nih.gov/pubmed/37124541
http://dx.doi.org/10.3389/fonc.2023.1072480
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author Lei, Yihui
Lin, Li
Cheng, Shuyu
Shao, Qiming
Ding, Chenchun
Zuo, Renjie
Chen, Weiping
Liao, Quan
Liu, Guoyan
author_facet Lei, Yihui
Lin, Li
Cheng, Shuyu
Shao, Qiming
Ding, Chenchun
Zuo, Renjie
Chen, Weiping
Liao, Quan
Liu, Guoyan
author_sort Lei, Yihui
collection PubMed
description 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.
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spelling pubmed-101405932023-04-29 Acute inflammatory reaction during anti-angiogenesis therapy combined with immunotherapy as a possible indicator of the therapeutic effect: Three case reports and literature review Lei, Yihui Lin, Li Cheng, Shuyu Shao, Qiming Ding, Chenchun Zuo, Renjie Chen, Weiping Liao, Quan Liu, Guoyan Front Oncol Oncology 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. Frontiers Media S.A. 2023-04-14 /pmc/articles/PMC10140593/ /pubmed/37124541 http://dx.doi.org/10.3389/fonc.2023.1072480 Text en Copyright © 2023 Lei, Lin, Cheng, Shao, Ding, Zuo, Chen, Liao and Liu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Lei, Yihui
Lin, Li
Cheng, Shuyu
Shao, Qiming
Ding, Chenchun
Zuo, Renjie
Chen, Weiping
Liao, Quan
Liu, Guoyan
Acute inflammatory reaction during anti-angiogenesis therapy combined with immunotherapy as a possible indicator of the therapeutic effect: Three case reports and literature review
title Acute inflammatory reaction during anti-angiogenesis therapy combined with immunotherapy as a possible indicator of the therapeutic effect: Three case reports and literature review
title_full Acute inflammatory reaction during anti-angiogenesis therapy combined with immunotherapy as a possible indicator of the therapeutic effect: Three case reports and literature review
title_fullStr Acute inflammatory reaction during anti-angiogenesis therapy combined with immunotherapy as a possible indicator of the therapeutic effect: Three case reports and literature review
title_full_unstemmed Acute inflammatory reaction during anti-angiogenesis therapy combined with immunotherapy as a possible indicator of the therapeutic effect: Three case reports and literature review
title_short Acute inflammatory reaction during anti-angiogenesis therapy combined with immunotherapy as a possible indicator of the therapeutic effect: Three case reports and literature review
title_sort acute inflammatory reaction during anti-angiogenesis therapy combined with immunotherapy as a possible indicator of the therapeutic effect: three case reports and literature review
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10140593/
https://www.ncbi.nlm.nih.gov/pubmed/37124541
http://dx.doi.org/10.3389/fonc.2023.1072480
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