Literature DB >> 35173881

Efficacy and mechanism of osimertinib combined with bevacizumab in the treatment of postoperative EGFR positive stage II-IIIA lung adenocarcinoma.

Jian Bao1, Zhengsheng Wu2, Congjun Zhang3, Mingjun Zhang4, Yi Wang1, Hongxia Li1, Xiang Sun1, Junfeng Gao1, Lei Ge1, Yuzhi Li1, Hao Wang2, Qianying Guo2.   

Abstract

OBJECTIVE: To explore the efficacy and mechanism of osimertinib combined with bevacizumab in treating postoperative epidermal growth factor receptor (EGFR) positive stage II-IIIA lung adenocarcinoma.
METHODS: In this retrospective study, one hundred and thirty patients with postoperative EGFR positive stage II-IIIA lung adenocarcinoma were divided into two groups according to different treatment methods. Patients treated with osimertinib alone were included in the single group (65 patients). Patients treated with bevacizumab on the basis of the single group were included in the joint group (65 patients). The short-term efficacy, side effects and survival results of the two groups were counted. The changes of serum vascular endothelial growth factor, serum tumor markers and life quality before and after the treatment were observed.
RESULTS: The ORR (66.15%) and DCR (86.15%) in the joint group were significantly higher than those in the single group (47.69% and 70.77%) (both P<0.05). The serum levels of VEGFA, VEGFB, VEGFC, BFGF, HDGF, SDF-1, CEA, CA153, CYFRA21-1 and CA199 in the joint group were lower than those in the single group after the treatment (all P<0.05). No significant difference was shown in the incidence of adverse reactions such as rash, diarrhea, constipation, albuminuria, hypertension and interstitial pneumonia between the joint group and the single group (all P>0.05). After the treatment, the ZPS score of the joint group was lower than that of the single group, and the KPS score was higher than that of the single group (both P<0.05). There was no significant difference in the two-year median DFS and the one or two-year DFS rate between the joint group and the single group (all P>0.05).
CONCLUSION: Osimertinib combined with bevacizumab in the treatment of postoperative EGFR positive stage II-IIIA lung adenocarcinoma has evident short-term efficacy and mild side effects, which is helpful in improving the disease control rate and life quality. The mechanism may be related to the regulation of serum CEA, CA153, CYFRA21-1, CA199 levels and inhibition of VEGFA, VEGFB, VEGFC, BFGF, HDGF, and SDF-1 levels. AJTR
Copyright © 2022.

Entities:  

Keywords:  EGFR mutation; bevacizumab; efficacy; lung adenocarcinoma; osimertinib; stage II-IIIA; tumor marker; vascular endothelial growth factor

Year:  2022        PMID: 35173881      PMCID: PMC8829594     

Source DB:  PubMed          Journal:  Am J Transl Res        ISSN: 1943-8141            Impact factor:   4.060


  22 in total

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Review 2.  The next tier of EGFR resistance mutations in lung cancer.

Authors:  Hannah L Tumbrink; Alena Heimsoeth; Martin L Sos
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Review 3.  Bevacizumab as first-line treatment in HER2-negative advanced breast cancer: pros and cons.

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Review 4.  Beyond bevacizumab: a review of targeted agents in metastatic small bowel adenocarcinoma.

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Review 5.  Targeting EGFRL858R/T790M and EGFRL858R/T790M/C797S resistance mutations in NSCLC: Current developments in medicinal chemistry.

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6.  Erlotinib alone or with bevacizumab as first-line therapy in patients with advanced non-squamous non-small-cell lung cancer harbouring EGFR mutations (JO25567): an open-label, randomised, multicentre, phase 2 study.

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Review 7.  Atezolizumab in combination with bevacizumab, paclitaxel and carboplatin for the first-line treatment of patients with metastatic non-squamous non-small cell lung cancer, including patients with EGFR mutations.

Authors:  Martin Reck; Geetha Shankar; Anthony Lee; Shelley Coleman; Mark McCleland; Vassiliki A Papadimitrakopoulou; Mark A Socinski; Alan Sandler
Journal:  Expert Rev Respir Med       Date:  2019-12-12       Impact factor: 3.772

Review 8.  Development of EGFR TKIs and Options to Manage Resistance of Third-Generation EGFR TKI Osimertinib: Conventional Ways and Immune Checkpoint Inhibitors.

Authors:  Leilei Wu; Linping Ke; Zhenshan Zhang; Jinming Yu; Xue Meng
Journal:  Front Oncol       Date:  2020-12-18       Impact factor: 6.244

9.  Atezolizumab with bevacizumab, paclitaxel and carboplatin was effective for patients with SMARCA4-deficient thoracic sarcoma.

Authors:  Hayato Kawachi; Kei Kunimasa; Yoji Kukita; Harumi Nakamura; Keiichiro Honma; Takahisa Kawamura; Takako Inoue; Motohiro Tamiya; Hanako Kuhara; Kazumi Nishino; Yu Mizote; Takashi Akazawa; Hideaki Tahara; Toru Kumagai
Journal:  Immunotherapy       Date:  2021-05-25       Impact factor: 4.196

Review 10.  First Biologic Drug in the Treatment of RAS Wild-Type Metastatic Colorectal Cancer: Anti-EGFR or Bevacizumab? Results From a Meta-Analysis.

Authors:  Alessandro Ottaiano; Alfonso De Stefano; Monica Capozzi; Anna Nappi; Chiara De Divitiis; Carmela Romano; Lucrezia Silvestro; Antonino Cassata; Rossana Casaretti; Salvatore Tafuto; Michele Caraglia; Massimiliano Berretta; Guglielmo Nasti; Antonio Avallone
Journal:  Front Pharmacol       Date:  2018-05-03       Impact factor: 5.810

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