PMID- 36872054 OWN - NLM STAT- MEDLINE DCOM- 20230307 LR - 20230325 IS - 1999-6187 (Electronic) IS - 1009-3419 (Print) IS - 1009-3419 (Linking) VI - 26 IP - 2 DP - 2023 Feb 20 TI - [Initial Treatment of Aumolertinib in Combination with Bevacizumab for Advanced NSCLC with Primary EGFR T790M Mutation: A Report of Three Cases and Literature Review]. PG - 158-164 LID - 10.3779/j.issn.1009-3419.2023.101.04 [doi] AB - With the development of sequencing technology, the detection rate of non-small cell lung cancer (NSCLC) with primary epidermal growth factor receptor (EGFR) T790M mutation is increasing. However, the first-line treatment for primary EGFR T790M-mutated NSCLC still lacks standard recommendations. Here, we reported three advanced NSCLC cases with EGFR-activating mutation and primary T790M mutation. The patients were initially treated with Aumolertinib combination with Bevacizumab; among which, one case was discontinued Bevacizumab due to bleeding risk after treatment for three months. Treatment was switched to Osimertinib after ten months of treatment. Another case switched to Osimertinib and discontinued Bevacizumab after thirteen months of treatment. The best effect response in all three cases was partial response (PR) after initial treatment. Two cases progressed after first-line treatment and progression-free survival (PFS) was eleven months and seven months respectively. The other one patient had persistent response after treatment, and the treatment duration has reached nineteen months. Two cases had multiple brain metastases before administration and the best response to intracranial lesions was PR. The intracranial PFS was fourteen months and not reached (16+ months), respectively. There were no new adverse events (AEs), and no AEs of grade three or above were reported. In addition, we summarized the research progress of Osimertinib in the treatment of NSCLC with primary EGFR T790M mutation. In conclusion, Aumolertinib combined with Bevacizumab in the treatment of advanced NSCLC with primary EGFR T790M mutation has a high objective response rate (ORR) and control ability of intracranial lesions, which can be used as one of the initial options for first-line advanced NSCLC with primary EGFR T790M mutation.
. FAU - Yang, Xue AU - Yang X AD - Department of Medical Oncology, Tianjin Medical University General Hospital, Tianjin 300052, China. FAU - Meng, Fanlu AU - Meng F AD - Department of Medical Oncology, Tianjin Medical University General Hospital, Tianjin 300052, China. FAU - Zhong, Diansheng AU - Zhong D AD - Department of Medical Oncology, Tianjin Medical University General Hospital, Tianjin 300052, China. LA - chi PT - Case Reports PT - English Abstract PT - Journal Article PT - Review PL - China TA - Zhongguo Fei Ai Za Zhi JT - Zhongguo fei ai za zhi = Chinese journal of lung cancer JID - 101126433 RN - 3C06JJ0Z2O (osimertinib) RN - 2S9ZZM9Q9V (Bevacizumab) RN - T4RS462G19 (aumolertinib) RN - EC 2.7.10.1 (ErbB Receptors) RN - 0 (Protein Kinase Inhibitors) RN - EC 2.7.10.1 (EGFR protein, human) SB - IM MH - Humans MH - Bevacizumab MH - *Carcinoma, Non-Small-Cell Lung MH - ErbB Receptors MH - *Lung Neoplasms MH - Mutation MH - Protein Kinase Inhibitors PMC - PMC10033243 OTO - NOTNLM OT - Aumolertinib OT - Bevacizumab OT - Lung neoplasms OT - Primary T790M EDAT- 2023/03/06 06:00 MHDA- 2023/03/08 06:00 PMCR- 2023/02/20 CRDT- 2023/03/05 21:12 PHST- 2023/03/05 21:12 [entrez] PHST- 2023/03/06 06:00 [pubmed] PHST- 2023/03/08 06:00 [medline] PHST- 2023/02/20 00:00 [pmc-release] AID - 10.3779/j.issn.1009-3419.2023.101.04 [doi] PST - ppublish SO - Zhongguo Fei Ai Za Zhi. 2023 Feb 20;26(2):158-164. doi: 10.3779/j.issn.1009-3419.2023.101.04.