scholarly journals Combination treatment with bevacizumab plus erlotinib for meningeal carcinomatosis of afatinib-resistant EGFR mutated lung cancer without T790M mutation: a case report

2021 ◽  
Vol 0 (0) ◽  
pp. 0-0
Author(s):  
Shinji Chiba ◽  
Masachika Akiyama ◽  
Kazuhiro Yakuwa ◽  
Hideomi Sato ◽  
Kunio Hirano ◽  
...  
2021 ◽  
pp. 107815522110191
Author(s):  
Pinar Gursoy

Introduction Most patients with non-small-cell lung cancer tumors that have epidermal growth factor receptor (EGFR) mutations have deletion mutations in exon 19 or exon 21, or both.In recent years, targeted therapies in lung cancer have increased survival, but the development of resistance to these drugs poses a major problem. Thesubstitution of methionineforthreonine at position 790 (T790M) mutation,is primarily responsible for this resistance. However, after osimertinib used in T790M positivepatients treatment options are generally limited to chemotherapy. Case report We reported the efficacy of erlotinib, which we reapplied due to the disappearance of the resistance mutation after osimertinib in a 68-year-old patient using osimertinib after erlotinib. Management and outcome: In the patient using erlotinib due to exon 19 deletion when progression was observed and T790M positivity was detected, osimertinib treatment was initiated. However, when T790M was found to be negative with rebiopsy in progression after osimertinib, a complete response was achieved by restarting erlotinib. Discussion The strategy of restarting erlotinib treatment with negative T790M mutation detected in biopsies of patients with osimertinib resistance may be an acceptable treatment option.


2015 ◽  
Vol 10 (1) ◽  
pp. 386-388 ◽  
Author(s):  
HIROKO WATANABE ◽  
TOMOHIRO TAMURA ◽  
KATSUNORI KAGOHASHI ◽  
NORIO TAKAYASHIKI ◽  
KOICHI KURISHIMA ◽  
...  

2015 ◽  
Vol 10 (1) ◽  
pp. 93-101 ◽  
Author(s):  
Yosuke Togashi ◽  
Hidetoshi Hayashi ◽  
Masato Terashima ◽  
Marco A de Velasco ◽  
Kazuko Sakai ◽  
...  

Lung Cancer ◽  
2020 ◽  
Vol 139 ◽  
pp. 28-34
Author(s):  
Masayuki Takeda ◽  
Kazuko Sakai ◽  
Hidetoshi Hayashi ◽  
Kaoru Tanaka ◽  
Koji Haratani ◽  
...  

2014 ◽  
Vol 4 (1) ◽  
pp. 13-17
Author(s):  
Seigo Minami ◽  
Naoki Matsushiro ◽  
Takashi Sato ◽  
Suguru Yamamoto ◽  
Yoshitaka Ogata ◽  
...  

2021 ◽  
Vol 2021 ◽  
pp. 1-9
Author(s):  
Milan Zhang ◽  
Weifeng Ma ◽  
Huiqin Liu ◽  
Yushu Jiang ◽  
Lingzhi Qin ◽  
...  

Osimertinib has demonstrated promising efficacy against leptomeningeal metastasis (LM) associated with T790M-positive non-small-cell lung cancer (NSCLC). However, the effect of cerebrospinal fluid’s (CSF’s) epidermal growth factor receptor (EGFR) T790M mutation on osimertinib efficacy remains unclear.Seventy-eight patients were studied with EGFR-mutated NSCLC and LM. Case data were collected and EGFR mutation status of circulating cell-free DNA from paired CSF, and plasma of 23 patients with LM was detected using droplet digital PCR. The median overall survival (mOS) was 8.08 months (95% CI: 6.07–10.09) in the study. Forty-four osimertinib-treated patients had an improved mOS of 13.15 (95% CI: 5.74–20.57) and a median progression-free survival (PFS) of 9.50 months (95% CI: 6.77–12.23) when compared with patients treated with first- or second-generation EGFR-TKI (mOS = 3.00 months (95% CI: 1.32–4.68) and median PFS = 1.50 months (95% CI: 0.00–3.14)). In the osimertinib group, mOS values for CSF with and without T790M mutation were 22.15 months (95% CI: 9.44–34.87) and 13.39 months (95% CI: 7.01–19.76), respectively, with no statistical differences. Regardless of the CSF T790M mutation status, osimertinib demonstrated significant efficacy against LM associated with NSCLC.


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