EGFR-TKI rechallenge in patients with EGFR-mutated non-small-cell lung cancer who progressed after first-line osimertinib treatment: A multicenter retrospective observational study

被引:5
作者
Araki, Taisuke [1 ]
Kanda, Shintaro [2 ]
Obara, Miho [3 ]
Agatsuma, Toshihiko [4 ]
Kakizaki, Yumiko [5 ]
Hama, Mineyuki [6 ]
Yamamoto, Hiroshi [7 ]
Takada, Munetake [8 ]
Yamamoto, Manabu [9 ]
Matsuo, Akemi [10 ]
Kondo, Daichi [11 ]
Komatsu, Masamichi [1 ]
Sonehara, Kei [1 ]
Tateishi, Kazunari [1 ]
Hanaoka, Masayuki [1 ]
Koizumi, Tomonobu [2 ]
机构
[1] Shinshu Univ, Sch Med, Dept Internal Med 1, 3-1-1 Asahi, Matsumoto, Nagano 3908621, Japan
[2] Shinshu Univ, Dept Hematol & Med Oncol, Sch Med, 3-1-1 Asahi, Matsumoto, Nagano 3908621, Japan
[3] Shinshu Univ Hosp, Dept Pharm, 3-1-1 Asahi, Matsumoto, Nagano 3908621, Japan
[4] Shinshu Ueda Med Ctr, Dept Resp Med, 1-27-21 Midorigaoka, Ueda, Nagano 3868610, Japan
[5] Yamanashi Prefectural Cent Hosp, Lung Canc & Resp Dis Ctr, 1-1-1 Fujimi, Kofu, Yamanashi 4008506, Japan
[6] Japanese Red Cross Soc Suwa Hosp, Dept Resp Med, 5-11-50 Kogandori, Suwa, Nagano 3928510, Japan
[7] Iida Municipal Hosp, Dept Resp Med, 438 Yawatamachi, Iida, Nagano 3950814, Japan
[8] Jiseikai Aizawa Hosp, Dept Resp Med, 2-5-1 Honjo, Matsumoto, Nagano 3908510, Japan
[9] Japanese Red Cross Soc Nagano Hosp, Dept Resp Med, 5-22-1 Wakasato, Nagano, Nagano 3808582, Japan
[10] Shinonoi Gen Hosp, Minaminagano Med Ctr, Dept Resp Med, 666-1 Shinonoiai, Nagano 3888004, Japan
[11] Hokushin Gen Hosp, Dept Resp Med, 1-5-63 Nishi, Nakano, Nagano 3838505, Japan
关键词
Non -small -cell lung cancer; Epidermal growth factor receptor tyrosine; kinase inhibitor; Osimertinib; Rechallenge; Resistance; INHIBITORS;
D O I
10.1016/j.resinv.2024.01.002
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Rechallenge therapy with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) is known to confer some clinical benefit for patients with metastatic EGFR-mutated non-small cell lung cancer (NSCLC). However, little is known about the efficacy of EGFR-TKI rechallenge after resistance to first-line (1L) osimertinib. This study aimed to assess the efficacy and safety of EGFR-TKI rechallenge therapy after resistance to 1L osimertinib in a Japanese clinical setting. Methods: Between April 2018 and August 2022, 26 patients who progressed after treatment with 1L osimertinib and received EGFR-TKI rechallenge were included in this multicenter retrospective analysis. Patients in whom 1L osimertinib was discontinued owing to toxicity and had subsequent disease progression were also included in the analysis. Results: Overall, the objective response rate for rechallenge therapy was 23.1%. The disease control rate was 53.9%, and the median progression-free survival (PFS) was 3.4 months. Patients who discontinued 1L osimertinib for toxicity had a higher response rate (42.9% vs. 15.8%) and longer PFS than those who discontinued it due to disease progression (median: 11.4 vs. 2.7 months, P = 0.001). Three patients (11.5%) developed rechallenge therapy-associated pneumonitis, two of which were grade >= 3. Conclusions: Rechallenge with EGFR-TKI after 1L osimertinib resistance showed limited clinical efficacy. However, it could be considered as a subsequent salvage therapeutic option for patients in whom 1L osimertinib was discontinued owing to toxicity.
引用
收藏
页码:262 / 268
页数:7
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