Osimertinib for patients with poor performance status and EGFR T790M mutation-positive advanced non-small cell lung cancer: a phase II clinical trial

被引:21
|
作者
Nakashima, Kazuhisa [1 ,2 ]
Ozawa, Yuichi [3 ]
Daga, Haruko [4 ]
Imai, Hisao [5 ]
Tamiya, Motohiro [6 ]
Tokito, Takaaki [7 ]
Kawamura, Takahisa [1 ]
Akamatsu, Hiroaki [3 ]
Tsuboguchi, Yuko [4 ]
Takahashi, Toshiaki [1 ]
Yamamoto, Nobuyuki [3 ]
Mori, Keita [8 ]
Murakami, Haruyasu [1 ]
机构
[1] Shizuoka Canc Ctr, Div Thorac Oncol, Shizuoka, Japan
[2] Shimane Univ, Div Med Oncol & Resp Med, Dept Internal Med, Fac Med, 89-1 Enya Cho, Izumo, Shimane, Japan
[3] Wakayama Med Univ, Internal Med 3, Wakayama, Japan
[4] Osaka City Gen Hosp, Dept Med Oncol, Osaka, Japan
[5] Gunma Prefectural Canc Ctr, Div Resp Med, Ota, Gunma, Japan
[6] Osaka Int Canc Inst, Dept Thorac Oncol, Osaka, Japan
[7] Kurume Univ, Sch Med, Dept Med, Div Respirol Neurol & Rheumatol, Fukuoka, Japan
[8] Shizuoka Canc Ctr, Clin Res Ctr, Shizuoka, Japan
关键词
EGFR T790M mutation-positive; Non-small-cell lung cancer; Osimertinib; Poor performance status; 1ST-LINE TREATMENT; OPEN-LABEL; STANDARD CHEMOTHERAPY; ERLOTINIB; MULTICENTER; GEMCITABINE; CISPLATIN; GEFITINIB;
D O I
10.1007/s10637-020-00943-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osimertinib is a molecularly targeted agent used to treat non-small cell lung cancer (NSCLC) patients with an epidermal growth factor receptor (EGFR) T790M mutation. However, its efficacy and safety profile when patients have poor performance status (PS) is unknown. Therefore, we conducted an open-label, multi-center, single-arm phase II study to evaluate its efficacy and safety in EGFR T790M mutation-positive NSCLC patients with Eastern Cooperative Oncology Group PS scores of between 2 and 4. Patients received 80 mg of osimertinib once daily. Our primary endpoint was progression-free survival. Eighteen patients were enrolled between June 2017 and November 2018. The median age was 77 years (range: 55-85 years). Ten, six, and two patients had PS scores of 2, 3, and 4, respectively. All patients had adenocarcinoma with common EGFR mutations and had been treated with first- or second-generation EGFR- tyrosine kinase inhibitors previously. The overall median progression-free survival was 7.0 months (90% confidence interval: 5.5-8.9 months). The overall response rate and median overall survival were 53% and 12.7 months, respectively. Moreover, improved PS scores were observed in 72% of the patients. Although the incidence of grade 3 adverse events was low, with no grade 4 or 5 events observed, three patients required treatment cessation due to the development of interstitial lung disease. Osimertinib therapy could be beneficial for EGFR T790M mutation-positive advanced NSCLC patients with poor PS. This trial was registered with the Japan Registry of Clinical Trials on March 12, 2019 (trial no. jRCT1041180081).
引用
收藏
页码:1854 / 1861
页数:8
相关论文
共 50 条
  • [1] Osimertinib for patients with poor performance status and EGFR T790M mutation-positive advanced non-small cell lung cancer: a phase II clinical trial
    Kazuhisa Nakashima
    Yuichi Ozawa
    Haruko Daga
    Hisao Imai
    Motohiro Tamiya
    Takaaki Tokito
    Takahisa Kawamura
    Hiroaki Akamatsu
    Yuko Tsuboguchi
    Toshiaki Takahashi
    Nobuyuki Yamamoto
    Keita Mori
    Haruyasu Murakami
    Investigational New Drugs, 2020, 38 : 1854 - 1861
  • [2] Osimertinib for EGFR T790M mutation-positive non-small cell lung cancer
    Soejima, Kenzo
    Yasuda, Hiroyuki
    Hirano, Toshiyuki
    EXPERT REVIEW OF CLINICAL PHARMACOLOGY, 2017, 10 (01) : 31 - 38
  • [3] Osimertinib for patients with EGFR T790M mutation-positive non-small-cell lung cancer and a poor performance status
    Nakashima, Kazuhisa
    Kimura, Madoka
    Akamatsu, Hiroaki
    Daga, Haruko
    Imai, Hisao
    Taira, Tetsuhiko
    Ko, Ryo
    Hisamatsu, Yasushi
    Nishino, Kazumi
    Sugimoto, Takeya
    Miyashita, Yosuke
    Takahashi, Toshiaki
    Kumagai, Toru
    Yamamoto, Nobuyuki
    Murakami, Haruyasu
    JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2019, 49 (07) : 671 - 675
  • [4] Osimertinib for patients with EGFR T790M mutation-positive non-small-cell lung cancer who have poor performance status
    Kimura, Madoka
    Nishino, Kazumi
    Imamura, Fumio
    Nakashima, Kazuhisa
    Takahashi, Toshiaki
    Sugimoto, Takeya
    Akamatsu, Hiroaki
    Yamamoto, Nobuyuki
    Daga, Haruko
    Imai, Hisao
    Taira, Tetsuhiko
    Miyashita, Yosuke
    Ko, Ryo
    Hisamatsu, Yasushi
    Murakami, Haruyasu
    ANNALS OF ONCOLOGY, 2018, 29
  • [5] Osimertinib for the Treatment of Metastatic EGFR T790M Mutation-Positive Non-Small Cell Lung Cancer
    Khozin, Sean
    Weinstock, Chana
    Blumenthal, Gideon M.
    Cheng, Joyce
    He, Kun
    Zhuang, Luning
    Zhao, Hong
    Charlab, Rosane
    Fan, Ingrid
    Keegan, Patricia
    Pazdur, Richard
    CLINICAL CANCER RESEARCH, 2017, 23 (09) : 2131 - 2135
  • [6] Targeting the Gatekeeper: Osimertinib in EGFR T790M Mutation-Positive Non-Small Cell Lung Cancer
    Skoulidis, Ferdinandos
    Papadimitrakopoulou, Vassiliki A.
    CLINICAL CANCER RESEARCH, 2017, 23 (03) : 618 - 622
  • [7] Osimertinib in Japanese patients with EGFR T790M mutation-positive advanced non-small-cell lung cancer: AURA3 trial
    Akamatsu, Hiroaki
    Katakami, Nobuyuki
    Okamoto, Isamu
    Kato, Terufumi
    Kim, Young Hak
    Imamura, Fumio
    Shinkai, Masaharu
    Hodge, Rachel A.
    Uchida, Hirohiko
    Hida, Toyoaki
    CANCER SCIENCE, 2018, 109 (06): : 1930 - 1938
  • [8] An evaluation of aumolertinib for the treatment of EGFR T790M mutation-positive non-small cell lung cancer
    Wang, Jingyi
    Wu, Lin
    EXPERT OPINION ON PHARMACOTHERAPY, 2022, 23 (06) : 647 - 652
  • [9] Phase II trial of alternating osimertinib with gefitinib in patients with EGFR-T790M mutation positive advanced non-small cell lung cancer (Oscillate)
    Mersiades, Antony
    Pavlakis, Nick
    Kao, Steven
    John, Tom
    Lee, Chee Khoon
    Dawson, Sarah-Jane
    Wong, Stephen
    Tan, Lavinia
    Yip, Sonia
    Brown, Chris
    Livingstone, Ann
    Cheung, Yvonne
    Jurkovic, Hannora
    Stockler, Martin
    ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, 2018, 14 : 199 - 200
  • [10] Real-world osimertinib for EGFR mutation-positive non-small-cell lung cancer with acquired T790M mutation
    Imamura, Fumio
    Kimura, Madoka
    Yano, Yukihiro
    Mori, Masahide
    Suzuki, Hidekazu
    Hirashima, Tomonori
    Ihara, Shouichi
    Komuta, Kiyoshi
    Shiroyama, Takayuki
    Nagatomo, Izumi
    Kumagai, Toru
    FUTURE ONCOLOGY, 2020, 16 (21) : 1537 - 1546