Does dose reduction of afatinib affect treatment outcomes of patients with EGFR-mutant metastatic non-small cell lung cancer in real-world clinical practice?

被引:2
|
作者
Poh, Mau Ern [1 ]
Chai, Chee Shee [2 ]
Liam, Chong Kin [1 ]
Ho, Gwo Fuang [3 ]
Pang, Yong Kek [1 ]
Hasbullah, Harissa Husainy [4 ,5 ]
Tho, Lye Mun [6 ]
Nor, Ibtisam Muhamad [5 ]
Ho, Kean Fatt [7 ]
Thiagarajan, Muthukkumaran [5 ]
Samsudin, Azlina [8 ]
Omar, Azza [9 ]
Ong, Choo Khoon [10 ]
Soon, Sing Yang [11 ]
Tan, Sin Nee [12 ]
How, Soon Hin [12 ,13 ]
机构
[1] Univ Malaya, Fac Med, Dept Med, Kuala Lumpur 50603, Malaysia
[2] Univ Malaysia Sarawak, Fac Med & Hlth Sci, Dept Med, Sarawak, Malaysia
[3] Univ Malaya, Fac Med, Clin Oncol Unit, Kuala Lumpur, Malaysia
[4] Univ Teknol Mara, Fac Med, Shah Alam, Selangor, Malaysia
[5] Gen Hosp Kuala Lumpur, Oncol & Radiotherapy Dept, Kuala Lumpur, Malaysia
[6] Beacon Hosp, Dept Clin Oncol, Petaling Jaya, Selangor, Malaysia
[7] Mt Miriam Canc Hosp, George Town, Malaysia
[8] Hosp Sultanah Nur Zahirah, Dept Med, Terengganu, Malaysia
[9] Hosp Raja Perempuan Zainab II, Med Dept, Resp Unit, Kota Baharu, Kelantan, Malaysia
[10] Gleneagles Hosp Penang, George Town, Malaysia
[11] Sarawak Heart Ctr, Sarawak, Malaysia
[12] Hosp Tengku Ampuan Afzan, Dept Med, Kuantan, Pahang, Malaysia
[13] Int Islamic Univ Malaysia, Kulliyyah Med, Pahang, Malaysia
关键词
Adenocarcinoma; resource-limited settings; survival; treatment outcome; tyrosine kinase inhibitors (TKIs); 1ST-LINE TREATMENT; ADVANCED NSCLC; SURVIVAL-DATA; OPEN-LABEL; ADENOCARCINOMA; GEFITINIB; SAFETY;
D O I
10.21037/tlcr-23-691
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Afatinib can be started at a dose lower than the recommended starting dose of 40 mg/day for the treatment of epidermal growth factor receptor ( EGFR )-mutant non -small cell lung cancer (NSCLC), however treatment outcomes in real -world clinical practice remains unclear. Methods: This retrospective study of patients with NSCLC from 18 major hospitals (public, private or university teaching hospitals) enrolled in Malaysia's National Cardiovascular and Thoracic Surgical Database (NCTSD) assessed the efficacy of lower doses of afatinib on treatment outcomes in a real -world clinical practice. Data on clinical characteristics, afatinib dosing, and treatment outcomes for patients included in NCTSD from 1(st) January 2015 to 31(st) December 2020 were analyzed. Results: Of the 133 patients studied, 94.7% had adenocarcinoma. Majority of the patients (60.9%) had EGFR exon 19 deletion and 23.3% had EGFR exon 21 L858R point mutation. The mean age of patients was 64.1 years and majority (83.5%) had Eastern Cooperative Oncology Group performance status of 2-4 at diagnosis. The most common afatinib starting doses were 40 mg (37.6%), 30 mg (29.3%), and 20 mg (26.3%) once daily (OD), respectively. A quarter of patients had dose reduction (23.3%) due to side effects or cost constraints. Majority of the patients had partial response to afatinib (63.2%) whilst 2.3% had complete response. Interestingly, the objective response rate was significantly higher (72.3%) with afatinib OD doses of less than 40 mg compared to 40 mg (54.0%) (P=0.032). Patients on lower doses of afatinib were two times more likely to achieve an objective response [odds ratio =2.64; 95% confidence interval (CI): 1.20-5.83; P=0.016]. These patients had a numerically but not statistically longer median time to treatment failure (TTF). Median TTF (95% CI) for the overall cohort was 12.4 (10.02-14.78) months. Median overall survival (95% CI) was 21.30 (15.86-26.75) months. Conclusions: Lower afatinib doses (<40 mg OD) could be equally effective as standard dose in patients with EGFR -mutant advanced NSCLC and may be more suited to Asian patients, minimizing side effects that may occur at higher dosages of afatinib leading to dose interruptions and affecting treatment outcomes.
引用
收藏
页码:307 / 320
页数:14
相关论文
共 50 条
  • [1] Real-World Pattern of Treatment and Clinical Outcomes of EGFR-Mutant Non-Small Cell Lung Cancer in a Single Academic Centre in Quebec
    Agulnik, Jason S.
    Kasymjanova, Goulnar
    Pepe, Carmela
    Hurry, Manjusha
    Walton, Ryan N.
    Sakr, Lama
    Cohen, Victor
    Small, David
    CURRENT ONCOLOGY, 2021, 28 (06) : 5179 - 5191
  • [2] Afatinib as First-Line Treatment in Elderly Patients with EGFR-Mutant Non-Small Cell Lung Cancer: Real-World Data Analysis
    Chen, Yen-Ting
    Yen, Chia-Te
    Wu, Wen-Jui
    Yang, Sheng-Hsiung
    INTERNATIONAL JOURNAL OF GERONTOLOGY, 2022, 16 (03) : 266 - 270
  • [3] Real-world analysis of first-line afatinib in patients with EGFR-mutant non-small cell lung cancer and brain metastasis: survival and prognostic factors
    Kim, Jehun
    Jang, Tae Won
    Choi, Chang Min
    Kim, Mi Hyun
    Lee, Sung Yong
    Park, Cheol Kyu
    Chang, Yoon Soo
    Lee, Kye Young
    Kim, Seung Joon
    Yang, Sei Hoon
    Ryu, Jeong Seon
    Lee, Jeong Eun
    Lee, Shin Yup
    Park, Chan Kwon
    Lee, Sang Hoon
    Jang, Seung Hun
    Yoon, Seong Hoon
    TRANSLATIONAL LUNG CANCER RESEARCH, 2023, 12 (06) : 1197 - +
  • [4] Real-world assessment of afatinib for patients with EGFR-positive non-small cell lung cancer
    Igawa, Satoshi
    Ono, Taihei
    Kasajima, Masashi
    Kusuhara, Seiichiro
    Otani, Sakiko
    Fukui, Tomoya
    Yokoba, Masanori
    Kubota, Masaru
    Katagiri, Masato
    Mitsufuji, Hisashi
    Sasaki, Jiichiro
    Naoki, Katsuhiko
    INVESTIGATIONAL NEW DRUGS, 2020, 38 (06) : 1906 - 1914
  • [5] A real-world cohort study of first-line afatinib in patients with EGFR-mutant advanced non-small cell lung cancer in Vietnam
    Pham, Cam Phuong
    Nguyen, Thi Thai Hoa
    Do, Anh Tu
    Nguyen, Tuan Khoi
    Hoang, Thi Anh Thu
    Le, Tuan Anh
    Vuong, Dinh Thy Hao
    Nguyen, Dac Nhan Tam
    Dang, Van Khiem
    Nguyen, Thi Oanh
    Pham, Van Luan
    Nguyen, Minh Hai
    Vo, Thi Huyen Trang
    Do, Hung Kien
    Vu, Ha Thanh
    Nguyen, Thi Thuy Hang
    Pham, Van Thai
    Trinh, Le Huy
    Nguyen, Khac Dung
    Nguyen, Hoang Gia
    Truong, Cong Minh
    Pham, Tran Minh Chau
    Nguyen, Thi Bich Phuong
    BMC CANCER, 2024, 24 (01)
  • [6] The Difference in Clinical Outcomes Between Osimertinib and Afatinib for First-Line Treatment in Patients with Advanced and Recurrent EGFR-Mutant Non-Small Cell Lung Cancer in Taiwan
    Huang, Yen-Hsiang
    Hsu, Kuo-Hsuan
    Tseng, Jeng-Sen
    Yang, Tsung-Ying
    Chen, Kun-Chieh
    Su, Kang-Yi
    Yu, Sung-Liang
    Chen, Jeremy J. W.
    Chang, Gee-Chen
    TARGETED ONCOLOGY, 2022, 17 (03) : 295 - 306
  • [7] Clinical Predictors of Response to EGFR Tyrosine Kinase inhibitors in Patients with EGFR-Mutant Non-Small Cell Lung Cancer
    Fukihara, Jun
    Watanabe, Naohiro
    Taniguchi, Hiroyuki
    Kondoh, Yasuhiro
    Kimura, Tomoki
    Kataoka, Kensuke
    Matsuda, Toshiaki
    Yokoyama, Toshiki
    Hasegawa, Yoshinori
    ONCOLOGY, 2014, 86 (02) : 86 - 93
  • [8] Efficacy and Safety of Afatinib for EGFR-mutant Non-small Cell Lung Cancer, Compared with Gefitinib or Erlotinib
    Kim, Youjin
    Lee, Se-Hoon
    Ahn, Jin Seok
    Ahn, Myung-Ju
    Park, Keunchil
    Sun, Jong-Mu
    CANCER RESEARCH AND TREATMENT, 2019, 51 (02): : 502 - 509
  • [9] Real-world Afatinib Outcomes in Advanced Non-small Cell Lung Cancer Harboring EGFR Mutations
    Chen, Chi-Han
    Chang, John Wen-Cheng
    Chang, Ching-Fu
    Huang, Chen-Yang
    Yang, Cheng-Ta
    Kuo, Chih-Hsi Scott
    Fang, Yueh-Fu
    Hsu, Ping-Chih
    Wu, Chiao-En
    ANTICANCER RESEARCH, 2022, 42 (04) : 2145 - 2157
  • [10] Real World Diagnosis and Treatment Outcomes in Patients with EGFR-Mutant Metastatic Lung Cancer
    Li, T.
    Ma, W.
    Tian, E.
    Li, Q.
    JOURNAL OF THORACIC ONCOLOGY, 2019, 14 (10) : S1066 - S1067