Clinical Experience With 75-mg Dose of Erlotinib for Mutated Metastatic EGFR Non-small Cell Lung Cancer

被引:0
|
作者
Aren, Osvaldo [1 ]
Samtani, Suraj [2 ,3 ]
Frelinghuysen, Micahel [4 ]
Burotto, Mauricio [1 ,5 ]
机构
[1] Bradford Hill Invest Ctr, Med Oncol Dept, Santiago, Chile
[2] Univ Desarrollo, Fac Med Clin Alemana, Med Oncol Dept, Santiago, Chile
[3] Inst Nacl Canc, Med Oncol Dept, Santiago, Chile
[4] Hosp Clin Reg Concepcion, Radiat Oncol Unit, Concepcion, Chile
[5] Clin Univ Los Andes, Med Oncol Dept, Santiago, Chile
关键词
lung cancer; target therapy; erlotinib; GROWTH-FACTOR RECEPTOR; PHASE-I; 1ST-LINE TREATMENT; TYROSINE KINASE; OPEN-LABEL; CHEMOTHERAPY; MULTICENTER; MUTATIONS; INHIBITOR; GEFITINIB;
D O I
10.1097/MJT.0000000000001074
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Non-small cell lung cancer (NSCLC) remains the leading cause of cancer death worldwide, although important advances in target therapy have been developed in the past few years. Erlotinib is a reversible epidermal growth factor receptor (EGFR) inhibitor, which was approved at its maximum tolerated dose of 150 mg/d determined from the initial phase I study. Studies suggest that the optimal biological dose of erlotinib should be lower and dependent on different variables. Study Question: We aimed to evaluate the response rates and toxicity with 75 mg/d dose of erlotinib in South American patients. Method: We performed a retrospective review of 18 patients with histologically proven (+) EGFR (+) mutation metastatic NSCLC (mNSCLC) treated with 75 mg/d erlotinib as starting dose. Measures and Outcomes: Clinical information, including toxicity grade 1-4, drug discontinuation, clinical evolution and radiological evaluation, and overall survival (OS), was revised. Results: Patients received 75 mg/d of erlotinib as starting dose. Sixteen (89%) patients were treated in first-line treatment and 2 (11%) in second-line treatment. Mean age was 62 years (range 36-89 years), and 50% patients were female. Sixteen percent of the patients had brain metastases at first diagnosis. All patients had mutation positive EGFR, 12 (66%) had Del19 and 6 (34%) exon 21 mutation. Median progression-free survival was 17 months and OS 23 months. The main grade 1-2 toxicities were rash (44%) and diarrhea (22%). No grade 3-4 toxicity and no cases of drug discontinuation were reported. Conclusions: In South American population with mutated mNSCLC, a dose of 75 mg/d of erlotinib was well tolerated. This dose resulted in comparable benefits in progression-free survival and OS when compared to those reported in the literature with the standard dose. More studies are needed to explore the use of adjusted doses of biological agents in different ethnic backgrounds.
引用
收藏
页码:E375 / E379
页数:5
相关论文
共 50 条
  • [21] RELAY, ramucirumab plus erlotinib versus placebo plus erlotinib in untreated EGFR-mutated metastatic non-small cell lung cancer: exposure-response relationship
    Nakagawa, Kazuhiko
    Garon, Edward B.
    Gao, Ling
    Callies, Sophie
    Zimmermann, Annamaria
    Walgren, Richard
    Visseren-Grul, Carla
    Reck, Martin
    CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2022, 90 (02) : 137 - 148
  • [22] Small Cell Lung Cancer Transformation following Treatment in EGFR-Mutated Non-Small Cell Lung Cancer
    Mambetsariev, Isa
    Arvanitis, Leonidas
    Fricke, Jeremy
    Pharaon, Rebecca
    Baroz, Angel R.
    Afkhami, Michelle
    Koczywas, Marianna
    Massarelli, Erminia
    Salgia, Ravi
    JOURNAL OF CLINICAL MEDICINE, 2022, 11 (05)
  • [23] Clinical experience with erlotinib in non-small-cell lung cancer
    Felip, Enriqueta
    Rosell, Rafael
    DRUGS OF TODAY, 2006, 42 (03) : 147 - 156
  • [24] Checkpoint Inhibitors in Metastatic EGFR-Mutated Non-Small Cell Lung Cancer A Meta-Analysis
    Lee, Chee Khoon
    Man, Johnathan
    Lord, Sally
    Links, Matthew
    Gebski, Val
    Mok, Tony
    Yang, James Chih-Hsin
    JOURNAL OF THORACIC ONCOLOGY, 2017, 12 (02) : 403 - 407
  • [25] High-dose, weekly erlotinib is not an effective treatment in EGFR-mutated non-small cell lung cancer-patients with acquired extracranial progressive disease on standard dose erlotinib
    Kuiper, J. L.
    Heideman, D. A. M.
    Thunnissen, E.
    van Wijk, A. W.
    Postmus, P. E.
    Smit, E. F.
    EUROPEAN JOURNAL OF CANCER, 2014, 50 (07) : 1399 - 1401
  • [26] EGFR testing and erlotinib use in non-small cell lung cancer patients in Kentucky
    Larson, Kara L.
    Huang, Bin
    Chen, Quan
    Tucker, Thomas
    Schuh, Marissa
    Arnold, Susanne M.
    Kolesar, Jill M.
    PLOS ONE, 2020, 15 (08):
  • [27] Outcomes and Prognostic Factors in Patients with EGFR Mutant Metastatic Non-Small Cell Lung Cancer Who Treated with Erlotinib
    Dogan, Izzet
    Khanmammadov, Nijat
    Ahmed, Melin Aydan
    Yildiz, Anil
    Saip, Pinar
    Aydiner, Adnan
    Vatansever, Sezai
    CLINICAL CANCER INVESTIGATION JOURNAL, 2022, 11 (04): : 5 - 9
  • [28] Patterns of initial and intracranial failure in metastatic EGFR-mutant non-small cell lung cancer treated with erlotinib
    Patel, Suchit H.
    Rimner, Andreas
    Foster, Amanda
    Zhang, Zhigang
    Woo, Kaitlin M.
    Yu, Helena A.
    Riely, Gregory J.
    Wu, Abraham J.
    LUNG CANCER, 2017, 108 : 109 - 114
  • [29] SECOND LINE ERLOTINIB IN NON-SMALL CELL LUNG CANCER: A LOCAL EXPERIENCE
    Smith, C. F.
    Garcia-Alonso, Angel
    Drury, G.
    Gostage, A.
    Smith, N.
    JOURNAL OF THORACIC ONCOLOGY, 2011, 6 (06) : S1180 - S1181
  • [30] Durable Response to Double Dose Osimertinib 160mg in EGFR-Mutated Non-Small Cell Lung Cancer With Brain Metastases
    Nam, M.
    Kim, L.
    Jung, C. M.
    Park, J.
    Chae, Y. K.
    JOURNAL OF THORACIC ONCOLOGY, 2021, 16 (10) : S1095 - S1095