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
  • [41] Erlotinib-Induced Cardiomyopathy in a Patient with Metastatic Non-Small Cell Lung Cancer
    Nagashio, Kenji
    Tajiri, Kazuko
    Sato, Kimi
    Ieda, Masaki
    INTERNATIONAL HEART JOURNAL, 2021, 62 (05) : 1171 - 1175
  • [42] Dacomitinib for the first-line treatment of patients with EGFR-mutated metastatic non-small cell lung cancer
    Santarpia, Mariacarmela
    Menis, Jessica
    Chaib, Imane
    Cao, Maria Gonzalez
    Rosell, Rafael
    EXPERT REVIEW OF CLINICAL PHARMACOLOGY, 2019, 12 (09) : 831 - 840
  • [43] Treatment of Non-Small Cell Lung Cancer with Atypical EGFR Mutations
    Wells, Leah
    Qin, Angel
    CURRENT TREATMENT OPTIONS IN ONCOLOGY, 2023, 24 (12) : 1978 - 1993
  • [44] Meta-analysis of Targeted Therapies in EGFR-mutated Non-Small Cell Lung Cancer
    Qureshi, Zaheer
    Altaf, Faryal
    Jamil, Abdur
    Siddique, Rimsha
    AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2025, 48 (01): : 44 - 54
  • [45] Critical points in the management of EGFR-mutated non-small cell lung cancer
    Casaluce, Francesca
    Gridelli, Cesare
    JOURNAL OF THORACIC DISEASE, 2022, 14 (06) : 1748 - 1752
  • [46] Second and later-line erlotinib use in non-small cell lung cancer: real world outcomes and practice patterns overtime in Canada
    Perdrizet, Kirstin
    Sutradhar, Rinku
    Li, Qing
    Liu, Ning
    Earle, Craig C.
    Leighl, Natasha B.
    JOURNAL OF THORACIC DISEASE, 2021, 13 (09) : 5419 - 5429
  • [47] Gefitinib and Erlotinib in Metastatic Non-Small Cell Lung Cancer: A Meta-Analysis of Toxicity and Efficacy of Randomized Clinical Trials
    Burotto, Mauricio
    Manasanch, Elisabet E.
    Wilkerson, Julia
    Fojo, Tito
    ONCOLOGIST, 2015, 20 (04) : 400 - 410
  • [48] Erlotinib versus Pemetrexed for Pretreated Non-Squamous Non-Small Cell Lung Cancer Patients in Clinical Practice
    Zugazagoitia, J.
    Puente, J.
    Gonzalez-Larriba, J. L.
    Manzano, A.
    Sotelo, M.
    Hernandez, S.
    Sanz, J.
    Perez, P.
    Diaz-Rubio, E.
    ONCOLOGY, 2013, 84 (05) : 255 - 264
  • [49] Clinical Impact of two Different Diagnostic Strategies in the First- and Second-Line Treatment of Locally Advanced or Metastatic EGFR-Mutated Non-Small Cell Lung Cancer
    Gancitano, Giovanni
    Ravasio, Roberto
    Cattelino, Lorenzo
    Di Procolo, Paolo
    Cortinovis, Diego
    FARMECONOMIA-HEALTH ECONOMICS AND THERAPEUTIC PATHWAYS, 2020, 21 (01) : 1 - 9
  • [50] Afatinib is Especially Effective Against Non-small Cell Lung Cancer Carrying an EGFR Exon 19 Deletion
    Banno, Eri
    Togashi, Yosuke
    Kobayashi, Yoshihisa
    Hayashi, Hidetoshi
    Mitsudomi, Tetsuya
    Nishio, Kazuto
    ANTICANCER RESEARCH, 2015, 35 (04) : 2005 - 2008