Abstract | AIM: METHODS: A prospective, multicenter, phase II clinical trial was carried out in patients aged ≥75 years with epidermal growth factor receptor-mutant non-small cell lung cancer. Initially, 100 mg/day erlotinib was administered orally; if well tolerated, it was increased to 150 mg/day. The primary end-point was progression-free survival, and secondary end-points were the response rate, overall survival and change in quality of life ("Care Notebook" questionnaire). RESULTS: The median progression-free survival was 17.8 months, response rate was 63.6% and median overall survival was 27.8 months. The change in the quality of life after 6 weeks was assessed in 72.7% of the patients. Fatigue, pain, anxiety and deterioration in daily activities were found in at least 40% of the patients. Despite the therapeutic effect of 100 mg/day erlotinib, many patients required dose reduction, and in some, the quality of life could not be maintained. CONCLUSIONS:
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Authors | Yukari Tsubata, Takeshi Masuda, Kosuke Hamai, Masaya Taniwaki, Akari Tanino, Takamasa Hotta, Megumi Hamaguchi, Shunichi Hamaguchi, Masahiro Yamasaki, Nobuhisa Ishikawa, Kazunori Fujitaka, Akihisa Sutani, Takeshi Isobe |
Journal | Geriatrics & gerontology international
(Geriatr Gerontol Int)
Vol. 21
Issue 10
Pg. 881-886
(Oct 2021)
ISSN: 1447-0594 [Electronic] Japan |
PMID | 34378299
(Publication Type: Clinical Trial, Phase II, Journal Article, Multicenter Study)
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Copyright | © 2021 The Authors. Geriatrics & Gerontology International published by John Wiley & Sons Australia, Ltd on behalf of Japan Geriatrics Society. |
Chemical References |
- Erlotinib Hydrochloride
- ErbB Receptors
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Topics |
- Aged
- Antineoplastic Combined Chemotherapy Protocols
- Carcinoma, Non-Small-Cell Lung
(drug therapy, genetics)
- ErbB Receptors
(genetics, therapeutic use)
- Erlotinib Hydrochloride
(therapeutic use)
- Humans
- Lung Neoplasms
(drug therapy, genetics)
- Mutation
- Prospective Studies
- Quality of Life
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