Does dose reduction of afatinib affect treatment outcomes of patients with EGFR-mutant metastatic non-small cell lung cancer in real-world clinical practice?
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 retro...
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my.unimas.ir.444202024-03-05T01:47:35Z http://ir.unimas.my/id/eprint/44420/ Does dose reduction of afatinib affect treatment outcomes of patients with EGFR-mutant metastatic non-small cell lung cancer in real-world clinical practice? Mau, Ern Poh Chai, Chee Shee Chong, Kin Liam Go, Fuang Ho Yong, Kek Pang Harissa, Husainy Hasbullah Lye, Mun Tho Ibtisam, Muhamad Nor Kean, Fatt Ho Muthukkumaran, Thiagarajan Azlina, Samsudin Azza, Omar Choo, Khoon Ong Sing, Yang Soon Sin, Nee Tan Soon, Hin How R Medicine (General) RC0254 Neoplasms. Tumors. Oncology (including Cancer) RZ Other systems of medicine 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 1st January 2015 to 31st 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. AME Publishing Company 2024-02-28 Article PeerReviewed text en http://ir.unimas.my/id/eprint/44420/3/Does%20dose.pdf Mau, Ern Poh and Chai, Chee Shee and Chong, Kin Liam and Go, Fuang Ho and Yong, Kek Pang and Harissa, Husainy Hasbullah and Lye, Mun Tho and Ibtisam, Muhamad Nor and Kean, Fatt Ho and Muthukkumaran, Thiagarajan and Azlina, Samsudin and Azza, Omar and Choo, Khoon Ong and Sing, Yang Soon and Sin, Nee Tan and Soon, Hin How (2024) Does dose reduction of afatinib affect treatment outcomes of patients with EGFR-mutant metastatic non-small cell lung cancer in real-world clinical practice? Translational Lung Cancer Research, 13 (2). pp. 307-320. ISSN 2218-6751 https://tlcr.amegroups.org/article/view/83673/html https://dx.doi.org/10.21037/tlcr-23-691 |
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R Medicine (General) RC0254 Neoplasms. Tumors. Oncology (including Cancer) RZ Other systems of medicine |
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R Medicine (General) RC0254 Neoplasms. Tumors. Oncology (including Cancer) RZ Other systems of medicine Mau, Ern Poh Chai, Chee Shee Chong, Kin Liam Go, Fuang Ho Yong, Kek Pang Harissa, Husainy Hasbullah Lye, Mun Tho Ibtisam, Muhamad Nor Kean, Fatt Ho Muthukkumaran, Thiagarajan Azlina, Samsudin Azza, Omar Choo, Khoon Ong Sing, Yang Soon Sin, Nee Tan Soon, Hin How Does dose reduction of afatinib affect treatment outcomes of patients with EGFR-mutant metastatic non-small cell lung cancer in real-world clinical practice? |
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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 1st January 2015 to 31st 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. |
format |
Article |
author |
Mau, Ern Poh Chai, Chee Shee Chong, Kin Liam Go, Fuang Ho Yong, Kek Pang Harissa, Husainy Hasbullah Lye, Mun Tho Ibtisam, Muhamad Nor Kean, Fatt Ho Muthukkumaran, Thiagarajan Azlina, Samsudin Azza, Omar Choo, Khoon Ong Sing, Yang Soon Sin, Nee Tan Soon, Hin How |
author_facet |
Mau, Ern Poh Chai, Chee Shee Chong, Kin Liam Go, Fuang Ho Yong, Kek Pang Harissa, Husainy Hasbullah Lye, Mun Tho Ibtisam, Muhamad Nor Kean, Fatt Ho Muthukkumaran, Thiagarajan Azlina, Samsudin Azza, Omar Choo, Khoon Ong Sing, Yang Soon Sin, Nee Tan Soon, Hin How |
author_sort |
Mau, Ern Poh |
title |
Does dose reduction of afatinib affect treatment outcomes of
patients with EGFR-mutant metastatic non-small cell lung cancer
in real-world clinical practice? |
title_short |
Does dose reduction of afatinib affect treatment outcomes of
patients with EGFR-mutant metastatic non-small cell lung cancer
in real-world clinical practice? |
title_full |
Does dose reduction of afatinib affect treatment outcomes of
patients with EGFR-mutant metastatic non-small cell lung cancer
in real-world clinical practice? |
title_fullStr |
Does dose reduction of afatinib affect treatment outcomes of
patients with EGFR-mutant metastatic non-small cell lung cancer
in real-world clinical practice? |
title_full_unstemmed |
Does dose reduction of afatinib affect treatment outcomes of
patients with EGFR-mutant metastatic non-small cell lung cancer
in real-world clinical practice? |
title_sort |
does dose reduction of afatinib affect treatment outcomes of
patients with egfr-mutant metastatic non-small cell lung cancer
in real-world clinical practice? |
publisher |
AME Publishing Company |
publishDate |
2024 |
url |
http://ir.unimas.my/id/eprint/44420/3/Does%20dose.pdf http://ir.unimas.my/id/eprint/44420/ https://tlcr.amegroups.org/article/view/83673/html https://dx.doi.org/10.21037/tlcr-23-691 |
_version_ |
1792658566062014464 |
score |
13.18916 |