2023
DOI: 10.1097/md.0000000000034572
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A meta-analysis for the efficacy and safety of icotinib combined with radiotherapy in treating brain metastases of non-small cell lung cancer

Bo Zhang

Abstract: Background: Currently, the therapies for brain metastases of non-small cell lung cancer (NSCLC) mainly include whole brain radiotherapy and icotinib. For exploring the efficacy and safety of radiotherapy and icotinib, a meta-analysis was performed based on a series of data. Method: A systematic search was performed on PubMed, Web of Science, Cochrane Library, China National Knowledge Infrastructure and Wanfang Database. The search time was set from the … Show more

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Cited by 1 publication
(4 citation statements)
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“…Two papers (31,34) used it for 8 weeks, one (33) for 4 weeks, one (36) for 12 weeks, and one (26) did not specify the duration. Nine other papers (18,19,21,23,28,32,35,37,38) used 125 mg of erlotinib orally, except for one (19), of which four (18,19,21,38) were administered until disease progression or intolerable toxicity, two (23,37) were administered for 4 weeks, two (32,35) were administered for 2 weeks, and one (28) was not elucidated for duration of administration; four papers (20,24,27,29) used oral 125 mg icotinib, of which two papers (27,29) used it until disease progression or intolerable toxicity, one paper (20) used it for 4 weeks, and one paper (24) did not elaborate on the duration of continued use. One paper (30) used oral 80 mg osimertinib until disease progression or intolerable toxicity.…”
Section: Study Selection and Characteristicsmentioning
confidence: 99%
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“…Two papers (31,34) used it for 8 weeks, one (33) for 4 weeks, one (36) for 12 weeks, and one (26) did not specify the duration. Nine other papers (18,19,21,23,28,32,35,37,38) used 125 mg of erlotinib orally, except for one (19), of which four (18,19,21,38) were administered until disease progression or intolerable toxicity, two (23,37) were administered for 4 weeks, two (32,35) were administered for 2 weeks, and one (28) was not elucidated for duration of administration; four papers (20,24,27,29) used oral 125 mg icotinib, of which two papers (27,29) used it until disease progression or intolerable toxicity, one paper (20) used it for 4 weeks, and one paper (24) did not elaborate on the duration of continued use. One paper (30) used oral 80 mg osimertinib until disease progression or intolerable toxicity.…”
Section: Study Selection and Characteristicsmentioning
confidence: 99%
“…One paper (30) used oral 80 mg osimertinib until disease progression or intolerable toxicity. Seven studies (20,21,25,31,34,38,40) included patients with EGFR mutations, and 14 studies (19, 22-24, 26-28, 30, 32, 33, 35-37, 39) omitted the description of the EGFR status among patients. One article (18) reported EGFR rates, where the experimental and control groups displayed rates of 54.7 and 44.7%, respectively.…”
Section: Study Selection and Characteristicsmentioning
confidence: 99%
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