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オノ マキコ
ONO Makiko
小野 麻紀子 所属 医学部 医学科(東京女子医科大学病院) 職種 准教授 |
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| 論文種別 | 原著 |
| 言語種別 | 英語 |
| 査読の有無 | 査読あり |
| 表題 | Addressing the knowledge gap in the genomic landscape and tailored therapeutic approaches to adolescent and young adult cancers. |
| 掲載誌名 | 正式名:ESMO open 略 称:ESMO Open ISSNコード:20597029/20597029 |
| 巻・号・頁 | 9(8),pp.103659 |
| 著者・共著者 | N Hayashi, M Ono, I Fukada, M Yamazaki, N Sato, M Hosonaga, X Wang, K Kaneko, H Arakawa, E Habano, A Kuga, A Kataoka, A Ueki, K Kiyotani, A Tonooka, K Takeuchi, T Kogawa, S Kitano, T Takano, M Watanabe, S Mori, S Takahashi |
| 発行年月 | 2024/08 |
| 概要 | BACKGROUND:Adolescents and young adults (AYAs) represent a small proportion of patients with cancer. The genomic profiles of AYA patients with cancer are not well-studied, and outcomes of genome-matched therapies remain largely unknown.PATIENTS AND METHODS:We investigated differences between Japanese AYA and older adult (OA) patients in genomic alterations, therapeutic evidence levels, and genome-matched therapy usage by cancer type. We also assessed treatment outcomes.RESULTS:AYA patients accounted for 8.3% of 876 cases. Microsatellite instability-high and/or tumor mutation burden was less common in AYA patients (1.4% versus 7.7% in OA; P = 0.05). However, BRCA1 alterations were more common in AYA patients with breast cancer (27.3% versus 1.7% in OA; P = 0.01), as were MYC alterations in AYA patients with colorectal cancer (23.5% versus 5.8% in OA; P = 0.02) and sarcoma (31.3% versus 3.4% in OA; P = 0.01). Genome-matched therapy use was similar between groups, with overall survival tending to improve in both. However, in AYA patients, the small number of patients prevented statistical significance. Comprehensive genomic profiling-guided genome-matched therapy yielded encouraging results, with progression-free survival of 9.0 months in AYA versus 3.7 months in OA patients (P = 0.59).CONCLUSION:Our study suggests that tailored therapeutic approaches can benefit cancer patients regardless of age. |
| DOI | 10.1016/j.esmoop.2024.103659 |
| PMID | 39137480 |