非小细胞肺癌术后分子靶向药物辅助治疗。

IF 2.4 3区 医学 Q3 ONCOLOGY International Journal of Clinical Oncology Pub Date : 2024-12-18 DOI:10.1007/s10147-024-02671-4
Tomohiro Miyoshi, Masahiro Tsuboi
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引用次数: 0

摘要

分子靶向药物在晚期肺癌中的疗效已得到证实,其适应症最近已扩大到包括可切除肺癌的围手术期治疗。对于表皮生长因子受体(EGFR)突变阳性的患者,根据ADAURA试验的结果,在日本可以使用EGFR-酪氨酸激酶抑制剂(EGFR- tkis)进行术后辅助治疗。除EGFR-TKIs外,TKIs靶向间变性淋巴瘤激酶(ALK)并在转染期间重排(RET)的术后辅助治疗有望建立。另一方面,对于单纯通过手术完全治愈癌症的患者,由于辅助化疗是无效的,因此必须考虑疗效与不良反应之间的平衡,需要进一步的研究来确定必要和足够的剂量以及适当的给药时间。此外,辅助化疗的费用近来也成为一个不容忽视的问题。因此,开发生物标志物来有效地缩小从辅助化疗中获益的患者是势在必行的。
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Postoperative adjuvant therapy with molecularly targeted agents for non-small cell lung cancer.

The efficacy of molecularly targeted agents has been established in advanced lung cancer, and their indications have recently expanded to include perioperative treatment of resectable lung cancer. For epidermal growth factor receptor (EGFR) mutation-positive patients, postoperative adjuvant therapy with EGFR-tyrosine kinase inhibitors (EGFR-TKIs) is available in Japan following the results of the ADAURA trial. In addition to EGFR-TKIs, postoperative adjuvant therapy with TKIs targeting anaplastic lymphoma kinase (ALK) and rearranged during transfection (RET) is expected to be established. On the other hand, because adjuvant chemotherapy is ineffective in patients who have been completely cured of cancer through surgery alone, the balance between efficacy and adverse effects must be considered, and further studies will be needed to determine the necessary and sufficient dosage and the appropriate duration of administration. In addition, the cost of adjuvant chemotherapy has recently become an issue that cannot be overlooked. Therefore, it will be imperative to develop biomarkers to effectively narrow down the patients who benefit from adjuvant chemotherapy.

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来源期刊
CiteScore
6.80
自引率
3.00%
发文量
175
审稿时长
2 months
期刊介绍: The International Journal of Clinical Oncology (IJCO) welcomes original research papers on all aspects of clinical oncology that report the results of novel and timely investigations. Reports on clinical trials are encouraged. Experimental studies will also be accepted if they have obvious relevance to clinical oncology. Membership in the Japan Society of Clinical Oncology is not a prerequisite for submission to the journal. Papers are received on the understanding that: their contents have not been published in whole or in part elsewhere; that they are subject to peer review by at least two referees and the Editors, and to editorial revision of the language and contents; and that the Editors are responsible for their acceptance, rejection, and order of publication.
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