Concurrent chemoradiotherapy with weekly low-dose carboplatin for cisplatin-ineligible patients with head and neck squamous cell carcinoma: survival analysis based on 2-year follow-up data.

IF 2.4 3区 医学 Q3 ONCOLOGY
Yushi Ueki, Yuki Ohno, Shusuke Ohshima, Yusuke Yokoyama, Jo Omata, Takeshi Takahashi, Ryusuke Shodo, Keisuke Yamazaki, Kohei Ohtaki, Kohei Saijo, Ryoko Tanaka, Nao Takahashi, Ryuichi Okabe, Arata Horii
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引用次数: 0

Abstract

Background: As a follow-up study to our prospective phase II trial of concurrent chemoradiotherapy (CCRT) with weekly low-dose carboplatin for cisplatin-ineligible patients with head and neck squamous cell carcinoma (HNSCC), we assessed long-term survival (minimum follow-up of 2-year) and subgroup analysis by age and renal function.

Methods: A prospective phase II study on CCRT with weekly low-dose carboplatin for cisplatin-ineligible HNSCC in 30 patients who were aged (≥ 75-year-old patients with 40 mL/min estimated glomerular filtration rate [eGFR] or better) or had renal dysfunction (< 75-year-old patients with 30-60 mL/min eGFR) was performed between July 2019 and January 2022 at three tertiary hospitals. Survival outcomes were investigated 2 years after this phase 2 trial were investigated. Furthermore, we compared the treatment outcome between ≥ 75 years group and < 75 years group.

Results: The median follow-up time was 41.5 months. The 2-year recurrence-free survival (RFS) and 2-year overall survival (OS) rates of all patients were 70% and 86.7%, respectively. The 2-year RFS and OS of patients ≥ 75 years old was 92.3% and 100%, respectively, whereas those of patients < 75 years old was 52.9% (p = 0.175) and 76% (p = 0.157), respectively, showing no significant differences between the groups.

Conclusion: CCRT with weekly low-dose carboplatin in patients with cisplatin-ineligible HNSCC showed favorable survival outcomes irrespective of age and renal function. This study highlights a potentially promising treatment option for cisplatin-ineligible HNSCC patients.

Trial registration: jRCTs031190028.

不适合顺铂治疗的头颈部鳞状细胞癌患者同步放化疗每周低剂量卡铂:基于2年随访数据的生存分析
背景:作为一项前瞻性II期试验的随访研究,我们对不符合顺铂治疗条件的头颈部鳞状细胞癌(HNSCC)患者进行了同步放化疗(CCRT),每周低剂量卡铂治疗,评估了长期生存率(最少随访2年),并根据年龄和肾功能进行了亚组分析。方法:2019年7月至2022年1月,在三家三级医院进行了一项前瞻性II期研究,在30名年龄(≥75岁,估计肾小球滤过率[eGFR]为40 mL/min或更高)或肾功能不全(< 75岁,eGFR为30-60 mL/min)的患者中,采用CCRT联合每周低剂量卡铂治疗顺铂不合格的HNSCC。在2期试验进行2年后,对生存结果进行了调查。此外,我们比较了≥75岁组的治疗结果和结果:中位随访时间为41.5个月。所有患者的2年无复发生存率(RFS)和2年总生存率(OS)分别为70%和86.7%。≥75岁患者的2年RFS和OS分别为92.3%和100%,而患者的2年RFS和OS则分别为92.3%和100%。结论:CCRT联合每周低剂量卡铂治疗不符合顺铂治疗条件的HNSCC患者,无论年龄和肾功能如何,均显示出良好的生存结果。这项研究强调了对不适合顺铂治疗的HNSCC患者的潜在有希望的治疗选择。试验注册号:jRCTs031190028。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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