Genomic Medicine, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Breast Medical Oncology, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Cancer Sci. 2023 Dec;114(12):4632-4642. doi: 10.1111/cas.15993. Epub 2023 Oct 19.
Cancer genomic profile (CGP) testing, which is covered by the national health insurance system in Japan, has been introduced as a routine clinical practice. However, the effects of CGP testing on prognoses remain unclear. Drug accessibility rates and prognoses after CGP testing were retrospectively investigated in 713 patients who underwent CGP testing examined by our molecular tumor board between November 2019 and October 2022,. Overall survival (OS) was examined using the log-rank test and the Kaplan-Meier method. The median age of patients (326 males and 387 females) was 58 years (12-85 years). CGP testing revealed one or more gene mutations in 681 cases (95.5%), among which actionable gene mutations were detected in 439 (61.6%). Although treatment options were recommended for 285 cases (40.0%) by the molecular tumor board, only 45 received treatment based on their gene mutations. During the median observation period of 8.6 months, 351 (49.2%) patients died of the exacerbation of existing diseases. No significant differences were observed in OS between patients treated with and without genomically matched therapy (p = 0.285). According to clinical responses to treatment based on gene mutations, median OS was significantly longer in patients who achieved partial response and stable disease (26.5 months; 95% CI 14.4-38.6) than in those with progressive disease and not evaluated (9.8 months; 95% CI 5.8-13.8, p = 0.013). Responses to treatment based on gene mutations may improve prognoses, and it is important to increase the drug accessibility rate after CGP testing.
癌症基因组分析(CGP)检测已被纳入日本国家医疗保险体系,作为常规临床实践。然而,CGP 检测对预后的影响仍不清楚。我们回顾性调查了 2019 年 11 月至 2022 年 10 月期间,分子肿瘤委员会对 713 名患者进行 CGP 检测后的药物可及性和预后。采用对数秩检验和 Kaplan-Meier 方法检测总生存期(OS)。患者的中位年龄(326 名男性和 387 名女性)为 58 岁(12-85 岁)。681 例(95.5%)患者的 CGP 检测发现一个或多个基因突变,其中 439 例(61.6%)检测到可操作基因突变。尽管分子肿瘤委员会建议为 285 例(40.0%)患者推荐治疗方案,但只有 45 例患者根据基因突变接受治疗。在中位观察期 8.6 个月内,351 例(49.2%)患者死于现有疾病恶化。接受和未接受基因匹配治疗的患者的 OS 无显著差异(p=0.285)。根据基因突变的治疗临床反应,获得部分缓解和稳定疾病的患者的中位 OS 明显长于疾病进展和未评估的患者(26.5 个月;95%CI 14.4-38.6),差异有统计学意义(p=0.013)。基于基因突变的治疗反应可能改善预后,增加 CGP 检测后的药物可及性非常重要。