Prognostic impact of cancer genomic profile testing for advanced or metastatic solid tumors in clinical practice

Cancer Sci. 2023 Dec;114(12):4632-4642. doi: 10.1111/cas.15993. Epub 2023 Oct 19.

Abstract

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.

Keywords: advanced solid tumor; cancer genomic profile test; clinical response; genomically matched therapy; precision cancer medicine.

MeSH terms

  • Female
  • Genomics / methods
  • Humans
  • Male
  • Middle Aged
  • Mutation
  • Neoplasms* / genetics
  • Neoplasms, Second Primary*
  • Prognosis
  • Retrospective Studies