Molecular residual disease and efficacy of adjuvant chemotherapy in patients with colorectal cancer

Daisuke Kotani(National Cancer Center Hospital East), Eiji Oki(Kyushu University), Yoshiaki Nakamura(National Cancer Center Hospital East), Hiroki Yukami(National Cancer Center Hospital East), Saori Mishima(National Cancer Center Hospital East), Hideaki Bando(National Cancer Center Hospital East), Hiromichi Shirasu(Shizuoka Cancer Center), Kentaro Yamazaki(Shizuoka Cancer Center), Jun Watanabe(Yokohama City University Medical Center), Masahito Kotaka, Keiji Hirata(University of Occupational and Environmental Health Japan), Naoya Akazawa(Sendai Medical Center), Kozo Kataoka(Hyogo University), Shruti Sharma(Natera (United States)), Vasily N. Aushev(Natera (United States)), Alexey Aleshin(Natera (United States)), Toshihiro Misumi(National Cancer Center Hospital East), Hiroya Taniguchi(Aichi Cancer Center), Ichiro Takemasa(Sapporo Medical University), Takeshi Kato(Osaka National Hospital), Masaki Mori(Tokai University), Takayuki Yoshino(National Cancer Center Hospital East)
Nature Medicine
January 1, 2023
Cited by 464Open Access
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Abstract

Despite standard-of-care treatment, more than 30% of patients with resectable colorectal cancer (CRC) relapse. Circulating tumor DNA (ctDNA) analysis may enable postsurgical risk stratification and adjuvant chemotherapy (ACT) treatment decision-making. We report results from GALAXY, which is an observational arm of the ongoing CIRCULATE-Japan study (UMIN000039205) that analyzed presurgical and postsurgical ctDNA in patients with stage II-IV resectable CRC (n = 1,039). In this cohort, with a median follow-up of 16.74 months (range 0.49-24.83 months), postsurgical ctDNA positivity (at 4 weeks after surgery) was associated with higher recurrence risk (hazard ratio (HR) 10.0, P < 0.0001) and was the most significant prognostic factor associated with recurrence risk in patients with stage II or III CRC (HR 10.82, P < 0.001). Furthermore, postsurgical ctDNA positivity identified patients with stage II or III CRC who derived benefit from ACT (HR 6.59, P < 0.0001). The results of our study, a large and comprehensive prospective analysis of ctDNA in resectable CRC, support the use of ctDNA testing to identify patients who are at increased risk of recurrence and are likely to benefit from ACT.


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