{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,8]],"date-time":"2026-10-08T16:26:30Z","timestamp":1791476790053,"version":"4.3.4"},"reference-count":38,"publisher":"American Medical Association (AMA)","issue":"9","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Oncol"],"published-print":{"date-parts":[[2026,9,1]]},"abstract":"<jats:sec id=\"ab-coi260032-4\">\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>The benefit of adjuvant chemotherapy (ACT) following curative resection of colorectal liver metastases (CRLM) remains uncertain, with no consistent overall survival (OS) benefit and optimal patient selection for postsurgical treatment not established.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-coi260032-5\">\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To evaluate the association between circulating tumor DNA (ctDNA)\u2013defined molecular residual disease (MRD) and survival outcomes and whether MRD status is associated with differential benefit from ACT in resected CRLM.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-coi260032-6\">\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>This prospective analysis included patients with resected CRLM enrolled in the CIRCULATE-Japan GALAXY study between May 2020 and July 2024 with available ctDNA results 2 to 10 weeks after surgery. Analyses were landmarked at 70 days and conducted separately for patients receiving neoadjuvant chemotherapy (NAC) and those undergoing upfront surgery. Data were analyzed from January to April 2026.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-coi260032-7\">\n                    <jats:title>Exposures<\/jats:title>\n                    <jats:p>Postsurgical ACT vs observation. ctDNA was assessed using a personalized, tumor-informed assay.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-coi260032-8\">\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>Disease-free survival (DFS) and OS, evaluated using Cox proportional hazards models.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-coi260032-9\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Of 298 included patients, the median (range) age was 67 (33-85) years, and 192 (64.4%) were male. The median (range) follow-up was 43.2 (1-68) months. In the upfront surgery cohort (n\u2009=\u2009191), postsurgical MRD positivity was associated with worse DFS (hazard ratio [HR], 4.14; 95% CI, 2.69-6.36;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001) and OS (HR, 9.13; 95% CI, 4.44-18.78;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001) compared with MRD negativity. Among patients with postsurgical MRD positivity, ACT was associated with improved DFS (HR, 0.07; 95% CI, 0.02-0.24;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001; 48-month DFS: 37.5% [95% CI, 15.4-59.8] vs not reached) and OS (HR, 0.27; 95% CI, 0.08-0.88;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009=\u2009.03; 48-month OS: 65.3% [95% CI, 30.8-85.7] vs 32.9% [95% CI, 17.4-49.3]) compared with observation. In contrast, among patients with MRD negativity, ACT was not associated with improved DFS (HR, 0.69; 95% CI, 0.32-1.50;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009=\u2009.36) or OS (HR, 0.54; 95% CI, 0.10-2.88;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009=\u2009.47) benefit. In the NAC cohort (n\u2009=\u2009107), postsurgical MRD positivity remained prognostic, with inferior DFS (HR, 4.82; 95% CI, 2.92-7.97;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001) and OS (HR, 9.43; 95% CI, 2.78-31.96;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001). ACT was not associated with improved DFS or OS regardless of MRD status. ctDNA positivity at the post-NAC presurgical time point was associated with worse OS (HR, 11.42; 95% CI, 1.58-1452.50;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009=\u2009.009).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-coi260032-10\">\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>In this prognostic study, postsurgical ctDNA-defined MRD identified patients with resected CRLM who derived OS benefit from ACT. In contrast, patients with MRD negativity experienced favorable long-term OS without clear benefit from ACT. These findings support prospective validation of ctDNA-guided adjuvant strategies, particularly in patients with CRLM undergoing upfront surgery.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jamaoncol.2026.2191","type":"journal-article","created":{"date-parts":[[2026,7,3]],"date-time":"2026-07-03T15:30:21Z","timestamp":1783092621000},"page":"950","source":"Crossref","is-referenced-by-count":2,"title":["Circulating Tumor DNA Status and Adjuvant Chemotherapy in Resected Colorectal Liver Metastases"],"prefix":"10.1001","volume":"12","author":[{"given":"Kozo","family":"Kataoka","sequence":"first","affiliation":[{"name":"Division of Lower GI Surgery, Department of Gastroenterological Surgery, Hyogo Medical University, Nishinomiya, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kazuma","family":"Ito","sequence":"additional","affiliation":[{"name":"Division of Lower GI Surgery, Department of Gastroenterological Surgery, Hyogo Medical University, Nishinomiya, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yoshiaki","family":"Nakamura","sequence":"additional","affiliation":[{"name":"Department of Oncology, University of Oxford, Oxford, United Kingdom"},{"name":"Translational Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jun","family":"Watanabe","sequence":"additional","affiliation":[{"name":"Department of Colorectal Surgery, Kansai Medical University, Hirakata, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Naoya","family":"Akazawa","sequence":"additional","affiliation":[{"name":"Department of Gastroenterological Surgery, Sendai City Medical Center Sendai Open Hospital, Sendai, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jun","family":"Nagata","sequence":"additional","affiliation":[{"name":"Department of Surgery, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mitsuru","family":"Yokota","sequence":"additional","affiliation":[{"name":"Department of General Surgery, Kurashiki Central Hospital, Kurashiki, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kentaro","family":"Kato","sequence":"additional","affiliation":[{"name":"Department of Surgery, Teine-Keijinkai Hospital, Sapporo, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Masahito","family":"Kotaka","sequence":"additional","affiliation":[{"name":"Gastrointestinal Cancer Center, Sano Hospital, Kobe, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tadayoshi","family":"Hashimoto","sequence":"additional","affiliation":[{"name":"Department of Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kentaro","family":"Yamazaki","sequence":"additional","affiliation":[{"name":"Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Sunto-gun, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yoshinori","family":"Kagawa","sequence":"additional","affiliation":[{"name":"Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan"},{"name":"Department of Gastroenterological Surgery, Osaka General Medical Center, Osaka, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Saori","family":"Mishima","sequence":"additional","affiliation":[{"name":"Department of Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Koji","family":"Ando","sequence":"additional","affiliation":[{"name":"Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Masaaki","family":"Miyo","sequence":"additional","affiliation":[{"name":"Department of Gastroenterological Surgery, Graduate School of Medicine, The University of Osaka, Suita, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hiroki","family":"Yukami","sequence":"additional","affiliation":[{"name":"Cancer Chemotherapy Center, Osaka Medical and Pharmaceutical University, Takatsuki, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Arkarachai","family":"Fungtammasan","sequence":"additional","affiliation":[{"name":"Natera, Austin, Texas"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shruti","family":"Sharma","sequence":"additional","affiliation":[{"name":"Natera, Austin, Texas"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J. 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