Evidence map›Paper›PMID 41973053›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2026

Circulating Tumor DNA Dynamics in Patients with Liver-Limited Metastatic Colorectal Cancer Resected after First-Line Systemic Treatment.

Roberto Moretto, Vittorio Studiale, Seung Won Hyun, Guglielmo Vetere, Farahnaz Islam, Martina Carullo, Veronica Conca, Christine Lo, Daniel Neems, Hala Boulos and 14 more

Abstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Roberto Moretto *Unit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.ORCID 0000-0001-8456-9269
Vittorio Studiale *Unit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.ORCID 0009-0005-7840-558X
Seung Won HyunTempus AI, Inc., Chicago, Illinois, USA.ORCID 0009-0006-4505-3423
Guglielmo VetereUnit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.ORCID 0000-0001-6943-2897
Farahnaz IslamTempus AI, Inc., Chicago, Illinois, USA.ORCID 0000-0002-8331-9871
Martina CarulloUnit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.ORCID 0000-0003-2846-2517
Veronica ConcaUnit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.ORCID 0000-0001-7713-4005
Christine LoTempus AI, Inc., Chicago, Illinois, USA.ORCID 0000-0003-0969-9973
Daniel NeemsTempus AI, Inc., Chicago, Illinois, USA.ORCID 0009-0004-7623-891X
Hala BoulosTempus AI, Inc., Chicago, Illinois, USA.ORCID 0009-0007-8585-4265
Dana F DeSantisTempus AI, Inc., Chicago, Illinois, USA.ORCID 0000-0001-5875-4962
Marco Maria GermaniUnit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.ORCID 0000-0002-1036-5869
Ada TaravellaUnit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.ORCID 0009-0000-2153-3867
Matteo LandiUnit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.ORCID 0000-0003-3789-5840
Filippo GhelardiMedical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0009-0001-1820-4402
Maria Caterina De GrandisMedical Oncology 1, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.ORCID 0009-0003-5480-7045
Sabina MurgioniMedical Oncology 1, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.ORCID 0000-0002-4682-9872
John AbranTempus AI, Inc., Chicago, Illinois, USA.ORCID 0000-0003-3592-349X
Kate SasserTempus AI, Inc., Chicago, Illinois, USA.ORCID 0009-0009-2804-1684
Filippo PietrantonioMedical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0002-8530-8420
Victoria L ChiouTempus AI, Inc., Chicago, Illinois, USA.ORCID 0009-0009-3364-2740
Chithra SangliTempus AI, Inc., Chicago, Illinois, USA.ORCID 0009-0000-1234-7122
Halla NimeiriTempus AI, Inc., Chicago, Illinois, USA.ORCID 0000-0002-8760-6456
Chiara CremoliniUnit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.ORCID 0000-0002-0520-4841

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeResection of liver metastases improves survival in patients with metastatic colorectal cancer (mCRC) with liver-limited disease (LLD), but relapse remains common. Postresection circulating tumor DNA (ctDNA) is a valid prognostic biomarker; however, no data are available regarding the prognostic effect of presurgery ctDNA after upfront chemotherapy. EXPERIMENTAL

designPatients (N = 116) with initially unresectable mCRC with LLD who underwent resection after upfront chemotherapy were included. Patients were sequenced with a tumor-naïve ctDNA-based minimal residual disease (MRD) assay at baseline (before chemotherapy), before surgery, and after surgery.

resultsPresurgery ctDNA status was not significantly associated with relapse-free survival (RFS). However, exploratory analyses demonstrated that a ≥50% reduction in variant allele frequency from baseline to before surgery was independently associated with improved RFS (median RFS: 21.0 vs. 9.8 months; HR: 2.19; P = 0.014), aligned with multivariate analysis (P = 0.022). Postsurgery ctDNA positivity was strongly predictive of recurrence (HR: 6.66; P < 0.001), with 100% specificity and 56.4% sensitivity. ctDNA dynamics from before to after surgery further stratified recurrence risk, regardless of adjuvant chemotherapy status. ctDNA dynamics from before to after surgery further stratified recurrence risk. Quantitative ctDNA measures (predicted tumor fragments per million) also correlated with RFS.

conclusionsUse of a tumor-naïve MRD assay increased the accuracy of detecting ctDNA after chemotherapy treatment, when a significant drop of ctDNA amount is expected compared with tests routinely used in metastatic disease. Presurgery ctDNA dynamics were prognostic with respect to RFS and may help stratify patients' prognosis prior to resection, potentially informing personalized treatment decisions.

Indexed as

Biomarkers, TumorCirculating Tumor DNAColorectal NeoplasmsLiver NeoplasmsNeoplasm Recurrence, LocalAdultAgedAntineoplastic Combined Chemotherapy ProtocolsFemaleHepatectomyHumansMaleMiddle AgedNeoplasm, ResidualPrognosisBiomarkers, TumorCirculating Tumor DNA

Identifiers

PMID41973053
PMCPMC13376887

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.