Evidence map›Paper›PMID 40565003›Full record

ReviewInternational journal of molecular sciences2025

Precision Oncology Framework Using Circulating Tumor Cells.

Fumihiko Kakizaki, Kyoichi Oshiro, Yuya Enoki, Kana Kawanishi, Norikazu Masuda, Hisatsugu Maekawa, Jun Matsubayashi, Masahiro Kawashima, Hiroyuki Miyoshi, Yukitoshi Takemura and 1 more

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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

11 authors.

Fumihiko KakizakiDepartment of Personalized Cancer Medicine, Graduate School of Medicine, Kyoto University, 53 Shogoin-Kawahara-cho, Sakyo-Ku, Kyoto 606-8507, Japan.ORCID 0000-0003-2017-6700
Kyoichi OshiroAFI Corporation, Medical Innovation Center, Building, Kyoto University, 53 Shogoin-Kawahara-cho, Sakyo-Ku, Kyoto 606-8507, Japan.
Yuya EnokiDepartment of Personalized Cancer Medicine, Graduate School of Medicine, Kyoto University, 53 Shogoin-Kawahara-cho, Sakyo-Ku, Kyoto 606-8507, Japan.
Kana KawanishiDepartment of Breast Surgery, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawahara-cho, Sakyo-Ku, Kyoto 606-8507, Japan.
Norikazu MasudaDepartment of Breast Surgery, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawahara-cho, Sakyo-Ku, Kyoto 606-8507, Japan.
Hisatsugu MaekawaDepartment of Personalized Cancer Medicine, Graduate School of Medicine, Kyoto University, 53 Shogoin-Kawahara-cho, Sakyo-Ku, Kyoto 606-8507, Japan.
Jun MatsubayashiDepartment of Personalized Cancer Medicine, Graduate School of Medicine, Kyoto University, 53 Shogoin-Kawahara-cho, Sakyo-Ku, Kyoto 606-8507, Japan.
Masahiro KawashimaDepartment of Breast Surgery, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawahara-cho, Sakyo-Ku, Kyoto 606-8507, Japan.
Hiroyuki MiyoshiDepartment of Personalized Cancer Medicine, Graduate School of Medicine, Kyoto University, 53 Shogoin-Kawahara-cho, Sakyo-Ku, Kyoto 606-8507, Japan.ORCID 0000-0001-7400-0714
Yukitoshi TakemuraDepartment of Personalized Cancer Medicine, Graduate School of Medicine, Kyoto University, 53 Shogoin-Kawahara-cho, Sakyo-Ku, Kyoto 606-8507, Japan.
Kazutaka ObamaDepartment of Personalized Cancer Medicine, Graduate School of Medicine, Kyoto University, 53 Shogoin-Kawahara-cho, Sakyo-Ku, Kyoto 606-8507, Japan.ORCID 0000-0003-2924-6701

Funding

Japan Agency for Medical Research and Development 23zf0227002h0001
6 · The paper itself

Abstract

Circulating tumor cells (CTCs) are multifaceted biomarkers with significant potential for precision oncology, offering opportunities to refine diagnoses and personalize treatments across various cancer types, including colorectal and breast cancer. CTC assays serve as reliable prognostic indicators, even during chemotherapy and/or molecularly targeted therapies. Notably, CTCs exhibit heterogeneity that gradually develops during carcinogenesis and becomes more pronounced in advanced disease stages. These intra- and intertumoral heterogeneities pose challenges, particularly when drug-resistant clones emerge following therapy. The dynamic behavior of CTCs provides valuable insights into treatment response and prognosis. Extensive efforts have led to the development of technologies for effective CTC isolation, accelerating their clinical implementation. While both CTC and circulating tumor DNA (ctDNA) tests offer prognostic value, they reflect different aspects of tumor biology: CTC counts indicate tumor progression, while ctDNA levels correlate with tumor burden. The combined analysis is expected to yield complementary insights. CTC tests are feasible in general hospitals and may serve as tumor markers comparable to, or even superior to, conventional markers such as carcinoembryonic antigen (CEA) and carbohydrate antigen 19-9 (CA19-9) for colorectal cancer, and CA15-3 for breast cancer. Early incorporation of CTC tests into routine blood panels appears to be a rational and promising approach.

Indexed as

Biomarkers, TumorNeoplasmsNeoplastic Cells, CirculatingPrecision MedicineBreast NeoplasmsCirculating Tumor DNAColorectal NeoplasmsHumansPrognosisBiomarkers, TumorCirculating Tumor DNAbreast cancercolorectal cancerCTCctDNAprecision oncology

Identifiers

PMID40565003
PMCPMC12192747

What OpenQuestion holds

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Registered trials

None linked

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.