Evidence map›Paper›PMID 38083992›Full record

ArticleCancer science2024

Postoperative recurrence detection using individualized circulating tumor DNA in upper tract urothelial carcinoma.

Daichi Tamura, Masakazu Abe, Hayato Hiraki, Noriyuki Sasaki, Akiko Yashima-Abo, Daiki Ikarashi, Renpei Kato, Yoichiro Kato, Shigekatsu Maekawa, Mitsugu Kanehira and 9 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
6.0field-weighted citation impact, top 3% of its field
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

19 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Renaissance of farnesyltransferase inhibitors in cancer.Journal of translational medicine · 2026
    Review
  4. Article
  5. Review
  6. Review
  7. Prediction of Postoperative Intravesical Recurrence Using Urine DNA Monitoring in Nonmuscular-Invasive Urothelial Bladder Cancer.International journal of urology : official journal of the Japanese Urological Association · 2026
    Article
  8. Review
  9. Current Status and Future Perspectives of Molecular Residual Disease Testing in Genitourinary Cancers.International journal of urology : official journal of the Japanese Urological Association · 2025
    Review
  10. Article
  11. Article
  12. Article
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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

19 authors at 3 institutions in 1 country.

Daichi TamuraDepartment of Urology, Iwate Medical University School of Medicine, Yahaba, Japan.ORCID https://orcid.org/0000-0001-9498-9996
Masakazu AbeDepartment of Urology, Iwate Medical University School of Medicine, Yahaba, Japan.
Hayato HirakiDivision of Biomedical Research and Development, Iwate Medical University Institute for Biomedical Sciences, Yahaba, Japan.
Noriyuki SasakiDivision of Biomedical Research and Development, Iwate Medical University Institute for Biomedical Sciences, Yahaba, Japan.
Akiko Yashima-AboDivision of Biomedical Research and Development, Iwate Medical University Institute for Biomedical Sciences, Yahaba, Japan.
Daiki IkarashiDepartment of Urology, Iwate Medical University School of Medicine, Yahaba, Japan.
Renpei KatoDepartment of Urology, Iwate Medical University School of Medicine, Yahaba, Japan.
Yoichiro KatoDepartment of Urology, Iwate Medical University School of Medicine, Yahaba, Japan.
Shigekatsu MaekawaDepartment of Urology, Iwate Medical University School of Medicine, Yahaba, Japan.
Mitsugu KanehiraDepartment of Urology, Iwate Medical University School of Medicine, Yahaba, Japan.
Ryo TakataDepartment of Urology, Iwate Medical University School of Medicine, Yahaba, Japan.ORCID https://orcid.org/0000-0002-4860-8942
Kazuhiro MaejimaLaboratory for Cancer Genomics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Shota SasagawaLaboratory for Cancer Genomics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Masashi FujitaLaboratory for Cancer Genomics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Yutaka SuzukiDepartment of Computational Biology and Medical Sciences, The University of Tokyo, Kashiwa, Japan.
Hidewaki NakagawaLaboratory for Cancer Genomics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.ORCID https://orcid.org/0000-0003-1807-772X
Takeshi IwayaDepartment of Clinical Oncology, Iwate Medical University School of Medicine, Yahaba, Japan.
Satoshi S NishizukaDivision of Biomedical Research and Development, Iwate Medical University Institute for Biomedical Sciences, Yahaba, Japan.
Wataru ObaraDepartment of Urology, Iwate Medical University School of Medicine, Yahaba, Japan.ORCID https://orcid.org/0000-0003-2720-9640
Iwate Medical University · JPRIKEN Center for Integrative Medical Sciences · JPThe University of Tokyo · JP

Funding

Iwate Prefectural Regional Innovation GrantJapan Society for the Promotion of Science 21K07223Japan Society for the Promotion of Science 21K09353Keiryokai Research Grant 133
6 · The paper itself

Abstract

Biomarkers that could detect the postoperative recurrence of upper tract urothelial carcinoma (UTUC) have not been established. In this prospective study, we aim to evaluate the utility of individualized circulating tumor DNA (ctDNA) monitoring using digital PCR (dPCR) as a tumor recurrence biomarker for UTUC in the perioperative period. Twenty-three patients who underwent radical nephroureterectomy (RNU) were included. In each patient, whole exome sequencing by next-generation sequencing and TERT promoter sequencing of tumor DNA were carried out. Case-specific gene mutations were selected from sequencing analysis to examine ctDNA by dPCR analysis. We also prospectively collected plasma and urine ctDNA from each patient. The longitudinal variant allele frequencies of ctDNA during the perioperative period were plotted. Case-specific gene mutations were detected in 22 cases (96%) from ctDNA in the preoperative samples. Frequently detected genes were TERT (39%), FGFR3 (26%), TP53 (22%), and HRAS (13%). In all cases, we obtained plasma and urine samples for 241 time points and undertook individualized ctDNA monitoring for 2 years after RNU. Ten patients with intravesical recurrence had case-specific ctDNA detected in urine at the time of recurrence. The mean lead time of urinary ctDNA in intravesical recurrence was 60 days (range, 0-202 days). Two patients with distal metastasis had case-specific ctDNA in plasma at the time of metastasis. In UTUC, tumor-specific gene mutations can be monitored postoperatively as ctDNA in plasma and urine. Individualized ctDNA might be a minimally invasive biomarker for the early detection of postoperative recurrence.

Indexed as

Carcinoma, Transitional CellCirculating Tumor DNAUrinary Bladder NeoplasmsBiomarkersBiomarkers, TumorHumansNeoplasm Recurrence, LocalProspective StudiesBiomarkersBiomarkers, TumorCirculating Tumor DNAcase-specific mutationcirculating tumor DNAdigital PCRpostoperative monitoringupper tract urothelial carcinoma

Identifiers

PMID38083992
PMCPMC10859621
OpenAlexW4389608227

What OpenQuestion holds

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Registered trials

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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.