Evidence map›Paper›PMID 41574789›Full record

ArticleJapanese journal of clinical oncology2026

Role of clonal lineage analysis via next-generation sequencing in identifying the origin of multiple cancers and guiding treatment options.

Rie Shimoyachi, Aya Takimoto, Taichi Yoshida, Koji Fukuda, Kazuhiro Shimazu, Daiki Taguchi, Naoaki Kodama, Tomohiro Matsumoto, Toshiki Wakabayashi, Kazuhiro Imai and 2 more

Abstract readCase Reports
In one paragraph

Article in Japanese journal of clinical oncology, 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

12 authors.

Rie ShimoyachiDepartment of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo1-1-1, Akita 010-8543, Japan.
Aya TakimotoDepartment of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo1-1-1, Akita 010-8543, Japan.
Taichi YoshidaDepartment of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo1-1-1, Akita 010-8543, Japan.
Koji FukudaDepartment of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo1-1-1, Akita 010-8543, Japan.
Kazuhiro ShimazuDepartment of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo1-1-1, Akita 010-8543, Japan.
Daiki TaguchiDepartment of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo1-1-1, Akita 010-8543, Japan.
Naoaki KodamaDepartment of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo1-1-1, Akita 010-8543, Japan.
Tomohiro MatsumotoDepartment of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo1-1-1, Akita 010-8543, Japan.
Toshiki WakabayashiDepartment of Surgery, Akita City Hospital, Kawamotomatsuoka-machi 4-30, 010-0933, Japan.
Kazuhiro ImaiDepartment of Thoracic Surgery, Akita University Graduate School of Medicine, Akita 010-8543, Japan.
Hiroshi NanjyoDepartment of Pathology, Akita University Hospital, Hondo1-1-1, Akita 010-8543, Japan.
Hiroyuki ShibataDepartment of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo1-1-1, Akita 010-8543, Japan.ORCID 0000-0003-3581-3506

Funding

Department of Clinical Oncology
6 · The paper itself

Abstract

Multiple cancers occur in the same individual, such as hereditary breast and ovarian cancer (HBOC) syndrome and Lynch syndrome. Here, we report a patient with HBOC syndrome who developed four different cancer types (pancreatic cancer, right lung adenocarcinoma, prostate cancer, and left lung adenocarcinoma) within a relatively short period of 6.5 years. In HBOC syndrome, the lung adenocarcinoma is rare, and the tumors were initially suspected to be lung metastases from pancreatic cancer, respectively. The pathological analysis results in each of the three lesions were inconsistent. A whole-exome analysis was performed on all three tumors using next-generation sequencing (NGS). The results showed that many of the deletion mutations found in pancreatic cancer were not present in other lung tumors. Homologous recombination is required for the repair of deletion mutations, but this function is impaired in HBOC syndrome. Deletions occurring in the primary tumor are irreversible and should be inherited in metastatic lesions. Therefore, we hypothesized that these three cancers arose independently, that each lung tumor was a primary tumor rather than a metastasis of pancreatic cancer, and that their resection would be curative. This assumption was reasonable, as no new lesions were observed in a 10-year follow-up study since the onset of pancreatic cancer. Tracking genetic traits using NGS helps understand the origins and progression of malignant tumors.

Indexed as

AdenocarcinomaHigh-Throughput Nucleotide SequencingLung NeoplasmsNeoplasms, Multiple PrimaryPancreatic NeoplasmsAdenocarcinoma of LungFemaleHumansMaleMiddle Agedhereditary breast and ovarian cancer syndromelung adenocarcinomamultiple primary cancernext-generation sequencingpancreatic cancer

Identifiers

PMID41574789
PMCPMC13070523

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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.