Evidence map›Paper›PMID 38524651›Full record

ArticleInternational cancer conference journal2024

A case of hereditary breast and ovarian cancer syndrome of initially presented as cancer of unknown primary with lymph node metastases unveiled by genetic analysis.

Juri Yamada, Koji Fukuda, Tae Sugawara, Kenichi Makino, Kazuhiro Shimazu, Taichi Yoshida, Daiki Taguchi, Hanae Shinozaki, Yukihiro Terada, Hiroshi Nanjo and 1 more

Open access · hybridAbstract read
In one paragraph

Article in International cancer conference journal, 2024. 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
1.6field-weighted citation impact, top 39% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

11 authors at 2 institutions in 1 country.

Juri YamadaDepartment of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo 1-1-1, Akita, Japan.
Koji FukudaDepartment of Obstetrics and Gynecology, Graduate School of Medicine, Akita University, Akita, Japan.
Tae SugawaraDepartment of Obstetrics and Gynecology, Graduate School of Medicine, Akita University, Akita, Japan.
Kenichi MakinoDepartment of Obstetrics and Gynecology, Graduate School of Medicine, Akita University, Akita, Japan.
Kazuhiro ShimazuDepartment of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo 1-1-1, Akita, Japan.
Taichi YoshidaDepartment of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo 1-1-1, Akita, Japan.
Daiki TaguchiDepartment of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo 1-1-1, Akita, Japan.
Hanae ShinozakiDepartment of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo 1-1-1, Akita, Japan.
Yukihiro TeradaDepartment of Obstetrics and Gynecology, Graduate School of Medicine, Akita University, Akita, Japan.
Hiroshi NanjoDepartment of Pathology, Akita University Hospital, Akita, Japan.
Hiroyuki ShibataDepartment of Clinical Oncology, Graduate School of Medicine, Akita University, Hondo 1-1-1, Akita, Japan.
Akita University · JPAkita University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer of unknown primary (CUP) is a heterogeneous disease concept involving various malignant tumors. Understanding its pathophysiology is often difficult, together with its treatment. Here, we present a case of CUP with abdominal lymph node enlargement and elevated carbohydrate antigen 125 levels. It initially resembled a favorable prognosis type similar to ovarian cancer, but metastases were observed in cervical lymph nodes, indicating a somewhat atypical CUP compared to the typical ovarian cancer-like CUP. We identified a germline Breast Cancer 1 (BRCA1) p.L63* variant through a family history inquiry and BRCA analysis, indicating hereditary breast and ovarian cancer syndrome. The patient achieved near-complete remission with platinum-based therapy followed by poly (ADP-ribose) polymerase (PARP) inhibitor. The variant has shown sensitivity in both clinical and pathogenic reports in the ClinVar database of the National Institutes of Health. No clinical studies reported on the efficacy of PARP inhibitors specific to this variant, but our case demonstrated the sensitivity of platinum-based therapy followed by PARP inhibitor. Reports of CUP in hereditary breast and ovarian cancer syndrome are very rare, with only a single report in the literature.

Indexed as

BRCA1 variantCancer of unknown primaryHBOC syndromeHomologous recombination deficiencyPARP inhibitor

Identifiers

PMID38524651
PMCPMC10957858
OpenAlexW4391691112

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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.