Evidence map›Paper›PMID 35545933›Full record

ArticleThoracic cancer2022

Use of a highly sensitive lung cancer compact panel to detect KRAS G12D in the wash fluid from a lung tumor: A case report.

Daisuke Minami, Nagio Takigawa, Yasuhiro Nakajima, Nobuaki Miyahara, Yasuyuki Mizumori, Mitsuhiro Ueda, Seiji Nakamura, Fumihiko Suzuki, Yoshiharu Sato, Kei Morikawa and 1 more

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In one paragraph

Article in Thoracic cancer, 2022. 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
0.6field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

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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

11 authors at 5 institutions in 1 country.

Daisuke MinamiDepartment of Respiratory Medicine, Himeji Saint Mary's Hospital, Himeji, Japan.ORCID 0000-0001-8130-1478
Nagio TakigawaDepartment of Internal Medicine, Himeji Saint Mary's Hospital, Himeji, Japan.
Yasuhiro NakajimaDepartment of Respiratory Medicine, Himeji Saint Mary's Hospital, Himeji, Japan.
Nobuaki MiyaharaDepartment of Internal Medicine, Himeji Saint Mary's Hospital, Himeji, Japan.
Yasuyuki MizumoriDepartment of Respiratory Medicine, National Hospital Organization Himeji Medical Center, Himeji, Japan.
Mitsuhiro UedaDepartment of Thoracic Surgery, National Hospital Organization Himeji Medical Center, Japan.
Seiji NakamuraDNA Chip Research Inc, Japan.
Fumihiko SuzukiDNA Chip Research Inc, Japan.
Yoshiharu SatoDNA Chip Research Inc, Japan.
Kei MorikawaDivision of Respiratory Medicine, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.
Arihiko KanehiroDepartment of Internal Medicine, Himeji Saint Mary's Hospital, Himeji, Japan.
Himeji University · JPDNA Chip Research (Japan) · JPHimeji Medical Center · JPKawasaki Medical School · JPSt. Marianna University School of Medicine · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Here, we report a case of a pulmonary invasive mucinous adenocarcinoma harboring KRAS G12D, diagnosed from tumor samples containing a very small amount of tumor cells using next-generation sequencing (NGS) and the recently developed Lung Cancer Compact Panel. A 79-year-old woman without any respiratory symptoms underwent chest computed tomography, which revealed a tumor in the left lower lobe. During endobronchial ultrasound (EBUS)-guided transbronchial biopsy (TBB) using a guide sheath (GS), a sufficient specimen for pathological diagnosis could not be obtained because the patient had a severe cough and pulmonary bullae located adjacent to the tumor. In the absence of EBUS transbronchial biopsy findings using a guide sheath, brush cytology was used to categorize the tumor as class II (Papanicolaou classification). However, the wash fluid from the cytological examination contained enough cells to obtain sufficient nucleic acid for use in sequencing analysis. The latter revealed KRAS G12D expression. Although the patient underwent surgery without pathological evidence, the evaluation of the surgical specimen confirmed a diagnosis of pulmonary invasive mucinous adenocarcinoma. Use of the Lung Cancer Compact Panel enabled the detection of KRAS G12D in the wash fluid of a brush cytology sample and thus a diagnosis of pulmonary invasive mucinous adenocarcinoma.

Indexed as

Adenocarcinoma, MucinousAdenocarcinoma of LungLung NeoplasmsAgedBronchoscopyFemaleHumansImage-Guided BiopsyProto-Oncogene Proteins p21(ras)KRAS protein, humanProto-Oncogene Proteins p21(ras)KRAS G12Dlung cancer compact panelpulmonary invasive mucinous adenocarcinoma

Identifiers

PMID35545933
PMCPMC9161320
OpenAlexW4280566002

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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.