Evidence map›Paper›PMID 40322207›Full record

ArticleCancer diagnosis & prognosis

Multicenter Retrospective Analysis of Pulmonary Sarcomatoid Carcinoma Clinically Diagnosed Using Small Biopsy Specimens.

Minehiko Inomata, Takeshi Tsuda, Tomomi Ichikawa, Masahiro Matsumoto, Isami Mizushima, Kenji Azechi, Naoki Takata, Nozomu Murayama, Zenta Seto, Kotaro Tokui and 6 more

Abstract read
In one paragraph

Article in Cancer diagnosis & prognosis. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

16 authors.

Minehiko InomataFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
Takeshi TsudaDepartment of Respiratory Medicine, Toyama Prefectural Central Hospital, Toyama, Japan.
Tomomi IchikawaRespiratory and Allergy Medicine, Toyama Red Cross Hospital, Toyama, Japan.
Masahiro MatsumotoDepartment of Respiratory Medicine, Toyama Prefectural Central Hospital, Toyama, Japan.
Isami MizushimaDepartment of Respiratory Medicine, Toyama Prefectural Central Hospital, Toyama, Japan.
Kenji AzechiDepartment of Respiratory Medicine, Toyama Prefectural Central Hospital, Toyama, Japan.
Naoki TakataFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
Nozomu MurayamaFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
Zenta SetoFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
Kotaro TokuiFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
Yasuaki MasakiDepartment of Respiratory Medicine, Toyama Prefectural Central Hospital, Toyama, Japan.
Seisuke OkazawaFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
Shingo ImanishiFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
Toshiro MiwaFirst Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
Ryuji HayashiDepartment of Medical Oncology, Toyama University Hospital, Toyama, Japan.
Hirokazu TaniguchiDepartment of Respiratory Medicine, Toyama Prefectural Central Hospital, Toyama, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aim: Pulmonary sarcomatoid carcinoma is a rare disease known for its aggressiveness, with numerous studies evaluating the efficacy of various therapeutic approaches. However, pulmonary sarcomatoid carcinoma is histologically defined according to WHO classification based on surgical specimens, whereas in clinical practice, most cases of advanced lung cancer are diagnosed based on small biopsy specimens. This retrospective study aimed to present the clinical course of patients diagnosed with pulmonary sarcomatoid carcinoma based on small biopsy specimens. Patients and Methods: Data of patients who were diagnosed with pulmonary sarcomatoid carcinoma based on small biopsy specimens and treated with platinum-doublet chemotherapy and/or an immune checkpoint inhibitor-containing regimen between 2005 and 2022 were analyzed. Results: Data from 12 patients were analyzed, including five patients treated with platinum-doublet chemotherapy and 11 patients treated with an immune checkpoint inhibitor-containing regimen. The median progression-free survival among the five patients treated with platinum-doublet chemotherapy was 1.5 months [95% confidence interval (CI)=0.7-4.1]. Of these, four patients subsequently received immune checkpoint inhibitor-containing therapy. The median overall survival from the initiation of platinum-doublet chemotherapy in these five patients was 14.7 months (95%CI=1.2-16.2). In contrast, 11 patients treated with immune checkpoint inhibitor therapy showed a median progression-free survival and overall survival of 8.9 months [95%CI=0.3-not estimated (NE)] and 10.8 months (95%CI=1.0-NE), respectively. Conclusion: Pulmonary sarcomatoid carcinoma diagnosed based on small biopsy specimens is refractory to platinum-doublet chemotherapy, and immune checkpoint inhibitor therapy may improve the prognosis.

Indexed as

diagnosisprognosispulmonary sarcomatoid carcinomaSmall biopsy specimens

Identifiers

PMID40322207
PMCPMC12046660

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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.