Evidence map›Paper›PMID 32754323›Full record

ArticleMolecular and clinical oncology2020

Value of TTF-1 expression in non-squamous non-small-cell lung cancer for assessing docetaxel monotherapy after chemotherapy failure.

Akira Takeuchi, Tetsuya Oguri, Yoriko Yamashita, Kazuki Sone, Satoshi Fukuda, Osamu Takakuwa, Takehiro Uemura, Ken Maeno, Yoshitsugu Inoue, Sayaka Yamamoto and 8 more

Abstract read
In one paragraph

Article in Molecular and clinical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

18 authors.

Akira TakeuchiDepartment of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Tetsuya OguriDepartment of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Yoriko YamashitaExperimental Pathology and Tumor Biology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Kazuki SoneDepartment of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Satoshi FukudaDepartment of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Osamu TakakuwaEducation and Research Center for Advanced Medicine, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Takehiro UemuraDepartment of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Ken MaenoDepartment of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Yoshitsugu InoueDepartment of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Sayaka YamamotoDepartment of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Hirono NishiyamaDepartment of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Kensuke FukumitsuDepartment of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Yoshihiro KanemitsuDepartment of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Tomoko TajiriDepartment of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Hirotsugu OhkuboDepartment of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Masaya TakemuraDepartment of Education and Research Center for Community Medicine, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Yutaka ItoDepartment of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
Akio NiimiDepartment of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Docetaxel is one of the standard second/third-line treatments for non-small-cell lung cancer (NSCLC) following a failed response to prior cytotoxic chemotherapy. The predictive biomarker for the effectiveness of docetaxel therapy remains undetermined. However, thyroid transcription factor-1 (TTF-1) is known to be a good prognostic factor for a variety of chemotherapies. To investigate the association between TTF-1 expression and docetaxel monotherapy outcome, 82 patients with non-squamous NSCLC who received second/third-line docetaxel monotherapy were retrospectively screened. All backgrounds were well-balanced whether or not tumor TTF-1 was expressed, and the present clinical outcomes were similar to those reported by previous clinical studies. A better clinical outcome was indicated in TTF-1 positive compared with TTF-1 negative patients, with disease control rates of 69% vs. 42%, respectively (P=0.03) and median overall survival of 393 days vs. 221.5 days, respectively (P<0.01). Furthermore, progression free survival tended to be longer in TTF-1 positive compared with TTF-1 negative patients (median, 100 days vs. 67 days; P=0.09). Multivariate analysis revealed that TTF-1 positivity was a unique significant predictor for assessing overall survival after docetaxel monotherapy. TTF-1 positivity may be useful for predicting survival outcome in patients who received docetaxel monotherapy after failure of prior chemotherapy.

Indexed as

cytotoxic chemotherapydocetaxelnon-squamous non-small-cell lung cancersecond-line chemotherapythyroid transcription factor-1

Identifiers

PMID32754323
PMCPMC7391830

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.