Evidence map›Paper›PMID 27330309›Full record

ArticleOncoTargets and therapy2016

Sequential measurements of serum matrix metalloproteinase 9 to monitor chemotherapy responses in patients with advanced non-small-cell lung cancer.

Xiaojuan Qiao, Xiaoran Zhai, Jinghui Wang, Xiaoting Zhao, Xinjie Yang, Jialin Lv, Li Ma, Lina Zhang, Yue Wang, Shucai Zhang and 1 more

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2016. 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
0.4field-weighted citation impact, top 35% 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, 4 citations in OpenAlex.

  1. Article
  2. Review
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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 2 institutions in 2 countries.

Xiaojuan QiaoDepartment of Cellular and Molecular Biology, Beijing Chest Hospital, Capital Medical University, Beijing, People's Republic of China; Department of Cellular and Molecular Biology, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing, People's Republic of China; Health Care Ward, The First Hospital Affiliated to Inner Mongolia Medical University, Hohhot, People's Republic of China.
Xiaoran ZhaiDepartment of Cellular and Molecular Biology, Beijing Chest Hospital, Capital Medical University, Beijing, People's Republic of China; Department of Cellular and Molecular Biology, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing, People's Republic of China.
Jinghui WangDepartment of Medical Oncology, Beijing Chest Hospital, Capital Medical University, Beijing, People's Republic of China.
Xiaoting ZhaoDepartment of Cellular and Molecular Biology, Beijing Chest Hospital, Capital Medical University, Beijing, People's Republic of China; Department of Cellular and Molecular Biology, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing, People's Republic of China.
Xinjie YangDepartment of Medical Oncology, Beijing Chest Hospital, Capital Medical University, Beijing, People's Republic of China.
Jialin LvDepartment of Medical Oncology, Beijing Chest Hospital, Capital Medical University, Beijing, People's Republic of China.
Li MaDepartment of Cellular and Molecular Biology, Beijing Chest Hospital, Capital Medical University, Beijing, People's Republic of China; Department of Cellular and Molecular Biology, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing, People's Republic of China.
Lina ZhangDepartment of Cellular and Molecular Biology, Beijing Chest Hospital, Capital Medical University, Beijing, People's Republic of China; Department of Cellular and Molecular Biology, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing, People's Republic of China.
Yue WangDepartment of Cellular and Molecular Biology, Beijing Chest Hospital, Capital Medical University, Beijing, People's Republic of China; Department of Cellular and Molecular Biology, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing, People's Republic of China.
Shucai ZhangDepartment of Medical Oncology, Beijing Chest Hospital, Capital Medical University, Beijing, People's Republic of China.
Wentao YueDepartment of Cellular and Molecular Biology, Beijing Chest Hospital, Capital Medical University, Beijing, People's Republic of China; Department of Cellular and Molecular Biology, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing, People's Republic of China.
Beijing Chest Hospital · CNCapital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMatrix metalloproteinase 9 (MMP-9) plays an important role in tumor invasion and metastasis, including lung cancer. However, whether variations in serum MMP-9 levels can serve as a biomarker for monitoring chemotherapy curative effect remains unclear. This study was designed to investigate the association between variations in serum MMP-9 levels and chemotherapy curative effect in patients with lung cancer. PATIENTS AND

methodsA total of 82 patients with advanced lung cancer were included. All newly diagnosed patients were treated with platinum-based doublet chemotherapy. Serial measurements of serum MMP-9 levels were performed by enzyme-linked immunosorbent assay. In this manner, we chose four time points to examine the association, including before chemotherapy, and 3 weeks after the beginning of the first, second, and fourth cycles of chemotherapy.

resultsCompared with the serum level of MMP-9 before progressive disease, patients with progressive disease had elevated serum levels of MMP-9. Compared with the previous time point of collecting specimens, the serum levels of MMP-9 in the patients with a complete response/partial response/stable disease decreased or were maintained stable. The differences of variation in serum MMP-9 levels in patients with different chemotherapy curative effects were all statistically significant after one cycle, two cycles, and four cycles (after one cycle: P<0.001; after two cycles: P<0.001; after four cycles: P=0.01). However, patients with small-cell lung cancer did not exhibit similar test results.

conclusionThe variation in serum MMP-9 levels in patients with non-small-cell lung cancer during chemotherapy was closely related to chemotherapy curative effect and could be useful to monitor chemotherapy curative effect for a small portion of patients.

Indexed as

chemotherapylung adenocarcinomalung squamous carcinomaprognosistreatment monitoring

Identifiers

PMID27330309
PMCPMC4898419
OpenAlexW2418580641

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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.