Evidence map›Paper›PMID 26884883›Full record

ArticleInternational journal of clinical and experimental pathology2015

(99m)Tc-3P-RGD2 SPECT to monitor early response to bevacizumab therapy in patients with advanced non-small cell lung cancer.

Bin Chen, Guoqing Zhao, Qingjie Ma, Bin Ji, Tiefeng Ji, Hua Xin, Shi Gao

Abstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Advances in Clinical Oncology Research onFrontiers in oncology · 2022
    Review
  3. Review
  4. Biodistribution and Internal Radiation Dosimetry ofCancer biotherapy & radiopharmaceuticals · 2018
    Article
  5. Imaging of Integrin αCancer biotherapy & radiopharmaceuticals · 2017
    Article
  6. Clinical study ofOncotarget · 2017
    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

7 authors.

Bin ChenDepartment of Nuclear Medicine, China-Japan Union Hospital, Jilin University Changchun, Jilin, China.
Guoqing ZhaoDepartment of Nuclear Medicine, China-Japan Union Hospital, Jilin University Changchun, Jilin, China.
Qingjie MaDepartment of Nuclear Medicine, China-Japan Union Hospital, Jilin University Changchun, Jilin, China.
Bin JiDepartment of Nuclear Medicine, China-Japan Union Hospital, Jilin University Changchun, Jilin, China.
Tiefeng JiDepartment of Nuclear Medicine, China-Japan Union Hospital, Jilin University Changchun, Jilin, China.
Hua XinDepartment of Thoracic Surgery, China-Japan Union Hospital, Jilin University Changchun, Jilin, China.
Shi GaoDepartment of Nuclear Medicine, China-Japan Union Hospital, Jilin University Changchun, Jilin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study assessed the predictive value of (99m)Tc-3(poly-(ethylene glycol), PEG) 4-arginine-glycine-aspartic ((99m)Tc-3P-RGD2) single photon emission computed tomography (SPECT) for the early identification of response to antiangiogenic treatment with bevacizumab in patients with advanced non-small cell lung cancer (NSCLC). Patients with advanced NSCLC treated with bevacizumab were prospectively studied with (99m)Tc-3P-RGD2 SPECT before and after 2 weeks from start of treatment. The tumor response was evaluated with RECIST criteria and related to observed change in the tumor to non-tumor (T/N) ratio for the largest known lesion. Receiver operating characteristic (ROC) curve analysis was used to determine T/N ratio changes with regard to predicting response to bevacizumab therapy. Change in T/N ratio was also related to progression-free survival (PFS) and overall survival (OS). Twenty-six patients were included, and 23 were finally assessable for metabolic response evaluation with (99m)Tc-3P-RGD2 SPECT. The cut-off value of T/N ratio change defined by ROC analysis was 24.4%. The sensitivity, specificity, and negative predictive value of (99m)Tc-3P-RGD2 SPECT for predicting tumor response were 81.8%, 91.7%, and 84.6%, respectively. Using the cut-off value defined by ROC analysis on (99m)Tc-3P-RGD2 SPECT, metabolic non-progressive disease patients (mNP) showed prolonged PFS (5.6 months versus 3.4 months; P < 0.001) and OS (17.1 months versus 8.6 months; P < 0.001) than metabolic progressive disease patients (mP). (99m)Tc-3P-RGD2 SPECT scan is a promising test to predict tumor response in patients with advanced non-small cell lung cancer early in the course of bevacizumab therapy.

Indexed as

AdultAgedAngiogenesis InhibitorsArea Under CurveBevacizumabCarcinoma, Non-Small-Cell LungDisease-Free SurvivalFemaleHumansKaplan-Meier EstimateLung NeoplasmsMaleMiddle AgedNeoplasm StagingOrganotechnetium CompoundsPeptides, CyclicAngiogenesis InhibitorsBevacizumabOrganotechnetium CompoundsPeptides, CyclicRadiopharmaceuticalstechnetium 99m (HYNIC-3PRGD(2))(tricine)(TPPTS)99mTc-3P-RGD2bevacizumabnon-small cell lung cancerresponseSPECT

Identifiers

PMID26884883
PMCPMC4730096

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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.