Evidence map›Paper›PMID 27604790›Full record

Trial reportEuropean journal of nuclear medicine and molecular imaging2017

Volume-based predictive biomarkers of sequential FDG-PET/CT for sunitinib in cancer of unknown primary: identification of the best benefited patients.

Yifei Ma, Wei Xu, Ruojing Bai, Yiming Li, Hongyu Yu, Chunshan Yang, Huazheng Shi, Jian Zhang, Jidong Li, Chenguang Wang and 1 more

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in European journal of nuclear medicine and molecular imaging, 2017. 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
–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

3 citing papers in PubMed.

  1. Observational
  2. Article
  3. 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

11 authors.

Yifei MaDepartment of Orthorpedic Oncology, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai, 200003, China.
Wei XuDepartment of Orthorpedic Oncology, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai, 200003, China.
Ruojing BaiDepartment of Geriatrics, Tianjin Medical University General Hospital, Laboratory of Neuro-Trauma and Neurodegenerative Disorder, Geriatrics Institute, Tianjin, 300352, China.
Yiming LiDepartment of Neuro-oncology, Neurosurgery Institute, Beijing, 100000, China.
Hongyu YuDepartment of Pathology, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai, 200003, China. yuhongyucz@aliyun.com.
Chunshan YangDepartment of PET/CT Radiology, Panorama Medical Imaging Center, Shanghai, China.
Huazheng ShiDepartment of PET/CT Radiology Center, Number 85 Hospital of PLA, 1328 Huashan Road, Shanghai, 200004, China.
Jian ZhangDepartment of PET/CT Radiology Center, Number 85 Hospital of PLA, 1328 Huashan Road, Shanghai, 200004, China.
Jidong LiDepartment of Stomatology, The First People's Hospital of Shangqiu, Shangqiu, 476100, Henan Province, China.
Chenguang WangDepartment of Radiology, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai, 200003, China.
Jianru XiaoDepartment of Orthorpedic Oncology, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai, 200003, China. jianruxiao83@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo test the performance of sequential

methodsCUP patients were enrolled for sequential PET/CT scanning for sunitinib and a control group. Univariate and multivariate analysis were applied to test the efficacy of sunitinib therapy in CUP patients. Next, sequential analyses involving PET/CT parameters were performed to identify and validate sensitive PET/CT biomarkers for sunitinib therapy. Finally, time-dependent receiver operating characteristic (TDROC) analyses were performed to compare the predictive accuracy.

resultsMultivariate analysis proved that sunitinib group had significantly improved survival (p < 0.01) as compared to control group. After cycle 2 of therapy, multivariate analysis identified volume-based PET/CT parameters as sensitive biomarkers for sunitinib (p < 0.01). TDROC curves demonstrated whole-body total lesion glycolysis reduction (Δ WTLG) and follow-up WTLG to have good accuracy for efficacy prediction. This evidence was validated after cycle 4 of therapy with the same method.

conclusionSunitinib therapy proved effective in treatment of CUP. PET/CT volume-based parameters may help predict outcome of sunitinib therapy, in which Δ WTLG and follow-up WTLG seem to be sensitive biomarkers for sunitinib efficacy. Patients with greater reduction and lower WTLG at follow-up seem to have better survival outcome.

Indexed as

Fluorodeoxyglucose F18Patient SelectionAdultAntineoplastic AgentsBiomarkersChinaFemaleHumansIndolesMaleMiddle AgedNeoplasms, Unknown PrimaryOutcome Assessment, Health CarePositron Emission Tomography Computed TomographyPrevalencePrognosisAntineoplastic AgentsBiomarkersFluorodeoxyglucose F18IndolesPyrrolesRadiopharmaceuticalsSunitinibCancer of unknown primarySunitinibSurvival predictionVolume-based PET/CT parameters

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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.