Evidence map›Paper›PMID 29625604›Full record

ArticleBMC cancer2018

Apatinib for advanced sarcoma: results from multiple institutions' off-label use in China.

Lu Xie, Wei Guo, Ye Wang, Taiqiang Yan, Tao Ji, Jie Xu

3 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in BMC cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 40 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 5 pooled it
8.6field-weighted citation impact, top 2% 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.

NCT04044378 phase1 / phase2withdrawnnot on this mapstarted 2019, after this paper: background citation

Famitinib Malate (SHR1020) Plus Camrelizumab (SHR 1210) Versus Famitinib Malate Alone Versus Famitinib Malate Plus Ifosfamide Locally Advanced, Unresectable or Metastatic Osteosarcoma Progression Upon Chemotherapy: A Phase Ib/II Randomized and Controlled Dose-Escalation Trial

TypeinterventionalSponsorPeking University People's HospitalRan2019 to 2022Enrolled0ConditionsEffect of Drugs, Progression, Pediatric CancerArmsFamitinib, Ifosfamide, Camrelizumab
NCT04260113 nacompletednot on this mapstarted 2019, after this paper: background citation

The Effectivity and Toxicity of Apatinib for Unresectable Advanced Chondrosarcoma: a Multicentric Retrospective Study

TypeinterventionalSponsorPeking University People's HospitalRan2019 to 2020Enrolled40ConditionsEfficacy, Toxicity, DrugArmsApatinib Mesylate
NCT06751251 active not recruitingnot on this mapstarted 2025, after this paper: background citation

The Exploration of OX40 (CD134) Expression Levels in Sarcoma Specimens and Its Clinical Application in Prognosis Determination

TypeobservationalSponsorPeking University People's HospitalRan2025 to 2026Enrolled200ConditionsSarcoma, Biomarkers, ProgressionArmsIHC: Immunohistochemistry, RNA-seq
3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 5 syntheses or guidelines pooled it, 63 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Lu XiePeking University People's Hospital, Peking, China.
Wei GuoPeking University People's Hospital, Peking, China. bonetumor@163.com.ORCID 0000-0003-2471-5767
Ye WangPeking University Shougang Hospital, Peking, China.
Taiqiang YanPeking University International Hospital, Peking, China.
Tao JiPeking University People's Hospital, Peking, China.
Jie XuPeking University People's Hospital, Peking, China.
Peking University · CNPeking University Shougang Hospital · CN

Funding

National Natural Science Foundation of China 81402382
6 · The paper itself

Abstract

backgroundAnti-angiogenesis Tyrosine kinase inhibitors (TKIs) have been proved to show promising effects on prolonging progression-free survival (PFS) for advanced sarcoma after failure of standard multimodal Therapy. Methylsulfonic apatinib is one of those TKIs which specifically inhibits VEGFR-2. This paper summarizes the experience of three Peking University affiliated hospitals in off-label use of apatinib in the treatment of extensively pre-treated sarcoma.

methodsWe retrospectively analysed files of patients with advanced sarcoma not amenable to curative treatment, who were receiving an apatinib-containing regimen between June 1, 2015 and December 1, 2016. Fifty-six patients were included: 22 osteosarcoma, 10 Ewing's sarcoma, 3 chondrosarcoma and 21 soft tissue sarcoma.

resultsWith median follow-up time of 6 months (range, 0.7-18.0 m), thirty-five (62.5%) patients had partial response, and disease was stable in 11 (19.6%). The 4-month and 6-month progression-free survival rates were 46.3 and 36.5%, respectively. The median duration of response was 3.8 months (95% CI 1.9-5.6 m), with much variability among disease subtypes. The median overall survival was 9.9 months (95% CI 7.6-12.2 m). Grade 3 and 4 toxicities were observed in 8 (14.3%) patients, the most common being hypertension, pneumothorax, wound-healing problems, anorexia, and rash or desquamation.

conclusionsApatinib might be effective, with a high objective response rate, in an off-label study of sarcoma patients with advanced, previously treated disease. The duration of response was consistent with reports in different subtypes of sarcomas. Prospective trials of apatinib in the treatment of selected subtypes of sarcomas are needed.

trial registrationRetrospectively registered in the Medical Ethics Committee of Peking University People's Hospital, Peking University Shougang Hospital and Peking University International Hospital. The trial registration number is 2017PHB176-03 and the date of registration is January 20th 2017.

Indexed as

AdolescentAdultAntineoplastic AgentsChildChinaFollow-Up StudiesHumansMiddle AgedMolecular Targeted TherapyNeoplasm GradingNeoplasm MetastasisNeoplasm StagingOff-Label UseProportional Hazards ModelsProtein Kinase InhibitorsPyridinesAntineoplastic AgentsapatinibProtein Kinase InhibitorsPyridinesVascular Endothelial Growth Factor Receptor-2ApatinibChondrosarcomaEwing sarcomaOsteosarcomaSoft-tissue sarcomaTyrosine-kinase inhibitor

Identifiers

PMID29625604
PMCPMC5889565
OpenAlexW2799341684

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.