Evidence map›Paper›PMID 30559126›Full record

Trial reportThe oncologist2019

Apatinib for Advanced Osteosarcoma after Failure of Standard Multimodal Therapy: An Open Label Phase II Clinical Trial.

Lu Xie, Jie Xu, Xin Sun, Xiaodong Tang, Taiqiang Yan, Rongli Yang, Wei Guo

5 registry-linked trialsOpen access · bronzeAbstract readClinical Trial, Phase II
In one paragraph

Trial report in The oncologist, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 5 registered trials, which are not on this map. Cited by 82 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed, 3 pooled it
10.3field-weighted citation impact, top 1% 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.

NCT03359018 phase2completednot on this map

Apatinib Mesylate Plus Anti-PD1 Therapy (SHR-1210) in Locally Advanced, Unresectable or Metastatic Osteosarcoma(APFAO)Refractory to Chemotherapy : a Single Institution, Open-label, Phase 2 Trial

TypeinterventionalSponsorPeking University People's HospitalRan2018 to 2020Enrolled43ConditionsProgression-free Survival, Overall Survival, Clinical Benefit Rate, ToxicityArmsApatinib, SHR-1210
NCT04044378 phase1 / phase2withdrawnnot on this map

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 map

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

TypeinterventionalSponsorPeking University People's HospitalRan2019 to 2020Enrolled40ConditionsEfficacy, Toxicity, DrugArmsApatinib Mesylate
NCT04690231 nacompletednot on this mapstarted 2020, after this paper: background citation

Apatinib+Ifosfamide and Etoposide (IE) Versus IE Alone for Relapsed or Refractory Osteosarcoma: a Real-world Study in Two Centers in China

TypeinterventionalSponsorPeking University People's HospitalRan2020 to 2021Enrolled79ConditionsEffect of Drug, Toxicity, Drug, Secondary ResistanceArmsApatinib Mesylate, ifosfamide and etoposide
NCT07479732 phase1 / phase2recruitingnot on this mapstarted 2026, after this paper: background citation

Safety and Efficacy of Apatinib Combined With Irinotecan Liposome Injection in the Treatment of Recurrent or Metastatic Osteosarcoma: A Single-Arm, Open-Label, Prospective Multicenter Clinical Study

TypeinterventionalSponsorPeking University People's HospitalRan2026 to 2028Enrolled56ConditionsOsteosarcoma, Osteosarcoma MetastaticArmsLiposomal Irinotecan, Apatinib in arm1
3 · Its place in the literature

Who cites it

82 citing papers in PubMed, 3 syntheses or guidelines pooled it, 124 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Randomized Double-Blind Phase II Study of Regorafenib in Patients With Metastatic Osteosarcoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2019
    Trial
  9. Article
  10. Review
  11. Article
  12. Review
  13. Sarcomas in Adolescents and Young Adults.Current oncology reports · 2026
    Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article

22 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 1 country.

Lu XieMusculoskeletal Tumor Center, Peking University People's Hospital, Beijing, People's Republic of China.ORCID 0000-0001-7241-1915
Jie XuMusculoskeletal Tumor Center, Peking University People's Hospital, Beijing, People's Republic of China.
Xin SunMusculoskeletal Tumor Center, Peking University People's Hospital, Beijing, People's Republic of China.
Xiaodong TangMusculoskeletal Tumor Center, Peking University People's Hospital, Beijing, People's Republic of China.
Taiqiang YanMusculoskeletal Tumor Center, Peking University People's Hospital, Beijing, People's Republic of China.
Rongli YangMusculoskeletal Tumor Center, Peking University People's Hospital, Beijing, People's Republic of China.
Wei GuoMusculoskeletal Tumor Center, Peking University People's Hospital, Beijing, People's Republic of China bonetumor@163.com.
Peking University · CNPeking University People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAntiangiogenesis tyrosine kinase inhibitors (TKIs) have been shown to prolong progression-free survival (PFS) in advanced osteosarcoma. Methylsulfonic apatinib is a TKI that specifically inhibits vascular endothelial growth factor receptor-2. We aim to assess apatinib in patients with advanced high-grade osteosarcoma progressing upon chemotherapy. MATERIALS AND

methodsThis phase II trial was conducted at Peking University People's Hospital. We enrolled participants (≥16 years of age) with progressive relapsed or unresectable osteosarcoma. Participants received 750 mg or 500 mg of apatinib according to body surface area once daily until disease progression or unacceptable toxicity. The primary endpoint was objective response rate and PFS at 4 months.

resultsA total of 37 participants were finally included into the analysis. Until final follow-up, the objective response rate (complete response + partial response) was 43.24% (16/37). The 4-month PFS rate was 56.76% (95% confidence interval [CI], 39.43%-70.84%). Median PFS and overall survival were 4.50 (95% CI, 3.47-6.27) and 9.87 (95% CI 7.97-18.93) months, respectively. Toxic effects led to dose reductions or interruptions in a total of 25 of 37 (67.57%) patients. The most common grade 3-4 adverse events were pneumothorax in six (16.22%) patients, wound dehiscence in four (10.81%), proteinuria in three (8.11%), diarrhea in three (8.11%), and palmar-plantar erythrodysesthesia syndrome in three (8.11%). No other serious adverse events were reported during the trial. There were no treatment-related deaths.

conclusionApatinib is a sensitive drug for advanced osteosarcoma with a high response rate after failure of chemotherapy, with similar duration of response compared to other TKIs. IMPLICATIONS FOR PRACTICE: For advanced osteosarcoma progressing upon chemotherapy, antiangiogenesis tyrosine kinase inhibitors (TKIs) have been proved to be effective in prolonging the progression-free survival in previous multicenter trials and have been included into new National Comprehensive Cancer Network guidelines as second-line therapy. Apatinib is a TKI that specifically inhibits vascular endothelial growth factor receptor-2, which is domestically made in China. This phase II trial supports the use of apatinib in patients with advanced osteosarcoma progressing after chemotherapy.

Indexed as

AdolescentAdultAntineoplastic AgentsFemaleHumansMaleMiddle AgedOsteosarcomaPrognosisProgression-Free SurvivalProspective StudiesPyridinesYoung AdultAntineoplastic AgentsapatinibPyridinesApatinibMetastasisOsteosarcomaRefractory to chemotherapyUnresectable

Identifiers

PMID30559126
PMCPMC6656465
OpenAlexW2904481169

What OpenQuestion holds

Textmetadata
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.