Evidence map›Paper›PMID 29334610›Full record

Trial reportCancer research and treatment2018

Phase II Study of Dovitinib in Patients with Castration-Resistant Prostate Cancer (KCSG-GU11-05).

Yoon Ji Choi, Hye Sook Kim, Se Hoon Park, Bong-Seog Kim, Kyoung Ha Kim, Hyo Jin Lee, Hong Suk Song, Dong-Yeop Shin, Ha Young Lee, Hoon-Gu Kim and 3 more

Open access · diamondAbstract readClinical Trial, Phase IIComparative StudyMulticenter Study
In one paragraph

Trial report in Cancer research and treatment, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
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  6. Targeted RNA Degradation as a Promising Therapeutic Strategy.International journal of molecular sciences · 2025
    Review
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  9. Dysregulated microRNAs in prostate cancer:Iranian journal of basic medical sciences · 2024
    Article
  10. Impact of cell plasticity on prostate tumor heterogeneity and therapeutic response.American journal of clinical and experimental urology · 2024
    Review
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  12. 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

13 authors at 10 institutions in 1 country.

Yoon Ji ChoiDivision of Oncology/Hematology, Department of Internal Medicine, Korea University Anam Hospital, Seoul, Korea.
Hye Sook KimDivision of Oncology/Hematology, Department of Internal Medicine, Korea University Anam Hospital, Seoul, Korea.
Se Hoon ParkDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Bong-Seog KimDivision of Hemato-Oncology, Department of Internal Medicine, Veterans Health Service Medical Center, Seoul, Korea.
Kyoung Ha KimDivision of Hematology-Oncology, Department of Internal Medicine, Soonchunhyang University Hospital, Soonchunhyang University College of Medicine, Seoul, Korea.
Hyo Jin LeeDepartment of Internal Medicine, Chungnam National University School of Medicine, Daejeon, Korea.
Hong Suk SongDivision of Hematology/Oncology, Department of Internal Medicine, Keimyung University Dongsan Medical Center, Daegu, Korea.
Dong-Yeop ShinDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Ha Young LeeDongnam Institute of Radiological and Medical Sciences, Busan, Korea.
Hoon-Gu KimDepartment of Internal Medicine, Gyeongsang Institute of Health Sciences, Gyeongsang National University Changwon Hospital, Gyeongsang National University College of Medicine, Changwon, Korea.
Kyung Hee LeeDepartment of Hemato-oncology, Yeungnam Medical Center, Daegu, Korea.
Jae Lyun LeeDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Kyong Hwa ParkDivision of Oncology/Hematology, Department of Internal Medicine, Korea University Anam Hospital, Seoul, Korea.
Gyeongsang National University · KRKorea University · KRSungkyunkwan University · KRChungnam National University · KRDongnam Institute of Radiological & Medical Sciences · KRKeimyung University · KRSeoul National University Hospital · KRSoonchunhyang University Hospital Seoul · KRVeterans Health Service Medical Center · KRYeungnam University Medical Center · KR

Funding

Ministry of Health and Welfare 1720150
6 · The paper itself

Abstract

purposeFibroblast growth factor (FGF) signals are important in carcinogenesis and progression of prostate cancer. Dovitinib is an oral, pan-class inhibitor of vascular endothelial growth factor receptor (VEGFR), platelet-derived growth factor receptor, and fibroblast growth factor receptor (FGFR). We evaluated the efficacy and toxicity of dovitinib in men with metastatic castration resistant prostate cancer (mCRPC). MATERIALS AND

methodsThis study was a single-arm, phase II, open-label, multicenter trial of dovitinib 500 mg/day (5-days-on/2-days-off schedule). The primary endpointwas 16-week progression-free survival (PFS). Secondary endpoints were overall survival (OS), toxicity and prostate-specific antigen (PSA) response rate. Biomarker analyses for VEGFR2, FGF23, and FGFR2 using multiplex enzyme-linked immunosorbent assay was performed.

resultsForty-four men were accrued from 11 hospitals. Eighty percent were post-docetaxel. Median PSA was 100 ng/dL, median age was 69, 82% had bone metastases, and 23% had liver metastases. Median cycles of dovitinibwas 2 (range, 0 to 33). Median PFSwas 3.67 months (95% confidence interval [CI], 1.36 to 5.98) and median OS was 13.70 months (95% CI, 0 to 27.41). Chemotherapy-naïve patients had longer PFS (17.90 months; 95% CI, 9.23 to 28.57) compared with docetaxel-treated patients (2.07 months; 95% CI, 1.73 to 2.41; p=0.001) and the patients with high serum VEGFR2 level over median level (7,800 pg/mL) showed longer PFS compared with others (6.03 months [95% CI, 4.26 to 7.80] vs. 1.97 months [95% CI, 1.79 to 2.15], p=0.023). Grade 3 related adverse events were seen in 40.9% of patients. Grade 1-2 nausea, diarrhea, fatigue, anorexia, and all grade thrombocytopenia are common.

conclusionDovitinib showed modest antitumor activity with manageable toxicities in men with mCRPC. Especially, patients who were chemo-naïve benefitted from dovitinib.

Indexed as

AgedAged, 80 and overBenzimidazolesBiomarkers, TumorDocetaxelDrug Administration ScheduleFibroblast Growth Factor-23Fibroblast Growth FactorsHumansMaleMiddle AgedNeoplasm MetastasisProstatic Neoplasms, Castration-ResistantProtein Kinase InhibitorsQuinolonesReceptor, Fibroblast Growth Factor, Type 24-amino-5-fluoro-3-(5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl)quinolin-2(1H)-oneBenzimidazolesBiomarkers, TumorDocetaxelFGF23 protein, humanFGFR2 protein, humanFibroblast Growth Factor-23Fibroblast Growth FactorsKDR protein, humanProtein Kinase InhibitorsQuinolonesReceptor, Fibroblast Growth Factor, Type 2Vascular Endothelial Growth Factor Receptor-2BiomarkersCastration-Resistant Prostatic NeoplasmDovitinib

Identifiers

PMID29334610
PMCPMC6192917
OpenAlexW2782399048

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.