Evidence map›Paper›PMID 32208957›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2020

Phase I Study of the Mutant IDH1 Inhibitor Ivosidenib: Safety and Clinical Activity in Patients With Advanced Chondrosarcoma.

William D Tap, Victor M Villalobos, Gregory M Cote, Howard Burris, Filip Janku, Olivier Mir, Murali Beeram, Andrew J Wagner, Liewen Jiang, Bin Wu and 7 more

Open access · bronzeAbstract readClinical Trial, Phase IMulticenter Study
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed, 2 pooled it
10.5field-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.

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

102 citing papers in PubMed, 2 syntheses or guidelines pooled it, 153 citations in OpenAlex.

  1. Pooled it
  2. [Update and interpretation of 2021 National Comprehensive Cancer Network (NCCN) "Clinical Practice Guidelines for Bone Tumors"].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2021
    Guideline
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  11. Clinical advancement in the management of mutant isocitrate dehydrogenase (EJC supplements : EJC : official journal of EORTC, European Organization for Research and Treatment of Cancer ... [et al.] · 2026
    Article
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42 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

17 authors at 10 institutions in 2 countries.

William D TapMemorial Sloan Kettering Cancer Center, New York, NY.
Victor M VillalobosUniversity of Colorado Anschutz Medical Campus, Aurora, CO.
Gregory M CoteCenter for Sarcoma and Connective Tissue Oncology, Massachusetts General Hospital Cancer Center, Boston, MA.
Howard BurrisSarah Cannon Research Institute, Nashville, TN.
Filip JankuPhase I Clinical Trials Program, Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX.
Olivier MirDepartment of Ambulatory Care, Gustave Roussy Cancer Campus, Villejuif, France.
Murali BeeramSTART Center for Cancer Care, San Antonio, TX.
Andrew J WagnerCenter for Sarcoma and Bone Oncology, Dana-Farber Cancer Institute, Boston, MA.
Liewen JiangAgios Pharmaceuticals, Cambridge, MA.
Bin WuAgios Pharmaceuticals, Cambridge, MA.
Sung ChoeAgios Pharmaceuticals, Cambridge, MA.
Katharine YenAgios Pharmaceuticals, Cambridge, MA.
Camelia GliserAgios Pharmaceuticals, Cambridge, MA.
Bin FanAgios Pharmaceuticals, Cambridge, MA.
Sam AgrestaAgios Pharmaceuticals, Cambridge, MA.
Shuchi S PandyaAgios Pharmaceuticals, Cambridge, MA.
Jonathan C TrentSylvester Comprehensive Cancer Center, University of Miami, Miami, FL.
Agios Pharmaceuticals (United States) · USCenter for Health Care Services · USDana-Farber Cancer Institute · USInstitut Gustave Roussy · FRMassachusetts General Hospital · USMemorial Sloan Kettering Cancer Center · USSarah Cannon · USSylvester Comprehensive Cancer Center · USThe University of Texas MD Anderson Cancer Center · USUniversity of Colorado Anschutz Medical Campus · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Tumor Biology Research ProgramP30CA240139 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Daniel Bilbao · 2019 to 2026
$24.1M
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA240139
6 · The paper itself

Abstract

purposeSurgery is the primary therapy for localized chondrosarcoma; for locally advanced and/or metastatic disease, no known effective systemic therapy exists. Mutations in the isocitrate dehydrogenase 1/2 (IDH1/2) enzymes occur in up to 65% of chondrosarcomas, resulting in accumulation of the oncometabolite D-2-hydroxyglutarate (2-HG). Ivosidenib (AG-120) is a selective inhibitor of mutant IDH1 approved in the United States for specific cases of acute myeloid leukemia. We report outcomes of patients with advanced chondrosarcoma in an ongoing study exploring ivosidenib treatment. PATIENTS AND

methodsThis phase I multicenter open-label dose-escalation and expansion study of ivosidenib monotherapy enrolled patients with mutant

resultsTwenty-one patients (escalation, n = 12; expansion, n = 9) with advanced chondrosarcoma received ivosidenib (women, n = 8; median age, 55 years; range, 30-88 years; 11 had received prior systemic therapy). Treatment-emergent adverse events (AEs) were mostly grade 1 or 2. Twelve patients experienced grade ≥ 3 AEs; only one event was judged treatment related (hypophosphatemia, n = 1). Plasma 2-HG levels decreased substantially in all patients (range, 14%-94.2%), to levels seen in healthy individuals. Median progression-free survival (PFS) was 5.6 months (95% CI, 1.9 to 7.4 months); the PFS rate at 6 months was 39.5%. Eleven (52%) of 21 patients experienced stable disease.

conclusionIn patients with chondrosarcoma, ivosidenib showed minimal toxicity, substantial 2-HG reduction, and durable disease control. Future studies of ivosidenib monotherapy or rational combination approaches should be considered in patients with advanced mutant

Indexed as

AdultAgedAged, 80 and overChondrosarcomaEnzyme InhibitorsFemaleGlycineHumansMaleMiddle AgedPyridinesEnzyme InhibitorsGlycineivosidenibPyridines

Identifiers

PMID32208957
PMCPMC7238491
OpenAlexW3013135065

What OpenQuestion holds

Textmetadata
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.