Evidence map›Paper›PMID 20862746›Full record

Trial reportCancer2011

Phase 2 trial of the histone deacetylase inhibitor romidepsin for the treatment of refractory multiple myeloma.

Ruben Niesvizky, Scott Ely, Tomer Mark, Sangeeta Aggarwal, Janice L Gabrilove, John J Wright, Selina Chen-Kiang, Joseph A Sparano

Abstract readClinical Trial, Phase II
In one paragraph

Trial report in Cancer, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
8.2field-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.

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

56 citing papers in PubMed, 132 citations in OpenAlex.

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  10. Dual HDAC/BRD4 Inhibitors Relieves Neuropathic Pain by Attenuating Inflammatory Response in Microglia After Spared Nerve Injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
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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

8 authors at 6 institutions in 1 country.

Ruben NiesvizkyDepartment of Medicine, Division of Hematology Oncology, Center of Excellence of Lymphoma and Myeloma, Weill Cornell Medical College/New York Presbyterian Hospital, New York, New York, USA. run9001@med.cornell.edu
Scott Ely
Tomer Mark
Sangeeta Aggarwal
Janice L Gabrilove
John J Wright
Selina Chen-Kiang
Joseph A Sparano
Albert Einstein College of Medicine · USCornell University · USNational Institutes of Health · USNew York Hospital Queens · USNewYork–Presbyterian Hospital · USTisch Cancer Institute

Funding

EXPLOITING NOVEL THERAPEUTIC TARGETS IN MULTIPLE MYELOMA (K23M)K23CA109260 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI NIESVIZKY, RUBEN · 2004 to 2008
$680k
Therapeutic Strategies in Disorders of HematopoiesisK24CA100287 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI GABRILOVE, JANICE L · 2003 to 2007
$679k
NCI NIH HHS K23 CA109260NCI NIH HHS K24 CA100287NCI NIH HHS K24 CA100287-02NCI NIH HHS N01 CM062204NCI NIH HHS N01-CM-62204
6 · The paper itself

Abstract

backgroundEpigenetic dysregulation is a hallmark of cancer, including multiple myeloma. Inhibitors of histone deacetylases (HDACs) induce DNA hyperacetylation by inhibiting removal of acetyl groups from amino tails on histone proteins, thereby uncoiling condensed chromatin favoring transcription of silenced genes, including tumor suppressor genes. Romidepsin is an HDAC inhibitor that exhibits antiproliferative and apoptotic effects against multiple myeloma cell lines.

methodsA phase 2 trial was performed of romidepsin in patients with multiple myeloma who were refractory to standard therapy. Treatment was comprised of romidepsin (13 mg/m²) given as a 4-hour intravenous infusion on Days 1, 8, and 15 every 28 days). Thirteen patients received a median of 2 cycles of therapy (range, 1-7 cycles).

resultsAlthough no patients had an objective response, 4 of 12 patients with secretory myeloma exhibited evidence of M-protein stabilization, and several other patients experienced improvement in bone pain and resolution of hypercalcemia.

conclusionsThe results of the current study demonstrate that romidepsin, as a single agent, is unlikely to be associated with a response rate of ≥30% in patients with refractory myeloma, although there was some clinical evidence suggesting a biological effect associated with therapy.

Indexed as

AgedBone and BonesDepsipeptidesDrug Administration ScheduleFemaleHistone Deacetylase InhibitorsHumansMaleMiddle AgedMultiple MyelomaMyeloma ProteinsPainRetreatmentDepsipeptidesHistone Deacetylase Inhibitorsmultiple myeloma M-proteinsMyeloma Proteinsromidepsin

Identifiers

PMID20862746
PMCPMC3010462
OpenAlexW2010833137

What OpenQuestion holds

Textmetadata
LicenceTDM
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.