Evidence map›Paper›PMID 29184451›Full record

ArticleClinical pharmacology : advances and applications2017

Population pharmacokinetics of pomalidomide in patients with relapsed or refractory multiple myeloma with various degrees of impaired renal function.

Yan Li, Xiaomin Wang, Edward O'Mara, Meletios A Dimopoulos, Pieter Sonneveld, Katja C Weisel, Jeffrey Matous, David S Siegel, Jatin J Shah, Elisabeth Kueenburg and 5 more

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

Article in Clinical pharmacology : advances and applications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 19% 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.

NCT01575925 phase1completednot on this map

A Phase 1 Multi-Center, Open-Label, Dose-Escalation Study to Determine the Pharmacokinetics and Safety of Pomalidomide When Given in Combination With Low Dose Dexamethasone in Subjects With Relapsed or Refractory Multiple Myeloma and Impaired Renal Function

TypeinterventionalSponsorCelgeneRan2012 to 2018Enrolled25ConditionsMultiple Myeloma, Renal ImpairmentArms4 mg Oral POM + 40 mg Oral DEX, 2 mg Oral POM + 40 mg Oral DEX
NCT02045017 phase2completednot on this map

A Phase 2 Multicenter, Open-label Study to Determine the Efficacy and Safety of Pomalidomide (CC-4047) in Combination With Low-Dose Dexamethasone in Subjects With Relapsed or Refractory Multiple Myeloma and Moderate or Severe Renal Impairment Including Subjects Undergoing Hemodialysis

TypeinterventionalSponsorCelgeneRan2014 to 2021Enrolled81ConditionsMultiple MyelomaArmsPomalidomide and Dexamethasone
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 16 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

15 authors at 4 institutions in 3 countries.

Yan LiTranslational Development and Clinical Pharmacology, Celgene Corporation, Summit, NJ, USA.
Xiaomin WangNon-Clinical Development and Drug Metabolism and Pharmacokinetics, Celgene Corporation, Summit, NJ, USA.
Edward O'MaraTranslational Development and Clinical Pharmacology, Celgene Corporation, Summit, NJ, USA.
Meletios A DimopoulosDepartment of Clinical Therapeutics, National and Kapodistrian University of Athens, Athens, Greece.
Pieter SonneveldDepartment of Hematology, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
Katja C WeiselDepartment of Hematology, University Hospital Tübingen, Tübingen, Germany.
Jeffrey MatousDepartment of Hematology/Oncology, Colorado Blood Cancer Institute, Denver, CO, USA.
David S SiegelMyeloma Division, John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, NJ, USA.
Jatin J ShahDepartment of Lymphoma/Myeloma, Division of Cancer Medicine, MD Anderson Cancer Center, Houston, TX, USA.
Elisabeth KueenburgGlobal Clinical R&D, Celgene Corporation, Summit, NJ, USA.
Lars SternasGlobal Clinical R&D, Celgene Corporation, Summit, NJ, USA.
Chloe CavanaughGlobal Clinical R&D, Celgene Corporation, Summit, NJ, USA.
Mohamed ZakiGlobal Clinical R&D, Celgene Corporation, Summit, NJ, USA.
Maria PalmisanoTranslational Development and Clinical Pharmacology, Celgene Corporation, Summit, NJ, USA.
Simon ZhouTranslational Development and Clinical Pharmacology, Celgene Corporation, Summit, NJ, USA.
Erasmus MC Cancer Institute · NLHackensack University Medical Center · USNational and Kapodistrian University of Athens · GRThe University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pomalidomide is an immunomodulatory drug for treatment of relapsed or refractory multiple myeloma (rrMM) in patients who often have comorbid renal conditions. To assess the impact of renal impairment on pomalidomide exposure, a population pharmacokinetics (PPK) model of pomalidomide in rrMM patients with various degrees of impaired renal function was developed. Intensive and sparse pomalidomide concentration data collected from two clinical studies in rrMM patients with normal renal function, moderately impaired renal function, severely impaired renal function not requiring dialysis, and with severely impaired renal function requiring dialysis were pooled over the dose range of 2 to 4 mg, to assess specifically the influence of the impaired renal function as a categorical variable and a continuous variable on pomalidomide clearance and plasma exposure. In addition, pomalidomide concentration data collected on dialysis days from both the withdrawal (arterial) side and from the returning (venous) side of the dialyzer, from rrMM patients with severely impaired renal function requiring dialysis, were used to assess the extent to which dialysis contributes to the removal of pomalidomide from blood circulation. PPK analyses demonstrated that moderate to severe renal impairment not requiring dialysis has no influence on pomalidomide clearance or plasma exposure, as compared to those patients with normal renal function, while pomalidomide exposure increased approximately 35% in patients with severe renal impairment requiring dialysis on nondialysis days. In addition, dialysis increased total body pomalidomide clearance from 5 L/h to 12 L/h, indicating that dialysis will significantly remove pomalidomide from the blood circulation. Thus, pomalidomide should be administered post-dialysis on the days of dialysis.

Indexed as

hemodialysispomalidomidepopulation pharmacokineticsrenal impairment

Identifiers

PMID29184451
PMCPMC5685150
OpenAlexW2767255960

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.