Evidence map›Paper›PMID 21791469›Full record

Trial reportHaematologica2011

Genetic factors underlying the risk of bortezomib induced peripheral neuropathy in multiple myeloma patients.

Sophie L Corthals, Rowan Kuiper, David C Johnson, Pieter Sonneveld, Roman Hajek, Bronno van der Holt, Florence Magrangeas, Hartmut Goldschmidt, Gareth J Morgan, Hervé Avet-Loiseau

2 registry-linked trialsAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Haematologica, 2011. 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 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT00200681 phase3completednot on this map

Etude Multicentrique Ouverte Randomisée de Phase III Comparant l'Association de VELCADE®-Dexaméthasone à la Chimiothérapie de Type VAD Pour le Traitement Des Patients Porteurs de Myélome Multiple de Novo Jusqu'à l'âge de 65 Ans

TypeinterventionalSponsorNantes University HospitalRan2005 to 2008Enrolled493ConditionsMultiple MyelomaArmsVelcade
NCT02478476 unknown statusnot on this mapstarted 2015, after this paper: background citation

DNA Single Nucleotide Polymorphisms as Predictors of Platinum and Taxane Related Adverse Events in Ovarian, Fallopian Tube, and Peritoneal Cancer Patients

TypeobservationalSponsorOvaGene Oncology, Inc.Ran2015 to 2017Enrolled75ConditionsOvarian Neoplasms, Fallopian Tube Neoplasms, Peritoneal Neoplasms
3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  12. A Genome-Wide Association Study Identifies a Novel Locus for Bortezomib-Induced Peripheral Neuropathy in European Patients with Multiple Myeloma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    Article
  13. Low serum vitamin D occurs commonly among multiple myeloma patients treated with bortezomib and/or thalidomide and is associated with severe neuropathy.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2016
    Article
  14. Review
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  16. Article
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  18. Lupus nephritis: the evolving role of novel therapeutics.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2014
    Review
  19. Review
  20. Article
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

10 authors.

Sophie L CorthalsErasmus Medical Center, Rotterdam, The Netherlands.
Rowan Kuiper
David C Johnson
Pieter Sonneveld
Roman Hajek
Bronno van der Holt
Florence Magrangeas
Hartmut Goldschmidt
Gareth J Morgan
Hervé Avet-Loiseau

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bortezomib induced peripheral neuropathy is a dose-limiting side effect and a major concern in the treatment of multiple myeloma. To identify genetic risk factors associated with the development of this side effect in bortezomib treated multiple myeloma patients, a pharmacogenetic association study was performed using a discovery set (IFM 2005-01; n = 238) and a validation set (HOVON65/GMMG-HD4 and a Czech dataset; n = 231). After multiplicity correction, none of the 2,149 single nucleotide polymorphisms tested revealed any significant association with bortezomib induced peripheral neuropathy. However, 56 single nucleotide polymorphisms demonstrated an association with bortezomib induced peripheral neuropathy with pointwise, uncorrected significance. Pathway analysis of these polymorphisms demonstrated involvement of neurological disease (FDR <20%). Also a clear enrichment of major bortezomib metabolizing genes was found. Univariate evaluation of these 56 polymorphisms in the validation set demonstrated one single nucleotide polymorphism with pointwise significance: rs619824 in CYP17A1. (IFM 2005-01 clinicaltrials.gov identifier: NCT00200681; HOVON-65/GMMG-HD4 isrctn.org identifier: ISRCTN64455289).

Indexed as

Multiple MyelomaPeripheral Nervous System DiseasesPolymorphism, Single NucleotideAntineoplastic AgentsBoronic AcidsBortezomibFemaleHumansMalePyrazinesRisk FactorsAntineoplastic AgentsBoronic AcidsBortezomibPyrazines

Identifiers

PMID21791469
PMCPMC3208695

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.