Evidence map›Paper›PMID 33629189›Full record

Trial reportSupportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer2021

The influence of brain metastases on the central nervous system effects of methylnaltrexone: a post hoc analysis of 3 randomized, double-blind studies.

Darren M Brenner, Neal E Slatkin, Nancy Stambler, Robert J Israel, Paul H Coluzzi

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Trial
  2. 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

5 authors at 5 institutions in 1 country.

Darren M BrennerNorthwestern University Feinberg School of Medicine, Chicago, IL, USA. Darren-brenner@northwestern.edu.ORCID http://orcid.org/0000-0002-8577-7278
Neal E SlatkinUniversity of California, Riverside, School of Medicine, Riverside, CA, USA.ORCID https://orcid.org/0000-0002-4389-7343
Nancy StamblerProgenics Pharmaceuticals, Inc., a subsidiary of Lantheus Holdings, Inc., New York, NY, USA.
Robert J IsraelBausch Health US, LLC, Bridgewater, NJ, USA.ORCID https://orcid.org/0000-0002-4150-2336
Paul H ColuzziUCI Health, Orange, CA, USA.
Bausch Health (United States) · USNorthwestern University · USProgenics Pharmaceuticals (United States) · USUC Irvine Health · USUniversity of California, Riverside · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePeripherally acting μ-opioid receptor antagonists such as methylnaltrexone (MNTX, Relistor

methodsThis post hoc analysis of pooled data from 3 randomized, placebo-controlled trials included cancer patients with OIC who received MNTX or placebo. Endpoints included changes from baseline in pain scores, rescue-free laxation (RFL) within 4 or 24 h of the first dose, and treatment-emergent adverse events (TEAEs), including those potentially related to opioid withdrawal symptoms.

resultsAmong 356 cancer patients in the pooled population, 47 (MNTX n = 27; placebo n = 20) had brain metastases and 309 (MNTX n = 172; placebo n = 137) did not have brain metastases. No significant differences in current pain, worst pain, or change in pain scores from baseline were observed between patients treated with MNTX or placebo. Among patients with brain metastases, a significantly greater proportion of patients who received MNTX versus placebo achieved an RFL within 4 h after the first dose (70.4% vs 15.0%, respectively, p = 0.0002). TEAEs were similar between treatment groups and were generally gastrointestinal in nature and not related to opioid withdrawal.

conclusionFocal disruptions of the BBB caused by brain metastases did not appear to alter central nervous system penetrance of MNTX.

Indexed as

Analgesics, OpioidBrain NeoplasmsAdultAgedAged, 80 and overCentral Nervous SystemConstipationDouble-Blind MethodFemaleHumansMaleMiddle AgedNaltrexoneQuaternary Ammonium CompoundsAnalgesics, OpioidmethylnaltrexoneNaltrexoneQuaternary Ammonium CompoundsAnalgesicsConstipationMethylnaltrexoneNarcotic antagonistsOpioidPain management

Identifiers

PMID33629189
PMCPMC8295095
OpenAlexW3131856787

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.