Evidence map›Paper›PMID 38563855›Full record

ArticleJournal of neuro-oncology2024

Sex differences in adverse events in Medicare individuals ≥ 66 years of age post glioblastoma treatment.

Mantas Dmukauskas, Gino Cioffi, Kristin A Waite, Andrew E Sloan, Corey Neff, Mackenzie Price, Quinn T Ostrom, Jill S Barnholtz-Sloan

Open access · hybridAbstract read
In one paragraph

Article in Journal of neuro-oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Observational
  2. Review
  3. Article
  4. 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

8 authors at 3 institutions in 1 country.

Mantas DmukauskasTrans Divisional Research Program, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA.
Gino CioffiTrans Divisional Research Program, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA.
Kristin A WaiteTrans Divisional Research Program, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA.
Andrew E SloanNeuroscience Service Line and Piedmont Brain Tumor Center, Piedmont Health, Atlanta, GA, USA.
Corey NeffDepartment of Neurosurgery, Duke University School of Medicine, Durham, NC, USA.
Mackenzie PriceDepartment of Neurosurgery, Duke University School of Medicine, Durham, NC, USA.
Quinn T OstromDepartment of Neurosurgery, Duke University School of Medicine, Durham, NC, USA.
Jill S Barnholtz-SloanTrans Divisional Research Program, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA. jill.barnholtz-sloan@nih.gov.
Duke University · USNational Cancer Institute · USDivision of Cancer Epidemiology and Genetics

Funding

General Studies of EpidemiologyZIACP010167 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI KRAFT, PETER · 2009 to 2025
$9.2M
NCI NIH HHS HHSN261201800009CNCI NIH HHS HHSN261201800009INCI NIH HHS HHSN261201800015CNCI NIH HHS HHSN261201800015INCI NIH HHS HHSN261201800032CNCI NIH HHS HHSN261201800032I
6 · The paper itself

Abstract

purposeGlioblastoma (GB) is the most common primary malignant brain tumor with the highest incidence occurring in older adults with a median age at diagnosis of 64 years old. While treatment often improves survival it brings toxicities and adverse events (AE). Here we identify sex differences in treatment patterns and AE in individuals ≥ 66 years at diagnosis with GB.

methodsUsing the SEER-Medicare dataset sex differences in adverse events were assessed using multivariable logistic regression performed to calculate the male/female odds ratio (M/F OR) and 95% confidence intervals [95% CI] of experiencing an AE adjusted for demographic variables and Elixhauser comorbidity score.

resultsMales with GB were more likely to receive standard of care (SOC; Surgery with concurrent radio-chemotherapy) [20%] compared to females [17%], whereas females were more likely to receive no treatment [26%] compared to males [21%]. Females with GB receiving SOC were more likely to develop gastrointestinal disorders (M/F OR = 0.76; 95% CI,0.64-0.91, p = 0.002) or blood and lymphatic system disorders (M/F OR = 0.79; 95% CI,0.66-0.95, p = 0.012). Males with GB receiving SOC were more likely to develop cardiac disorders (M/F OR = 1.21; 95% CI,1.02-1.44, p = 0.029) and renal disorders (M/F OR = 1.65; 95% CI,1.37-2.01, p < 0.001).

conclusionsSex differences for individuals, 66 years and older, diagnosed with GB exist in treatment received and adverse events developed across different treatment modalities.

Indexed as

Brain NeoplasmsGlioblastomaMedicareAgedAged, 80 and overCombined Modality TherapyFemaleHumansMaleSEER ProgramSex CharacteristicsSex FactorsUnited StatesAdverse eventsGliomaSEER-MedicareSex difference

Identifiers

PMID38563855
PMCPMC11093825
OpenAlexW4393397144

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.