Evidence map›Paper›PMID 38347093›Full record

Trial reportBritish journal of cancer2024

Germline predictors for bevacizumab induced hypertensive crisis in ECOG-ACRIN 5103 and BEATRICE.

Fei Shen, Guanglong Jiang, Santosh Philips, Erica Cantor, Laura Gardner, Gloria Xue, Geneva Cunningham, Nawal Kassem, Anne O'Neill, David Cameron and 4 more

Open access · greenAbstract readClinical Trial, Phase III
In one paragraph

Trial report in British journal of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 97% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

14 authors at 5 institutions in 3 countries.

Fei Shen *Indiana University School of Medicine, Indianapolis, IN, USA.ORCID 0000-0003-1545-0955
Guanglong Jiang *Indiana University School of Medicine, Indianapolis, IN, USA.ORCID 0000-0002-9233-052X
Santosh PhilipsIndiana University School of Medicine, Indianapolis, IN, USA.
Erica CantorIndiana University School of Medicine, Indianapolis, IN, USA.
Laura GardnerIndiana University School of Medicine, Indianapolis, IN, USA.
Gloria XueIndiana University School of Medicine, Indianapolis, IN, USA.
Geneva CunninghamIndiana University School of Medicine, Indianapolis, IN, USA.
Nawal KassemIndiana University School of Medicine, Indianapolis, IN, USA.
Anne O'NeillDana Farber Cancer Institute - ECOG-ACRIN Biostatistics Center, Boston, MA, USA.
David CameronEdinburgh Cancer Research Centre, Edinburgh, United Kingdom.
Thomas M SuterSwiss Cardiovascular Center, Bern University Hospital, Inselspital, Bern, Switzerland.
Kathy D MillerIndiana University School of Medicine, Indianapolis, IN, USA.ORCID 0000-0002-7125-883X
George W SledgeCaris Life Science, Dalla, TX, USA.
Bryan P SchneiderIndiana University School of Medicine, Indianapolis, IN, USA. bpschnei@iu.edu.ORCID 0000-0003-1868-7739
Indiana University School of MedicineCaris Life Sciences (United States) · USDana-Farber Cancer Institute · USEdinburgh Cancer Research · GBUniversity Hospital of Bern · CH

Funding

Project-006U10CA180820 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI Peter J ODwyer · 2014 to 2026
$167.6M
Statistics CoreU10CA180794 · NCI · DANA-FARBER CANCER INST · PI PAUL J CATALANO · 2014 to 2026
$111.2M
Tumor Microenvironment and Metastasis ProgramP30CA082709 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI David W Clapp · 1999 to 2026
$59.3M
ECOG-ACRIN Biospecimen Bank to Support NCTNU24CA196172 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI STANLEY R. HAMILTON, Scott D Jewell · 2015 to 2026
$41.1M
NCI NIH HHS P30 CA082709NCI NIH HHS U10 CA180794NCI NIH HHS U10 CA180820NCI NIH HHS U24 CA196172Susan G. Komen for the Cure, Komen Wyoming Affiliate (Wyoming Affiliate of Susan G. Komen for the Cure) SAC110056Vera Bradley Foundation for Breast Cancer (Vera Bradley Foundation for Breast Cancer, Inc.) BPS
6 · The paper itself

Abstract

backgroundBevacizumab is a beneficial therapy in several advanced cancer types. Predictive biomarkers to better understand which patients are destined to benefit or experience toxicity are needed. Associations between bevacizumab induced hypertension and survival have been reported but with conflicting conclusions.

methodsWe performed post-hoc analyses to evaluate the association in 3124 patients from two phase III adjuvant breast cancer trials, E5103 and BEATRICE. Differences in invasive disease-free survival (IDFS) and overall survival (OS) between patients with hypertension and those without were compared. Hypertension was defined as systolic blood pressure (SBP) ≥ 160 mmHg (n = 346) and SBP ≥ 180 mmHg (hypertensive crisis) (n = 69). Genomic analyses were performed to evaluate germline genetic predictors for the hypertensive crisis.

resultsHypertensive crisis was significantly associated with superior IDFS (p = 0.015) and OS (p = 0.042), but only IDFS (p = 0.029; HR = 0.28) remained significant after correction for prognostic factors. SBP ≥ 160 mmHg was not associated with either IDFS or OS. A common single-nucleotide polymorphism, rs6486785, was significantly associated with hypertensive crisis (p = 8.4 × 10

conclusionBevacizumab-induced hypertensive crisis is associated with superior outcomes and rs6486785 predicted an increased risk of this key toxicity.

Indexed as

Breast NeoplasmsHypertensionHypertensive CrisisBevacizumabFemaleGerm CellsHumansBevacizumab

Identifiers

PMID38347093
PMCPMC11014938
OpenAlexW4391751780

What OpenQuestion holds

Textmetadata
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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.