Evidence map›Paper›PMID 26463708›Full record

Trial reportClinical cancer research : an official journal of the American Association for Cancer Research2016

Association of Variants in Candidate Genes with Lipid Profiles in Women with Early Breast Cancer on Adjuvant Aromatase Inhibitor Therapy.

Cesar A Santa-Maria, Amanda Blackford, Anne T Nguyen, Todd C Skaar, Santosh Philips, Steffi Oesterreich, James M Rae, Zeruesenay Desta, Jason Robarge, Norah Lynn Henry and 8 more

Open access · bronzeAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Clinical cancer research : an official journal of the American Association for Cancer Research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
2.0field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Targeting tumor metabolism to augment CD8Journal of pharmaceutical analysis · 2025
    Review
  6. Review
  7. Association between the aromatase (Archives of endocrinology and metabolism · 2024
    Article
  8. Review
  9. [Reconsideration of the third-generation non-steroidal aromatase inhibitors in pediatrics].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. 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

18 authors at 5 institutions in 1 country.

Cesar A Santa-MariaJohns Hopkins University School of Medicine, Baltimore, Maryland.
Amanda BlackfordJohns Hopkins University School of Medicine, Baltimore, Maryland.
Anne T NguyenIndiana University School of Medicine, Indianapolis, Indiana.
Todd C SkaarIndiana University School of Medicine, Indianapolis, Indiana.
Santosh PhilipsIndiana University School of Medicine, Indianapolis, Indiana.
Steffi OesterreichUniversity of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania.
James M RaeUniversity of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan.
Zeruesenay DestaIndiana University School of Medicine, Indianapolis, Indiana.
Jason RobargeIndiana University School of Medicine, Indianapolis, Indiana.
Norah Lynn HenryUniversity of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan.
Anna M StornioloIndiana University School of Medicine, Indianapolis, Indiana.
Daniel F HayesUniversity of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan.
Roger S BlumenthalJohns Hopkins University School of Medicine, Baltimore, Maryland.
Pamela OuyangJohns Hopkins University School of Medicine, Baltimore, Maryland.
Wendy S PostJohns Hopkins University School of Medicine, Baltimore, Maryland.
David A FlockhartIndiana University School of Medicine, Indianapolis, Indiana.
Vered StearnsJohns Hopkins University School of Medicine, Baltimore, Maryland. vstearn1@jhmi.edu.
Consortium on Breast Cancer Pharmacogenomics (COBRA)
Indiana University School of MedicineJohns Hopkins University · USIndiana University – Purdue University Indianapolis · USUniversity of Baltimore · USUPMC Hillman Cancer Center · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
Michigan Institute for Clinical and Health Research (MCHR)UL1TR000433 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MASHOUR, GEORGE ALEXANDER · 2012 to 2016
$49.9M
TAMAXIFEN PHARMACOGENETICSU01GM061373 · NIGMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI FLOCKHART, DAVID ALASTAIR · 2000 to 2009
$17.0M
Indiana University Comprehensive Training in Clinical PharmacologyT32GM008425 · NIGMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI Zeruesenay Desta, Michael Thomas Eadon · 1992 to 2026
$7.7M
Genetic Predictors of Anti-Estrogen Clinical Activity in Breast Cancer PatientsR01GM099143 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RAE, JAMES MICHAEL · 2011 to 2015
$1.6M
NCATS NIH HHS UL1 TR000433NCI NIH HHS P30 CA006973NCI NIH HHS P30 CA06973NIGMS NIH HHS 1R01GM099143NIGMS NIH HHS R01 GM099143NIGMS NIH HHS T32 GM008425NIGMS NIH HHS U01 GM061373
6 · The paper itself

Abstract

purposeAromatase inhibitors can exert unfavorable effects on lipid profiles; however, previous studies have reported inconsistent results. We describe the association of single-nucleotide polymorphisms (SNP) in candidate genes with lipid profiles in women treated with adjuvant aromatase inhibitors. EXPERIMENTAL

designWe conducted a prospective observational study to test the associations between SNPs in candidate genes in estrogen signaling and aromatase inhibitor metabolism pathways with fasting lipid profiles during the first 3 months of aromatase inhibitor therapy in postmenopausal women with early breast cancer randomized to adjuvant letrozole or exemestane. We performed genetic association analysis and multivariable linear regressions using dominant, recessive, and additive models.

resultsA total of 303 women had complete genetic and lipid data and were evaluable for analysis. In letrozole-treated patients, SNPs in CYP19A1, including rs4646, rs10046, rs700518, rs749292, rs2289106, rs3759811, and rs4775936 were significantly associated with decreases in triglycerides by 20.2 mg/dL and 39.3 mg/dL (P < 0.00053), respectively, and with variable changes in high-density lipoprotein (HDL-C) from decreases by 4.2 mg/dL to increases by 9.8 mg/dL (P < 0.00053).

conclusionsVariants in CYP19A1 are associated with decreases in triglycerides and variable changes in HDL-C in postmenopausal women on adjuvant aromatase inhibitors. Future studies are needed to validate these findings, and to identify breast cancer survivors who are at higher risk for cardiovascular disease with aromatase inhibitor therapy.

Indexed as

Genetic VariationAdultAgedAged, 80 and overAntineoplastic Agents, HormonalAromatase InhibitorsBreast NeoplasmsChemotherapy, AdjuvantFemaleGenetic Association StudiesHumansLipid MetabolismLipidsMiddle AgedNeoplasm StagingPharmacogeneticsAntineoplastic Agents, HormonalAromatase InhibitorsLipids

Identifiers

PMID26463708
PMCPMC4794377
OpenAlexW2219237924

What OpenQuestion holds

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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.