Evidence map›Paper›PMID 23684373›Full record

SynthesisCancer treatment reviews2014

Metabolic complications with the use of mTOR inhibitors for cancer therapy.

Shanthi Sivendran, Neeraj Agarwal, Benjamin Gartrell, Jian Ying, Kenneth M Boucher, Toni K Choueiri, Guru Sonpavde, William K Oh, Matthew D Galsky

Open access · greenAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Cancer treatment reviews, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

39 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Insulin and cancer: a tangled web.The Biochemical journal · 2022
    Review
  16. Review
  17. Phenformin as an Anticancer Agent: Challenges and Prospects.International journal of molecular sciences · 2019
    Review
  18. Article
  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

9 authors at 7 institutions in 1 country.

Shanthi SivendranHematology/Oncology Medical Specialists, Lancaster General Health, Lancaster, PA, United States.
Neeraj Agarwal
Benjamin Gartrell
Jian Ying
Kenneth M Boucher
Toni K Choueiri
Guru Sonpavde
William K Oh
Matthew D Galsky
Huntsman Cancer Institute · USIcahn School of Medicine at Mount Sinai · USAlbert Einstein College of Medicine · USDana-Farber Cancer Institute · USLancaster General Hospital · USUniversity of Alabama at Birmingham · USUniversity of Utah · US

Funding

Novel Approach to Facilitate Decisions in Patients w/ Muscle Invasive Bladder CAR21CA176551 · NCI · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI DIEFENBACH, MICHAEL A, GALSKY, MATTHEW · 2015 to 2016
$450k
NCI NIH HHS R21 CA176551
6 · The paper itself

Abstract

backgroundmTOR inhibitors are now approved by regulatory agencies for the treatment of a variety of malignancies. The risk of metabolic complications with these agents is not well characterized.

methodsPubMed was searched for articles published from 2001 until 2011. Eligible studies included prospective randomized trials evaluating temsirolimus, everolimus, and ridaforolimus in patients with all solid tumor malignancies. Sixteen eligible phase II clinical trials and 8 randomized controlled clinical trials were included in a systematic review and meta-analysis and the number of metabolic related AEs (hyperglycemia, hypercholesterolemia, and hypertriglyceridemia) was extracted. Incidence rates and incident rate ratios were calculated.

findingsTwenty-four trials, including 4261 patients, were included in the calculation of the incidence rate. The average incidence rate of all grade metabolic related events was 0.70 (95% CI, 0.47, 0.93). The average incidence rate of serious (grade 3 and 4) metabolic related adverse events was 0.11 (95% CI, 0.08, 0.15). The incidence rate ratio (IRR) of a metabolic adverse event with mTOR inhibitor therapy compared with control was 2.93 (95% CI, 2.33, 3.70) and of serious grade 3 and 4 metabolic adverse events was 4.58 (95% CI, 2.86, 7.34). The IRR of all grade hyperglycemia was 2.95 (95% CI, 2.14, 4.05) and of grade 3-4 hyperglycemia was 5.25 (95% CI, 3.07, 9.00). The IRR of all grade hypertriglyceridemia was 2.49 (95% CI, 1.76, 3.52) and of grade 3-4 hypertriglyceridemia was 2.01 (95% CI, 0.65, 6.27). The IRR of all grade hypercholesterolemia was 3.35 (95% CI, 2.17, 5.18) and of grade 3-4 hypercholesterolemia was 6.51 (95% CI, 1.48, 28.59). These findings suggest a statistically significant increase in the risk of hyperglycemia, hypercholesterolemia (all grades and grade 3 and 4), and all grade hypertriglyceridemia associated with mTOR therapy when compared with control.

interpretationThe risk of all grade and grade 3-4, hyperglycemia, hypercholesterolemia, and hypertriglyceridemia, are increase in patients treated with mTOR inhibitors compared with control.

Indexed as

Antibiotics, AntineoplasticDyslipidemiasEverolimusHumansHyperglycemiaIncidenceNeoplasmsRandomized Controlled Trials as TopicSirolimusTOR Serine-Threonine KinasesAntibiotics, AntineoplasticEverolimusMTOR protein, humanridaforolimusSirolimustemsirolimusTOR Serine-Threonine KinasesAdverse eventsCancerEverolimusMetabolicmTOR inhibitorRidaforolimusTemsirolimus

Identifiers

PMID23684373
PMCPMC4744486
OpenAlexW2051725201

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.