Evidence map›Paper›PMID 16283381›Full record

Trial reportJournal of cancer research and clinical oncology2006

Effects of doxorubicin-containing chemotherapy and a combination with L-carnitine on oxidative metabolism in patients with non-Hodgkin lymphoma.

Raimund Waldner, Claudia Laschan, Alfred Lohninger, Martin Gessner, Heinz Tüchler, Marlies Huemer, Wolfgang Spiegel, Heidrun Karlic

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of cancer research and clinical oncology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 41 citations in OpenAlex.

  1. Cardioprotective interventions for cancer patients receiving anthracyclines.The Cochrane database of systematic reviews · 2011
    Pooled it
  2. Pooled it
  3. Article
  4. The Role of the Natural Antioxidant Mechanism in Sperm Cells.Reproductive sciences (Thousand Oaks, Calif.) · 2022
    Review
  5. Review
  6. Review
  7. Review
  8. African Vegetables (Oxidative medicine and cellular longevity · 2020
    Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. The role of antioxidants in the era of cardio‑oncology.Cancer chemotherapy and pharmacology · 2013
    Review
  16. Chemotherapy-induced cardiotoxicity.Current heart failure reports · 2012
    Review
  17. Role of carnitine in cancer chemotherapy-induced multiple organ toxicity.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2010
    Article
  18. 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 2 institutions in 1 country.

Raimund Waldner3rd Department of Medicine, Hanusch Hospital, Vienna, Austria.
Claudia Laschan
Alfred Lohninger
Martin Gessner
Heinz Tüchler
Marlies Huemer
Wolfgang Spiegel
Heidrun Karlic
Hanusch Hospital · ATMedical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeChemotherapy regimens based on anthracycline (doxorubicin) are well established in lymphoma therapy. The purpose of this study was to examine the effects of L-carnitine with a view to reducing cytotoxic side-effects.

methods20 patients were scheduled to receive 3 g L-carnitine before each chemotherapy cycle, followed by 1 g L-carnitine/day during the following 21 days, while 20 patients received a placebo (randomized controlled trial). The plasma lipid profile and relative mRNA levels of key enzymes of oxidative metabolism (carnitine acyltransferases) were measured at three points of time. In addition to the clinical parameters we used the mRNA of white blood cells to evaluate the toxic effects on cardiomyocytes.

resultsIn the present study no cardiotoxicity of anthracycline therapy was detected. Carnitine treated patients showed a rise in plasma carnitine which led to an increase of relative mRNA levels from CPT1A (liver isoform of carnitine palmitoyltransferase) and OCTN2 (carnitine transporter). Following chemotherapy, an activation of carnitine acyltransferases was associated with a stimulation of OCTN2 in both groups.

conclusionBiochemical and molecular analyses indicated a stimulation of oxidative metabolism in white blood cells through carnitine uptake.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarnitineCarnitine AcyltransferasesCarnitine O-PalmitoyltransferaseDoxorubicinHumansLeukocytesLipid PeroxidationLymphoma, Non-HodgkinOrganic Cation Transport ProteinsOxidation-ReductionRNA, MessengerSolute Carrier Family 22 Member 5Time FactorsVitamin B ComplexCarnitineCarnitine AcyltransferasesCarnitine O-PalmitoyltransferaseDoxorubicinOrganic Cation Transport ProteinsRNA, MessengerSLC22A5 protein, humanSolute Carrier Family 22 Member 5Vitamin B Complex

Identifiers

PMID16283381
PMCPMC12161048
OpenAlexW2036493045

What OpenQuestion holds

Textmetadata
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.