Evidence map›Paper›PMID 18208791›Full record

ReviewClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2008

Cardiac toxicity: old and new issues in anti-cancer drugs.

M Sereno, A Brunello, A Chiappori, J Barriuso, E Casado, C Belda, J de Castro, J Feliu, M González-Barón

Abstract readReview
PubMed Publisher
In one paragraph

Review in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.7field-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

19 citing papers in PubMed, 65 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Intense bitterness of molecules: Machine learning for expediting drug discovery.Computational and structural biotechnology journal · 2021
    Article
  6. Antitumor profiles and cardiac electrophysiological effects of aurora kinase inhibitor ZM447439.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2019
    Article
  7. Article
  8. Proinflammatory Cytokines Mediate GPCR Dysfunction.Journal of cardiovascular pharmacology · 2017
    Review
  9. Radiotherapy and anthracyclines - cardiovascular toxicity.Contemporary oncology (Poznan, Poland) · 2015
    Review
  10. Article
  11. Cardiomyocyte autophagy and cancer chemotherapy.Journal of molecular and cellular cardiology · 2014
    Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Review
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 4 institutions in 3 countries.

M SerenoOncology Department, La Paz Hospital, Madrid, Spain. mariasereno@yahoo.es
A Brunello
A Chiappori
J Barriuso
E Casado
C Belda
J de Castro
J Feliu
M González-Barón
Hospital Universitario La Paz · ESMedica (Italy) · ITMoffitt Cancer Center · USYahoo (Spain) · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although rare, cardiotoxicity is a significant complication of cancer treatment. The incidence and severity of cardiovascular side effects are dependent on the type of drugs used, dose and schedule employed, and age of patients, as well as the presence of coexisting cardiac diseases and previous mediastinal irradiation. Classically, anthracyclines are among one of the most active agents in oncology, but their use is often hampered by their cumulative dose-limiting cardiotoxicity. In the past decade, combination therapy with new drugs such as taxanes or anti- EGFR, and Her-2 therapy as a single agent have also resulted in unexpected cardiotoxicity. Cardiac damage can be secondary to an alteration of cardiac rhythm, changes in blood pressure and ischaemia, and can also alter the ability of the heart to contract and/or relax. The clinical spectrum of these toxicities can range from subclinical abnormalities to being catastrophic, life-threatening and sometimes fatal. Knowledge of this toxicity can aid clinicians to choose the optimal and least toxic regimen suitable for an individual patient. In this work we present an exhaustive review of the cardiovascular side effects associated to new anticancer drugs, from new formulations of anthracyclines to tyrosine kinase inhibitors and monoclonal antibodies.

Indexed as

Angiogenesis InhibitorsAnthracyclinesAntineoplastic AgentsAromatase InhibitorsCapecitabineDeoxycytidineErb-b2 Receptor Tyrosine KinasesErbB ReceptorsFluorouracilHeart DiseasesHumansOrganoplatinum CompoundsOxaliplatinTaxoidsAngiogenesis InhibitorsAnthracyclinesAntineoplastic AgentsAromatase InhibitorsCapecitabineDeoxycytidineErb-b2 Receptor Tyrosine KinasesErbB ReceptorsFluorouracilOrganoplatinum CompoundsOxaliplatinTaxoids

Identifiers

PMID18208791
OpenAlexW2087504337

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.