Evidence map›Paper›PMID 28275118›Full record

Observational studyThe oncologist2017

Modern Management of Anthracycline-Induced Cardiotoxicity in Lymphoma Patients: Low Occurrence of Cardiotoxicity with Comprehensive Assessment and Tailored Substitution by Nonpegylated Liposomal Doxorubicin.

Jacopo Olivieri, Gian Piero Perna, Caterina Bocci, Claudia Montevecchi, Attilio Olivieri, Pietro Leoni, Guido Gini

Open access · bronzeAbstract readObservational Study
In one paragraph

Observational study in The oncologist, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Cardiac complications of cancer therapies.Advances in cancer research · 2022
    Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. The Role of Biomarkers in Cardio-Oncology.Journal of cardiovascular translational research · 2020
    Review
  16. Cardiotoxicity of Anthracyclines.Frontiers in cardiovascular medicine · 2020
    Review
  17. Article
  18. The breast cancer patient in the cardioncology unit.Journal of thoracic disease · 2018
    Review
  19. Article
  20. 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

7 authors at 2 institutions in 1 country.

Jacopo OlivieriClinica di Ematologia, Università Politecnica delle Marche, Ancona, Italy jacopo.olivieri@hotmail.it.
Gian Piero PernaCardiologia Subintensiva, Presidio "G.M. Lancisi", Azienda Ospedaliero-Universitaria "Ospedali Riuniti" di Ancona, Italy.
Caterina BocciClinica di Ematologia, Università Politecnica delle Marche, Ancona, Italy.
Claudia MontevecchiClinica di Ematologia, Università Politecnica delle Marche, Ancona, Italy.
Attilio OlivieriClinica di Ematologia, Università Politecnica delle Marche, Ancona, Italy.
Pietro LeoniClinica di Ematologia, Università Politecnica delle Marche, Ancona, Italy.
Guido GiniClinica di Ematologia, Università Politecnica delle Marche, Ancona, Italy.
Marche Polytechnic University · ITOspedali Riuniti di Ancona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAnthracyclines (AC) are still undeniable drugs in lymphoma treatment, despite occasionally causing cardiotoxicity. Liposomal AC may reduce cardiotoxicity while retaining clinical efficacy; also, biomarker monitoring during chemotherapy allows early detection of cardiac damage, enabling strategies to prevent left ventricular ejection fraction (LVEF) deterioration. MATERIALS AND

methodsWe conducted a prospective observational trial in a real-life population of lymphoma patients, combining advanced echocardiography and biomarkers (Troponin I [TnI]) for early detection of cardiotoxicity; we applied a prespecified policy to minimize cardiotoxicity, selecting patients with higher baseline risk to replace doxorubicin with nonpegylated liposomal doxorubicin (NPLD) and starting cardioprotective treatment when subclinical cardiotoxicity was detected.

resultsNinety-nine patients received ≥1 cycle of chemotherapy (39 with NPLD): 38 (NPLD = 34) were older than 65 years. At baseline, the NPLD subgroup had more cardiovascular risk factors and comorbidities than the doxorubicin subgroup. After treatment, echocardiographic parameters did not worsen in the NPLD subgroup; significant LVEF reduction occurred in two patients treated with doxorubicin. Over treatment course, TnI rises increased linearly in the doxorubicin subgroup but modestly in the NPLD subgroup. At doxorubicin doses >200 mg/m

conclusionA comprehensive strategy to prevent, detect, and treat cardiotoxicity allows an optimal management of the lymphoma with low incidence of cardiac complications.

Indexed as

AdolescentAdultAgedAged, 80 and overAnthracyclinesAntineoplastic Combined Chemotherapy ProtocolsCardiotoxicityDoxorubicinDrug Delivery SystemsFemaleHeartHeart DiseasesHodgkin DiseaseHumansLiposomesMaleAnthracyclinesDoxorubicinliposomal doxorubicinLiposomesPolyethylene GlycolsAnthracyclinesBiomarkersCardiotoxicityDoxorubicinHodgkin DiseaseLymphomaNon‐Hodgkin

Identifiers

PMID28275118
PMCPMC5388379
OpenAlexW2592721950

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.