Evidence map›Paper›PMID 28756613›Full record

Trial reportMedical oncology (Northwood, London, England)2017

Phase II study of paclitaxel associated with lipid core nanoparticles (LDE) as third-line treatment of patients with epithelial ovarian carcinoma.

Silvia R Graziani, Carolina G Vital, Aleksandra T Morikawa, Brigitte M Van Eyll, Hezio J Fernandes Junior, Roberto Kalil Filho, Raul C Maranhão

Open access · greenAbstract readClinical Trial, Phase II
PubMed Publisher
In one paragraph

Trial report in Medical oncology (Northwood, London, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.8field-weighted citation impact, top 6% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Nanotheranostics for gynecological cancers: a path forward for Africa.Medical oncology (Northwood, London, England) · 2024
    Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Nanodrugs Targeting T Cells in Tumor Therapy.Frontiers in immunology · 2022
    Review
  13. Review
  14. Review
  15. Review
  16. Nanomedicines for Endometriosis: Lessons Learned from Cancer Research.Small (Weinheim an der Bergstrasse, Germany) · 2021
    Review
  17. Review
  18. 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 1 institution in 1 country.

Silvia R GrazianiHeart Institute (InCor) of the Medical School Hospital, University of São Paulo, São Paulo, SP, Brazil.
Carolina G VitalHeart Institute (InCor) of the Medical School Hospital, University of São Paulo, São Paulo, SP, Brazil.
Aleksandra T MorikawaHeart Institute (InCor) of the Medical School Hospital, University of São Paulo, São Paulo, SP, Brazil.
Brigitte M Van EyllArnaldo Vieira de Carvalho Cancer Institute, São Paulo, SP, Brazil.
Hezio J Fernandes JuniorArnaldo Vieira de Carvalho Cancer Institute, São Paulo, SP, Brazil.
Roberto Kalil FilhoHeart Institute (InCor) of the Medical School Hospital, University of São Paulo, São Paulo, SP, Brazil.
Raul C MaranhãoHeart Institute (InCor) of the Medical School Hospital, University of São Paulo, São Paulo, SP, Brazil. ramarans@usp.br.
Universidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian cancer is often diagnosed at advanced stages, when poorly responsive to standard treatment. First-line treatment consists in schemes including cytoreductive surgery followed by adjuvant chemotherapy schemes with platinum and taxane derivatives. Second-line regimens are based on gemcitabine and liposomal doxorubicin. Third line is often not worthwhile because of the high toxicity with poor response to treatment. Previously, we showed that paclitaxel (PTX) carried in non-protein lipid core nanoparticles (LDE) resembling the chemical structure of LDL has remarkably reduced toxicity. Here, the hypothesis was tested whether PTX-LDE could safely benefit patients in third-line treatment setting. Fourteen women unresponsive to second-line chemotherapy for ovarian cancer, aged 61 ± 10 years, clinical stage IV and TqNqM1, were included. PTX-LDE was administered at 175 mg/m

Indexed as

AdultAgedAntineoplastic Combined Chemotherapy ProtocolsCarcinomaCarcinoma, Ovarian EpithelialChemotherapy, AdjuvantDeoxycytidineDisease-Free SurvivalDisease ProgressionDoxorubicinFemaleGemcitabineHumansLipidsNanoparticlesNeoplasms, Glandular and EpithelialDeoxycytidineDoxorubicinGemcitabineLipidsliposomal doxorubicinPaclitaxelPolyethylene GlycolsDrug delivery and cancerDrug targeting and cancerLDL receptorsOvarian cancer treatmentSolid lipid particles

Identifiers

PMID28756613
OpenAlexW2739712695

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.