Evidence map›Paper›PMID 31074244›Full record

ArticleJournal of gynecologic oncology2019

Early experiences with PD-1 inhibitor treatment of platinum resistant epithelial ovarian cancer.

Marius C Normann, Martin Türzer, Lien My Diep, Jan Oldenburg, Beata Gajdzik, Olesya Solheim, Erik Rud

Open access · diamondAbstract read
In one paragraph

Article in Journal of gynecologic oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 pooled it
1.7field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 2 syntheses or guidelines pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  12. How to use immune checkpoint inhibitor in ovarian cancer?Journal of gynecologic oncology · 2019
    Article
  13. Article
  14. Review
  15. Blocking CD47-SIRPα Signal Axis as Promising Immunotherapy in Ovarian Cancer.Cancer control : journal of the Moffitt Cancer Center
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Marius C NormannAleris Cancer Center, Oslo, Norway.ORCID https://orcid.org/0000-0001-6230-8738
Martin TürzerAleris Cancer Center, Oslo, Norway.ORCID https://orcid.org/0000-0003-4626-547X
Lien My DiepOslo University Hospital, Center for Biostatistics and Epidemiology, Oslo, Norway.ORCID https://orcid.org/0000-0003-2086-4909
Jan OldenburgAleris Cancer Center, Oslo, Norway.ORCID https://orcid.org/0000-0002-4454-905X
Beata GajdzikAleris Cancer Center, Oslo, Norway.ORCID https://orcid.org/0000-0002-6316-8121
Olesya SolheimDepartment of Gynecology, Oslo University Hospital, Oslo, Norway.ORCID https://orcid.org/0000-0003-1936-3453
Erik RudDepartment of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo, Norway. erik.rud@ous-hf.no.ORCID https://orcid.org/0000-0002-3740-2519
Cancer Registry of Norway · NOOslo University Hospital · NOAkershus University Hospital · NO

Funding

Aleris Hospital
6 · The paper itself

Abstract

objectiveIn this study, we evaluated the toxicity and clinical efficacy of nivolumab, a programmed cell death protein 1 (PD-1) inhibitor, on patients with platinum resistant ovarian cancer.

methodsEvery second week, 18 patients with platinum resistance ovarian cancer received nivolumab until disease progression occurred. We assessed toxicity, disease control rate, progression free survival (PFS) and overall survival (OS). Radiological response evaluation according to irRECIST was performed every 12th week, while clinical evaluation was done every second week.

resultsThe disease control rate was 44% (95% confidence interval [CI]=19-87) as 8 showed stable disease, 6 showed progressive disease and 4 died before the first radiological response evaluation. The median OS was 30 weeks (95% CI=14-42; range, 3-95), and PFS was 15 weeks (95% CI=13-17). The median follow-up time was 30 weeks (range, 3-123). The rate of grade 2-5 adverse events was 28% (5 out of 18). Two patients (11%) developed grade 2 and 3 adverse events, respectively, while no grade 4 events were observed. One patient died from intestinal perforation, believed to be caused by concomitant bevacizumab rather than nivolumab.

conclusionThis study shows few adverse events, and promising clinical efficacy when using nivolumab for ovarian cancer.

Indexed as

Administration, IntravenousAgedAntineoplastic Agents, ImmunologicalCarcinoma, Ovarian EpithelialDrug Resistance, NeoplasmFemaleHumansMiddle AgedNivolumabOvarian NeoplasmsPlatinumProgrammed Cell Death 1 ReceptorProspective StudiesAntineoplastic Agents, ImmunologicalNivolumabPDCD1 protein, humanPlatinumProgrammed Cell Death 1 ReceptorImmunotherapyOvarian Cancer

Identifiers

PMID31074244
PMCPMC6543107
OpenAlexW2918892827

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.