Evidence map›Paper›PMID 32107407›Full record

ArticleScientific reports2020

Hyperprogression under Immune Checkpoint Inhibitor: a potential role for germinal immunogenetics.

Sadal Refae, Jocelyn Gal, Patrick Brest, Damien Giacchero, Delphine Borchiellini, Nathalie Ebran, Frederic Peyrade, Joël Guigay, Gérard Milano, Esma Saada-Bouzid

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 24 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 3 pooled it
2.4field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 3 syntheses or guidelines pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Review
  6. Hyperprogressive disease in patients with advanced cancer treated with immune checkpoint inhibitors.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Hyperprogressive Disease: Main Features and Key Controversies.International journal of molecular sciences · 2021
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Sadal RefaeUniversity Côte d'Azur, Centre Antoine Lacassagne, Oncopharmacology Unit, Nice, France.
Jocelyn GalUniversity Côte d'Azur, Centre Antoine Lacassagne, Epidemiology and Biostatistics Department, Nice, France.
Patrick BrestUniversity Côte d'Azur, Centre Antoine Lacassagne, CNRS, Inserm, Ircan, FHU-Oncoage, Nice, F-06189, France.
Damien GiaccheroUniversity Côte d'Azur, Centre Antoine Lacassagne, Medical Oncology Department, Nice, France.
Delphine BorchielliniUniversity Côte d'Azur, Centre Antoine Lacassagne, Medical Oncology Department, Nice, France.
Nathalie EbranUniversity Côte d'Azur, Centre Antoine Lacassagne, Oncopharmacology Unit, Nice, France.
Frederic PeyradeUniversity Côte d'Azur, Centre Antoine Lacassagne, Medical Oncology Department, Nice, France.
Joël GuigayUniversity Côte d'Azur, Centre Antoine Lacassagne, Medical Oncology Department, Nice, France.
Gérard MilanoUniversity Côte d'Azur, Centre Antoine Lacassagne, Oncopharmacology Unit, Nice, France. gerard.milano@nice.unicancer.fr.
Esma Saada-BouzidUniversity Côte d'Azur, Centre Antoine Lacassagne, Medical Oncology Department, Nice, France.
Centre Antoine Lacassagne · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyperprogressive disease (HPD), an unexpected acceleration of tumor growth kinetics, is described in cancer patients treated with anti-PD-1/anti-PD-L1 agents. Here, our aim was to take into consideration the host and explore whether single nucleotide polymorphisms (SNPs) in key genes involved in immune response might predispose to HPD. DNA was extracted from blood-samples from 98 patients treated under CPI monotherapy. Four candidate genes (PD-1, PD-L1, IDO1 and VEGFR2) and 15 potential SNPs were selected. The TGK

Indexed as

AdultAgedAged, 80 and overAntineoplastic AgentsB7-H1 AntigenCell ProliferationDisease ProgressionFemaleHumansImmune Checkpoint InhibitorsImmunogeneticsMaleMiddle AgedNeoplasmsPolymorphism, Single NucleotideProgrammed Cell Death 1 ReceptorAntineoplastic AgentsB7-H1 AntigenCD274 protein, humanImmune Checkpoint InhibitorsKDR protein, humanProgrammed Cell Death 1 ReceptorVascular Endothelial Growth Factor Receptor-2

Identifiers

PMID32107407
PMCPMC7046673
OpenAlexW3009627109

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.