Evidence map›Paper›PMID 32101722›Full record

ReviewTrends in cancer2020

Hyperprogression and Immunotherapy: Fact, Fiction, or Alternative Fact?

Jacob J Adashek, Ishwaria M Subbiah, Ignacio Matos, Elena Garralda, Arjun K Menta, Dhakshina Moorthy Ganeshan, Vivek Subbiah

Open access · hybridAbstract readReview
In one paragraph

Review in Trends in cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

79 citing papers in PubMed, 135 citations in OpenAlex.

  1. A Phase II Trial of Guadecitabine plus Atezolizumab in Metastatic Urothelial Carcinoma Progressing after Initial Immune Checkpoint Inhibitor Therapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
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  12. Efficacy assessment in phase I clinical trials: endpoints and challenges.Annals of oncology : official journal of the European Society for Medical Oncology · 2025
    Review
  13. Review
  14. Review
  15. Article
  16. Primary and Acquired Resistance to Immunotherapy with Checkpoint Inhibitors in NSCLC: From Bedside to Bench and Back.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
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  19. Review
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19 more citing papers are in PubMed but not listed here.

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 4 institutions in 2 countries.

Jacob J AdashekUniversity of South Florida, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL, USA.
Ishwaria M SubbiahThe University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Ignacio MatosVall Hebron Institute, Madrid, Spain.
Elena GarraldaVall Hebron Institute, Madrid, Spain.
Arjun K MentaThe University of Texas at Austin, Austin, TX, USA.
Dhakshina Moorthy GaneshanThe University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Vivek SubbiahThe University of Texas MD Anderson Cancer Center, Houston, TX, USA. Electronic address: vsubbiah@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USVall d'Hebron Institut de Recerca · ESThe University of Texas at Austin · USUniversity of South Florida · US

Funding

Discovery of the next-generation RET-targeted drugs based on nicotinamide scaffoldR01CA273168 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI FUNDA MERIC-BERNSTAM, Herman O Sintim · 2022 to 2026
$2.9M
Blocking tumor progression in therapy-responsive RET aberration-associated cancerR01CA242845 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI AHNERT, JORDI RODON, MOOERS, BLAINE H. M. · 2020 to 2024
$1.9M
NCI NIH HHS R01 CA242845NCI NIH HHS R01 CA273168
6 · The paper itself

Abstract

Immunotherapy (IO) has altered the therapeutic landscape for multiple cancers. There are emerging data from retrospective studies on a subset of patients who do not benefit from IO, instead experiencing rapid progression with dramatic acceleration of disease trajectory, termed 'hyperprogressive disease' (HPD). The incidence of HPD ranges from 4% to 29% from the studies reported. Biological basis and mechanisms of HPD are currently being elucidated, with one theory involving the Fc region of antibodies. Another group has shown EGFR and MDM2/MDM4 amplifications in patients with HPD. This phenomenon has polarized oncologists who debate that this could still reflect the natural history of the disease. Thus, prospective studies are urgently needed to confirm the underlying biology, predict patients who are susceptible to HPD, and determine the modality of therapy post progression.

Indexed as

AnimalsClinical Trials as TopicDisease ProgressionHumansImmune Checkpoint InhibitorsImmunoglobulin Fab FragmentsImmunoglobulin Fc FragmentsImmunotherapyMiceModels, ImmunologicalNeoplasm ProteinsNeoplasmsNivolumabProgression-Free SurvivalRetrospective StudiesTreatment OutcomeImmune Checkpoint InhibitorsImmunoglobulin Fab FragmentsImmunoglobulin Fc FragmentsNeoplasm ProteinsNivolumabcancer clinical trialshyperprogressive diseaseimmune checkpoint inhibitorsimmunotherapy

Identifiers

PMID32101722
PMCPMC9726601
OpenAlexW3005152261

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.