Evidence map›Paper›PMID 33916696›Full record

ReviewInternational journal of molecular sciences2021

Hyperprogressive Disease: Main Features and Key Controversies.

Hugo Arasanz, Miren Zuazo, Ana Bocanegra, Luisa Chocarro, Ester Blanco, Maite Martínez, Idoia Morilla, Gonzalo Fernández, Lucía Teijeira, Pilar Morente and 8 more

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
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  12. Article
  13. Review
  14. Systemic CD4 Immunity and PD-L1/PD-1 Blockade Immunotherapy.International journal of molecular sciences · 2022
    Review
  15. Article
  16. CAR-T Cells for the Treatment of Lung Cancer.Life (Basel, Switzerland) · 2022
    Review
  17. Article
  18. Article
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

18 authors at 2 institutions in 1 country.

Hugo ArasanzOncoimmunology Group, Navarrabiomed, Fundación Miguel Servet-Public University of Navarre, IdiSNA, 31008 Pamplona, Spain.ORCID 0000-0001-6838-6702
Miren ZuazoOncoimmunology Group, Navarrabiomed, Fundación Miguel Servet-Public University of Navarre, IdiSNA, 31008 Pamplona, Spain.
Ana BocanegraOncoimmunology Group, Navarrabiomed, Fundación Miguel Servet-Public University of Navarre, IdiSNA, 31008 Pamplona, Spain.
Luisa ChocarroOncoimmunology Group, Navarrabiomed, Fundación Miguel Servet-Public University of Navarre, IdiSNA, 31008 Pamplona, Spain.ORCID 0000-0001-7384-9847
Ester BlancoOncoimmunology Group, Navarrabiomed, Fundación Miguel Servet-Public University of Navarre, IdiSNA, 31008 Pamplona, Spain.ORCID 0000-0002-2980-7137
Maite MartínezDepartment of Medical Oncology, Complejo Hospitalario de Navarra-IdiSNA, 31008 Pamplona, Spain.
Idoia MorillaDepartment of Medical Oncology, Complejo Hospitalario de Navarra-IdiSNA, 31008 Pamplona, Spain.
Gonzalo FernándezOncoimmunology Group, Navarrabiomed, Fundación Miguel Servet-Public University of Navarre, IdiSNA, 31008 Pamplona, Spain.
Lucía TeijeiraDepartment of Medical Oncology, Complejo Hospitalario de Navarra-IdiSNA, 31008 Pamplona, Spain.
Pilar MorenteOncoimmunology Group, Navarrabiomed, Fundación Miguel Servet-Public University of Navarre, IdiSNA, 31008 Pamplona, Spain.
Miriam EchaideOncoimmunology Group, Navarrabiomed, Fundación Miguel Servet-Public University of Navarre, IdiSNA, 31008 Pamplona, Spain.
Natalia CastroDepartment of Medical Oncology, Complejo Hospitalario de Navarra-IdiSNA, 31008 Pamplona, Spain.
Leticia FernándezOncoimmunology Group, Navarrabiomed, Fundación Miguel Servet-Public University of Navarre, IdiSNA, 31008 Pamplona, Spain.
Maider GarnicaOncoimmunology Group, Navarrabiomed, Fundación Miguel Servet-Public University of Navarre, IdiSNA, 31008 Pamplona, Spain.
Pablo RamosOncoimmunology Group, Navarrabiomed, Fundación Miguel Servet-Public University of Navarre, IdiSNA, 31008 Pamplona, Spain.
David EscorsOncoimmunology Group, Navarrabiomed, Fundación Miguel Servet-Public University of Navarre, IdiSNA, 31008 Pamplona, Spain.
Grazyna KochanOncoimmunology Group, Navarrabiomed, Fundación Miguel Servet-Public University of Navarre, IdiSNA, 31008 Pamplona, Spain.
Ruth VeraDepartment of Medical Oncology, Complejo Hospitalario de Navarra-IdiSNA, 31008 Pamplona, Spain.
Universidad Publica de Navarra · ESComplejo Hospitalario de Navarra · ES

Funding

Asociación Española Contra el Cáncer (AECC) CLJUN19010ARASAsociación Española Contra el Cáncer (AECC) PROYE16001ESCODepartamento de Salud de Navarra BMED 050-2019Instituto de Salud Carlos III ISCIII-FEDER, FIS. PI17/02119
6 · The paper itself

Abstract

Along with the positioning of immunotherapy as a preferential treatment for a wide variety of neoplasms, a new pattern of response consisting in a sudden acceleration of tumor growth has been described. This phenomenon has received the name of "hyperprogressive disease", and several definitions have been proposed for its identification, most of them relying on radiological criteria. However, due to the fact that the cellular and molecular mechanisms have not been elucidated yet, there is still some debate regarding whether this fast progression is induced by immunotherapy or only reflects the natural course of some highly aggressive neoplasms. Moreover, contradictory results of trials including patients with different cancer types suggest that both the incidence, the associated factors and the implications regarding prognosis might differ depending on tumor histology. This article intends to review the main publications regarding this matter and critically approach the most controversial aspects.

Indexed as

ImmunotherapyNeoplasmsHumansImmune Checkpoint InhibitorsPrognosisImmune Checkpoint Inhibitorscancercheckpoint inhibitorshyperprogressive diseaseimmunotherapysolid tumors

Identifiers

PMID33916696
PMCPMC8038385
OpenAlexW3151754693

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.