Evidence map›Paper›PMID 29725330›Full record

ArticleFrontiers in immunology2018

Hyperprogressive Disease in Anorectal Melanoma Treated by PD-1 Inhibitors.

Marjorie Faure, Philippe Rochigneux, Daniel Olive, Sébastien Taix, Isabelle Brenot-Rossi, Marine Gilabert

Abstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

27 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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  4. Article
  5. The immune checkpoint inhibitors treatment of head and neck squamous cell carcinoma: an expert consensus.Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2022
    Article
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  12. Article
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  15. Hyperprogression: A novel response pattern under immunotherapy.Clinical and translational medicine · 2020
    Review
  16. Review
  17. Article
  18. Prognostic model for patient survival in primary anorectal mucosal melanoma: stage at presentation determines relevance of histopathologic features.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2020
    Article
  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

6 authors.

Marjorie FaureMedical Oncology Department, Paoli-Calmettes Institute, Aix-Marseille University, Marseille, France.
Philippe RochigneuxMedical Oncology Department, Paoli-Calmettes Institute, Aix-Marseille University, Marseille, France.
Daniel OliveTeam Immunity and Cancer, Centre de Recherche en Cancérologie de Marseille (CRCM), INSERM, U1068, CNRS, UMR7258, Paoli-Calmettes Institute, Aix-Marseille University, Marseille, France.
Sébastien TaixPathology Department, Paoli-Calmettes Institute, Aix-Marseille University, Marseille, France.
Isabelle Brenot-RossiNuclear Medicine Department, Paoli-Calmettes Institute, Aix-Marseille University, Marseille, France.
Marine GilabertMedical Oncology Department, Paoli-Calmettes Institute, Aix-Marseille University, Marseille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 5-year survival rate of primary anorectal malignant melanoma is less than 20%. Optimal treatment of this condition remains controversial regarding locally disease, and whether any preferential survival benefit arises from either abdominoperineal resection or wide local excision remains unknown. The majority of patients progress to metastatic disease, and for decades, the use of chemotherapies, such as platines or dacarbazine, has been advocated to improve overall survival. The therapeutic use of new checkpoint inhibitors in a variety of trials has provided evidence for an antitumoral effect of PD-1 and/or CTL4 inhibitors in mucosal melanomas, but these treatments must still be further evaluated. Some anecdotal occurrences of rapid progression [i.e., hyperprogressive disease (HPD)] while using these immune agents have been described, suggesting potentially deleterious effects of these drugs for some patients. We report a 77-year-old male metastatic anorectal melanoma patient presenting with HPD over 2 months of a PD1 inhibitor treatment course and document this HPD blood phenotype.

Indexed as

AgedAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalDisease ProgressionFatal OutcomeHumansMaleMelanomaNeoplasm Recurrence, LocalRectal NeoplasmsAntibodies, Monoclonal, HumanizedAntineoplastic Agents, Immunologicalpembrolizumabanti-PD1hyperprogressionimmune checkpoint inhibitorsimmunomonitoringmelanoma

Identifiers

PMID29725330
PMCPMC5916968

What OpenQuestion holds

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Registered trials

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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.