Evidence map›Paper›PMID 38130914›Full record

ArticleSAGE open medical case reports2023

Lichenoid drug reaction after ipilimumab/nivolumab combination therapy: A case report.

Zonía Robenne Moore, Dalit Zajdman-Faitelson, Arely Tamariz Campillo, Diana Karen Brito Bustillos, Sonia Toussaint-Caire, Cristina Berumen-Glinz

Open access · goldAbstract readCase Reports
In one paragraph

Article in SAGE open medical case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 25% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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 at 1 institution in 2 countries.

Zonía Robenne MooreUniversity of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.ORCID https://orcid.org/0000-0003-2133-7545
Dalit Zajdman-FaitelsonDermatology Department, Manuel Gea González General Hospital, Tlalpan, CDMX, Mexico.
Arely Tamariz CampilloDermatology Department, Manuel Gea González General Hospital, Tlalpan, CDMX, Mexico.
Diana Karen Brito BustillosDermatopathology Department, Manuel Gea González General Hospital, Tlalpan, CDMX, Mexico.
Sonia Toussaint-CaireDermatopathology Department, Manuel Gea González General Hospital, Tlalpan, CDMX, Mexico.
Cristina Berumen-GlinzDermatology Department, Manuel Gea González General Hospital, Tlalpan, CDMX, Mexico.
Hospital General Dr. Manuel Gea Gonzalez · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nivolumab (PD-1 inhibitor) and ipilumumab (CTLA-4 inhibitor) are recently approved checkpoint inhibitors for treatment of non-small cell lung cancer. Immune-related adverse events related to the usage of checkpoint inhibitors are growing with their popularity. We present the case of a patient in combination treatment of nivolumab and ipilimumab who developed a lichenoid drug reaction, notable because it worsened to a bullous lichenoid drug reaction. Treatment with prednisone and withdrawal of checkpoint inhibitors aided in clinical resolution. Initial presentation of a lichenoid reaction that progressed to a bullous, desquamated presentation indicates the possibility of the prodromal rash progressing to a Stevens-Johnson Syndrome-like dermatosis. When dermatologists are consulted for rashes developed during checkpoint-inhibitor therapy, they should be aware that early treatment may prevent progression to bullae formation and desquamation and develop their treatment plans with this in mind.

Indexed as

Bullous lichenoid drug reactioncombination therapyipilimumabmesotheliomanivolumab

Identifiers

PMID38130914
PMCPMC10734355
OpenAlexW4390072510

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.