Evidence map›Paper›PMID 32193712›Full record

ReviewCurrent treatment options in oncology2020

Cutaneous Adverse Events of Anti-PD-1 Therapy and BRAF Inhibitors.

Subashini Sharon Gnanendran, Lauren Maree Turner, James Austin Miller, Shelley Ji Eun Hwang, Andrew Charles Miller

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current treatment options in oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–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

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Survivorship Issues in Adult Patients With Histiocytic Neoplasms.Journal of the National Comprehensive Cancer Network : JNCCN · 2021
    Review
  7. Eczematous Drug Eruptions.American journal of clinical dermatology · 2021
    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

5 authors.

Subashini Sharon GnanendranDermatology Department, The Canberra Hospital, Australian National University, Level 2, Building 6, Canberra, Australian Capital Territory, Australia.
Lauren Maree TurnerANU Medical School, Australian National University, Acton, Canberra, ACT, 2600, Australia.
James Austin MillerANU Medical School, Australian National University, Acton, Canberra, ACT, 2600, Australia. James.Miller@anu.edu.au.
Shelley Ji Eun HwangDermatology Department, The Canberra Hospital, Australian National University, Level 2, Building 6, Canberra, Australian Capital Territory, Australia.
Andrew Charles MillerDermatology Department, The Canberra Hospital, Australian National University, Level 2, Building 6, Canberra, Australian Capital Territory, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

opinion statementThe treatment of advanced melanoma has undergone a dramatic transformation over the last decade with the advent of targeted and immunomodulatory therapies. This transition from cytotoxic chemotherapy has yielded improvements in both survival and quality of life; yet despite their therapeutic advantages, these treatments have been associated with a diverse range of cutaneous adverse events (AEs). These range from relatively benign eczematous conditions to more severe inflammatory and bullous disorders, and can include induction of second malignancies. AEs can result in serious morbidity and risk of mortality if not recognised and managed early. As a consequence of their novelty, and rapid uptake, these agents have been subject to intense scrutiny and there is a general understanding that cutaneous AEs should be anticipated in treatment plans. Dermatologists should be integrated into management teams to assist in the development of treatment protocols for anticipated common AEs and to provide expert management of more severe, rare or unusual AEs. Our experience has shown a reduction in treatment interruptions, more rapid recognition of unusual AEs and improved management pathways for patients suffering cutaneous AEs.

Indexed as

Biomarkers, TumorDisease ManagementDisease SusceptibilityHumansImmune Checkpoint InhibitorsMolecular Targeted TherapyNeoplasmsProgrammed Cell Death 1 ReceptorProtein Kinase InhibitorsProto-Oncogene Proteins B-rafSkin DiseasesBiomarkers, TumorBRAF protein, humanImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorProtein Kinase InhibitorsProto-Oncogene Proteins B-rafAdverse eventAnti-PD-1Anti-programmed cell death protein 1 inhibitorBRAFComplicationCutaneousDermatologicalDermatologyImmune therapyImmunotherapyMelanomaMelanoma treatmentPD1

Identifiers

What OpenQuestion holds

Textmetadata
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.