Evidence map›Paper›PMID 36125617›Full record

ReviewCurrent treatment options in oncology2022

Advanced Acral Melanoma Therapies: Current Status and Future Directions.

Yiqun Zhang, Shijie Lan, Di Wu

Open access · hybridAbstract readReview
In one paragraph

Review in Current treatment options in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  5. Review
  6. Article
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  11. A bibliometric analysis of global research on microbial immune microenvironment in melanoma from 2012 to 2022.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2024
    Review
  12. Article
  13. Adjuvant Therapy in Acral Melanoma: A Systematic Review.Clinical, cosmetic and investigational dermatology · 2024
    Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. 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

3 authors at 1 institution in 1 country.

Yiqun ZhangCancer Center, The First Hospital of Jilin University, 1 Xinmin St, Changchun, 130021, China.
Shijie LanCancer Center, The First Hospital of Jilin University, 1 Xinmin St, Changchun, 130021, China.
Di WuCancer Center, The First Hospital of Jilin University, 1 Xinmin St, Changchun, 130021, China. wudi1971@jlu.edu.cn.ORCID 0000-0002-0742-0556
Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

opinion statementMelanoma is one of the deadliest malignancies. Its incidence has been significantly increasing in most countries in recent decades. Acral melanoma (AM), a peculiar subgroup of melanoma occurring on the palms, soles, and nails, is the main subtype of melanoma in people of color and is extremely rare in Caucasians. Although great progress has been made in melanoma treatment in recent years, patients with AM have shown limited benefit from current therapies and thus consequently have worse overall survival rates. Achieving durable therapeutic responses in this high-risk melanoma subtype represents one of the greatest challenges in the field. The frequency of BRAF mutations in AM is much lower than that in cutaneous melanoma, which prevents most AM patients from receiving treatment with BRAF inhibitors. However, AM has more frequent mutations such as KIT and CDK4/6, so targeted therapy may still improve the survival of some AM patients in the future. AM may be less susceptible to immune checkpoint inhibitors because of the poor immunogenicity. Therefore, how to enhance the immune response to the tumor cells may be the key to the application of immune checkpoint inhibitors in advanced AM. Anti-angiogenic drugs, albumin paclitaxel, or interferons are thought to enhance the effectiveness of immune checkpoint inhibitors. Combination therapies based on the backbone of PD-1 are more likely to provide greater clinical benefits. Understanding the molecular landscapes and immune microenvironment of AM will help optimize our combinatory strategies.

Indexed as

MelanomaSkin NeoplasmsAlbuminsAngiogenesis InhibitorsCutaneous Malignant MelanomaHumansImmune Checkpoint InhibitorsImmunotherapyInterferonsPaclitaxelProgrammed Cell Death 1 ReceptorProto-Oncogene Proteins B-rafTumor MicroenvironmentAlbuminsAngiogenesis InhibitorsImmune Checkpoint InhibitorsInterferonsPaclitaxelProgrammed Cell Death 1 ReceptorProto-Oncogene Proteins B-rafAcral melanomaCombination therapyImmunotherapyTargeted therapy

Identifiers

PMID36125617
PMCPMC9526689
OpenAlexW4297855270

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.