Evidence map›Paper›PMID 42313150›Full record

ReviewPathologie (Heidelberg, Germany)2026

[Therapy of melanoma : Current standards and future perspectives].

Isabel Hariri, Jessica C Hassel

Abstract readEnglish AbstractReview
PubMed Publisher
In one paragraph

Review in Pathologie (Heidelberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Isabel HaririKlinik für Dermatologie sowie nationales Zentrum für Tumorerkrankungen (NCT) Heidelberg, Medizinische Fakultät Heidelberg, Universität Heidelberg, Im Neuenheimer Feld 440, 69120, Heidelberg, Deutschland. isabel.hariri@med.uni-heidelberg.de.ORCID http://orcid.org/0009-0004-1165-3979
Jessica C HasselKlinik für Dermatologie sowie nationales Zentrum für Tumorerkrankungen (NCT) Heidelberg, Medizinische Fakultät Heidelberg, Universität Heidelberg, Im Neuenheimer Feld 440, 69120, Heidelberg, Deutschland. jessica.hassel@med.uni-heidelberg.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMelanoma is an aggressive skin cancer with a rising incidence. While early-stage disease can often be managed successfully with surgical intervention alone, advanced stages require immunotherapies and, where appropriate, targeted treatments, which have significantly improved prognosis and overall survival.

objectivesThis review summarizes current therapeutic standards and emerging developments in melanoma treatment and evaluates their clinical relevance. MATERIALS AND

methodsA systematic literature search was conducted up to 2025, including guidelines, clinical trials, and review articles on surgical, immunological, and targeted therapies.

resultsSurgical resection remains the standard of care in early-stage melanoma. In advanced stages, immune checkpoint inhibitors (PD‑1, CTLA‑4, LAG-3) reduce recurrence risk in the adjuvant and neoadjuvant settings and improve overall survival in metastatic disease. Local and intralesional therapies (e.g., T‑VEC, Daromun) complement systemic approaches. In BRAF-V600-mutant melanoma, combinations of BRAF and MEK inhibitors are effective and are particularly used in cases of rapidly progressing disease. Novel approaches such as bispecific antibodies, cell-based therapies, and various tumor-specific vaccines show promising results in early clinical studies.

conclusionsMultimodal treatment strategies have fundamentally improved the prognosis of melanoma. Therapy selection should be individualized based on molecular markers and disease stage. Future developments aim to integrate combination strategies, personalized immunotherapeutic approaches, and the overcoming of resistance mechanisms.

Indexed as

Bispecific antibodiesImmune checkpoint inhibitorsImmunotherapyMolecular targeted therapyProto-oncogene proteins B‑raf

Identifiers

PMID42313150

What Socratic 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 Socratic graph.