Evidence map›Paper›PMID 42726384›Full record

ReviewCurrent treatment options in oncology2026

Recent Advances in Tumor-Infiltrating Lymphocyte Therapy for Melanoma.

Huihua Zeng, Wuxuan Mei, Changchun Zeng

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current treatment options in oncology, 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

3 authors.

Huihua ZengDepartment of General Medicine, Shenzhen Longhua District Central Hospital, the Affiliated Longhua Hospital of Shenzhen University, Shenzhen, 518110, China.
Wuxuan MeiXianning Medical College, Hubei University of Science and Technology, Xianning, 437100, China.
Changchun ZengDepartment of Medical Laboratory, Shenzhen Longhua District Central Hospital, the Affiliated Longhua Hospital of Shenzhen University, Shenzhen, 518110, China. zengchch@glmu.edu.cn.ORCID http://orcid.org/0000-0002-9489-0627

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

opinion statementMelanoma is the most aggressive form of skin cancer and remains a leading cause of skin cancer-related mortality. The therapeutic landscape of melanoma has been revolutionized by the advent of immune checkpoint inhibitors (ICIs), resulting in significant improvements in patient survival. Nevertheless, treatment-related toxicities, resistance mechanisms, and disease progression remain major barriers to durable clinical benefit, highlighting an ongoing unmet medical need. Tumor-infiltrating lymphocyte (TIL) therapy has emerged as a clinically active immunotherapeutic strategy for melanoma, particularly in patients with advanced or refractory disease. Continuous advances in biological understanding, manufacturing technologies, and clinical development have further strengthened its therapeutic potential. This review summarizes the biological basis of TIL therapy and outlines the manufacturing process from tumor procurement to lymphodepletion, TIL infusion, and interleukin-2 support. We then review current clinical evidence for conventional TIL products, including lifileucel, TM001, LM103, HS-IT101, and GC101, highlighting their efficacy and safety profiles. Emerging combination strategies integrating immune checkpoint inhibitors, targeted therapies, and oncolytic adenoviruses are also reviewed. In addition, advances in genetically engineered TILs, such as OBX-115, KSQ-001EX, and IOV-4001, are reviewed. Moreover, this review covers recent advances for improving therapeutic outcomes, including safety optimization, product optimization, next-generation engineered TILs, and predictive biomarkers. Challenges and future directions of TIL therapy in melanoma are also discussed. Overall, TIL therapy constitutes a rapidly evolving and clinically potent treatment modality for melanoma.

Indexed as

Immunotherapy, AdoptiveLymphocytes, Tumor-InfiltratingMelanomaSkin NeoplasmsBiomarkers, TumorCombined Modality TherapyDisease ManagementHumansImmune Checkpoint InhibitorsImmunotherapyTreatment OutcomeBiomarkers, TumorImmune Checkpoint InhibitorsAdoptive cell therapy (ACT)BiomarkersMelanomaTherapyTumor-infiltrating lymphocytes (TILs)

Identifiers

PMID42726384

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.