Evidence map›Paper›PMID 41706365›Full record

ReviewCurrent oncology reports2026

Pleural Mesothelioma: Current Therapeutic Strategies and Future Directions.

Haoxuan Tang, Xingchen Lu, Shiyang Wu, Guo-Liang Lu, Jingyuan Wen, Ming Q Wei, Xianyi Sha, Zhiwen Zhang

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current oncology reports, 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

8 authors.

Haoxuan TangSchool of Pharmaceutical Sciences, Key laboratory of smart drug delivery (Ministry of Education), State Key Laboratory of Advanced Drug Formulations for Overcoming Delivery Barriers, Fudan University, Shanghai, 201203, China.
Xingchen LuSchool of Pharmaceutical Sciences, Key laboratory of smart drug delivery (Ministry of Education), State Key Laboratory of Advanced Drug Formulations for Overcoming Delivery Barriers, Fudan University, Shanghai, 201203, China.
Shiyang WuSchool of Pharmaceutical Sciences, Key laboratory of smart drug delivery (Ministry of Education), State Key Laboratory of Advanced Drug Formulations for Overcoming Delivery Barriers, Fudan University, Shanghai, 201203, China. wushiyang@fudan.edu.cn.
Guo-Liang LuThe University of Auckland, Auckland, 1142, New Zealand.
Jingyuan WenThe University of Auckland, Auckland, 1142, New Zealand.
Ming Q WeiMenzies Health Institute, School of Medical Science, Griffith University, Southport, QLD, 4215, Australia.
Xianyi ShaSchool of Pharmaceutical Sciences, Key laboratory of smart drug delivery (Ministry of Education), State Key Laboratory of Advanced Drug Formulations for Overcoming Delivery Barriers, Fudan University, Shanghai, 201203, China.
Zhiwen ZhangSchool of Pharmaceutical Sciences, Key laboratory of smart drug delivery (Ministry of Education), State Key Laboratory of Advanced Drug Formulations for Overcoming Delivery Barriers, Fudan University, Shanghai, 201203, China. zhangzhiwen@fudan.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewPleural mesothelioma (PM) is a rare yet highly aggressive cancer. It is typically diagnosed at an advanced stage, leaving patients with limited curative options. In this review, we highlight emerging frameworks for patient stratification and summarize advances in conventional therapy, targeted therapy and immunotherapy for PM, and provide some feasible considerations in this challenging field. RECENT

findingsRecently, targeted therapies, including biomarker-driven therapies and gene-modulating strategies, have shown early clinical activity in molecularly defined patient subgroups. By contrast, immune checkpoint-based approaches have begun to reshape the treatment landscape, demonstrating survival benefit across histologic subtypes and progressing toward frontline use, whereas cancer vaccines, cellular therapies, and oncolytic viruses remain in early stages of clinical development with limited clinical impact to date. In parallel, advances in drug delivery systems such as intrapleural administration, gene delivery platforms, and nanosystems are being explored to improve pleural targeting and potentially mitigate resistance and systemic toxicity. The therapeutic paradigm for PM is shifting toward precision and multimodal treatment. However, many emerging approaches require further validation before broad clinical adoption. With collaborative clinical efforts and translational innovation, more effective treatment strategies may be realized for PM patients.

Indexed as

MesotheliomaMesothelioma, MalignantPleural NeoplasmsCombined Modality TherapyDrug Delivery SystemsHumansImmunotherapyMolecular Targeted TherapyChemotherapyDrug deliveryImmunotherapyPleural mesotheliomaTargeted therapy

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.