Evidence map›Paper›PMID 42902326›Full record

ReviewJournal of hematology & oncology2026

Cancer metastasis: biological mechanisms, therapeutic bottlenecks, and emerging interventions.

Huali Ye, Yuquan Wei, Xuemei He, Xiawei Wei

Abstract readReview
In one paragraph

Review in Journal of hematology & 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

4 authors.

Huali YeLaboratory of Aging Research and Immunology, State Key Laboratory of Biotherapy and Cancer Center, National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Yuquan WeiLaboratory of Aging Research and Immunology, State Key Laboratory of Biotherapy and Cancer Center, National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Xuemei HeLaboratory of Aging Research and Immunology, State Key Laboratory of Biotherapy and Cancer Center, National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, Chengdu, Sichuan, China. hexuemei1116@126.com.
Xiawei WeiLaboratory of Aging Research and Immunology, State Key Laboratory of Biotherapy and Cancer Center, National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, Chengdu, Sichuan, China. xiaweiwei@scu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastatic cancer remains a major clinical challenge, which is driven by the continuous adaptation of disseminated tumor cells to diverse tissue environments and therapeutic pressures. Although current treatments, including conventional therapies, small-molecule drugs, antibody-drug conjugates, and immunotherapies, have improved clinical outcomes in selected patients, they rarely achieve durable disease control, largely because each stage of the metastatic cascade presents distinct therapeutic bottlenecks. This review examines these bottlenecks and identifies therapeutic vulnerabilities that can be targeted at each metastatic stage. Cross-stage adaptive programs, encompassing genetic, epigenetic, metabolic, immune, and microenvironmental alterations, are linked to the specific modes of therapeutic failure they drive, thereby connecting underlying mechanisms with their corresponding clinical consequences. Emerging therapeutic strategies are discussed in the context of the metastatic stage, and general design principles for combination regimens are proposed. We also highlight the potential of liquid biopsy-guided dynamic treatment adjustment and advanced preclinical models to inform patient selection, treatment timing, and the design of therapies aimed at overcoming resistance. By integrating metastatic biology, mechanisms of therapeutic failure, and emerging interventions, this review provides a framework for understanding and targeting the bottlenecks that limit durable disease control in metastatic cancer.

Indexed as

Neoplasm MetastasisNeoplasmsAnimalsAntineoplastic AgentsHumansTumor MicroenvironmentAntineoplastic AgentsAdaptive programsCombination therapyMolecular mechanismsTherapeutic resistanceTumor metastasis

Identifiers

PMID42902326
PMCPMC13685084

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.