Evidence map›Paper›PMID 40904097›Full record

ReviewCancer discovery2025

Histologic Transformation in Cancer: The Path for Clinical Translation.

Ioannis Vathiotis, Avisek Banerjee, Utsav Sen, Felix C Saalfeld, Debdatta Halder, Andriani Charpidou, Konstantinos N Syrigos, Hidehito Horinouchi, Ashutosh K Tewari, Mark A Dawson and 2 more

Abstract readReview
In one paragraph

Review in Cancer discovery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
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

12 authors.

Ioannis Vathiotis *Third Department of Internal Medicine, Sotiria Thoracic Diseases Hospital of Athens, National and Kapodistrian University of Athens, Athens, Greece.ORCID 0000-0002-1772-5986
Avisek Banerjee *Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0001-5697-6721
Utsav SenDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0001-7970-0357
Felix C SaalfeldClinic for Internal Medicine I, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.ORCID 0000-0002-4095-8649
Debdatta HalderDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0009-0004-0780-7832
Andriani CharpidouThird Department of Internal Medicine, Sotiria Thoracic Diseases Hospital of Athens, National and Kapodistrian University of Athens, Athens, Greece.ORCID 0000-0002-5107-6430
Konstantinos N SyrigosThird Department of Internal Medicine, Sotiria Thoracic Diseases Hospital of Athens, National and Kapodistrian University of Athens, Athens, Greece.ORCID 0000-0002-3474-1363
Hidehito HorinouchiDepartment of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID 0000-0001-9090-801X
Ashutosh K TewariDepartment of Urology, Icahn School of Medicine at Mount Sinai Hospital, New York, New York.ORCID 0000-0002-3146-4524
Mark A DawsonPeter MacCallum Cancer Centre, Melbourne, Australia.ORCID 0000-0002-5464-5029
Martin WermkeClinic for Internal Medicine I, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.ORCID 0000-0002-4844-4087
Triparna SenDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0003-4673-7481

Funding

Targeting replication stress signaling to overcome immune evasion in small cell lung cancerR01CA258784 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SEN, TRIPARNA · 2021 to 2025
$2.4M
Defining and overcoming lineage plasticity in lung cancerR01CA289410 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SEN, TRIPARNA · 2025 to 2025
$631k
Jazz Pharmaceuticals (Greenwich Biosciences)National Cancer Institute (NCI) R01CA258784National Cancer Institute (NCI) R01CA289410NCI NIH HHS R01 CA258784NCI NIH HHS R01 CA289410
6 · The paper itself

Abstract

Lineage plasticity, a critical hallmark of cancer progression, enables tumor cells to evade inhibition of primary oncogenic pathways through histologic transformation. This adaptive process, driven by stemness-associated features and epigenetic reprogramming, poses significant challenges in treatment. Using non-small cell lung cancer and prostate cancer as models, we examine the utility of tissue and liquid biopsies in detecting histologic transformations and tailoring treatments to specific subtypes, which has profound clinical implications, potentially improving outcomes in patients with advanced, therapy-resistant disease. We also discuss emerging therapeutic strategies, including novel molecular targets, and address ongoing clinical challenges in managing treatment-emergent histologic transformation. SIGNIFICANCE: The advent of highly effective molecularly targeted therapies results in increased recognition of treatment-emergent histologic transformation. This review not only summarizes current evidence on diagnosis and management of lineage plasticity but also explores therapeutic strategies under study, outlining a framework for clinical translation and successful drug development.

Indexed as

Cell Transformation, NeoplasticNeoplasmsHumansTranslational Research, Biomedical

Identifiers

PMID40904097
PMCPMC12412897

What OpenQuestion holds

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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.