Evidence map›Paper›PMID 38539487›Full record

ArticleCancers2024

Stem Cell Origin of Cancer: Clinical Implications beyond Immunotherapy for Drug versus Therapy Development in Cancer Care.

Shi-Ming Tu, Anup K Trikannad, Sruthi Vellanki, Munawwar Hussain, Nazish Malik, Sunny R Singh, Anusha Jillella, Sri Obulareddy, Sindhu Malapati, Sajjad A Bhatti and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 31% of its field
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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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 at 1 institution in 1 country.

Shi-Ming TuDivision of Hematology and Oncology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Anup K TrikannadDivision of Hematology and Oncology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Sruthi VellankiDivision of Hematology and Oncology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Munawwar HussainDivision of Hematology and Oncology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Nazish MalikDivision of Hematology and Oncology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Sunny R SinghDivision of Hematology and Oncology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Anusha JillellaDivision of Hematology and Oncology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Sri ObulareddyDivision of Hematology and Oncology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Sindhu MalapatiDivision of Hematology and Oncology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.ORCID 0000-0001-9446-6036
Sajjad A BhattiDivision of Hematology and Oncology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Konstantinos ArnaoutakisDivision of Hematology and Oncology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.ORCID 0000-0001-5715-1000
Omar T AtiqDivision of Hematology and Oncology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
University of Arkansas for Medical Sciences · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although immunotherapy has revolutionized cancer care, there is still an urgent need to enhance its efficacy and ensure its safety. A correct cancer theory and proper scientific method empower pertinent cancer research and enable effective and efficient drug versus therapy development for patient care. In this perspective, we revisit the concept of immune privilege in a cancer cell versus normal cell, as well as in a cancer stem cell versus normal stem cell. We re-examine whether effective immunotherapies are efficacious due to their anti-cancer and/or immune modulatory mechanisms. We reassess why checkpoint inhibitors (CPIs) are not equal. We reconsider whether one can attribute the utility of immunotherapy to specific cancer subtypes and its futility to certain tumor/immune compartments, components, and microenvironments. We propose ways and means to advance immunotherapy beyond CPIs by combining anti-PD1/L1 with various other treatment modalities according to an appropriate scientific theory, e.g., stem cell origin of cancer, and based on available clinical evidence, e.g., randomized clinical trials. We predict that a stem cell theory of cancer will facilitate the design of better and safer immunotherapy with improved selection of its use for the right patient with the right cancer type at the right time to optimize clinical benefits and minimize potential toxic effects and complications.

Indexed as

cancer stem celldrug developmentimmune modulationimmune privilegeimmunotherapymultimodal therapy

Identifiers

PMID38539487
PMCPMC10969562
OpenAlexW4392863850

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.