Evidence map›Paper›PMID 38195534›Full record

ReviewMolecular cancer2024

Evolution of cell therapy for renal cell carcinoma.

Yufei Wang, Eloah Rabello Suarez, Gabriella Kastrunes, Najla Santos Pacheco de Campos, Rabia Abbas, Renata Schmieder Pivetta, Nithyassree Murugan, Ghanbar Mahmoodi Chalbatani, Vincent D'Andrea, Wayne A Marasco

Open access · goldAbstract readReview
In one paragraph

Review in Molecular cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
19.9field-weighted citation impact, top 1% 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

72 citing papers in PubMed, 85 citations in OpenAlex.

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12 more citing papers are in PubMed but not listed here.

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

10 authors at 6 institutions in 2 countries.

Yufei Wang *Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Eloah Rabello Suarez *Center for Natural and Human Sciences, Federal University of ABC, Santo Andre, SP, 09210-580, Brazil.
Gabriella KastrunesDepartment of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Najla Santos Pacheco de CamposCenter for Natural and Human Sciences, Federal University of ABC, Santo Andre, SP, 09210-580, Brazil.
Rabia AbbasDepartment of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Renata Schmieder PivettaCenter for Natural and Human Sciences, Federal University of ABC, Santo Andre, SP, 09210-580, Brazil.
Nithyassree MuruganDepartment of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Ghanbar Mahmoodi ChalbataniDepartment of Immunology, Mayo Clinic, Scottsdale, AZ, 85259, USA.
Vincent D'AndreaDepartment of Surgery, Brigham and Women's Hospital, Boston, MA, 02215, USA.
Wayne A MarascoDepartment of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA. Wayne_Marasco@dfci.harvard.edu.
Dana-Farber Cancer Institute · USHarvard University · USUniversidade Federal do ABC · BRBrigham and Women's Hospital · USMayo Clinic in Arizona · USUniversidade Federal de São Paulo · BR

Funding

U.S. Department of Defense W81XWH-21-1-0442U.S. Department of Defense W81XWH-21-1-0482
6 · The paper itself

Abstract

Treatment for renal cell carcinoma (RCC) has improved dramatically over the last decade, shifting from high-dose cytokine therapy in combination with surgical resection of tumors to targeted therapy, immunotherapy, and combination therapies. However, curative treatment, particularly for advanced-stage disease, remains rare. Cell therapy as a "living drug" has achieved hematological malignancy cures with a high response rate, and significant research efforts have been made to facilitate its translation to solid tumors. Herein, we overview the cellular therapies for RCC focusing on allogeneic hematopoietic stem cell transplantation, T cell receptor gene-modified T cells, chimeric antigen receptor (CAR) T cells, CAR natural killer (NK) cells, lymphokine-activated killer (LAK) cells, γδ T cells, and dendritic cell vaccination. We have also included perspectives for using other recent approaches, such as CAR macrophages, dendritic cell-cytokine induced killer cells and regulatory CAR-T cells to shed light on preclinical development of cell therapy and advancing cell therapy into clinic to achieve cures for RCC.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsCell- and Tissue-Based TherapyCombined Modality TherapyHumansImmunotherapyCAR-NKCAR-TCell therapyImmunotherapyRenal cell carcinoma (RCC)

Identifiers

PMID38195534
PMCPMC10775455
OpenAlexW4390767635

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.