Evidence mapPaperPMID 42507306Full record

ReviewJournal of the Egyptian National Cancer Institute2026

The promising role of engineered T lymphocytes in immunotherapy for high-grade serous ovarian carcinoma: a review of mechanisms, clinical landscape, and future strategies.

Dwi Faradina, Muhammad Rusda, Muhammad Fidel Ganis Siregar, Cut Adeya Adella, Agung Putra, Arya Tjipta Prananda, Dodi Suardi, Johny Marpaung, Felix Khosasi

Abstract readReview
In one paragraph

Review in Journal of the Egyptian National Cancer Institute, 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

9 authors.

Dwi FaradinaDepartment of Obstetrics and Gynecology, Faculty of Medicine, Universitas Sumatera Utara, Medan, Indonesia. dwifaradina@yahoo.com.ORCID http://orcid.org/0009-0001-5131-6692
Muhammad RusdaDepartment of Obstetrics and Gynecology, Faculty of Medicine, Universitas Sumatera Utara, Medan, Indonesia.ORCID http://orcid.org/0000-0002-2268-6838
Muhammad Fidel Ganis SiregarDepartment of Obstetrics and Gynecology, Faculty of Medicine, Universitas Sumatera Utara, Medan, Indonesia.ORCID http://orcid.org/0000-0002-2702-4091
Cut Adeya AdellaDepartment of Obstetrics and Gynecology, Faculty of Medicine, Universitas Sumatera Utara, Medan, Indonesia.ORCID http://orcid.org/0000-0002-6981-6441
Agung PutraStem Cell and Cancer Research (SCCR) Laboratory, Stem Cell and Cancer Research, Semarang, Indonesia.ORCID http://orcid.org/0000-0002-9822-3119
Arya Tjipta PranandaDepartment of Surgery, Faculty of Medicine, Universitas Sumatera Utara, Medan, Indonesia.ORCID http://orcid.org/0000-0002-0905-7404
Dodi SuardiDepartment of Obstetrics and Gynaecology, Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia.ORCID http://orcid.org/0000-0003-2066-9345
Johny MarpaungDepartment of Obstetrics and Gynecology, Faculty of Medicine, Universitas Sumatera Utara, Medan, Indonesia.ORCID http://orcid.org/0000-0001-5809-9814
Felix KhosasiFaculty of Medicine, Universitas Sumatera Utara, Medan, Indonesia.ORCID http://orcid.org/0009-0006-8828-861X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-grade serous ovarian carcinoma (HGSC) demonstrates poor prognosis with approximately 80% recurrence rates and significant chemotherapy resistance. Conventional checkpoint inhibitors show limited efficacy (10-15%), necessitating alternative immunotherapeutic approaches. Engineered T lymphocytes, particularly CAR-T and TCR-T cells, have emerged as promising strategies for HGSC. This literature review examines the promising role of engineered T lymphocytes in immunotherapy for HGSC. A comprehensive literature search was conducted across PubMed, Scopus, and Cochrane Library databases for peer-reviewed studies published between 2015 and 2025. Search terms included "engineered T lymphocytes," "CAR-T cells," "TCR-T cells," "ovarian cancer immunotherapy". CAR-T cells demonstrate promising preclinical antitumor activity in HGSC, with high-avidity T-cell clones showing robust efficacy. Engineered T lymphocytes demonstrate promising approaches across disease contexts. In high-grade serous ovarian carcinoma, Engineered T lymphocytes orchestrate tumor cell apoptosis through coordinated granzyme/perforin and Fas/FasL signaling, enabling rapid cytotoxic elimination of multiple tumor targets.

Indexed as

Cystadenocarcinoma, SerousImmunotherapyImmunotherapy, AdoptiveOvarian NeoplasmsT-LymphocytesAnimalsFemaleHumansCAR-T cellsImmunotherapy and cancerOvarian carcinomaTCR-T cells

Identifiers

PMID42507306
PMCPMC13407792

What Socratic holds

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LicenceCC BY
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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 Socratic graph.