Evidence map›Paper›PMID 42643436›Full record

ArticleFrontiers in immunology2026

Case Report: Primed dendritic cell immunotherapy for multiple solid tumors.

Jeffrey Jones, Aly Alrabaa, William Decker, Luis Ferbeyre, Gregorio Viramontes, Rafael Gonzalez, Elideth Angulo, Antonio Zamudio, Raul Hernandez, Stephen Noga and 7 more

Abstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 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

17 authors.

Jeffrey JonesDepartment of Urology or Immunology, Baylor College of Medicine, Houston, TX, United States.
Aly AlrabaaLong School of Medicine, University of Texas Health Science Center San Antonio, San Antonio, TX, United States.
William DeckerDepartment of Urology or Immunology, Baylor College of Medicine, Houston, TX, United States.
Luis FerbeyreImmunocine Cancer Center, Cancún, Q.R., Mexico.
Gregorio ViramontesImmunocine Cancer Center, Cancún, Q.R., Mexico.
Rafael GonzalezImmunocine Cancer Center, Cancún, Q.R., Mexico.
Elideth AnguloImmunocine Cancer Center, Cancún, Q.R., Mexico.
Antonio ZamudioImmunocine Cancer Center, Cancún, Q.R., Mexico.
Raul HernandezAmerimed Hospital, Cancún, Q.R., Mexico.
Stephen NogaImmunocine Cancer Center, Cancún, Q.R., Mexico.
Susana Hernandez-ReyesImmunocine Cancer Center, Cancún, Q.R., Mexico.
Paul ZhangOmega Precision Oncology, Houston, TX, United States.
Darryl SmithDepartment of Urology or Immunology, Baylor College of Medicine, Houston, TX, United States.
Ara KaramanianHALO Precision Diagnostics (Prostate Laser Center), Houston, TX, United States.
Luis TamaraUrology Section, Michael E DeBakey Veterans Affairs Medical Center, Houston, TX, United States.
Dalton GreenwoodImmunocine Cancer Center, Cancún, Q.R., Mexico.
Matthew HalpertImmunocine Cancer Center, Cancún, Q.R., Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many patients with advanced solid tumors ultimately develop resistance to conventional therapies, with especially limited options for those experiencing rapid progression or poor performance status, highlighting the need for personalized immunotherapies capable of inducing durable responses. In this retrospective case series, we describe the clinical course and outcomes of five adults (4 male, 1 female; median age 51 years [range, 39-62]) with metastatic solid tumors who achieved complete and durable remission following doubly loaded autologous dendritic cell therapy after failure of standard treatments, such as immune checkpoint inhibition, radiation, surgery, or endocrine therapy. Five patients, including prostate adenocarcinoma (n=1), malignant melanoma (n=2), triple-negative breast cancer (n=1), and urothelial carcinoma (n=1), were treated between July 2022 and March 2025 at a single-site referral-based immunotherapy center (Immunocine Cancer Center). Over the course of six weeks, patients received three vaccines of approximately 5-7 million modified dendritic cells injected adjacent to the lymph node draining to the tumor site. Follow-up ranged from 6 to 28 months, where radiographic response, clinical performance status, and tumor and available clinical and biological biomarkers were assessed. All five patients achieved complete radiographic remission confirmed by PET/CT or histology, with sustained responses ranging from 6 to 28 months and ongoing in all cases, and no grade 3 or higher adverse events observed. These observations support further evaluation of doubly-loaded autologous dendritic cell therapy in larger, controlled studies.

Indexed as

Cancer VaccinesDendritic CellsImmunotherapyAdultFemaleHumansMaleMelanomaMiddle AgedRetrospective StudiesTreatment OutcomeCancer Vaccinesbreast/ prostate adenocarcinomacancer immunotherapydendritic cell therapymetastatic melanomaurothelial carcinoma

Identifiers

PMID42643436
PMCPMC13503334

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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.