ReviewEClinicalMedicine2025
Therapeutic anti-cancer vaccines: a systematic review of prospective intervention trials for common hematological malignancies.
Review in EClinicalMedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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.
Who cites it
2 citing papers in PubMed.
- Advances in molecular pathobiology of PCNSL - towards clinical implementation of novel diagnostics and therapeutics.Biomarker research · 2026Review
- Clinical development of cancer vaccines.Nature medicine · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: This review comprehensively assesses all prospective trials on anti-cancer vaccines for common hematological malignancies by analyzing trial designs, endpoints, and whether these endpoints are met across these trials. Methods: We included onco prospective clinical trials involving therapeutic anti-cancer vaccines for hematological malignancies published up to May 2025. We excluded retrospective cohort studies, case reports, non-research opinion publications, and studies not related to hematological malignancies. Information sources: Embase, MEDLINE, Web of Science Core Collection, and ClinicalTrials.gov. All the included RCTs were assessed for bias using the Cochrane Handbook for Systematic Review of Interventions, version 6.2 and Cochrane risk-of-bias tool. Results were synthesized descriptively, using frequencies (%) and medians (interquartile range [IQR]). The study protocol utilized was recorded in the PROSPERO database (Registration ID. CRD42024504780). Findings: Out of 2856 studies screened, a total of 187 studies were included. The median sample size was 18 (IQR = 20), and 33/187 (18%) studies were randomized. Most utilized primary endpoints were translational and safety, of which the endpoint was met 65/81 (80%) and 51/74 (69%) of the time, respectively. In 35/187 (19%) of the total studies included, the primary endpoint was a clinical efficacy endpoint (PFS, OS, duration of remission, cancer response) of which, 11/35 (31%) of studies met their clinical primary endpoint. Of the 33 randomized studies, 24 measured a clinical endpoint as their primary endpoint. Besides BCG administration in AML, no vaccine trial met a clinical efficacy endpoint in a randomized trial. There was not a single instance in which a vaccine product demonstrated an improvement in overall survival. The risk of bias assessment for RCTs showed most studies at low or intermediate risk of bias. Interpretation: This systematic review of all therapeutic anti-cancer vaccine trials in common hematological malignancies shows that although vaccines generally demonstrate immunogenicity, they have mostly failed to show consistent anti-cancer activity. Limitations include a lack of quantitative synthesis due to heterogeneity of assessed interventions, small sample sizes in most studies, and a lack of clear endpoint description in some studies. Funding: None. PROSPERO Registration ID. CRD42024504780.
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Registered trials
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.