Evidence map›Paper›PMID 33916194›Full record

ArticleCancers2021

Clinical Activity of an hTERT-Specific Cancer Vaccine (Vx-001) in "Immune Desert" NSCLC.

Ioannis S Pateras, Athanasios Kotsakis, Margaritis Avgeris, Evangelia Baliou, Panagiotis Kouroupakis, Eleni Patsea, Vassilis Georgoulias, Jeanne Menez-Jamet, Jean-Pierre Kinet, Kostas Kosmatopoulos

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Therapeutic vaccines for advanced non-small cell lung cancer.The Cochrane database of systematic reviews · 2024
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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 8 institutions in 3 countries.

Ioannis S PaterasDepartment of Histology and Embryology, Medical School, National and Kapodistrian University of Athens, 11527 Athens, Greece.
Athanasios KotsakisDepartment of Medical Oncology, University General Hospital of Larissa, 41110 Larissa, Greece.
Margaritis AvgerisLaboratory of Clinical Biochemistry-Molecular Diagnostics, 2nd Department of Pediatrics, School of Medicine, National and Kapodistrian University of Athens, 11527 Athens, Greece.ORCID 0000-0002-2135-9886
Evangelia BaliouDepartment of Pathology, Athens Medical Center, 15126 Marousi, Greece.
Panagiotis KouroupakisDepartment of Hematology, Sismanogleion General Hospital of Athens, 15126 Marousi, Greece.
Eleni PatseaDepartment of Pathology, Metropolitan Hospital, 18547 Cholargos, Greece.
Vassilis GeorgouliasHellenic Oncology Research Group, 11474 Athens, Greece.
Jeanne Menez-JametVaxon Biotech, 75005 Paris, France.
Jean-Pierre KinetVaxon Biotech, 75005 Paris, France.
Kostas KosmatopoulosVaxon Biotech, 75005 Paris, France.
National and Kapodistrian University of Athens · GRVaxon Biotech (France) · FRAthens Medical Center · GRHarvard University · USHellenic Oncology Research Group · GRMetropolitan Hospital · GRSismanoglio General Hospital · GRUniversity Hospital of Larissa · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTumors can be separated into immunogenic/hot and non-immunogenic/cold on the basis of the presence of tumor-infiltrating lymphocytes (TILs), the expression of PD-L1 and the tumor mutation burden (TMB). In immunogenic tumors, TILs become unable to control tumor growth because their activity is suppressed by different inhibitory pathways, including PD-1/PD-L1. We hypothesized that tumor vaccines may not be active in the immunosuppressive microenvironment of immunogenic/hot tumors while they could be efficient in the immune naïve microenvironment of non-immunogenic/cold tumors.

methodsThe randomized phase II Vx-001-201 study investigated the effect of the Vx-001 vaccine as maintenance treatment in metastatic non-small cell lung cancer (NSCLC) patients. Biopsies from 131 (68 placebo and 63 Vx-001) patients were retrospectively analyzed for PD-L1 expression and TIL infiltration. TILs were measured as tumor-associated immune cells (TAICs), CD3-TILs, CD8-TILs and granzyme B-producing TILs (GZMB-TILs). Patients were distinguished into PD-L1(+) and PD-L1(-) and into TIL high and TIL low.

findingsThere was no correlation between PD-L1 expression and Vx-001 clinical activity. In contrast, Vx-001 showed a significant improvement of overall survival (OS) vs. placebo in TAIC low (21 vs. 8.1 months,

conclusionsThese results support the hypothesis that Vx-001 may be efficient in patients with non-immunogenic/cold but not with immunogenic/hot tumors.

Indexed as

cancer vaccinesgranzyme Bimmunologically cold tumorsmetastatic non-small cell lung cancertumor-infiltrating lymphocytesVx-001

Identifiers

PMID33916194
PMCPMC8037524
OpenAlexW3150824583

What OpenQuestion holds

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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.