Evidence map›Paper›PMID 28891906›Full record

ArticleJournal of immunotherapy (Hagerstown, Md. : 1997)2017

First-in-Human Treatment With a Dendritic Cell-targeting Lentiviral Vector-expressing NY-ESO-1, LV305, Induces Deep, Durable Response in Refractory Metastatic Synovial Sarcoma Patient.

Seth M Pollack, Hailing Lu, Sacha Gnjatic, Neeta Somaiah, Ryan B O'Malley, Robin L Jones, Frank J Hsu, Jan Ter Meulen

Open access · hybridAbstract readCase Reports
In one paragraph

Article in Journal of immunotherapy (Hagerstown, Md. : 1997), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

36 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. NY-ESO-1 antigen: A promising frontier in cancer immunotherapy.Clinical and translational medicine · 2024
    Review
  7. Article
  8. Article
  9. Review
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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

8 authors at 5 institutions in 3 countries.

Seth M Pollack*Clinical Research Division, Fred Hutchinson Cancer Research Center Department of †Medicine ¶Radiology, University of Washington, Seattle, WA ‡Immune Design, Seattle, WA, and South San Francisco, CA §Mount Sinai School of Medicine, Tisch Cancer Institute, New York, NY ∥MD Anderson Cancer Center, Houston, TX #Royal Marsden Hospital/Institute of Cancer Research, London, England.
Hailing Lu
Sacha Gnjatic
Neeta Somaiah
Ryan B O'Malley
Robin L Jones
Frank J Hsu
Jan Ter Meulen
Cancer Research Center · USIcahn School of Medicine at Mount Sinai · USRoyal Marsden Hospital · GBThe University of Texas MD Anderson Cancer Center · USUniversity of Washington · US

Funding

Adoptive T cell Therapy for Patients with NY-ESO-1 Expressing SarcomasK23CA175167 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI POLLACK, SETH M · 2013 to 2017
$859k
NCI NIH HHS K23 CA175167
6 · The paper itself

Abstract

Effective induction of antitumor T cells is a pivotal goal of cancer immunotherapy. To this end, lentiviral vectors (LV) are uniquely poised to directly prime CD8 T-cell responses via transduction of dendritic cells in vivo and have shown promise as active cancer therapeutics in preclinical tumor models. However, until now, significant barriers related to production and regulation have prevented their widespread use in the clinic. We developed LV305, a dendritic cell-targeting, integration-deficient, replication incompetent LV from the ZVex platform, encoding the full-length cancer-testis antigen NY-ESO-1. LV305 is currently being evaluated in phase 1 and 2 trials in metastatic recurrent cancer patients with NY-ESO-1 positive solid tumors as a single agent and in combination with anti-PD-L1. Here we report on the first patient treated with LV305, a young woman with metastatic, recurrent, therapy-refractive NY-ESO-1 synovial sarcoma. The patient developed a robust NY-ESO-1-specific CD4 and CD8 T-cell response after 3 intradermal injections with LV305, and subsequently over 85% disease regression that is continuing for >2.5 years posttherapy. No adverse events >grade 2 occurred. This case demonstrates that LV305 can be safely administered and has the potential to induce a significant clinical benefit and immunologic response in a patient with advanced stage cancer.

Indexed as

AdultAntigens, NeoplasmCancer VaccinesCD8-Positive T-LymphocytesDendritic CellsDrug Resistance, NeoplasmFemaleGenetic VectorsHumansImmunotherapy, AdoptiveLentivirusLung NeoplasmsMembrane ProteinsPneumonectomyProgrammed Cell Death 1 ReceptorRecurrenceAntigens, NeoplasmCancer VaccinesCTAG1B protein, humanMembrane ProteinsPDCD1 protein, humanProgrammed Cell Death 1 Receptor

Identifiers

PMID28891906
PMCPMC5733794
OpenAlexW2751401058

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.