Evidence map›Paper›PMID 32753545›Full record

Trial reportJournal for immunotherapy of cancer2020

Tumor infiltrating lymphocytes (TIL) therapy in metastatic melanoma: boosting of neoantigen-specific T cell reactivity and long-term follow-up.

Joost H van den Berg, Bianca Heemskerk, Nienke van Rooij, Raquel Gomez-Eerland, Samira Michels, Maaike van Zon, Renate de Boer, Noor A M Bakker, Annelies Jorritsma-Smit, Marit M van Buuren and 14 more

Open access · goldAbstract readClinical Trial, Phase IClinical Trial, Phase II
In one paragraph

Trial report in Journal for immunotherapy of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed, 3 pooled it
7.8field-weighted citation impact, top 2% 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

106 citing papers in PubMed, 3 syntheses or guidelines pooled it, 189 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. A systematic review of immunotherapy in high-grade glioma: learning from the past to shape future perspectives.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Pooled it
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  11. Molecular origin, discovery, validation and application of neoantigens.Asian journal of pharmaceutical sciences · 2026
    Review
  12. IL-2 Free Expansion of T Cells with Immunofilaments.Advanced healthcare materials · 2026
    Article
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  19. Article
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46 more citing papers are in PubMed but not listed here.

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

24 authors at 3 institutions in 3 countries.

Joost H van den BergBioTherapeutics Unit, Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0002-4928-8397
Bianca HeemskerkDivision of Molecular Oncology and Immunology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Nienke van RooijDivision of Molecular Oncology and Immunology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Raquel Gomez-EerlandDivision of Molecular Oncology and Immunology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Samira MichelsDivision of Molecular Oncology and Immunology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Maaike van ZonBioTherapeutics Unit, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Renate de BoerBioTherapeutics Unit, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Noor A M BakkerBioTherapeutics Unit, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Annelies Jorritsma-SmitDivision of Molecular Oncology and Immunology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Marit M van BuurenDivision of Molecular Oncology and Immunology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Pia KvistborgDivision of Molecular Oncology and Immunology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Hergen SpitsAIMM Therapeutics, Amsterdam, The Netherlands.
Remko SchotteAIMM Therapeutics, Amsterdam, The Netherlands.
Henk MalloDepartment of Medical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Matthias KargerDepartment of Medical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Joris A van der HageDepartment of Surgery, Leiden Universitair Medisch Centrum, Leiden, Zuid-Holland, The Netherlands.
Michel W J M WoutersSurgical Oncology, Antoni van Leeuwenhoek Nederlands Kanker Instituut, Amsterdam, The Netherlands.
Loes M PronkDepartment of Biometrics, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Marnix H Geukes FoppenDepartment of Medical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Christian U BlankDepartment of Medical Oncology, Netherlands Cancer Institute, Amsterdam, Noord-Holland, The Netherlands.
Jos H BeijnenDepartment of Pharmacy & Pharmacology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Bastiaan NuijenDepartment of Pharmacy & Pharmacology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Ton N SchumacherDivision of Molecular Oncology and Immunology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
John B A G HaanenDivision of Molecular Oncology and Immunology, Netherlands Cancer Institute, Amsterdam, The Netherlands j.haanen@nki.nl.
The Netherlands Cancer Institute · NLAIMM Therapeutics (Netherlands) · NLUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment of metastatic melanoma with autologous tumor infiltrating lymphocytes (TILs) is currently applied in several centers. Robust and remarkably consistent overall response rates, of around 50% of treated patients, have been observed across hospitals, including a substantial fraction of durable, complete responses. PURPOSE: Execute a phase I/II feasibility study with TIL therapy in metastatic melanoma at the Netherlands Cancer Institute, with the goal to assess feasibility and potential value of a randomized phase III trial. EXPERIMENTAL: Ten patients were treated with TIL therapy. Infusion products and peripheral blood samples were phenotypically characterized and neoantigen reactivity was assessed. Here, we present long-term clinical outcome and translational data on neoantigen reactivity of the T cell products.

resultsFive out of 10 patients, who were all anti-PD-1 naïve at time of treatment, showed an objective clinical response, including two patients with a complete response that are both ongoing for more than 7 years. Immune monitoring demonstrated that neoantigen-specific T cells were detectable in TIL infusion products from three out of three patients analyzed. For six out of the nine neoantigen-specific T cell responses detected in these TIL products, T cell response magnitude increased significantly in the peripheral blood compartment after therapy, and neoantigen-specific T cells were detectable for up to 3 years after TIL infusion.

conclusionThe clinical results from this study confirm the robustness of TIL therapy in metastatic melanoma and the potential role of neoantigen-specific T cell reactivity. In addition, the data from this study supported the rationale to initiate an ongoing multicenter phase III TIL trial.

Indexed as

AdultAgedFemaleFollow-Up StudiesHumansLymphocytes, Tumor-InfiltratingMaleMelanomaMiddle AgedT-Lymphocytesimmunotherapy, adoptivelymphocytes, tumor-infiltratingmelanoma

Identifiers

PMID32753545
PMCPMC7406109
OpenAlexW3047394062

What OpenQuestion holds

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Registered trials

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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.