Evidence map›Paper›PMID 28344888›Full record

ArticleOncoimmunology

Pre-emptive and therapeutic adoptive immunotherapy for nasopharyngeal carcinoma: Phenotype and effector function of T cells impact on clinical response.

Corey Smith, Victor Lee, Andrea Schuessler, Leone Beagley, Sweera Rehan, Janice Tsang, Vivian Li, Randal Tiu, David Smith, Michelle A Neller and 11 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 6% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
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  5. Article
  6. Adoptive T-cell therapy for virus-associated diseases.Clinical microbiology reviews · 2025
    Review
  7. Novel Therapeutic Development for Nasopharyngeal Carcinoma.Current oncology (Toronto, Ont.) · 2025
    Review
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  9. Review
  10. Article
  11. Article
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  13. Article
  14. Article
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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

21 authors at 6 institutions in 5 countries.

Corey SmithQIMR Berghofer Centre for Immunotherapy and Vaccine Development and Tumour Immunology Laboratory, Department of Immunology, QIMR Berghofer Medical Research Institute , Brisbane, Queensland, Australia.
Victor LeeDepartment of Clinical Oncology, Queen Mary Hospital, The University of Hong Kong , Hong Kong.
Andrea SchuesslerQIMR Berghofer Centre for Immunotherapy and Vaccine Development and Tumour Immunology Laboratory, Department of Immunology, QIMR Berghofer Medical Research Institute , Brisbane, Queensland, Australia.
Leone BeagleyQIMR Berghofer Centre for Immunotherapy and Vaccine Development and Tumour Immunology Laboratory, Department of Immunology, QIMR Berghofer Medical Research Institute , Brisbane, Queensland, Australia.
Sweera RehanQIMR Berghofer Centre for Immunotherapy and Vaccine Development and Tumour Immunology Laboratory, Department of Immunology, QIMR Berghofer Medical Research Institute , Brisbane, Queensland, Australia.
Janice TsangDepartment of Clinical Oncology, Queen Mary Hospital, The University of Hong Kong , Hong Kong.
Vivian LiDepartment of Clinical Oncology, Queen Mary Hospital, The University of Hong Kong , Hong Kong.
Randal TiuDepartment of Clinical Oncology, Queen Mary Hospital, The University of Hong Kong , Hong Kong.
David SmithQIMR Berghofer Centre for Immunotherapy and Vaccine Development and Tumour Immunology Laboratory, Department of Immunology, QIMR Berghofer Medical Research Institute , Brisbane, Queensland, Australia.
Michelle A NellerQIMR Berghofer Centre for Immunotherapy and Vaccine Development and Tumour Immunology Laboratory, Department of Immunology, QIMR Berghofer Medical Research Institute , Brisbane, Queensland, Australia.
Katherine K MatthewsQIMR Berghofer Centre for Immunotherapy and Vaccine Development and Tumour Immunology Laboratory, Department of Immunology, QIMR Berghofer Medical Research Institute , Brisbane, Queensland, Australia.
Emma GostickInstitute of Infection and Immunity, Cardiff University School of Medicine , Cardiff, UK.
David A PriceInstitute of Infection and Immunity, Cardiff University School of Medicine, Cardiff, UK; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Jacqueline BurrowsQIMR Berghofer Centre for Immunotherapy and Vaccine Development and Tumour Immunology Laboratory, Department of Immunology, QIMR Berghofer Medical Research Institute , Brisbane, Queensland, Australia.
Glen M BoyleQIMR Berghofer Centre for Immunotherapy and Vaccine Development and Tumour Immunology Laboratory, Department of Immunology, QIMR Berghofer Medical Research Institute , Brisbane, Queensland, Australia.
Daniel ChuaComprehensive Oncology Centre, Hong Kong Sanatorium Hospital , Hong Kong.
Benedict PanizzaDepartment of Otolaryngology-Head and Neck Surgery, The Princess Alexandra Hospital, University of Queensland , Brisbane, Queensland, Australia.
Sandro V PorcedduDepartment of Otolaryngology-Head and Neck Surgery, The Princess Alexandra Hospital, University of Queensland , Brisbane, Queensland, Australia.
John NichollsDepartment of Pathology, Queen Mary Hospital, The University of Hong Kong , Hong Kong.
Dora KwongDepartment of Clinical Oncology, Queen Mary Hospital, The University of Hong Kong , Hong Kong.
Rajiv KhannaQIMR Berghofer Centre for Immunotherapy and Vaccine Development and Tumour Immunology Laboratory, Department of Immunology, QIMR Berghofer Medical Research Institute , Brisbane, Queensland, Australia.
QIMR Berghofer Medical Research Institute · AUQueen Mary Hospital · CNUniversity of Hong Kong · HKCardiff University · GBThe University of Queensland · AUHong Kong Sanatorium and Hospital · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adoptive T cell therapy has emerged as a powerful strategy to treat human cancers especially haematological malignancies. Extension of these therapies to solid cancers remains a significant challenge especially in the context of defining immunological correlates of clinical responses. Here we describe results from a clinical study investigating autologous Epstein-Barr virus (EBV)-specific T cells generated using a novel AdE1-LMPpoly vector to treat patients with nasopharyngeal carcinoma (NPC) either pre-emptively in at-risk patients with no or minimal residual disease (N/MRD) or therapeutically in patients with active recurrent/metastatic disease (ARMD). Tolerability, safety and efficacy, including progression-free survival (PFS) and overall survival (OS), were evaluated following adoptive T-cell immunotherapy. Twenty-nine patients, including 20 with ARMD and nine with N/MRD, successfully completed T-cell therapy. After a median follow-up of 18.5 months, the median PFS was 5.5 months (95% CI 2.1 to 9.0 months) and the median OS was 38.1 months (95% CI 17.2 months to not reached). Post-immunotherapy analyses revealed that disease stabilization in ARMD patients was significantly associated with the functional and phenotypic composition of

Indexed as

Adoptive immunotherapyEpstein-Barr virusnasopharyngeal carcinomasafetyT cells

Identifiers

PMID28344888
PMCPMC5353921
OpenAlexW2571281044

What OpenQuestion holds

Textmetadata
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.