Evidence map›Paper›PMID 41298491›Full record

ArticleNature communications2025

Allogeneic iPSC-derived iNKT cells in recurrent head and neck cancer: a phase 1 trial.

Tomohisa Iinuma, Tomoya Kurokawa, Takahiro Aoki, Atsushi Onodera, Tominaga Fukazawa, Daisuke Yamada, Genta Kitahara, Momoko Okoshi, Munechika Yamaguchi, Hiroko Okura and 14 more

Abstract readClinical Trial, Phase I
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Invariant Natural Killer T Cell-Based Immunotherapy Using α-Galactosylceramide-Pulsed CD14European journal of case reports in internal medicine · 2026
    Article
  9. Review
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.

Tomohisa IinumaDepartment of Otorhinolaryngology, Head and Neck Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0002-9940-5520
Tomoya KurokawaDepartment of Otorhinolaryngology, Head and Neck Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.
Takahiro AokiDepartment of Medical Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0002-9148-2871
Atsushi OnoderaResearch Institute of Disaster Medicine, Chiba University, Chiba, Japan.
Tominaga FukazawaLaboratory for Developmental Genetics, RIKEN Center for Integrative Medical Science, Kanagawa, Japan.
Daisuke YamadaLaboratory for Developmental Genetics, RIKEN Center for Integrative Medical Science, Kanagawa, Japan.ORCID 0000-0003-1590-9922
Genta KitaharaLaboratory for Developmental Genetics, RIKEN Center for Integrative Medical Science, Kanagawa, Japan.
Momoko OkoshiLaboratory for Developmental Genetics, RIKEN Center for Integrative Medical Science, Kanagawa, Japan.
Munechika YamaguchiLaboratory for Developmental Genetics, RIKEN Center for Integrative Medical Science, Kanagawa, Japan.
Hiroko OkuraLaboratory for Developmental Genetics, RIKEN Center for Integrative Medical Science, Kanagawa, Japan.
Satoko SasakiLaboratory for Developmental Genetics, RIKEN Center for Integrative Medical Science, Kanagawa, Japan.
Yoshie SasakoLaboratory for Developmental Genetics, RIKEN Center for Integrative Medical Science, Kanagawa, Japan.
Sachiko KiraLaboratory for Developmental Genetics, RIKEN Center for Integrative Medical Science, Kanagawa, Japan.
Jafar SharifLaboratory for Developmental Genetics, RIKEN Center for Integrative Medical Science, Kanagawa, Japan.
Yukio TsuchiyamaLaboratory for Developmental Genetics, RIKEN Center for Integrative Medical Science, Kanagawa, Japan.
Midori KobayashiDepartment of Medical Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Norihiko KobayashiCenter for Advanced Medicine, Chiba University Hospital, Chiba, Japan.
Takuro HorikoshiDiagnostic Radiology and Radiation Oncology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Yosuke InabaClinical Research Center, Chiba University Hospital, Chiba, Japan.
Hideki HanaokaClinical Research Center, Chiba University Hospital, Chiba, Japan.
Yoshitaka OkamotoChiba Rosai Hospital, Chiba, Japan.
Toyoyuki HanazawaDepartment of Otorhinolaryngology, Head and Neck Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.
Haruhiko KosekiLaboratory for Developmental Genetics, RIKEN Center for Integrative Medical Science, Kanagawa, Japan. haruhiko.koseki@riken.jp.ORCID 0000-0001-8424-5854
Shinichiro MotohashiDepartment of Medical Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan. motohashi@faculty.chiba-u.jp.ORCID 0000-0002-9332-3129

Funding

Japan Agency for Medical Research and Development (AMED) JP15bm0304003Japan Agency for Medical Research and Development (AMED) JP19bk0104087Japan Agency for Medical Research and Development (AMED) JP22bk0104145
6 · The paper itself

Abstract

Invariant Natural killer T (iNKT) cells exhibit cytotoxic activity and immunomodulatory functions and have gained interest in cancer immunotherapy. We conducted a phase 1, first-in human clinical trial to evaluate the safety and efficacy of clinical-grade allogeneic iNKT cells generated from induced pluripotent stem cells (iPSC-iNKT cells) in patients with recurrent head and neck cancer (jRCT2033200116). The primary endpoint was the incidence of dose-limiting toxicity (DLT). The secondary endpoints were to assess safety and efficacy, as well as to evaluate immunological dynamics. iPSC-iNKT cells were administered intra-arterially to 10 patients. One subject developed grade 3 skin rash at the second dose, identified as DLT. No other severe adverse events were observed in any patients. Tumor progression was suppressed in two patients, in whom clonal expansion of memory- and effector-phenotype CD8

Indexed as

Head and Neck NeoplasmsImmunotherapy, AdoptiveInduced Pluripotent Stem CellsNatural Killer T-CellsNeoplasm Recurrence, LocalAdultAgedCD8-Positive T-LymphocytesFemaleHumansImmunotherapyInterferon-gammaMaleMiddle AgedInterferon-gamma

Identifiers

PMID41298491
PMCPMC12749447

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.