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Antitumor immune responses induced by anthracyclin in malignant lymphoma

Antitumor immune responses induced by anthracyclin in malignant lymphoma - Antitumor immune responses in malignant lymphoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000019939
Enrollment
10
Registered
2015-11-26
Start date
2015-01-09
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

malignant lymphoma

Interventions

None listed

Sponsors

Department of Advanced Cell and Molecular Therapy Kyushu University Hospital
Lead Sponsor
Laboratory of DNA Information Analysis, Human Genome Center, The Institute of Medical Science, The University of Tokyo Project Division of ALA Advanced Medical Research, The Institute of Medical Science, The University of Tokyo Department of Immunology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama Department of Cancer Therapy and Research, Graduate School of Medical Sciences, Kyushu University
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Adult patients who receive lymphoma tissue biopsy as daily medical practice 2) Patients who understand well and can agree with this study plan by himself

Exclusion criteria

Exclusion criteria: 1) Patients diagnosed as double cancer 2) Patients whom researchers judged inappropriate as a subject

Design outcomes

Primary

MeasureTime frame
The absolute number and ratio of IFNg-producing CD8+ TILs after treatment by anthracyclin agents or other anticancer drugs.

Secondary

MeasureTime frame
The ratio and absolute number of CD8+ TILs expressing PD-1 or CD137, the ratio and count of Treg to CD4+T cells. Clinical findings (age, sex, prognosis), Blood count and biochemistry analysis. TCR clonality of above CD8+ TILs and antitumor effects of genetically modified T cells to express engineered TCR. Tumor-specific antigens obtained by exome sequencing analysis data.

Countries

Japan

Contacts

Public ContactMutsunori Murahashi

Kyushu University Hospital Department of Advanced Cell and Molecular Therapy

murahashi.mutsunori.791@m.kyushu-u.ac.jp092-642-5996

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026