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Clinical study of a combined use of EGFR-TKI and autologous lymphocyte-activated killer cells (LAK) therapy for advanced non-small cell lung cancer.

Clinical study of a combined use of EGFR-TKI and autologous lymphocyte-activated killer cells (LAK) therapy for advanced non-small cell lung cancer. - Clinical study of a combined use of EGFR-TKI and autologous lymphocyte-activated killer cells (LAK) therapy for advanced non-small cell lung cancer.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000001966
Enrollment
10
Registered
2009-05-13
Start date
2009-05-01
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

non-small cell lung cancer

Interventions

Autologous Lymphocyte-Activated Killer cells (LAK) are injected on day0,day14,day28,day42,day56,day70. EGFR-TKI regulated dosage,regimen/day,oral daily.

Sponsors

Juntendo University, School of Medicine
Lead Sponsor
Seta Clinic Group
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Non-small cell lung cancer patients who are judged SD or PD for EGFR-TKI therapy based on RECIST Patients who have measurable lesion -Performance Status is 0-1 -Life-expectancy is more than 4 months. -No serious abnormality in bone marrow, liver and/or renal functions

Exclusion criteria

Exclusion criteria: Patients who have: -Previous history of hypersensitivity to EGFR-TKI -Uncontrolled infections -Active autoimmune diseases -Serious cardiac disease -Continuous systemic administration of steroids. -Other cancer who are pregnant, to be pregnant, or nursing mothers, and whom principle investigator or co-investigator judged to be inappropriate to participate in this study.

Design outcomes

Primary

MeasureTime frame
Antitumor effect

Secondary

MeasureTime frame
Progression-free survival Overall survival Survival rate Improvement of tumor-related markers QOL(FACT-BRM) Safety

Countries

Japan

Contacts

Public ContactYoshiteru Morio

Juntendo University, School of Medicine Department of Respiratory Medicine

ymorio@juntendo.ac.jp03-5802-1063

Outcome results

None listed

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