Human Leukocyte Antigen-A*2402-Restricted Tumor Vessel Specific Peptide Vaccination for Advanced Pancreatic Cancer
Information source: Tokyo University
Information obtained from ClinicalTrials.gov on November 03, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Pancreatic Cancer; Pancreas Neoplasms; Cancer of Pancreas; Neoplasms, Pancreatic; Pancreas Cancer
Intervention: VEGFR1-A24-1084 (SYGVLLWEI) (Biological)
Phase: Phase 1/Phase 2
Status: Recruiting
Sponsored by: Tokyo University Official(s) and/or principal investigator(s): Naohide Yamashita, MD, PhD, Study Director, Affiliation: Director, Research Hospital, Institute of Medical Science, Tokyo University
Overall contact: Hitomi Nagayama, MD,PhD, Phone: 81-3-5449-5772, Ext: 75185, Email: zephyrus@ims.u-tokyo.ac.jp
Summary
Feasibility and efficacy of combined modality intervention using chemotherapeutic agent
gemcitabine with anti-angiogenic peptide vaccination targeting VRGFR1 should be determined in
case of advanced/inoperable or therapy-resistant pancreatic cancer patients.
Gemcitabine 1,000mg/m2 BSA will be administered on day1, day8, day15, day29, day36, day43,
respectively.
HLA-A*2402-restricted VEGFR1-derived peptide (VEGFR1-A24-1084; SYGVLLWEI) emulsified with
Montanide ISA51 will be subcutaneously injected twice weekly for 8weeks (total 16 doses).
Clinical Details
Official title: Phase Ⅰ/Ⅱ Trial of Human Leukocyte Antigen (HLA)-A*2402-Restricted Vascular Endothelial Growth Factor Receptor 1 (VEGFR1)-Derived Peptide Vaccination Combined With Gemcitabine for Advanced Pancreatic Cancer
Study design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
Primary outcome: PhaseⅠ; safety (NCI CTCAE v.3)
PhaseⅡ;time to progression (RECIST)
Secondary outcome: Immune response (ELISPOT, Perforin/FoxP3 FACS, in vitro CTL assay etc.)Tumor regression(Imaging study, tumor marker, etc.)
Detailed description:
HLA-A*2402-restricted cytotoxic T lymphocyte (CTL) clones were obtained from healthy
volunteer donor peripheral blood.
These CTL clones showed potent cytotoxicities selectively against VEGFR1-expressing target
cells in HLA-class I-restricted manner.
Eligibility
Minimum age: 20 Years.
Maximum age: 85 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Heterozygote or homozygote of HLA-A*2402 allele
- Inoperable or recurrent pancreatic cancer with or without any prior therapy
- Difficult to continue the prior therapy due to treatment-related toxicities
- ECOG performance status 0-2
- Evaluable primary or metastatic lesion with RECIST criteria
- Clearance period from prior therapy more than 4 weeks
- Life expectancy more than 3 months
- Laboratory values as follows 2,000/μL100,000/μL
AST<150IU/L ALT<150IU/L Total bilirubin<3. 0mg/dl Serum creatinine<3. 0mg/dl
Exclusion Criteria:
- Pregnancy (refusal or inability to use effective contraceptives)
- Breastfeeding
- Active or uncontrolled infection
- Systemic use of corticosteroids or immunosuppressants
- Uncontrollable brain metastasis and/or meningeal infiltration
- Unhealed external wound
- Possibilities of complicated paralytic ileus or interstitial pneumonitis
- Decision of not eligible determined by principal investigator or attending doctor
Locations and Contacts
Hitomi Nagayama, MD,PhD, Phone: 81-3-5449-5772, Ext: 75185, Email: zephyrus@ims.u-tokyo.ac.jp
Research Hospital, The Institute of Medical Science, The University of Tokyo, Minato-ku, Tokyo 108-8639, Japan; Recruiting Hitomi Nagayama, MD,PhD, Principal Investigator
Additional Information
Related publications: Ishizaki H, Tsunoda T, Wada S, Yamauchi M, Shibuya M, Tahara H. Inhibition of tumor growth with antiangiogenic cancer vaccine using epitope peptides derived from human vascular endothelial growth factor receptor 1. Clin Cancer Res. 2006 Oct 1;12(19):5841-9. Nagayama H, Sato K, Morishita M, Uchimaru K, Oyaizu N, Inazawa T, Yamasaki T, Enomoto M, Nakaoka T, Nakamura T, Maekawa T, Yamamoto A, Shimada S, Saida T, Kawakami Y, Asano S, Tani K, Takahashi TA, Yamashita N. Results of a phase I clinical study using autologous tumour lysate-pulsed monocyte-derived mature dendritic cell vaccinations for stage IV malignant melanoma patients combined with low dose interleukin-2. Melanoma Res. 2003 Oct;13(5):521-30.
Starting date: May 2008
Ending date: April 2009
Last updated: May 22, 2008
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