CpG 7909 in Treating Patients Who Have Undergone Autologous Stem Cell Transplant

Lymphoma Clinical Trial

Official title:

CPG 7909 Oligodeoxynucleotides (ODNS) After Autologous Transplantation to Enhance Immune Reconstitution

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00369291
• Other study ID #: 2003LS014
• Secondary ID: UMN-0302M41542UM
• Status: Terminated
• Phase: Phase 1
• First received: August 24, 2006
• Last updated: November 27, 2017
• Start date: September 2003
• Est. completion date: May 2010

Study information

• Verified date: November 2017
• Source: Masonic Cancer Center, University of Minnesota
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Giving CpG 7909 after an autologous stem cell transplant may make a stronger immune response and prevent or delay the recurrence of cancer.

PURPOSE: This phase I trial is studying the side effects and best dose of CpG 7909 in treating patients who have undergone autologous stem cell transplant.

Description:

OBJECTIVES:

Primary

• Determine whether CpG 7909 enhances immune function, as measured by the response to keyhole limpet hemocyanin (neo-antigen) and tetanus toxoid (memory antigen), in patients who have undergone autologous stem cell transplantation.

Secondary

• Determine if dose escalation of CpG 7909, within a range of previously tested safe doses of CpG 7909, impacts upon the primary immune readouts.

OUTLINE: This is a non-randomized, dose-escalation study of CpG 7909.

Patients receive CpG 7909 subcutaneously (SC) on days 1, 7, and 14. Patients receive keyhole limpet hemocyanin SC and tetanus toxoid SC on day 7.

Cohorts of 3-6 patients receive escalating doses of Cp6 7909 until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. A total of 10 patients are treated at the MTD.

Blood is collected at baseline and at approximately day 40 for immunological studies, including immunoenzyme techniques, antibody response assays, and immunophenotyping.

After completion of study treatment, patients are followed every 3 months for 1 year.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 19
• Est. completion date: May 2010
• Est. primary completion date: May 2010
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients must have undergone autologous transplantation for non-Hodgkin's lymphoma (NHL), Hodgkin's disease, acute myelogenous leukemia (AML), germ cell tumors, or multiple myeloma.

• Patients must be eligible for and consent to participate in study MT1999 06 - Vaccination with tetanus toxoid and Keyhole Limpet Hemocyanin (KLH) to assess antigen specific immune responses (BB-IND 10430).

• Patients will be eligible to receive CpG 7909 and vaccines on or after day 60 post transplant. No patients are eligible for this protocol beyond day 74 post transplant. Therefore, all patients will start therapy on this protocol between days 60-74 post transplant to allow for patient scheduling flexibility.

• Patients must have engraftment and be independent of transfusion support or growth factor support.

• Patients must not have received platelet or red-cell transfusions in the previous week.

• Patients must have been continuously off all growth factors for at least 1 week.

• Unsupported counts must be:

• platelets = 50,000/ml

• Hgb = 9 gm/ul

• Absolute neutrophil count = 1000/µL

• Absolute lymphocyte count = 500/µL

• Patients must have a current performance status of 0-1 (Eastern Cooperative Oncology Group) or 70-100% (Karnofsky.

• Patients must be afebrile, off antibiotics therapeutic (not prophylactic), and free of evidence of active infection. Patients must be off intravenous (IV) hyperalimentation and IV fluids.

• Minimum laboratory values within 2 weeks of entry: Creatinine = 2.0 mg/dl or CrCl = 50 ml/min, Bilirubin, ALT = 2 x normal

• Age >18 years

• Patients receiving or scheduled to receive planned radiation therapy, growth factor therapy, or steroid therapy during the study period will be ineligible. Patients must have completed all planned post-transplant radiation therapy if applicable.

• Patients must be able to give written informed consent and agree to comply with the study parameters

• Patients must agree to use contraception during the study.

Exclusion Criteria:

Patients with one or more of the following:

• Active infection, or fever >38.2°C

• Significant nonmalignant disease including documented HIV infection, uncontrolled hypertension (diastolic blood presses >115 mmHg), unstable angina, congestive heart failure (NY Class II), poorly controlled diabetes, coronary angioplasty within 6 months, myocardial infarction with the last 6 months, or uncontrolled atrial or ventricular cardiac arrhythmias.

• Hematopoietic growth factors administered within 1 week of study entry.

• Expected to require additional cytotoxic therapy within 30 days of study

• Receiving other post-transplant investigational agents

• Patients with a history of autoimmune diseases will be ineligible for this protocol

• It is unknown whether CpG 7909 may exacerbate autoimmune disorders by its immunomodulatory effects. Therefore, subjects with a history of autoimmune disease should not receive CpG 7909. Controlled thyroid disease is permissible.

• Systemic corticosteroids or other immunosuppressants

• Pregnant or lactating (It is unlikely and probably unwise that a women of childbearing potential become pregnant this early after transplant, however; if any suspicion, a pregnancy test should be done)

• Not meeting one or more of the eligibility criteria, as listed above

Related Conditions & MeSH terms

• Germ Cell Tumor
• Leukemia
• Lymphoma
• Multiple Myeloma
• Multiple Myeloma and Plasma Cell Neoplasm
• Neoplasms, Germ Cell and Embryonal
• Neoplasms, Plasma Cell
• Plasmacytoma

Intervention

Biological:
• keyhole limpet hemocyanin
KLH is a foreign protein to humans, it will be used to assess the immune response to a neo-antigen given as a single injection, 1 mg subcutaneously in the arm (per MT1999-06).
• tetanus toxoid
Tetanus toxoid booster 0.5 ml intramuscularly (IM) in the opposite arm (per MT1999-06)

Locations

Country	Name	City	State
United States	Masonic Cancer Center at University of Minnesota	Minneapolis	Minnesota

Sponsors (1)

Lead Sponsor	Collaborator
Masonic Cancer Center, University of Minnesota

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Enhanced immune function as measured by response to keyhole limpet hemocyanin and tetanus toxoid	anti-KLH IgG	1 Month after vaccine
Secondary	Impact of dose escalation of CpG 7909 on primary immune readouts	Compare primary outcome between cohorts	At study completion