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Feasibility of Lymphocyte Reinfusion in Newly Diagnosed High Grade Gliomas

Feasibility of Lymphocyte Reinfusion in Newly Diagnosed High Grade Gliomas

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01653834
Enrollment
10
Registered
2012-07-31
Start date
2012-07-31
Completion date
2014-03-31
Last updated
2018-11-07

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

Conditions

Glioblastoma

Keywords

lymphopenia

Brief summary

This research study is being done to see if lymphocytes can be collected from patients with high grade gliomas before they start standard radiation and chemotherapy. (Lymphocytes are cells that normally circulate in the blood and are an essential part of the immune system). The investigators goal is to store these and give them back to the patient after radiation is completed. This is part of a larger effort that will attempt to preserve the immune system from the effects of radiation and chemotherapy.

Detailed description

The patients blood will be collected (apheresis) before starting the patients planned standard of care radiation therapy and chemotherapy: * An IV will be inserted into the vein in the patients arm. * The blood will be sent to a machine that removes the lymphocytes and returns the rest to the patient. * This procedure will last from 1 hour and 15 minutes to 4 hours. * During this time the patient will also be treated with a blood thinner to prevent the blood from clotting in the machine. * The lymphocytes will be counted and stored. If an insufficient number were collected, we will ask for another similar collection in about 1 week. * After the patient has completed the full 6 weeks of radiation, all of the lymphocytes will be returned to the patient through a simple intravenous infusion. A larger intravenous access (i.e. midline) might be needed. Any cells that are not reinfused will be stored for 1 year and then discarded. * Study bloods (10 ml) will be collected at the time of lymphocyte collection, prior lymphocyte reinfusion, and then every 2 weeks until week 20th. These blood samples will be stored and used for future analysis. Blood counts are obtained weekly as part of standard care for patients with this kind of brain tumor. For the first 14 weeks after the lymphocyte reinfusion we will be doing some extra tests on the routinely collected blood to see how the effective the reinfused lymphocytes are in raising the patients lymphocyte counts. These results will be available to the patients treating physician. At no time will this study interfere with the patients planned standard of care radiation and chemotherapy.

Interventions

PROCEDURELymphocyte harvesting & reinfusion

Lymphocytes will be collected and stored approximately one week prior to initiating concurrent radiation therapy (RT) and temozolomide (TMZ). Two lymphocyte collections are allowed. After the patient has completed 6 weeks of RT/TMZ, all of the collected lymphocytes will be re-infused. After lymphocyte re-infusion, Heme-8 and absolute lymphocyte count (ALC) will be checked per standard of care. The absolute increase in ALC as the primary endpoint will be assessed 4 weeks after lymphocyte re-infusion.

Sponsors

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* • Age≥18 year * New diagnosed high grade glioma * Post-operative treatment with standard RT/TMZ * Karnofsky performance status ≥ 60% * Normal bone marrow function with Hematocrit ≥ 30%, platelet ≥ 100K, ANC ≥ 1000, and absolute lymphocyte count ≥ 1000 prior entry to this study. Blood product transfusions are allowed.

Exclusion criteria

* Prior radiation therapy, chemotherapy, immunotherapy or therapy with biologic agents or hormonal therapy for their brain tumor are excluded. Glucocorticoid therapy is allowed. * Fresh CNS bleed, current anticoagulation use; and anti-VEGF therapy in past 6 weeks are excluded. * Patients must not have taken an ACE inhibitor within last 24 hours prior to apheresis.

Design outcomes

Primary

MeasureTime frameDescription
the feasibility of lymphocyte harvesting and reinfusion10 weeksthis will be considered a feasible approach if 5 of the 10 patients to be accrued have an absolute lymphocyte count increase of 300 cells per mm3 at 4 weeks after reinfusion.

Secondary

MeasureTime frameDescription
the number of lymphocytes that can be harvested in this pt population10 weeksthe number of lymphocytes harvested per patient
duration of lymphocyte rise following lymphocyte reinfusion10 weekshow long will lymphocyte counts remain elevated after reinfusion
changes in lymphocyte subtypes following collection and reinfusion10 weekschanges in lymphocyte subtype between collection and reinfusion as a result of freezing for storage.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026