Overview

In-Human CXCR4 Imaging of Blood Cancers Using [68Ga]-Pentixafor-PET

Status:
Recruiting
Trial end date:
2023-10-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to determine the uptake of the imaging agent [68Ga]-pentixafor with PET/CT scans in people with monoclonal gammopathy of undetermined significance (MGUS), smoldering multiple myeloma (SMM), and non-Hodgkin lymphoma (NHL).
Phase:
Early Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Memorial Sloan Kettering Cancer Center
Criteria
Inclusion Criteria:

Twenty patients with histologically proven treatment-naïve, therapy-refractory or relapsed
blood cancers meeting the below criteria will be included:

- Indolent B- or T-cell Non-Hodgkin lymphoma (including cutaneous lymphomas) and
measurable disease according to Lugano criteria

- MGUS/SMM according to IMWG definitions

- Age ≥18

- Negative serum pregnancy test for female volunteers of childbearing age and potential
(as defined by MSKCC Standards & Guidelines) from assays obtained <2 weeks prior to
study enrollment/intervention; or negative urine pregnancy test performed on the day
of intervention

- MSKCC patients

Exclusion Criteria:

- Breast-feeding

- History of renal functional disorders (chronic kidney disease with eGFR<30)

- Refusal or inability to tolerate the scanning procedure (e.g., due to claustrophobia)

- CNS lymphoma