Prophylactic Peripheral Blood Stem Cell Collection in Patients with Extensive Bone-Marrow Infiltration of Neuroendocrine Tumours Prior to Peptide Receptor Radionuclide Therapy with 177Lu-DOTATATE.
Amir SabetNicolai MaderJörg Thomas BittenbringFadi KhreishFrank GrünwaldHans Jürgen BiersackSamer EzziddinPublished in: Pharmaceuticals (Basel, Switzerland) (2021)
Peptide receptor radionuclide therapy (PRRT) of metastatic neuroendocrine tumors (NET) can be successfully repeated but may eventually be dose-limited. Since 177Lu-DOTATATE dose limitation may come from hematological rather than renal function, hematological peripheral blood stem cell backup might be desirable. Here, we report our initial experience of peripheral blood stem-cell collection (PBSC) in patients with treatment-related cytopenia and therefore high risk of bone-marrow failure. Five patients with diffuse bone-marrow infiltration of NET and relevant myelosuppression (≥grade 2) received PBSC before one PRRT cycle with 177Lu-DOTATATE (7.6 ± 0.8 GBq/cycle). Standard stem-cell mobilization with Granulocyte-colony stimulating factor (G-CSF) was applied, and successful PBSC was defined as a collection of >2 × 106/kg CD34+ cells. In case of initial failure, Plerixafor was administered in addition to G-CSF prior to apheresis. PBSC was successfully performed in all patients with no adverse events. Median cumulative activity was 44.8 GBq (range, 21.3-62.4). Three patients had been previously treated with PRRT, two of which needed the addition of Plerixafor for stem-cell mobilization. Only one of five patients required autologous peripheral blood stem-cell transplantation during the median follow up time of 28 months. PBSC collection seems to be feasible in NET with bone-marrow involvement and might be worth considering as a backup strategy prior to PRRT, in order to overcome dose-limiting bone-marrow toxicity.
Keyphrases
- bone marrow
- peripheral blood
- stem cells
- neuroendocrine tumors
- mesenchymal stem cells
- stem cell transplantation
- end stage renal disease
- newly diagnosed
- ejection fraction
- pet ct
- cell therapy
- chronic kidney disease
- squamous cell carcinoma
- small cell lung cancer
- high dose
- prognostic factors
- peritoneal dialysis
- oxidative stress
- smoking cessation
- low dose
- cerebrospinal fluid
- patient reported
- drug induced
- combination therapy
- oxide nanoparticles
- replacement therapy