28.06.2014 Views

Autologous Bone Marrow Transplantation - Blog Science Connections

Autologous Bone Marrow Transplantation - Blog Science Connections

Autologous Bone Marrow Transplantation - Blog Science Connections

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

Peripheral Stem Cell <strong>Transplantation</strong> 617<br />

Cryopreservation of Apheresis-Derived Stem Cells<br />

The 200-ml cell suspension collected per run was concentrated to 100<br />

ml and mixed with the same volume of Spinner-minimum essential medium<br />

supplemented with 20% dimethyl sulfoxide. The final 200-ml cell suspension<br />

was distributed into two 100-ml polyolefine bags (DELMED, Canton, MA) and<br />

frozen to -100°C in a computerized freezer (CRYOSON BV-6, Cryoson<br />

Deutschland GmbH, Schollkrippen, West Germany). The frozen cells were<br />

stored in the liquid phase of nitrogen until use.<br />

Thawing and Transplanting Apheresis-Derived Stem Cells<br />

The frozen bags were thawed by immersing them into a 40°C water bath.<br />

The cell suspension was immediately injected into the patient using a central<br />

line. Postthaw washing and spinning of cells was avoided to minimize the risk<br />

of cell clumping and stem cell loss. The total volume of cell suspension<br />

injected into the patient was in the range of 1500 ml and was given over 2<br />

hours. Forced diuresis was started after infusing 500 ml. The transfusion of<br />

the remaining free hemoglobin transiently impaired renal function (creatinine<br />

was raised to 2.0-2.5 mg/dl for 24-48 hours). In our experience this<br />

procedure produced no major risk to the patient, nor did the infusion of a<br />

cooled 6°C-8°C cell suspension into the right atrium of the heart cause any<br />

cardiac arrhythmia.<br />

Regimen 1<br />

Pretransplant Conditioning Regimens<br />

Total body irradiation (TBI) using a linear accelerator, superfractionated<br />

over 4 days at 120 cGy single dose up to a total of 1320-1440 cGy (lungs, 900<br />

cGy). Three single doses were administered per day at 8 AM., noon, and 4 P.M..<br />

Following TBI, cyclophosphamide (50 mg/kg) was given on each of 4<br />

consecutive days (total dose 200 mg/kg) (patients 1, 3, and 6).<br />

Regimen 2<br />

TBI, superfractionated over 3 days up to a total of 1200 cGy, followed by a<br />

single dose of melphalan (120 mg/m 2 ) (patient 4).<br />

Regimen 3<br />

Cyclophosphamide (1.5 g/m 2<br />

x 4), carmustine (300 mg/m 2 ), and<br />

etoposide (125 mg/m 2 x 3) (CBV regimen [22]) (patient 2).<br />

Regimen 4<br />

Mitoxantrone (12 mg/m 2<br />

x 2 days), carmustine (300 mg/m 2 ), and<br />

etoposide (125 mg/m 2 x 3 days) (patient 5).

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!