18.01.2013 Views

VI Autologous Bone Marrow Transplantation.pdf - Blog Science ...

VI Autologous Bone Marrow Transplantation.pdf - Blog Science ...

VI Autologous Bone Marrow Transplantation.pdf - Blog Science ...

SHOW MORE
SHOW LESS

Create successful ePaper yourself

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

TOXICITY<br />

Preparation Regimen<br />

The preparative regimens were generally well-tolerated. Most patients experienced<br />

mild to moderate nausea and vomiting during the administration of<br />

chemotherapy and fTBI. Mucositis was moderate to severe. Diarrhea was experienced<br />

by the majority of patients in the first two weeks after TBI. Almost all<br />

patients became febrile during the period of marrow hypoplasia and leukopenia<br />

and required multiple parenteral antibiotics including amphotericin B.<br />

Eight patients died within two months of ABMT while in the recovery<br />

phase. Six patients died from overwhelming sepsis despite aggressive antimicrobial<br />

therapy, one from hemorrhagic complications due to refractoriness to platelet<br />

transfusions, and one from pulmonary and hepatic failure.<br />

<strong>Marrow</strong> Infusion<br />

The infusion of bone marrow was well-tolerated. Patients were<br />

premedicated with acetaminophen, diphenhydramine and hydrocortisone. Hydration<br />

at 1.5 - 2 times maintenance was maintained for 24 hours with marrow<br />

infusion. Blood pressure and cardiac monitoring were carried out during bone<br />

marrow infusion.<br />

Five patients required a second infusion of MAb-treated marrow when engraftment<br />

appeared delayed. In each case, a moderately severe reaction occurred.<br />

In one patient this was manifest as hypotension associated with syncope.<br />

In the other patients, respiratory distress associated with pulmonary infiltrates<br />

developed several hours after the infusion. Each patient was treated with aggressive<br />

fluid and corticosteroid therapy, and all reactions were reversed without<br />

sequellae. No patient required intubation and mechanical ventilation. In<br />

each case engraftment followed the infusion of the treated "back-up" bone marrow.<br />

None of the patients with prolonged thrombopenia received "back-up"<br />

marrow.<br />

CFUS<br />

The effect of the MAb and C treatment on CFUS was determined by culture<br />

of cells in methylcellulose. The median recovery of CFU-GM progenitor cells<br />

was 38% (range 22-150) for the first CR group, 48% (range 1-190) for the second/<br />

third CR group and 87% (range 58-248) for the relapse group. Median recovery<br />

of BFU-E was 49% (range 29-136) for the first CR group, 69% (range 1-2500) for<br />

the second/third CR group and 100% (range 0-392) for the relapse group. Median<br />

recovery of CFU-MIX was 50% (range 17-60) for the first CR group, 37%<br />

(range 0-381) for the second/third CR group and 13% (range 0-249) for the relapse<br />

group.<br />

Engraftment<br />

A median number of 4.0 x 10 7<br />

cells/kg body weight (range 2.30 x 10 7<br />

to 8.23<br />

x 10 7<br />

) were infused into each first CR patient. The median number of cells transfused<br />

into the second/third CR group was 2.80 x 107 (range 7.50 x 10 6<br />

to 1.16 x<br />

10 s<br />

). A median number of 4.10 x 10 7<br />

cells/kg body weight (range 2.38 x 10 7<br />

to<br />

5.96 x 10 8<br />

) were infused into each first relapse patient.<br />

SIXTH INTERNATIONAL SYMPOSIUM ON AUTOLOGOUS BONE MARROW TRANSPLANTATION 23

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

Saved successfully!

Ooh no, something went wrong!