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

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1.2 Description of the study<br />

The treatment plan was the following:<br />

- Cyto-reductive surgery as wide as possible on day 0.<br />

- <strong>Bone</strong> marrow harvest on d21:l x 108 mononuclear cells/kg were harvested.<br />

A buffy coat was performed to reduce the volume to 100-150 ml. The<br />

marrow was then stored at 4° C.<br />

- On the afternoon of marrow harvest, high dose BCNU (800 mg/ m2) was<br />

administered over a 2-hour infusion.<br />

- The patient was discharged from the hospital on the following day.<br />

- Monitoring was organized on an out-patient basis with one weekly blood<br />

count, hepatic and renal biology, physical staging and chest X-ray.<br />

- Radiation therapy was scheduled approximately on day 45. The total delivered<br />

dose was 45 Gy in 19 days, using the 18 MV energy of a linear accelerator:<br />

24 Gy in 8 fractions to the whole subtentorial brain, followed by a localized<br />

boost of 21 Gy in 7 fractions to the tumor or tumor bed. Every radiotherapy field<br />

was designed using the dosimetry CT scan planning system.<br />

- Overall survival was chosen as the main evaluation criteria.<br />

- The first 16 treated patients also received an early post-operative chemotherapy<br />

given on day 3 after histology confirmation, combining. VM 26,150<br />

mg/m 2<br />

, BCNU, 100 mg/m 2<br />

in a 5 mn IV short infusion, through a peripheral<br />

venous access. PROCARBAZINE (day 3 to 10), 100 mg/m2/day, per os. This<br />

part of the chemotherapy program was deleted in March 1987 after the 16 first<br />

patients because of the difficulty of feasibility.<br />

2. Results<br />

2.1 Evaluation of the toxicity<br />

The toxicity observed in the 103 patients is similar to the first observations<br />

we presented and much lower in the most recently treated patients.<br />

2.1.1 <strong>Bone</strong> marrow harvest<br />

Following general anesthesia for bone marrow harvest, 3 of the first patients<br />

experienced a decrease of consciousness and enhancement of neurologic impairment<br />

or cranial hyperpressure which was suspected to be related to hydration<br />

administered during general anesthesia. The next patients received furosemide<br />

at the end of anesthesia and did not experienced these symptoms.<br />

2.1.2 Hematological toxicity<br />

Hematologic toxicity remained mild: 9 % of the patients experienced a grade<br />

4 aplasia for neutrophil (PMNN) and 6% for WBC. Grade 3 toxicity was observed<br />

in 16% of the patients for PMNN and in 21% for WBC. Thrombopenia<br />

grade 4 was observed in 10% of patients, grade 3 in 18% and grade 0,1 or 2 in 72<br />

%. For patients with grade 3 or 4, the mean duration of thrombopenia is 10 days.<br />

Nadir for WBC, neutrophils is on the second week while nadir for platelets on<br />

the third week.<br />

2.1.3 Extrahematological toxicity<br />

Immediate tolerance of BCNU was good. Nausea and vomiting were mild:<br />

31 grade 0,58 grade 1 and 2,9 grade 3.<br />

226 SIXTH INTERNATIONAL SYMPOSIUM ON AUTOLOGOUS BONE MARROW TRANSPLANTATION

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