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

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Intensive hydration to maintain high urine output was started 24 hours<br />

prior to intensification chemotherapy and continued for one week. Cyclophosphamide<br />

was infused intravenously over one hour on days 1,2, and 3.<br />

Etoposide was infused over four hours every 12 hours on days 1,2, and 3.<br />

Cisplatinwas administered over 2 hours on days 1,2, and 3.<br />

RESULTS<br />

Response<br />

Seventy-seven patients had measurable or assessable disease at the time of<br />

intensification. Three patients had no evidence of disease (NED) after surgical<br />

resection, these were not assessable for response to induction.<br />

Seventy-nine patients were treated with median 4 cycles of induction chemotherapy<br />

(77 patients with measurable disease and two NED patients). Seventy-nine<br />

percent (79%) received Adriamycin-based induction chemotherapy.<br />

Twenty-one percent (21%) were treated with Methotrexate chemotherapy combinations.<br />

Seven patients suffering early death during the intensive phase were considered<br />

treatment failures and scored as treatment related early deaths. Median duration<br />

of follow-up for the entire group of 80 patients is 83+ weeks (range, 13-<br />

283+). Median duration of follow-up for the 24 surviving patients is 172+<br />

weeks(range 74+-283+).<br />

Response to induction chemotherapy was 77%. Thirty-one percent (31%)<br />

were complete responders and 46% were partial responders. Twenty-three percent<br />

(23%) had nonresponsive stable disease.<br />

The "overall response" was defined as response in those patients with measurable<br />

disease who completed both induction and intensive phases. The three<br />

NED patients were censored from response evaluation. The "overall response"<br />

was 79%. Complete remission in 55% and partial response in 25%. Thirty-seven<br />

percent 37% of partial responders and 33% of stable disease patients to induction<br />

chemotherapy were converted to complete remission after the intensive<br />

phase.<br />

Median progression-free survival measured from beginning induction<br />

therapy is 50 weeks (95% confidence interval, 44 to 61 weeks)(Fig. 2). Median<br />

survival is 83 weeks (95% confidence interval, 68 to 110 weeks) (Fig. 3). Patients<br />

followed long term show that the progression-free interval and overall survival<br />

curves have reached a plateau after 142 weeks (2.7 years) and 180 weeks (3.5<br />

years) respectively, persisting at greater than 5 year follow-up. Characteristics of<br />

patients constituting the tail of the progression-free interval and survival curves<br />

reveal predominately one or two sites of parenchymal lung or regional nodal<br />

relapse at the time they started induction chemotherapy.<br />

Using univariate analysis, four features predicted for improved progression-free<br />

survival or overall survival. These include: (1) disease site distributed<br />

to lung or regional lymph nodes (P=.093 and .007); (2) one disease site (P=.030<br />

and .006); (3) disease-free interval (DFI) from diagnosis to detection of metastasis<br />

of greater or equal to 1 year (P=.038 and .042); (4) response to induction chemotherapy<br />

with complete response or no evidence of disease (P=.011 and .037).<br />

By multivariate analysis five variables were significant "negative" predic-<br />

Sixm INTERNATIONAL SYMPOSIUM ON AUTOLOGOUS BONE MARROW TRANSPLANTATION 119

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