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Abonour et al. 393<br />

DFS by Prognostic Category<br />

o.o v 10 20 30<br />

Category<br />

Good<br />

Intermediate<br />

Months of DFS<br />

cnsr<br />

22<br />

3<br />

event<br />

10<br />

14<br />

40<br />

tot<br />

32<br />

17<br />

1<br />

I 1<br />

50<br />

median<br />

Figure 1 • Disease-free survival based on prognostic category. Scores were calculate<br />

giving 1 point each for progressive or refractory disease before HDCT <strong>and</strong> 2 points fo<br />

absolute refractory disease or HCG >1000 before HDCT. 17<br />

7.2<br />

T<br />

60<br />

Thirty-two patients had a sco<br />

ofO (good risk category), <strong>and</strong> 17 patients scored 1-2 (intermediate risk group). Median s<br />

vival was Hot reached for the good category group.<br />

is of interest that six of the nine patients who had a partial response to first-line<br />

therapy <strong>and</strong> persistent elevation of their tumor marker were cured after HDCT,<br />

while one of the four patients who were cisplatin refractory was cured. Based on<br />

the multivariate analysis of prognostic factors, 32 patients were in the good<br />

category group <strong>and</strong> 17 patients were in the intermediate group (Fig. 1) According<br />

to this prognostic model, 1 point is given for progressive or refractory disease<br />

before high-dose chemotherapy <strong>and</strong> 2 points for absolute refractory disease or<br />

HCG >1000 before HDCT. Of the 32 patients in the low-risk category, 72% are<br />

currently free of disease compared with only 29% of those in the intermediate<br />

category. Ninety-one of the 98 planned cycles of HDCT were given with limited<br />

toxicity. Febrile neutropenia was seen in 58% of the cycles <strong>and</strong> documented<br />

infection in 18% of the cycles. Grade 3-4 gastrointestinal toxicity rate was 39%

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