CD38 positivity:
In an Italian study from 2001, it was shown in multivariate analysis that higher CD38 levels (cutoff here >30%) was correlated with shorter time to progression.
Dürig et al stidied the same in Nature in 2002 here. There was longer survival correlated with CD38 positivity (>20% positive) in univariate analysis but this did NOT hold up in multivariate analysis. Hgb and IgA levels did hold up, however.
It seems like a lot of the risk factors (CD38, IgA, hypermutations, sCD23, ZAP70 are closely correlated).
17p-
A nice study in Blood from 2009 looked at de novo 17p- CLL. In my opinion, the study showed that 17p- lends a poor prognosis but that it shouldn't be considered a stand-alone entity. Some reports have claimed that only Campath works for 17p- but this may be exaggerated, as shown in this study. Responses to rituximab, alkylators and fludarabine were acceptable to warrant these regimens in 17p-.
IGvH Hypermutations:
This study by Oscier et al (Blood, 2002) showed the risk associated with various risk factors, focusing on the IGvH mutations. The Hazard Ratios came to this. Unmutated patients had a 55% death rate at 10 years, compared to 6% for mutated patients.
This study by Oscier et al (Blood, 2002) showed the risk associated with various risk factors, focusing on the IGvH mutations. The Hazard Ratios came to this. Unmutated patients had a 55% death rate at 10 years, compared to 6% for mutated patients.
Staging
This study shows by Stilgenbauer in NEJM 2000 shows survival based on cytogenetics.
Treatment
Indications (NCCN)
fcg
Links
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