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Chronic Lymphocytic Leukemia - Alberta Health Services

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CLINICAL PRACTICE GUIDELINE LYHE-007<br />

Version 2<br />

six months of treatment are identified as having refractory disease. Those demonstrating PD more than<br />

six months after treatment has ended, who have previously achieved a CR or PR, are identified as having<br />

relapsed disease. (3)<br />

Table 3. Criteria for Identifying Treatment Response (3)<br />

Parameter Complete response Partial response Progressive disease<br />

(CR)<br />

(PR)<br />

(PD)<br />

Lymphadenopathy None >1.5 cm Decrease ≥50% Increase ≥50% or<br />

appearance of any new<br />

lesion<br />

Liver and/or spleen<br />

size<br />

Constitutional<br />

symptoms<br />

Polymorphonuclear<br />

leukocytes<br />

Normal size Decrease ≥50% Increase ≥50% or new<br />

enlargement when<br />

previously normal<br />

None Any Any Any<br />

>1.5 x 10 9 /L without<br />

need for exogenous<br />

growth factors<br />

>1.5 x 10 9 /L or >50%<br />

improvement over<br />

baseline without need for<br />

exogenous growth factors<br />

Circulating clonal B- None Decrease ≥50% over<br />

lymphocytes<br />

baseline<br />

Platelet count >100 x 10 9 /L without >100 x 10<br />

need for exogenous<br />

growth factors<br />

9 /L or increase<br />

≥50% over baseline<br />

Hemoglobin >110 g/L (untransfused >110 g/L or increase<br />

and without need for<br />

exogenous<br />

erythropoietin)<br />

≥50% over baseline<br />

Marrow Normocellular for age, No BM requirements to<br />

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