Criteria
Rai staging system[3]
0 = Clonal lymphocytosis (>5000 cells/microliter [>5 × 10⁹ cells/L]) in blood and/or >40% lymphocytes in bone marrow (low risk)
I = Lymphocytosis plus lymphadenopathy (intermediate risk)
II = Lymphocytosis plus hepatomegaly and/or splenomegaly, with or without lymphadenopathy (intermediate risk)
III = Lymphocytosis plus anemia (hemoglobin <11 g/dL) or hematocrit <33%, with or without organomegaly (high risk)
IV = Lymphocytosis plus thrombocytopenia (platelets <100,000/microliter [<100 × 10⁹/L]), with or without anemia or organomegaly (high risk)
Binet staging system[50]
A = Hemoglobin ≥10 g/dL and platelets ≥100,000/microliter (≥100 × 10⁹/L) and <3 lymphoid areas enlarged (low risk)
B = Hemoglobin ≥10 g/dL and platelets ≥100,000/microliter (≥100 × 10⁹/L) and ≥3 lymphoid areas enlarged (intermediate risk)
C = Presence of anemia (hemoglobin <10 g/dL) or thrombocytopenia (platelets <100,000/microliter [<100 × 10⁹/L]) with any number of lymphoid areas enlarged (high risk)
Chronic lymphocytic leukaemia international prognostic index (CLL-IPI)[40]
An international prognostic index for CLL developed by the CLL-IPI working group. The index combines genetic, biochemical, and clinical parameters into a prognostic model to stratify patients into four risk groups (low, intermediate, high, and very high).
The five prognostic factors used in the index are:
TP53 status (no abnormalities vs. del(17p) and/or TP53 mutation)
Immunoglobulin heavy chain (IgHV) mutational status (mutated vs. unmutated)
Serum beta2-microglobulin concentration (≤3.5 mg/L vs. >3.5 mg/L)
Clinical stage (Binet A or Rai 0 vs. Binet B to C or Rai I-IV)
Age (≤65 vs. >65 years)
The CLL-IPI utilizes modern prognostic factors and may provide improved prognostication in CLL; however, it requires further evaluation in prospective trials.
International workshop on chronic lymphocytic leukemia (iwCLL) treatment response criteria[2]
Complete remission (all of the criteria have to be met)
Group A parameters
Lymph nodes: none ≥1.5 cm
Liver and/or spleen size: spleen size <13 cm; liver size normal
Constitutional symptoms: none
Circulating lymphocyte count: normal
Group B parameters
Platelet count: ≥100 × 10⁹/L
Hemoglobin: ≥11.0 g/dL (untransfused and without erythropoietin)
Marrow: normocellular, no CLL cells, no B-lymphoid nodules
Neutrophil count: ≥1.5 × 10⁹/L
Partial remission (at least 2 of the parameters of group A and 1 parameter of group B need to improve if previously abnormal; if only 1 parameter of both groups A and B is abnormal before therapy, only 1 needs to improve)
Group A parameters
Lymph nodes: decrease ≥50% from baseline (sum of the products of 6 or fewer lymph nodes as evaluated by CT scans and physical exam in clinical trials or by physical exam in general practice)
Liver and/or spleen size: decrease ≥50% from baseline
Constitutional symptoms: any
Circulating lymphocyte count: decrease ≥50% from baseline
Group B parameters
Platelet count: ≥100 × 10⁹/L or increase ≥50% over baseline
Hemoglobin: ≥11 g/dL or increase ≥50% over baseline
Marrow: presence of CLL cells, or of B-lymphoid nodules, or not done
Progressive disease (at least 1 of the criteria of group A or group B has to be met)
Group A parameters
Lymph nodes: increase ≥50% from baseline or from response
Liver and/or spleen size: increase ≥50% from baseline or from response
Constitutional symptoms: any
Circulating lymphocyte count: increase ≥50% over baseline
Group B parameters
Platelet count: decrease of ≥50% from baseline secondary to CLL
Hemoglobin: decrease of ≥2 g/dL from baseline secondary to CLL
Marrow: increase of CLL cells by ≥50% on successive biopsies
Stable disease (all of the criteria have to be met; constitutional symptoms alone do not define progressive disease).
Group A parameters
Lymph nodes: change of -49% to +49%
Liver and/or spleen size: change of -49% to +49%
Constitutional symptoms: any
Circulating lymphocyte count: change of -49% to +49%
Group B parameters
Platelet count: change of -49 to +49%
Hemoglobin: increase <11.0 g/dL or <50% over baseline, or decrease <2 g/dL
Marrow: no change in marrow infiltrate
Use of this content is subject to our disclaimer