Table 1.

Clinical and laboratory characteristics of patients with MCL at diagnosis

VariableAll patients (n = 92)De novo MCL (n = 65)Secondary MCL (n = 27)
Age at MCL diagnosis (y), median (range) 60.4 (25.4-90.8) 60.4 (27.1-90.8) 60.0 (25.4-73.4) 
Males, n (%) 59 (64.1) 43 (66.2) 16 (59.3) 
Diagnosis, n (%)    
MCL 61 (66.3) 46 (70.7) 15 (55.6) 
MCL-AHN 31 (33.7) 19 (29.2) 12 (44.4) 
MDS/MPN-U 14 (45.2) 12 (18.5) 2 (7.4) 
CMML 8 (25.8) 2 (3.1) 6 (22.2) 
CEL/eosinophilia 3 (9.7) 2 (3.1) 1 (3.7) 
AML 3 (9.7) 1 (1.5) 2 (7.4) 
Multiple myeloma 1 (3.2) 1 (1.5) 
NHL 1 (3.2) 1 (1.5) 
Not specified 1 (3.2) 1 (3.7) 
C-findings, n/N (%)     
No C-findings present 13 (14) 8 (12.3) 5 (18.5) 
Hemoglobin < 10 g/dL 43 (46.7) 31 (47.7) 12 (44.4) 
Platelets < 100 × 109/L 46 (50.0) 30 (46.2) 16 (59.3) 
Absolute neutrophil count < 1 × 109/L 2 (2.2) 2 (3.1) 
Weight loss (> 10% in 6 mo) 41/85 (41.8) 37/61 (60.7) 4/24 (16.7) 
Albumin < 3.5 g/dL 26/83 (31.3) 21/57 (36.8) 5/26 (19.2) 
Hepatomegaly with ascites or portal hypertension 19/84 (22.6) 13/59 (22.0) 6/25 (24.0) 
Alkaline phosphatase > 150 U/L 47/87 (54.0) 31/60 (51.7) 16/27 (59.3) 
Osteolytic lesion(s) ≥ 2 cm 4/70 (5.7) 2/51 (3.9) 2/19 (10.5) 
Other relevant findings, n/N (%)     
Serum tryptase, μg/L median (range) 333.5 (50.9-7490) 308 (57.2-7490) 396 (50.9-1820) 
≥200 μg/L, n (%) 75 (81.5) 53 (81.5) 22 (81.5) 
Any PB MCs detectable, n/N (%) 11/89 (12.4) 8/63 (12.7) 3/26 (11.5) 
≥3% PB MCs 7/89 (7.9) 6/63 (9.5) 1/26 (3.8) 
≥10% PB MCs 4/89 (4.5) 4/63 (6.3) 0/26 (0) 
MC infiltration in BM aspirate smear, %; median (range)  30 (20-100) 30 (20-100) 30 (20-88) 
Abnormal karyotype, n/N (%) 10/60 (17) 7/38 (18.4) 3/22 (13.6) 
S/A/R mutations present, n/N (%) 16/36 (44) 9/24 (37.5) 7/12 (58.3) 
VariableAll patients (n = 92)De novo MCL (n = 65)Secondary MCL (n = 27)
Age at MCL diagnosis (y), median (range) 60.4 (25.4-90.8) 60.4 (27.1-90.8) 60.0 (25.4-73.4) 
Males, n (%) 59 (64.1) 43 (66.2) 16 (59.3) 
Diagnosis, n (%)    
MCL 61 (66.3) 46 (70.7) 15 (55.6) 
MCL-AHN 31 (33.7) 19 (29.2) 12 (44.4) 
MDS/MPN-U 14 (45.2) 12 (18.5) 2 (7.4) 
CMML 8 (25.8) 2 (3.1) 6 (22.2) 
CEL/eosinophilia 3 (9.7) 2 (3.1) 1 (3.7) 
AML 3 (9.7) 1 (1.5) 2 (7.4) 
Multiple myeloma 1 (3.2) 1 (1.5) 
NHL 1 (3.2) 1 (1.5) 
Not specified 1 (3.2) 1 (3.7) 
C-findings, n/N (%)     
No C-findings present 13 (14) 8 (12.3) 5 (18.5) 
Hemoglobin < 10 g/dL 43 (46.7) 31 (47.7) 12 (44.4) 
Platelets < 100 × 109/L 46 (50.0) 30 (46.2) 16 (59.3) 
Absolute neutrophil count < 1 × 109/L 2 (2.2) 2 (3.1) 
Weight loss (> 10% in 6 mo) 41/85 (41.8) 37/61 (60.7) 4/24 (16.7) 
Albumin < 3.5 g/dL 26/83 (31.3) 21/57 (36.8) 5/26 (19.2) 
Hepatomegaly with ascites or portal hypertension 19/84 (22.6) 13/59 (22.0) 6/25 (24.0) 
Alkaline phosphatase > 150 U/L 47/87 (54.0) 31/60 (51.7) 16/27 (59.3) 
Osteolytic lesion(s) ≥ 2 cm 4/70 (5.7) 2/51 (3.9) 2/19 (10.5) 
Other relevant findings, n/N (%)     
Serum tryptase, μg/L median (range) 333.5 (50.9-7490) 308 (57.2-7490) 396 (50.9-1820) 
≥200 μg/L, n (%) 75 (81.5) 53 (81.5) 22 (81.5) 
Any PB MCs detectable, n/N (%) 11/89 (12.4) 8/63 (12.7) 3/26 (11.5) 
≥3% PB MCs 7/89 (7.9) 6/63 (9.5) 1/26 (3.8) 
≥10% PB MCs 4/89 (4.5) 4/63 (6.3) 0/26 (0) 
MC infiltration in BM aspirate smear, %; median (range)  30 (20-100) 30 (20-100) 30 (20-88) 
Abnormal karyotype, n/N (%) 10/60 (17) 7/38 (18.4) 3/22 (13.6) 
S/A/R mutations present, n/N (%) 16/36 (44) 9/24 (37.5) 7/12 (58.3) 

CEL, chronic eosinophilic leukemia; CMML, chronic myelomonocytic leukemia; MDS/MPN-U, myelodysplastic syndrome/myeloproliferative neoplasm-unclassifiable; NHL, non-Hodgkin lymphoma.

Denominator is the total number of patients (92, 65, or 27 for full cohort, de novo, or secondary MCL, respectively) unless otherwise specified.

One patient did not have a BM biopsy but had >10% MCs in the PB.

or Create an Account

Close Modal
Close Modal