Table 2

Characteristics at the time of initiation of first-line therapy and their association with survival in 587 patients with symptomatic Waldenström macroglobulinemia

CharacteristicNo. (%) of patientsMedian survival95% CIP
Sex     
    Male 373 (64) 85 65-98  
    Female 212 (36) 89 79-110 .74 
Age     
    65 y or less 254 (43) 141 120-53  
    More than 65 y 333 (57) 56 49-63 < .001 
Criteria for treatment initiation     
    Cytopenia*     
        Absent 285 (49) 92 84-20  
        Present 300 (51) 77 60-90 .03 
    Organomegaly*     
        Absent 380 (65) 89 79-106  
        Present 207 (35) 80 64-143 .84 
    IgM-related symptoms*     
        Absent 506 (87) 84 74-98  
        Present 77 (13) 94 87-174 .27 
    Hyperviscosity*     
        Absent 401 (69) 85 79-103  
        Present 183 (31) 80 57-117 .35 
    Constitutional symptoms*     
        Absent 323 (56) 89 79-110  
        Present 255 (44) 85 60-119 .18 
Time from diagnosis to treatment initiation     
    Less than 4 mo 406 (83) 89 79-118  
    4 mo or more 181 (17) 85 54-106 .14 
Hemoglobin, g/dL*     
    11.5 or less 381 (65) 123 110-179  
    More than 11.5 205 (35) 72 62-84 < .001 
Platelet count, ×109/L*     
    100 or less 54 (9) 51 32-59  
    More than 100 531 (91) 90 83-116 < .001 
Absolute neutrophil count, ×109/L*     
    1.5 or less 53 (9) 46 27-74  
    More than 1.5 512 (91) 89 80-103 .002 
Serum monoclonal protein, g/dL*     
    7.0 or less 541 (93) 90 82-110  
    More than 7.0 43 (7) 49 37-62 .002 
Serum albumin, g/dL*     
    3.5 or less 197 (36) 79 55-89  
    More than 3.5 354 (64) 106 92-137 .001 
Serum β2-microglobulin, mg/L     
    3 or less 251 (44) 122 103-141  
    More than 3 326 (56) 63 55-83 < .001 
Treatment     
    Alkylating agents 369 (63) 85 74-103  
    Fludarabine (alone or in combination) 195 (33) 85 61-NR  
    Rituximab 23 (4) NR 30-NR .30 
CharacteristicNo. (%) of patientsMedian survival95% CIP
Sex     
    Male 373 (64) 85 65-98  
    Female 212 (36) 89 79-110 .74 
Age     
    65 y or less 254 (43) 141 120-53  
    More than 65 y 333 (57) 56 49-63 < .001 
Criteria for treatment initiation     
    Cytopenia*     
        Absent 285 (49) 92 84-20  
        Present 300 (51) 77 60-90 .03 
    Organomegaly*     
        Absent 380 (65) 89 79-106  
        Present 207 (35) 80 64-143 .84 
    IgM-related symptoms*     
        Absent 506 (87) 84 74-98  
        Present 77 (13) 94 87-174 .27 
    Hyperviscosity*     
        Absent 401 (69) 85 79-103  
        Present 183 (31) 80 57-117 .35 
    Constitutional symptoms*     
        Absent 323 (56) 89 79-110  
        Present 255 (44) 85 60-119 .18 
Time from diagnosis to treatment initiation     
    Less than 4 mo 406 (83) 89 79-118  
    4 mo or more 181 (17) 85 54-106 .14 
Hemoglobin, g/dL*     
    11.5 or less 381 (65) 123 110-179  
    More than 11.5 205 (35) 72 62-84 < .001 
Platelet count, ×109/L*     
    100 or less 54 (9) 51 32-59  
    More than 100 531 (91) 90 83-116 < .001 
Absolute neutrophil count, ×109/L*     
    1.5 or less 53 (9) 46 27-74  
    More than 1.5 512 (91) 89 80-103 .002 
Serum monoclonal protein, g/dL*     
    7.0 or less 541 (93) 90 82-110  
    More than 7.0 43 (7) 49 37-62 .002 
Serum albumin, g/dL*     
    3.5 or less 197 (36) 79 55-89  
    More than 3.5 354 (64) 106 92-137 .001 
Serum β2-microglobulin, mg/L     
    3 or less 251 (44) 122 103-141  
    More than 3 326 (56) 63 55-83 < .001 
Treatment     
    Alkylating agents 369 (63) 85 74-103  
    Fludarabine (alone or in combination) 195 (33) 85 61-NR  
    Rituximab 23 (4) NR 30-NR .30 

CI indicates confidence interval; and NR, not reached.

*

Data were unavailable for some patients.

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