Table 3.

Concordance rates between referral and expert diagnoses according to sampling procedures in 31 138 eligible cases

Lymphoma diagnosesCNB concordanceSurgical excision concordance
Overall concordance 76.9% (n = 7627/9924) 78.8% (n = 16 712/21 214)∗∗ 
Classified lymphoma 80.5% (n = 6844/8499) 80.4% (n = 15 086/18 760) 
Classified B-NHL 80.2% (n = 5110/6368) 79.2% (n = 9787/12 359) 
DLBCL NOS 86% (n = 2319/2698) 82.2% (n = 3290/4001)∗∗∗ 
TCRBCL 72.7% (n = 40/55) 69% (n = 78/113) 
HGBL 40.2% (n = 41/102) 44.7% (n = 42/94) 
BL 76.6% (n = 59/77) 81.3% (n = 78/96) 
Grade 3B FL 29.5% (n = 18/61) 44.8% (n = 95/212)∗ 
Grades 1, 2, and 3A FL 78.1% (n = 1665/2133) 82.6% (n = 3697/4475)∗∗∗ 
NMZL 63.4% (n = 192/303) 56.8% (n = 389/685) 
CLL/SLL 83.2% (n = 381/458) 79.8% (n = 1267/1587) 
MCL 83.4% (n = 331/397) 80.4% (n = 761/946) 
LPL/WD 76.2% (n = 64/84) 60% (n = 90/150)∗ 
Classified PTCL 63.5% (n = 345/543) 62.3% (n = 980/1572) 
PTCL NOS 61% (n = 94/154) 54.4% (n = 228/419) 
AITL 58.4% (n = 142/243) 64.6% (n = 565/874) 
ALCL ALK 68.1% (n = 49/72) 58.0% (n = 87/150) 
ALCL ALK+ 81.1% ( = 60/74) 77.5% (n = 100/129) 
Classified HL 87.5% (n = 1389/1588) 89.4% (n = 4319/4829)∗ 
cHL 89.9% (n = 1318/1466) 93.9% (n = 3944/4201)∗∗∗ 
NLPHL 58.2% (n = 71/122) 59.7% (n = 375/628) 
Nonlymphoid neoplasm 65.5% (n = 93/142) 63.6% (n = 196/308) 
Reactive lesion 63.6% (n = 337/530) 69.6% (n = 1222/1756)∗∗ 
Lymphoma diagnosesCNB concordanceSurgical excision concordance
Overall concordance 76.9% (n = 7627/9924) 78.8% (n = 16 712/21 214)∗∗ 
Classified lymphoma 80.5% (n = 6844/8499) 80.4% (n = 15 086/18 760) 
Classified B-NHL 80.2% (n = 5110/6368) 79.2% (n = 9787/12 359) 
DLBCL NOS 86% (n = 2319/2698) 82.2% (n = 3290/4001)∗∗∗ 
TCRBCL 72.7% (n = 40/55) 69% (n = 78/113) 
HGBL 40.2% (n = 41/102) 44.7% (n = 42/94) 
BL 76.6% (n = 59/77) 81.3% (n = 78/96) 
Grade 3B FL 29.5% (n = 18/61) 44.8% (n = 95/212)∗ 
Grades 1, 2, and 3A FL 78.1% (n = 1665/2133) 82.6% (n = 3697/4475)∗∗∗ 
NMZL 63.4% (n = 192/303) 56.8% (n = 389/685) 
CLL/SLL 83.2% (n = 381/458) 79.8% (n = 1267/1587) 
MCL 83.4% (n = 331/397) 80.4% (n = 761/946) 
LPL/WD 76.2% (n = 64/84) 60% (n = 90/150)∗ 
Classified PTCL 63.5% (n = 345/543) 62.3% (n = 980/1572) 
PTCL NOS 61% (n = 94/154) 54.4% (n = 228/419) 
AITL 58.4% (n = 142/243) 64.6% (n = 565/874) 
ALCL ALK 68.1% (n = 49/72) 58.0% (n = 87/150) 
ALCL ALK+ 81.1% ( = 60/74) 77.5% (n = 100/129) 
Classified HL 87.5% (n = 1389/1588) 89.4% (n = 4319/4829)∗ 
cHL 89.9% (n = 1318/1466) 93.9% (n = 3944/4201)∗∗∗ 
NLPHL 58.2% (n = 71/122) 59.7% (n = 375/628) 
Nonlymphoid neoplasm 65.5% (n = 93/142) 63.6% (n = 196/308) 
Reactive lesion 63.6% (n = 337/530) 69.6% (n = 1222/1756)∗∗ 

ALCL, anaplastic large cell lymphoma; BL, Burkitt lymphoma; CLL/SLL, chronic lymphocytic leukemia/small lymphocytic lymphoma; FL, follicular lymphoma; HGBL, high-grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements; cHL, classical HL; LPL/WD, lymphoplasmacytic lymphoma/Waldenström macroglobulinemia; MCL, mantle cell lymphoma; PTCL NOS, PTCL, not otherwise specified; TCRBCL, T-cell/histiocyte-rich B-cell lymphoma.

P value significance levels: ∗≤.05; ∗∗≤.01; ∗∗∗≤.0001.

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