TY - JOUR
T1 - Enhancing lymphoma diagnosis on core needle biopsies: Integrating immunohistochemistry with flow cytometry
AU - Bellesi, Silvia
AU - Schiaffini, Gabriele
AU - Contegiacomo, Andrea
AU - Maiolo, Elena
AU - Iacovelli, Camilla
AU - Malafronte, Rosalia
AU - D'Innocenzo, Simone
AU - Alma, Eleonora
AU - Bellisario, Flaminia
AU - Viscovo, Marcello
AU - Campana, Fabrizia
AU - De Filippis, Alessandra
AU - D'Alo', Francesco
AU - Larocca, Luigi Maria
AU - De Stefano, Valerio
AU - Iezzi, Roberto
AU - Hohaus, Stefan
PY - 2024
Y1 - 2024
N2 - Image-guided core needle biopsies (IG-CNB) represent a minimally invasive approach for obtaining tissue in patients with lymphadenopathy and suspected lymphoma. Despite their utility, diagnostic challenges persist, with lower efficacy compared with excisional biopsies. Our study aimed to evaluate the potential utility of incorporation of flow cytometry (FC) alongside immunohistochemistry (IHC) when performing IG-CNB for suspected lymphoproliferative diseases. Analyzing 170 consecutive cases, guided by ultrasound (n = 94) or computer tomography (n = 76), we employed a diagnostic algorithm, already established in our laboratory practice, utilizing three antibody cocktail-equipped tubes tailored for defining lymphomas, particularly those of B-cell origin. FC expedited the diagnostic process, yielding presumptive results in 87.6% of cases within 48 h, with a positive predictive value of 98%. Addition of FC to routine IHC enhanced the diagnostic rate from 91.2% to 95.3%, reducing IG-CNB failure rate by 45%, from 8.8% to 4.7%. This enhancement was particularly notable for deep-seated sites and in the setting of suspected disease recurrences. Consequently, FC emerges as a valuable adjunctive tool, allowing for the improvement of diagnostic performance, with a particular focus on the ability to quantify the expression of surface markers for targeted therapies, and holding the potential to diminish the necessity for repeat excisional biopsies subsequent to IG-CNB procedures.
AB - Image-guided core needle biopsies (IG-CNB) represent a minimally invasive approach for obtaining tissue in patients with lymphadenopathy and suspected lymphoma. Despite their utility, diagnostic challenges persist, with lower efficacy compared with excisional biopsies. Our study aimed to evaluate the potential utility of incorporation of flow cytometry (FC) alongside immunohistochemistry (IHC) when performing IG-CNB for suspected lymphoproliferative diseases. Analyzing 170 consecutive cases, guided by ultrasound (n = 94) or computer tomography (n = 76), we employed a diagnostic algorithm, already established in our laboratory practice, utilizing three antibody cocktail-equipped tubes tailored for defining lymphomas, particularly those of B-cell origin. FC expedited the diagnostic process, yielding presumptive results in 87.6% of cases within 48 h, with a positive predictive value of 98%. Addition of FC to routine IHC enhanced the diagnostic rate from 91.2% to 95.3%, reducing IG-CNB failure rate by 45%, from 8.8% to 4.7%. This enhancement was particularly notable for deep-seated sites and in the setting of suspected disease recurrences. Consequently, FC emerges as a valuable adjunctive tool, allowing for the improvement of diagnostic performance, with a particular focus on the ability to quantify the expression of surface markers for targeted therapies, and holding the potential to diminish the necessity for repeat excisional biopsies subsequent to IG-CNB procedures.
KW - core needle biopsy
KW - non-Hodgkin lymphoma
KW - flow cytometry
KW - diagnosis
KW - core needle biopsy
KW - non-Hodgkin lymphoma
KW - flow cytometry
KW - diagnosis
UR - http://hdl.handle.net/10807/282158
U2 - 10.1002/cyto.b.22185
DO - 10.1002/cyto.b.22185
M3 - Article
SN - 1552-4957
SP - N/A-N/A
JO - CYTOMETRY. PART B, CLINICAL CYTOMETRY
JF - CYTOMETRY. PART B, CLINICAL CYTOMETRY
ER -