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Accuracy of Pathologic Diagnosis in Patients With Lymphoma and Survival: A Prospective Analysis From Botswana.
- Source :
-
JCO global oncology [JCO Glob Oncol] 2021 Sep; Vol. 7, pp. 1620-1632. - Publication Year :
- 2021
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Abstract
- Purpose: With intense HIV epidemics, southern African countries have a high burden of classic Hodgkin lymphoma (CHL) and non-Hodgkin lymphoma (NHL). However, suboptimal access to pathology resources limits subtype classification. We sought to assess the diagnostic accuracy of specimens classified as lymphoma and to determine association between discordant pathologic diagnosis and overall survival.<br />Methods: Seventy patients with CHL or NHL and treated at three Botswana hospitals from 2010 to 2016 were analyzed. Local pathologic assessment relied primarily on morphology. All cases underwent secondary US hematopathology review, which is considered gold standard.<br />Results: The median follow-up was 58 months. The overall reclassification rate was 20 of 70 cases (29%). All 20 CHL cases were correctly classified in Botswana, and mixed cellularity was the most common subtype, diagnosed in 11 (55%) cases. Of 47 confirmed NHL cases, diffuse large B-cell lymphoma was the final US diagnosis in 28 cases (60%), another aggressive B-cell NHL in nine (19%), an indolent B-cell NHL in six (13%), and T-cell NHL in four (9%). Common types of diagnostic discordance included NHL subtype reclassification (11 of 20, 55%) and CHL reclassified as NHL (7 of 20, 35%). Concordant versus discordant diagnosis after secondary review was associated with improved 5-year overall survival (60.1% v 26.3%, P = .0066). Discordant diagnosis was independently associated with increased risk of death (adjusted hazard ratio 2.733; 95% CI, 1.102 to 6.775; P = .0300) even after stratifying results by CHL versus NHL.<br />Conclusion: In this single prospective cohort, discordant pathologic diagnosis was associated with a nearly three-fold increased risk of death. Limited access to relatively basic diagnostic techniques impairs treatment decisions and leads to poor patient outcomes in low-resource countries.<br />Competing Interests: Jason A. EfstathiouConsulting or Advisory Role: Blue Earth Diagnostics, AstraZeneca, Boston Scientific, Roivant, Merck, Myovant Sciences Bruce A. ChabnerStock and Other Ownership Interests: Alnylam, Loxo, PharmaMar, Blueprint Medicines, GlaxoSmithKline, Biomarin, Seattle Genetics, SpringWorks Therapeutics, Constellation PharmaceuticalsHonoraria: Bristol Myers SquibbConsulting or Advisory Role: PharmaMar, EMD Serono, Cyteir, Chugai PharmaExpert Testimony: LillyTravel, Accommodations, Expenses: PharmaMar Jeremy AbramsonConsulting or Advisory Role: Celgene, Novartis, AbbVie, Kite, a Gilead company, Genentech, EMD Serono, MorphoSys, Alimera Sciences, Karyopharm Therapeutics, Bristol Myers Squibb, C4 Therapeutics¸ BeiGene, AstraZeneca, Incyte, Bluebird Bio, Kymera, Epizyme, Genmab, MorphoSys, MustangBio, Ono Pharmaceutical, RegeneronResearch Funding: Seattle Genetics (Inst), AI Therapeutics (Inst), Bristol Myers Squibb/Celgene (Inst) Scott L. Dryden-PetersonPatents, Royalties, Other Intellectual Property: Royalties received from UpToDate, Inc for article on HIV Aliyah R. SohaniConsulting or Advisory Role: AbbVie, MersanaExpert Testimony: Levin PapantonioNo other potential conflicts of interest were reported.
Details
- Language :
- English
- ISSN :
- 2687-8941
- Volume :
- 7
- Database :
- MEDLINE
- Journal :
- JCO global oncology
- Publication Type :
- Academic Journal
- Accession number :
- 34860565
- Full Text :
- https://doi.org/10.1200/GO.21.00209