Laboratory Workup of Lymphoma in Adults: Guideline From the American Society for Clinical Pathology and the College of American Pathologists.


Journal

Archives of pathology & laboratory medicine
ISSN: 1543-2165
Titre abrégé: Arch Pathol Lab Med
Pays: United States
ID NLM: 7607091

Informations de publication

Date de publication:
01 03 2021
Historique:
accepted: 31 08 2020
pubmed: 12 11 2020
medline: 7 4 2021
entrez: 11 11 2020
Statut: ppublish

Résumé

The diagnostic workup of lymphoma continues to evolve rapidly as experience and discovery led to the addition of new clinicopathologic entities and techniques to differentiate them. The optimal clinically effective, efficient, and cost-effective approach to diagnosis that is safe for patients can be elusive, in both community-based and academic practice. Studies suggest that there is variation in practice in both settings. To develop an evidence-based guideline for the preanalytic phase of testing, focusing on specimen requirements for the diagnostic evaluation of lymphoma. The American Society for Clinical Pathology, the College of American Pathologists, and the American Society of Hematology convened a panel of experts in the laboratory workup of lymphoma to develop evidence-based recommendations. The panel conducted a systematic review of literature to address key questions. Using the Grading of Recommendations Assessment, Development, and Evaluation approach, recommendations were derived based on the available evidence, strength of that evidence, and key judgements as defined in the Grading of Recommendations Assessment, Development, and Evaluation Evidence to Decision framework. Thirteen guideline statements were established to optimize specimen selection, ancillary diagnostic testing, and appropriate follow-up for safe and accurate diagnosis of indolent and aggressive lymphoma. Primary diagnosis and classification of lymphoma can be achieved with a variety of specimens. Application of the recommendations can guide decisions on specimen suitability, diagnostic capabilities, and correct use of ancillary testing. Disease prevalence in patient populations, availability of ancillary testing, and diagnostic goals should be incorporated into algorithms tailored to each practice environment.

Identifiants

pubmed: 33175094
pii: 447620
doi: 10.5858/arpa.2020-0261-SA
doi:

Types de publication

Journal Article Practice Guideline

Langues

eng

Sous-ensembles de citation

IM

Pagination

269-290

Informations de copyright

© 2021 College of American Pathologists.

Déclaration de conflit d'intérêts

Authors' disclosures of potential conflicts of interest and author contributions are found in the Appendix at the end of this article.

Auteurs

Steven H Kroft (SH)

From the Department of Pathology, Froedtert Hospital and the Medical Colleges of Wisconsin, Milwaukee (Kroft).

Cordelia E Sever (CE)

Pathology Associates of Albuquerque, Albuquerque, New Mexico (Sever).

Adam Bagg (A)

The Department of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia (Bagg).

Brooke Billman (B)

Governance Services (Billman), College of American Pathologists, Northfield, Illinois.

Catherine Diefenbach (C)

The Department of Medicine, New York University School of Medicine, New York, New York (Diefenbach).

David M Dorfman (DM)

The Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts (Dorfman).

William G Finn (WG)

The Department of Pathology and Laboratory Medicine, Warde Medical Laboratory, Ann Arbor, Michigan (Finn).

Dita A Gratzinger (DA)

The Department of Pathology, Stanford Health Care, Stanford, California (Gratzinger).

Patricia A Gregg (PA)

The Department of Pathology, Lehigh Regional Medical Center, Lehigh Acres, Florida (Gregg).

John P Leonard (JP)

The Department of Hematology and Oncology, Weill Cornell Medical College, New York, New York (Leonard).

Sonali Smith (S)

The Department of Medicine, University of Chicago Medicine, Chicago, Illinois (Smith).

Lesley Souter (L)

Souter is in private practice in Wellandport, Ontario, Canada.

Ronald L Weiss (RL)

The Department of Pathology, ARUP Laboratories Inc, Salt Lake City, Utah (Weiss).

Christina B Ventura (CB)

The Pathology and Laboratory Quality Center (Ventura), College of American Pathologists, Northfield, Illinois.

Matthew C Cheung (MC)

The Department of Medicine, Odette Cancer Centre/Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada (Cheung).

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