-Author name in bold denotes the presenting author
-Asterisk * with author name denotes a Non-ASH member
Clinically Relevant Abstract denotes an abstract that is clinically relevant.

PhD Trainee denotes that this is a recommended PHD Trainee Session.

Ticketed Session denotes that this is a ticketed session.

1920 Diagnostic Test Accuracy of Bone Scintigraphy in the Diagnosis of Attr Amyloidosis: A Systematic Review and Meta-Analysis

Program: Oral and Poster Abstracts
Session: 652. MGUS, Amyloidosis, and Other Non-Myeloma Plasma Cell Dyscrasias: Clinical and Epidemiological: Poster I
Hematology Disease Topics & Pathways:
Research, Clinical Research, Plasma Cell Disorders, Diseases, Lymphoid Malignancies, Technology and Procedures, Imaging
Saturday, December 7, 2024, 5:30 PM-7:30 PM

Muayad Azzam, MD1*, Hassan Kawtharany2*, Jamil Nazzal, MD2*, Vishal Kukreti, MD, MSc3, Matthew D. Seftel, MD, FRCP, FRCPC, MPH4, Aseel Alkhader, MD2*, Qais Hamarsha, MD2*, Tala Khraise, MD5*, Mohammad Mahmoud AlMasri, MD6*, Hadi Khaled Abou Zeid, MD7*, Iktimal Alwan, MD8*, Noor Jaber2*, Mohammad Fraitekh9*, Noel Dasgupta, MD10*, Raymond Comenzo, MD11, Faizi Jamal, MD12*, Maria Adela Aguirre, MD, PhD13*, Deborah Boedicker14*, Naresh Bumma, MD15, Antonia Carroll, MD16*, Joselle Cook, MBBS17, Alfredo H. De La Torre, MD18, Angela Dispenzieri, MD17, Jack Khouri, MD19, Nelson Leung, MD17, Maria M. Picken, MD, PhD20*, Shahzad Raza, MD19, Vaishali Sanchorawala21, Hira Shaikh, MD22, Nitasha Sarswat, MD23*, Daulath Singh, MD24* and Reem A Mustafa, MD, PhD, MPH25*

1Evidence-Based Practice and Impact Center, Department of Internal Medicine, University of Kansas Medical Center, Overland Park, KS
2Evidence-Based Practice and Impact Center, Department of Internal Medicine, University of Kansas Medical Center, Kansas City, KS
3Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, ON, Canada
4Department of Medicine, University of British Columbia, Vancouver, CAN
5Northwest Health, Porter County, IN
6King Hussein Cancer Center, Amman, Jordan
7University of Balamand, Balamand, Lebanon
8AdventHealth, Tampa
9Blue Valley West, Overland Park, KS
10Indiana University, Bloomington, IN
11Division of Hematology/Oncology, John C. Davis Myeloma and Amyloid Program, Tufts Medical Center, Boston, MA
12Division of Cardiology, Department of Medicine, City of Hope National Medical Center, Duarte, CA
13Internal Medicine Department, Hospital Italiano de Buenos Aires, BUENOS AIRES, AL, ARG
14Mackenzie’s Mission, Great Falls, VA
15The Ohio State University Comprehensive Cancer Center, COLUMBUS, OH
16Department of Neurology and Neurophysiology, St Vincent’s Hospital, Sydney, AUS
17Division of Hematology, Mayo Clinic, Rochester, MN
18QEII Health Sciences Centre, Halifax, NS, CAN
19Department of Hematology and Medical Oncology, Cleveland Clinic Taussig Cancer Institute, Cleveland, OH
20Loyola University Medical Center, Maywood, IL
21Amyloidosis Center, Boston University Chobanian & Avedisian School of Medicine and Boston Medical Center, Boston, MA
22Division of Hematology, Oncology and Bone Marrow Transplantation, University of Iowa, Coralville, IA
23Advanced Heart Failure, Mechanical Circulatory Support and Transplantation, Division of Cardiology, The University of Chicago, Chicago, IL
24Mission Cancer + Blood, Des Moines, IA
25Division of Nephrology and Hypertension, Department of Internal Medicine, University of Kansas Medical Centre, Kansas City, KS

Introduction:

For cardiac transthyretin (ATTR) amyloidosis, bone scintigraphy has emerged as a noninvasive diagnostic tool. The use of different tracers, namely Pyrophosphate (PYP), 3,3-diphosphono-1,2-propanodicarboxylic acid (DPD), HydroxymethyleneDiphosphonate (HMDP), allow for the detection of amyloid deposits in the heart. The aim of this systematic review is to evaluate the diagnostic test accuracy of bone scintigraphy in ATTR and light chain (AL) amyloidosis.

Methods:

As part of the ASH AL Amyloidosis Diagnostic Guideline, we performed systematic reviews for 7 prioritized PICO questions related to the screening, diagnosis and organ involvement evaluation of AL amyloidosis. Electronic searches were conducted on PubMed, Embase, and the Cochrane Central Register of Controlled Trials from inception till January 2024. Two reviewers independently and in duplicate performed title and abstract screening and full text article screening on LASER AI, with conflicts resolved by a third reviewer.

Studies were eligible if they included patients that performed both a bone scintigraphy scan and an endomyocardial biopsy for suspicion of ATTR amyloidosis. Test positivity for the visual score was defined to be ≥2, for the heart over contralateral (H/CL) ratio it was > 1.5 at one hour and >1.3 at 3 hours. Diagnostic test accuracy measures of interest were sensitivity, specificity, positive and negative predictive value. Statistical analysis was performed on STATA 18.0. Grading of Recommendations Assessment, Development and Evaluation (GRADE) was used to assess the certainty of evidence.

Results:

After deduplication, we retrieved 29,237 studies from electronic databases. 12 studies with 1127 patients reported on visual score in patients suspected to have ATTR amyloidosis. The pooled sensitivity for visual score was 96% (95% CI 92.0-98.0) while specificity was 90% (95% CI 84.0-95.0) (Certainty of evidence (COE): Moderate ⨁⨁⨁◯). 3 studies reported on ATTR visual score in combination with evaluating for monoclonal gammopathy, the pooled sensitivity was decreased to 93% (95% CI 65-99) and while specificity increased to 99% (95% CI 80-100) (COE: Moderate ⨁⨁⨁◯). H/CL was evaluated in 5 studies with 189 patients; pooled sensitivity was 97% (95% CI 89.0-99.0) and specificity was 88% (95% CI 64-97) (COE: Low ⨁⨁◯◯).

We also performed subgroup analyses for the diagnostic test accuracy of visual score for the different tracers (PYP, DPD, HMDP) in patients suspected to have ATTR amyloidosis. DPD was found to have the highest sensitivity which was found to be 97% (95% CI 91.0-99.0) and a specificity of 95 (95% CI 86.0-98.0) (4 studies, n = 297 COE: Moderate ⨁⨁⨁◯). The sensitivity and specificity for PYP was 95% (95% CI 87.0-98.0) and 90% (95% CI 79.0-96.0) (7 studies, n = 377 COE: Moderate ⨁⨁⨁◯). 1 study reported on HMDP with a sensitivity and specificity of 79% (95% CI 49.0-95.0) and 100% (95% CI 59.0-100.0) (COE: Low ⨁⨁◯◯).

Conclusion:

Bone scintigraphy has a high sensitivity and specificity for the diagnosis of ATTR amyloidosis, particularly in patients without a monoclonal gammopathy.

Disclosures: Seftel: Astrazeneca: Other: Meal at CME event; Novartis: Other: Meal at CME event. Dasgupta: Siemens: Other: Adjudicator; Intellia: Other: Advisory board; Eidos: Other: Advisory Board; Alnylam: Other: Advisory Board; NovoNordisk: Other: Advisory Board; Astra Zeneca: Other: Advisory board. Jamal: Janssen: Consultancy. Aguirre: Pfizer: Honoraria; PTC Bio: Honoraria. Bumma: Amgen: Membership on an entity's Board of Directors or advisory committees, Speakers Bureau; sanofi: Honoraria, Membership on an entity's Board of Directors or advisory committees, Speakers Bureau; Janssen: Honoraria, Membership on an entity's Board of Directors or advisory committees, Speakers Bureau. Carroll: CSL Behring: Honoraria; Janssen: Other: Travel Support; Alnylam: Other: Advisory Committee. Cook: Geron Corp: Other: Held $600 Geron Stock for one week and sold without profit . Dispenzieri: HaemaloiX: Research Funding; Pfizer: Research Funding; Alnylam: Research Funding; Alexion: Consultancy, Research Funding; Takeda: Consultancy, Research Funding; BMS: Consultancy, Research Funding; Janssen: Research Funding. Khouri: Prothena: Honoraria; GPCR Therapeutics, Inc.: Honoraria; Janssen: Honoraria, Membership on an entity's Board of Directors or advisory committees, Other: Consultant; Legend: Membership on an entity's Board of Directors or advisory committees. Leung: Checkpoint Therapeutics: Current holder of stock options in a privately-held company; AbbVie: Current holder of stock options in a privately-held company. Raza: Pfizer: Consultancy, Honoraria; Prothena Biosciences: Consultancy; Kite Pharma: Consultancy. Sanchorawala: Pfizer, Janssen, Attralus, GateBio, Abbvie, BridgeBio: Consultancy; Proclara, Caelum, Abbvie, Janssen, Regeneron, Protego, Pharmatrace, Telix, Prothena, AstraZeneca, Nexcella: Membership on an entity's Board of Directors or advisory committees; Celgene, Millennium-Takeda, Janssen, Prothena, Sorrento, Karyopharm, Oncopeptide, Caelum, Alexion: Research Funding. Sarswat: Eidos: Consultancy, Membership on an entity's Board of Directors or advisory committees; Astra Zeneca: Membership on an entity's Board of Directors or advisory committees; Alnylam: Consultancy, Membership on an entity's Board of Directors or advisory committees; Pfizer: Consultancy, Membership on an entity's Board of Directors or advisory committees, Research Funding; Novo Nordisk: Consultancy, Membership on an entity's Board of Directors or advisory committees.

*signifies non-member of ASH