Abstract 4369484: Evaluating the Impact of Lutetium-177 Therapy on Bioprosthetic Heart Valves in Carcinoid Heart Disease

F Fatmaelzahraa Abdelfattah (Mayo Clinic Arizona, Phoenix, Arizona, United States) I Isabel Scalia (Mayo Clinic Arizona, Phoenix, Arizona, United States) J Juan Farina (Mayo Clinic, Phoenix, Arizona, United States) O Omar Ibrahim (Mayo Clinic, Phoenix, AZ, Phoenix, Arizona, United States) K Kamal Awad M Milagros Pereyra (Mayo Clinic Arizona, Phoenix, Arizona, United States) M Mohammed Tiseer Abbas (Mayo Clinic Arizona, Phoenix, Arizona, United States) S Sogol Attaripour Esfahani (Mayo Clinic, Phoenix, AZ, Phoenix, Arizona, United States) N Nima Baba Ali (Mayo clinic, Phoenix, Arizona, United States) H Hesham Sheashaa (Mayo Clinic, Phoenix, AZ, Phoenix, Arizona, United States) M Mahshad Razaghi (Mayo Clinic, Phoenix, AZ, Phoenix, Arizona, United States) R Reza Arsanjani (Mayo Clinic, Scottsdale, Arizona, United States) C Chadi Ayoub (Mayo Clinic, Scottsdale, Arizona, United States)

Abstract

Background: High serotonin from neuroendocrine tumors (NETs) can result in carcinoid heart disease (CaHD) with severe valve dysfunction, often requiring valve replacement surgery. Lutetium-177 (Lu-177), a targeted radioactive isotope therapy, is increasingly utilized in the treatment of NETs; however, there is limited data on its impact on bioprosthetic heart valves (BHVs) in CaHD. Methods: A retrospective review was conducted on all patients with stage IV metastatic NET who underwent BHV replacement at three tertiary centers in the United States. Patients were stratified by Lu-177 therapy, administered after valve replacement. A propensity matched cohort of CaHD patients with BHV who did not received Lu-177 was curated including age, sex, and baseline left ventricular ejection fraction. Serial transthoracic echocardiograms (TTEs) following surgery were evaluated for progression of BHV degeneration; rise in mean gradient or increase in grade of prosthetic/periprosthetic regurgitation (grade increase of ≥1 out of 5), from first TTE following surgery (TTE1) to most recent TTE (TTE2). Analysis was performed at the level of individual valves, recognizing that some patients had more than one valve implanted. To account for changes in Lu-177 exposure over time, we constructed a time-varying Cox proportional hazards model. Accounting for non-independence of multiple valves within the same patient, a clustered Cox model was fitted using robust standard errors. Mortality was compared between patients exposed to Lu-177 therapy and those not exposed. Results: 184 patients were identified, mean age 60.4 ± 10.3 years, 53.3 % male. Of these, 16 patients had Lu-177 therapy, with 45 individual BHVs within this group. Patients in the control group had a total of 60 BHVs. Across a median of 2.09 years [0.77-5.01] between TTE1 and TTE2, BHVs exposed to Lu-177 therapy demonstrated an increased risk of BHV degeneration (HR=2.44, 95% CI 1.05–5.69, p=0.038), accounting for the time between TTE1 and administration of Lu-177 and the non-independence of multiple BHVs within the same patient. There was no significant difference in mortality between the two cohorts (p=0.440). Conclusions: BHVs in patients with CaHD exposed to Lu-177 therapy demonstrated an increased risk of degeneration. These findings suggest an association between Lu-177 treatment and accelerated prosthetic valvular deterioration, warranting further investigation and close monitoring in this patient population.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (13)

F

Fatmaelzahraa Abdelfattah

Mayo Clinic Arizona, Phoenix, Arizona, United States

I

Isabel Scalia

Mayo Clinic Arizona, Phoenix, Arizona, United States

J

Juan Farina

Mayo Clinic, Phoenix, Arizona, United States

O

Omar Ibrahim

Mayo Clinic, Phoenix, AZ, Phoenix, Arizona, United States

K

Kamal Awad

M

Milagros Pereyra

Mayo Clinic Arizona, Phoenix, Arizona, United States

M

Mohammed Tiseer Abbas

Mayo Clinic Arizona, Phoenix, Arizona, United States

S

Sogol Attaripour Esfahani

Mayo Clinic, Phoenix, AZ, Phoenix, Arizona, United States

N

Nima Baba Ali

Mayo clinic, Phoenix, Arizona, United States

H

Hesham Sheashaa

Mayo Clinic, Phoenix, AZ, Phoenix, Arizona, United States

M

Mahshad Razaghi

Mayo Clinic, Phoenix, AZ, Phoenix, Arizona, United States

R

Reza Arsanjani

Mayo Clinic, Scottsdale, Arizona, United States

C

Chadi Ayoub

Mayo Clinic, Scottsdale, Arizona, United States