Phase II Study of <sup>177</sup> Lu-DOTATATE for Progressive Metastatic Pheochromocytomas and Paragangliomas: Interim Analysis of Efficacy, Safety, and Biomarkers

F Frank I. Lin J Jaydira Del Rivero J Jorge A. Carrasquillo A Abhishek Jha J Joy Zou I Inna Shamis S Sara Talvacchio B Baris Turkbey (2Molecular Imaging Branch, NCI, Center for Cancer Research, NIH, Bethesda, United States) E Erich P. Huang J Joanna Shih J Joanna Klubo-Gwiezdzinska E Esther Mena (1National Cancer Institute, Lymphoid Malignancies Branch, Bethesda, United States) L Liza Lindenberg (National Institutes of Health, Bethesda, MD) Y Yating Teng F Freddy E. Escorcia (Christopher H. Crane, MD, Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY; Theodore S. Hong, MD, FASCO, Harvard Medical School, Boston, Massachusetts; Freddy E. Escorcia, MD, PhD, Laboratory of Molecular Radiotherapy, National Institutes of Health, Bethesda, MD; and Laura A. Dawson, MD, Department of Radiation Oncology, University of Toronto, Toronto, Canada, Radiation Medicine Program, Princess Margaret Cancer Centre, University Health Network, Toronto, Canada) C Clara Chen (National Institutes of Health, Bethesda, MD) P Peter Herscovitch C Corina Millo P Peter L. Choyke K Karel Pacak

Abstract

PURPOSE 177 Lu-DOTA(0)-Tyr(3)-octreotate ( 177 Lu-DOTATATE) is a somatostatin receptor (SSTR)-targeting radiopharmaceutical that shows promise for treating metastatic pheochromocytomas/paragangliomas (PPGLs), a rare SSTR-expressing tumor. METHODS In the first stage of this two-stage Simon phase II trial, 36 PPGL patients with RECIST 1.1 progression within 12 months were prospectively recruited into two genetic cohorts (succinate dehydrogenase [ SDHx ]–mutated v apparent sporadic, 18 per cohort) and treated with four cycles of 177 Lu-DOTATATE. The primary end point was progression-free survival (PFS) rate at 6 months (from initiation of treatment). Secondary end points included safety, overall survival (OS), response rate, imaging/serum biomarkers, and antihypertensive medication reduction. Computed tomography/magnetic resonance imaging (CT/MRIs) and positron emission tomography (PET)-CTs ( 68 Ga-DOTATATE and 18 F-labeled fluorodeoxyglucose) were obtained after two and four cycles, then every 3 (CT/MRIs) to 6 months (PET/CTs). Patients with systolic blood pressure (SBP) &gt; 200 mmHg despite medical management were treated in the intensive care unit (ICU). RESULTS Six-month PFS rate for all patients was 0.861 (95% CI, 0.755 to 0.982), which was significantly lower ( P = .009) for SDHx at 0.72 (95% CI, 0.542 to 0.962) versus sporadic at 1.00 (95% CI, 1.0 to 1.0). Median PFS was 19.9 months (12.9 months SDHx v 24.3 months sporadic) and median OS was 51.7 months (31.2 months SDHx v not reached in sporadic). Best response was achieved on average 11.0 months after completing 177 Lu-DOTATATE. A 17% incidence of grade 3+ catecholamine release syndrome (CRS) was noted, which may benefit from preemptive ICU admission. Plasma chromogranin A and normetanephrine were the best tumor-marker surrogates and correlated well with changes in RECIST sum and total tumor lesion uptake on serial 68 Ga-DOTATATE PET-CT scans. CONCLUSION 177 Lu-DOTATATE demonstrated effectiveness and acceptable safety profile for progressive, metastatic PPGL. CRS may occur but can be mitigated through pretreatment with antihypertensives, and, when appropriate, intensified monitoring in the ICU with intravenous antihypertensives.

Article Details

Volume / Issue Vol. 43, Issue 28
Published October 01, 2025
Pages 3102-3112
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

F

Frank I. Lin

J

Jaydira Del Rivero

J

Jorge A. Carrasquillo

A

Abhishek Jha

J

Joy Zou

I

Inna Shamis

S

Sara Talvacchio

B

Baris Turkbey

2Molecular Imaging Branch, NCI, Center for Cancer Research, NIH, Bethesda, United States

E

Erich P. Huang

J

Joanna Shih

J

Joanna Klubo-Gwiezdzinska

E

Esther Mena

1National Cancer Institute, Lymphoid Malignancies Branch, Bethesda, United States

L

Liza Lindenberg

National Institutes of Health, Bethesda, MD

Y

Yating Teng

F

Freddy E. Escorcia

Christopher H. Crane, MD, Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY; Theodore S. Hong, MD, FASCO, Harvard Medical School, Boston, Massachusetts; Freddy E. Escorcia, MD, PhD, Laboratory of Molecular Radiotherapy, National Institutes of Health, Bethesda, MD; and Laura A. Dawson, MD, Department of Radiation Oncology, University of Toronto, Toronto, Canada, Radiation Medicine Program, Princess Margaret Cancer Centre, University Health Network, Toronto, Canada

C

Clara Chen

National Institutes of Health, Bethesda, MD

P

Peter Herscovitch

C

Corina Millo

P

Peter L. Choyke

K

Karel Pacak