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Dotatate PET/CT and 225Ac-Dotatate Therapy for Somatostatin Receptor-expressing Metastatic Breast Cancer
Gary A Ulaner1, Louis A VanderMolen1, Gary Li1
1From the Department of Molecular Imaging and Therapy, Hoag Family Cancer Institute, 16105 Sand Canyon Ave, Irvine, CA 92618 (G.A.U.); Department of Radiology and Translational Genomics (G.A.U.) and Department of Medicine (L.A.V.), University of Southern California, Los Angeles, Calif; and RayzeBio, San Diego, CA (G.L., D.F.).
Abstract:
Background Somatostatin receptors, and specifically somatostatin receptor type 2 (SSTR2), have primarily been associated with neuroendocrine tumors and have revolutionized the imaging and therapy of patients with these tumors. SSTR2 is expressed on other tumors at lower prevalence. Purpose To evaluate the potential of SSTR2-targeted imaging and therapy in patients with breast cancer. Materials and Methods In a preclinical experiment, SSTR2 expression was assessed in tissue microarrays of breast cancer samples using H-score analysis. H-scores higher than 50 (0-300 scale) were considered positive. Then, a prospective phase 2 clinical trial of SSTR2-targeted tetraazacyclododecane tetraacetic acid octreotate (Dotatate) PET/CT was performed in participants with biopsy-proven estrogen receptor (ER)-positive breast cancer from January to August 2023. A positive Dotatate PET/CT scan was defined as tumors with a Krenning score of 3 (avidity greater than liver) or 4 (avidity greater than spleen). The proportion of positive scans and the 95% CI were calculated. One participant with metastatic ER-positive breast cancer and a Krenning 4 Dotatate PET/CT result underwent treatment with SSTR2-targeted actinium 225 (225Ac) Dotatate. Results Preclinical microarrays demonstrated that 63 of 123 ER-positive breast cancer tissue samples (51% [95% CI: 42, 60]) but only 22 of 121 ER-negative breast cancer tissue samples (18% [95% CI: 12, 26]) were enriched for SSTR2 (P < .001). Thirty female participants (mean age, 66 years ± 15) with metastatic ER-positive breast cancer were accrued to the phase 2 SSTR2-targeted imaging trial and underwent Dotatate PET/CT. Dotatate PET/CT demonstrated that nine of 30 participants (30% [95% CI: 15, 49]) had tumors with Krenning scores of 3 or 4, indicating strong SSTR2 expression. SSTR2-targeted therapy with alpha-emitting 225Ac-Dotatate resulted in a near complete response in a heavily pretreated participant with metastatic ER-positive breast cancer and a Krenning 4 Dotatate PET result. Conclusion Molecular imaging targeting SSTR2 and radioligand therapy with SSTR2-targeted 225Ac-Dotatate enables a new therapeutic option for patients with metastatic breast cancer. Clinical trial registration no. NCT05880394 © RSNA, 2024 See also the editorial by Lin and Choyke in this issue.
Insights
Somatostatin receptor type 2 (SSTR2) imaging and therapy show promise for metastatic breast cancer. SSTR2-targeted Dotatate PET/CT identified eligible patients, and actinium 225 Dotatate therapy yielded a near complete response in one patient.
Area of Science:
- Oncology
- Nuclear Medicine
- Radiopharmaceutical Therapy
Background:
- Somatostatin receptor type 2 (SSTR2) is crucial for neuroendocrine tumor imaging and therapy.
- SSTR2 expression is observed in other tumor types, including breast cancer, at varying frequencies.
- Investigating SSTR2 as a target for breast cancer imaging and treatment is warranted.
Purpose of the Study:
- To assess the potential of SSTR2-targeted imaging and therapy in breast cancer patients.
- To evaluate SSTR2 expression in ER-positive and ER-negative breast cancer tissues.
- To determine the efficacy of SSTR2-targeted Dotatate PET/CT and radioligand therapy.
Main Methods:
- Preclinical assessment of SSTR2 expression in breast cancer tissue microarrays using H-score analysis.
- Prospective phase 2 clinical trial involving Dotatate PET/CT in metastatic ER-positive breast cancer patients.
- Treatment of one patient with metastatic ER-positive breast cancer using SSTR2-targeted actinium 225 (225Ac) Dotatate.
Main Results:
- SSTR2 enrichment was significantly higher in ER-positive (51%) versus ER-negative (18%) breast cancer tissues.
- Dotatate PET/CT identified 30% of metastatic ER-positive breast cancer patients with tumors showing strong SSTR2 expression (Krenning score 3 or 4).
- SSTR2-targeted 225Ac-Dotatate therapy achieved a near complete response in a heavily pretreated metastatic ER-positive breast cancer patient.
Conclusions:
- Molecular imaging targeting SSTR2 with Dotatate PET/CT is feasible in metastatic breast cancer.
- SSTR2-targeted radioligand therapy using 225Ac-Dotatate represents a novel therapeutic option.
- These findings open new avenues for personalized treatment strategies in metastatic breast cancer.
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