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Excellus BlueCross BlueShieldCommercial · Coverage · Cancer Treatment (Oncology) · NY · Oncology, Nuclear MedicineMedium impact

Radiopharmaceuticals for the Treatment of Cancer 6.01.44

Effective date
Sep 17, 2026
Identified
Jun 20, 2026

Summary

Policy 6.01.44 considers radiopharmaceutical treatments for cancer medically appropriate only within their FDA-approved regimen, and requests in excess of that regimen are considered investigational. Xofigo is considered medically appropriate for castration-resistant prostate cancer with symptomatic bone metastases and no known visceral metastatic disease or bulky regional lymph nodes greater than 3 cm on imaging within the past 30 days. Pluvicto, Lutathera, strontium-89 chloride, and HICON (sodium iodide I 131) are each considered medically appropriate only when their listed criteria are met. The September 18, 2025 review added a new Pluvicto indication and removed Azedra and Zevalin because both are no longer commercially available.

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What to do

Action · 9 steps
01Current version effective September 17, 2026: Billing team, confirm that each radiopharmaceutical request is within its FDA-approved regimen, because requests beyond that regimen are considered investigational.
02Before billing Xofigo, confirm the record documents castration-resistant prostate cancer, symptomatic bone metastases, and no known visceral metastatic disease or bulky regional lymph nodes greater than 3 cm on imaging within the past 30 days.
03Hematologic evaluation must be performed at baseline and before every Xofigo dose.
04Before the first Xofigo dose, ANC must be 1.5 x 10^9 per L or greater, platelets 100 x 10^9 per L or greater, and hemoglobin 10 g/dL or greater; before later doses, ANC must be 1 x 10^9 per L or greater and platelets 50 x 10^9 per L or greater.
05Before billing Pluvicto, confirm PSMA-positive metastatic castration-resistant prostate cancer, prior treatment with at least one androgen receptor pathway inhibitor (enzalutamide and/or abiraterone), one or two taxane-based regimens or appropriateness to delay taxane-based chemotherapy, and a PSMA PET/CT scan showing at least one PSMA-positive metastatic lesion and no PSMA-negative lesions.
06Before billing Lutathera, confirm the tumor type and Ki-67 limits, positive somatostatin receptor scintigraphy with correlative MRI or CT or a positive 68-Ga-Dotate PET scan, progression after somatostatin analogs, and the absence of the listed contraindications.
07When there is no metastatic disease, document a surgical or medical consult and the reason for inoperability.
08Before billing HICON, confirm remnant ablation criteria, one of the listed adjuvant criteria, or proven unresectable or metastatic disease.
09Before billing strontium-89 chloride, confirm bone pain in patients with confirmed skeletal metastases, and note that repeat doses are generally not recommended at intervals of less than 90 days.

Codes mentioned

77750791017900579403963749637596409A4641A9513A9517A9530A9600A9606A9607C9399C61C79.51C79.52D40.0V58.0Z85.46

Original notice

Radiopharmaceuticals for the Treatment of Cancer 6.01.44
excellusbcbs.com · Always check the source before changing claims.
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