
B7-H3 radiopharmaceutical enters first-in-human tumor trial
The first patient in the Phase 1/2a study received the investigational B7-H3-targeted radiopharmaceutical therapy at BAMF Health.
Section
Imaging research, modality advances, and clinical practice updates.

The first patient in the Phase 1/2a study received the investigational B7-H3-targeted radiopharmaceutical therapy at BAMF Health.

Vanderbilt Health researchers reported that MyProstateScore 2.0 Active Surveillance outperformed PSA-based testing and MRI for monitoring low-risk prostate cancer.

ARPA-H awarded Siemens Healthineers’ Varian business up to $60M over 5 years to advance photon Flash radiotherapy.

Researchers found that age and lifetime low-level alcohol exposure were associated with lower cortical perfusion and thinner cortex on MRI in healthy adults.

A JACR study found that gallium-68 PET radiotracer adoption widened rural access gaps for neuroendocrine tumor imaging, while copper-64 DOTATATE later reduced those differences.

A phase 2 DETECT study found that 99mTc-maraciclatide SPECT/CT imaging was concordant with surgical findings in 16 of 19 participants with suspected or confirmed endometriosis.

Researchers reported that ¹⁷⁷Lu-AKIR001 achieved complete remission in 40% of treated mice with pancreatic ductal adenocarcinoma xenografts.

The phase 2/3 trial is evaluating mangaciclanol, GE HealthCare’s investigational manganese-based MRI contrast agent.

Researchers found that lower preoperative diaphragmatic dome height on chest X-rays was associated with poorer 3-year survival after lung cancer surgery. The measurement may offer a low-cost way to identify higher-risk patients before lobectomy.

The IPAX BrIGHT trial is evaluating TLX101-Tx with lomustine versus lomustine alone in patients with recurrent glioblastoma.

Researchers found that ultrasound-enhanced fine-needle aspiration biopsy produced larger tissue samples than conventional fine-needle and core-needle biopsy in benign parotid gland tumors without reducing sample quality.

The DOORwaY90 study reported a 90% complete response rate and 99% best overall response rate for SIR-Spheres Y-90 resin microspheres.

The FDA assigned a September 11, 2026, PDUFA goal date for Pixclara, an investigational F-18 FET PET agent for glioma imaging.

The Phase 1 first-in-human trial is evaluating RYZ401, an Ac-225-labeled radiopharmaceutical targeting somatostatin receptors in neuroendocrine tumors and other solid tumors.