Lutetium-177 (¹⁷⁷Lu)
Lutetium-177 is a radioactive isotope of the element lutetium, widely used in theranostics (both therapy and diagnostics).
It emits:
- Beta particles (β⁻): Medium-energy electrons that travel a few millimeters in tissue, causing localized damage (useful for targeted therapy).
- Gamma photons: Allow imaging with scintigraphy (e.g., SPECT scans) to monitor the treatment distribution.
Key Characteristics
Property | Description |
---|---|
Half-life | ~6.7 days |
Beta energy (Eβmax) | 497 keV |
Gamma energy | 208 keV (11% abundance) |
Tissue penetration | 0.2 to 2 mm (depending on tissue density) |
Production | Produced by irradiating ytterbium-176 targets in nuclear reactors. |
Importance in Medicine
¹⁷⁷Lu is crucial for:
- Targeted radiotherapy: Attached to ligands that seek out specific cancer cells.
- Precision therapy: Short beta range minimizes damage to healthy tissues.
- Theranostics: Simultaneous imaging and treatment.
Current clinical uses:
- Prostate cancer (¹⁷⁷Lu-PSMA-617 therapy).
- Neuroendocrine tumors (¹⁷⁷Lu-DOTATATE therapy).
Emerging research:
- Applications in glioblastoma, breast cancer, and renal cancer where PSMA or similar targets are expressed.
Example: Application in Glioblastoma
Recent studies suggest PSMA is expressed not directly on GBM tumor cells, but on tumor-associated endothelial cells.
¹⁷⁷Lu-PSMA-617 therapy might:
- Damage tumor vasculature, starving the tumor.
- Bypass blood-brain barrier defects present in GBM.
Challenges:
- Variable PSMA expression.
- Need for controlled clinical trials.
- Safety concerns regarding radiation to normal brain tissue.
Case Report: A 42-year-old man with refractory GBM showed an excellent response to six doses of ¹⁷⁷Lu-PSMA-617 (100-150 mCi every 4–5 weeks), confirmed by MRI and ⁹⁹mTc-HYNIC-PSMA-11 scintigraphy 1)
Future directions:
- Larger trials.
- Better patient selection.
- Combination therapies.
A 37-year-old man, treated case of left temporal glioblastoma, presented with headache, seizures, and progressive right-sided weakness with MRI evidence of recurrence. Exploratory Ga-PSMA PET/CT demonstrated PSMA expression in the recurrent lesion; it was decided to treat this patient with Lu-PSMA-617. After 3 cycles of Lu-PSMA-617, Ga-PSMA PET/CT showed significant reduction in PSMA uptake and regression in size of lesion on MRI with improvement in patient's symptoms and performance status. Lu-/Ga-PSMA theranostics has potential in patients with recurrent glioblastoma when other therapeutic options are not feasible 2).