177Lu-PSMA Therapy, also known as Lutetium-177 Prostate-Specific Membrane Antigen Therapy, is a cutting-edge nuclear medicine treatment designed for patients with advanced or metastatic prostate cancer who have not responded well to conventional treatments such as surgery, radiation therapy, hormone therapy, or chemotherapy. This therapy uses a radioactive isotope (Lutetium-177) attached to a molecule that binds specifically to PSMA—a protein found in high levels on the surface of prostate cancer cells. By delivering radiation directly to cancerous cells, 177Lu-PSMA therapy targets and destroys tumors with minimal damage to surrounding healthy tissues. It is administered intravenously in multiple cycles, typically spaced 6–8 weeks apart, with the number of cycles ranging from 2 to 6, depending on patient response and clinical condition.
What is PSMA and Why is it Important?
PSMA (Prostate-Specific Membrane Antigen) is a cell surface protein that is significantly overexpressed in more than 90% of prostate cancer cases, particularly in metastatic or castration-resistant prostate cancer (mCRPC). This makes it an ideal target for imaging and therapy. The unique aspect of PSMA-targeted therapies is that they can selectively deliver therapeutic agents directly to prostate cancer cells, sparing normal tissue and enhancing treatment efficacy. 177Lu-PSMA-617, the most commonly used radioligand, combines Lutetium-177 (a beta-emitting radioisotope) with a PSMA-binding ligand, ensuring that the radioactive compound accumulates only where PSMA is present—primarily in prostate cancer lesions.
Who Can Benefit from 177Lu-PSMA Therapy?
177Lu-PSMA therapy is generally offered to patients who:
Have metastatic prostate cancer, especially castration-resistant (mCRPC)
Have failed or progressed after first-line treatments like hormone therapy or chemotherapy
Have confirmed PSMA-avid disease, seen on PSMA PET-CT scans
Are medically fit to undergo radionuclide therapy and can tolerate intravenous treatment
Do not have contraindications such as severe bone marrow suppression or renal impairment
This therapy is personalized—meaning patient suitability is carefully evaluated through clinical history, laboratory reports, and PSMA PET-CT imaging before initiating the treatment cycle.
How is 177Lu-PSMA Therapy Administered?
The treatment is typically delivered in outpatient settings and involves systemic injection of the radioligand under the supervision of a trained nuclear medicine team. The general protocol includes:
Pre-Therapy Evaluation
Blood tests to assess renal, liver, and bone marrow function
PSMA PET-CT scan to confirm PSMA-avid lesions
Review of prior treatments and imaging studies
Therapy Session
177Lu-PSMA is administered through an intravenous line
The injection typically takes 10–15 minutes
Post-injection, patients are monitored for a short time for any acute reactions
Radiation safety instructions are given before discharge
Treatment Cycle
Patients usually receive 2 to 6 cycles, each spaced 6–8 weeks apart
The total number of cycles depends on response to therapy and tolerability
Follow-Up
Clinical assessments
PSA level monitoring
Repeat imaging (such as PSMA PET-CT) to evaluate response
Side effect evaluation and supportive care as needed
What are the Benefits of 177Lu-PSMA Therapy?
Patients undergoing 177Lu-PSMA therapy can experience significant clinical improvement, including symptom relief and better quality of life.
Key Benefits:
• Targeted therapy – Directly binds to prostate cancer cells while sparing healthy tissue
• Reduced tumor burden – Helps in controlling disease progression in metastatic cases
• Pain relief – Especially beneficial for patients with bone metastases
• Improved survival outcomes – Has shown promising results in clinical trials
• Outpatient-based – Requires no hospital stay in most cases
• Well-tolerated – Lower toxicity compared to traditional chemotherapy
What Are the Possible Side Effects?
While 177Lu-PSMA therapy is generally well-tolerated, some patients may experience mild to moderate side effects. These may include:
Fatigue and weakness
Mild nausea or vomiting
Dry mouth (xerostomia) due to salivary gland uptake
Temporary decrease in blood cell counts (anemia, leukopenia, thrombocytopenia)
Rarely, renal impairment or liver function abnormalities
Most side effects are temporary and manageable, with appropriate supportive care.
Response Monitoring and Effectiveness
The effectiveness of 177Lu-PSMA therapy is typically measured through:
Decline in PSA levels – PSA (Prostate-Specific Antigen) levels are monitored throughout the therapy
Symptom relief – Especially pain reduction in bone metastases
Follow-up PET-CT or other imaging – To assess disease status post-treatment
Improvement in quality of life – Increased energy levels, appetite, and mobility
Studies have shown that over 60–70% of patients respond favorably to this therapy, with measurable drops in PSA levels and radiological evidence of disease stabilization or regression.
Precautions and Considerations
While the therapy is safe for most, certain precautions are necessary:
Radiation safety – Patients are advised to limit close contact with pregnant women and small children for a few days
Hydration – Encouraged before and after therapy to promote renal clearance of the radiotracer
Routine monitoring – Blood tests are conducted before each cycle to monitor for bone marrow suppression or kidney issues
Pre-existing conditions – Those with severe kidney or liver issues may need customized protocols
Conclusion
177Lu-PSMA Therapy represents a breakthrough in targeted treatment for advanced prostate cancer, especially for those who have exhausted conventional therapies. It harnesses the power of precision nuclear medicine, offering patients a chance to manage their disease effectively, with fewer side effects and improved quality of life. This innovative approach allows for personalized cancer care, aligning with the growing need for tailored and less toxic cancer treatment options. As research continues and accessibility expands, 177Lu-PSMA therapy is poised to become a cornerstone in the fight against metastatic prostate cancer.
Test information: Fasting: 2 hours
Reporting: Not applicable
In pre-work up, blood tests such as complete blood count (CBC), liver and kidney function tests (LFT, KFT), and serum electrolytes are to be carried out. The DTPA and salivary gland scans are performed to look for kidney and salivary gland functions.
68Ga-PSMA or 18F-PSMA PET/CT scan is done before and after every two cycles of 177Lu-PSMA therapy and after the entire treatment.
After 177Lu-PSMA therapy, every 2–3 weeks (depending on baseline conditions), blood cell count should be checked for up to 12 weeks. The serum PSA level is also checked periodically as a follow-up.
Every 6–8 weeks, basic liver and kidney profiles should be assessed.
During the first 2 days after therapy, the high activity level is excreted. Patients are advised to avoid contamination of toilets and flush the toilet twice. Patients should wash their hands after urination.
Patients should avoid soiling underclothing or areas around toilet bowls for 1 week following therapy. Considerably contaminated clothing should be washed separately.
Incontinent patients should be catheterized before therapy, and the catheter should be kept for 2 days after that. Urine bags should be emptied frequently. • Gloves and protective clothing should be worn by the person caring for catheterized patients (or providing any care involving close contact).
कुछ रक्त परीक्षण जैसे पूर्ण रक्त गणना (सीबीसी), यकृत और गुर्दा परीक्षण (एलएफटी, केएफटी), और सीरम इलेक्ट्रोलाइट्स प्रत्येक उपचार चक्र से पहले और अनुवर्ती उपचार पर किए जाते हैं। गुर्दे और लार ग्रंथि के कार्यों को देखने के लिए डीटीपीए और लार ग्रंथि स्कैन किए जाते हैं।
68Ga-PSMA या 18F-PSMA PET/CT स्कैन 177Lu-PSMA थेरेपी के हर दो चक्र से पहले और पूरे उपचार के बाद किया जाता है।
177Lu-PSMA चिकित्सा के बाद, प्रत्येक 2-3 सप्ताह (आधारभूत स्थितियों के आधार पर), 12 सप्ताह तक रक्त कोशिकाओं की संख्या की जाँच की जानी चाहिए। अनुवर्ती कार्रवाई के रूप में सीरम पीएसए स्तर की समय-समय पर जाँच की जाती है।
प्रत्येक 6-8 सप्ताह में, यकृत और गुर्दा प्रोफाइल का मूल्यांकन किया जाना चाहिए।
थेरेपी के बाद पहले 2 दिनों के दौरान, उच्च स्तर की रेडियोधर्मिता उत्सर्जित होती है। मरीजों को शौचालय के दूषित होने से बचने और शौचालय को दो बार फ्लश करने की सलाह दी जाती है। मरीजों को पेशाब के बाद हाथ धोना चाहिए।
थेरेपी के बाद 1 सप्ताह तक मरीजों को अपने नीचे के कपड़े या शौचालय के आसपास के क्षेत्रों को गंदा करने से बचना चाहिए। काफी दूषित कपड़ों को अलग से धोना चाहिए।
थेरेपी से पहले मूत्र के रोगियों को कैथीटेराइज किया जाना चाहिए, और कैथेटर को उसके बाद 2 दिनों तक रखा जाना चाहिए। यूरिन बैग को बार-बार खाली करना चाहिए।
कैथीटेराइज्ड रोगियों की देखभाल करने वाले (या निकट संपर्क मे देखभाल प्रदान करने वाले) व्यक्ति द्वारा दस्ताने और सुरक्षात्मक कपड़े पहने जाने चाहिए।
प्रसव की क्षमता वाली महिलाओं को उपचार के दौरान प्रभावी गर्भनिरोधक का उपयोग करना चाहिए और उसके बाद कम से कम 6 महीने तक गर्भधारण से बचना चाहिए।
पुरुष रोगियों को उपचार से पहले स्पर्म बैंकिंग पर विचार करना चाहिए।
After registration and payment, the patient's medical history is taken on the day of therapy, including checking referral, surgical and treatment details, investigation records, history of last meal, etc. Informed consent is also obtained at the same time.
The procedure is done in daycare. The patient is detained for 3-4 hours, and during this, intravenous fluid is given to achieve sufficient hydration and reduce the effect of the medicine on non-target organs.
While continuing the IV fluids, 177Lu-PSMA is infused slowly, and fluid administration continues.
Once therapy is completed, the patient is observed for some time and then discharged.
The patient may be called for the post-therapy scan on 3rd day from the therapy date.
* For details, please see service-related policies
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