Speaker
Dr
Manoj Gupta
(Rajiv Gandhi Cancer Institute and Research Centre, Delhi, India)
Description
Introduction
Prostate cancer patients with distant metastasis have a poor prognosis and developed resistance to all standard drugs at various time intervals. A therapeutic option which can alleviate symptoms and prolong survival is in-search for these patients. [177Lu] prostate specific membrane antigen ([177Lu]PSMA) is a novel drug based on the theranostic concept. Here, we have presented the safety and efficacy profile of one cycle of [177Lu]PSMA in metastatic castration-resistant prostate cancer (mCRPC) patients who have exhausted all standard therapeutic options.
Methods
Twenty-two patients treated with at least first line anti-androgens and docetaxel were treated with one cycle of [177Lu]PSMA therapy on a compassionate basis. Haemoglobin, total leukocyte counts, platelets and serum creatinine for toxicity profile while prostate-specific antigen (PSA), eastern cooperative oncology group (ECOG) performance status, visual analogue scale (VAS) and analgesic quantification scale (AQS) for therapeutic efficacy were recorded pre and 8 weeks post-therapy. Wilcoxon signed-rank and ANOVA tests were used for statistical analysis.
Results
Partial response (PR), stable disease (SD) and progressive disease (PD) for PSA were seen in 5 (22.7%), 13 (59.1%) and 4 (18.2%) patients respectively treated with mean 6.88GBq dose of [177Lu]PSMA. 8/22 (36.4%) patients showed ≥ 30% drop in PSA. Grade 3 haemoglobin toxicity was seen in 5/22 (22.7%) patients. No patient developed grade 4 haemoglobin toxicity. No patients had grade 3 or 4 leukocytopenia or thrombocytopenia. Wilcoxon signed-rank test showed statistical significant (p <0.05) difference in pre and post-treatment ECOG, VAS, AQS scores while it was insignificant for PSA (P > 0.05). ANOVA test showed a statistically significant difference in mean doses of [177Lu]PSMA used in three PSA response group while the difference was non-significant for other variables.
Conclusion
We concluded that [177Lu]PSMA therapy has adequate pain palliation in all end-stage mCRPC patients and it has the potential to become an effective therapeutic option in properly selected patients.
Keywords: [177Lu]PSMA, Safety, efficacy, mCRPC
Funding Agency | None |
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Email Address | docmanojgupta@yahoo.com |
Presentation Type | Contributed Oral |
Primary author
Dr
Manoj Gupta
(Rajiv Gandhi Cancer Institute and Research Centre, Delhi, India)
Co-authors
Mrs
Amita Gupta
(Rajiv Gandhi Cancer Institute and Research Centre, Delhi, India.)
Dr
Amitabh Singh
(Rajiv Gandhi Cancer Institute and Research Centre, Delhi, India.)
Prof.
Harish Chandra Goel
(Amity centre for radiation biology, Amity University, Noida, Uttar Pradesh India)
Dr
Kumar Deep Dutta
(Rajiv Gandhi Cancer Institute and Research Centre, Delhi, India.)
Dr
Partha Choudhury
(Rajiv Gandhi Cancer Institute and Research Centre, Delhi, India)
Dr
Sudhir Rawal
(Rajiv Gandhi Cancer Institute and Research Centre, Delhi, India,)
Dr
Vineet Talwar
(Rajiv Gandhi Cancer Institute and Research Centre, Delhi, India.)