Dose-Dense Docetaxel and Radium-223 in Bone-Dominant Metastatic Castration-Resistant Prostate Cancer

• Published in: Clinical genitourinary cancer Vol. 23; no. 4; p. 102368
• Main Authors: Connell, Brendan, Hwang, Clara, Folefac, Edmund, Lawlor, Christian, Koethe, Benjamin, Mathew, Paul
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.08.2025
• Subjects: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols - administration & dosage; Antineoplastic Combined Chemotherapy Protocols - adverse effects; Antineoplastic Combined Chemotherapy Protocols - therapeutic use; Bone metastases; Bone Neoplasms - drug therapy; Bone Neoplasms - secondary; Bone Neoplasms - therapy; Combination therapy; Docetaxel - administration & dosage; Docetaxel - adverse effects; Dose-Response Relationship, Drug; Efficacy; Granulocyte Colony-Stimulating Factor - administration & dosage; Humans; Lead-in cycle; Male; Maximum Tolerated Dose; Middle Aged; Prostatic Neoplasms, Castration-Resistant - drug therapy; Prostatic Neoplasms, Castration-Resistant - pathology; Prostatic Neoplasms, Castration-Resistant - therapy; Radium - administration & dosage; Radium - adverse effects; Safety; Treatment Outcome; Efficacy; Safety; Combination therapy; Bone metastases; Lead-in cycle
• ISSN: 1558-7673; 1938-0682; 1938-0682
• DOI: 10.1016/j.clgc.2025.102368

Disease progression in castration-resistant prostate cancer (CRPC) remains bone-dominant and docetaxel-responsive. Docetaxel and radium-223 would be a logical combination but myelosuppression is dose-limiting. Dose-dense schedules of docetaxel have comparable activity to bolus dosing with mitigated myelosuppression. We hypothesized that dose-dense docetaxel with standard radium-223 would be a feasible, safe and effective combination in bone-dominant metastatic CRPC. Subjects had progressive bone-predominant CRPC. Design was dose escalation plus expansion with 28-day cycles. Docetaxel was given every 2 weeks in a 4-week lead-in, then with Radium-223 every 4 weeks up to 6 cycles. Dose-levels (DL) included 1: docetaxel 40 mg/m2; 1a: docetaxel 40 mg/m2 with G-CSF on Day 16, 2a: docetaxel 50 mg/m2 with G-CSF on Day 16. The maximum tolerated dose (MTD) was defined as the highest (DL) of docetaxel achieved without dose-limiting toxicity (DLT). Markers of safety and efficacy were annotated. Forty-three subjects were enrolled (NCT03737370). The patient population included 21% black, 9% Asians, 93% had prior intensified hormonal therapy, 67% had bone pain, and 76% had ≥ 4 bone metastases. Seven patients dropped out during the 4-week docetaxel lead in. Neutropenia at DL 1 limited combination therapy. No (DLT) occurred at DL 1a (n = 6) or DL 2a (n = 5). Twenty-two patients were enrolled to an expansion cohort with docetaxel 50 mg/m2 with G-CSF on Day 16 (DL 2a), the designated MTD. Among 35 patients treated with the combination, there were no febrile neutropenia events. One patient had dose-limiting Grade 3 anemia. PSA50 response was 51.4% and PSA90 was 25.7%. Median progression-free survival was 11.7 months, and median overall survival was 20.1 months. A lead-in cycle and a dose-dense schedule of docetaxel with G-CSF enabled the combination with radium-223 in standard dose-intensities with minimal hematological toxicity. The regimen will likely combine logically and safely with hormone-intensification for study in high-risk/high-volume castration-sensitive metastatic disease. A dose-dense schedule of docetaxel 50 mg/m2 every 2 weeks with G-CSF on Day 16 permits combination with standard Ra-223 every 4 weeks, with preservation of dose-intensity of both agents in CRPC. The survival advantages demonstrated by both agents in CRPC warrants study of the dose-dense combination in castration-sensitive high-risk/high-volume disease where the therapeutic benefit may be disproportionately larger.