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Generation of Prostate Cancer Patient Derived Xenograft Models from Circulating Tumor Cells
Published on: October 20, 2015
Phase II Trial of Eribulin in Patients With Metastatic Hormone Refractory Prostate Cancer: A Trial of the ECOG-ACRIN
Mark N Stein1, Yu-Hui Chen2, Michael A Carducci3
1Columbia University Medical Center, New York, NY.
Background:
Eribulin mesylate, a synthetic analog of halichondrin B, is a novel tubulin-binding agent that inhibits cancer cell proliferation at low-nanomolar levels.
Methods:
In a multicenter ECOG trial, patients with progressive metastatic CRPC, ECOG 0-2 were treated with eribulin 1.4 mg/m as an IV bolus over 5 minutes on days 1 and 8 of a 21-day cycle. This noncomparative study stratified points to either a chemonaive (CN), prior-taxane (Tax) only, or 2 prior cytotoxic (TCx) chemotherapy arm. The trial was powered to detect a 50% PSA reduction using Consensus Criteria in at least 40% versus 20% (90% power, one-sided α=0.10) for the CN stratum and 25% versus. 10% (power 87%, one-sided α=0.10) for the Tax and TCx strata.
Results:
In total, 119 pts received treatment of which 116 were eligible for the primary response determination in this study. Median age 70 years (range, 45 to 88); median number of treatment cycles 4 (range, 1 to 20+); ECOG 0-1 90%. Confirmed PSA response rates (50% decline from baseline) were 29% (90% [18.2%, 41.2%]; P=0.20), 10% (90% [5.2%, 27.1%]; P=1.00), and 4% ([0.2%, 18.3%]; P=0.59) in the chemonaive stratum, the prior-taxane stratum, and the 2-prior-chemotherapy stratum, respectively. Median progression-free survival was 3.5 months (95% CI, 2.0, 5.9), 2.3 months (95% CI, 2.0, 2.9) and 3.7 months (95% CI, 2.1, 4.2) for the chemonaive stratum, the prior-taxane stratum and the 2-prior-chemotherapy stratum, respectively. Nonhematological toxicities of any grade (mainly grade 1 and 2) were fatigue (74%), neuropathy (40%), alopecia (39%), nausea (35%), and anorexia (34%). Common hematological toxicities were decreased leukocytes (75%), decreased neutrophils (72%), and decreased hemoglobin (66%). The most common grade ≥ 3 toxicities were decreased neutrophils (55%), decreased leukocytes (42%), sensory neuropathy (13%), and fatigue (11%). Overall, there was a 4% rate of febrile neutropenia.
Conclusions:
In summary, per the prespecified study endpoints, eribulin did not have adequate activity in chemotherapy naïve or chemotherapy pretreated patients with metastatic CRPC to support further study in this setting.
Insights
Eribulin mesylate showed limited efficacy in treating metastatic castration-resistant prostate cancer (CRPC). The study concluded that eribulin is not suitable for further investigation in this patient population.
Area of Science:
- Oncology
- Pharmacology
Background:
- Eribulin mesylate is a novel synthetic analog of halichondrin B.
- It functions as a tubulin-binding agent, inhibiting cancer cell proliferation.
- Demonstrates potent anti-cancer activity at low nanomolar concentrations.
Purpose of the Study:
- To evaluate the efficacy of eribulin mesylate in patients with metastatic castration-resistant prostate cancer (CRPC).
- To assess response rates and progression-free survival in different patient strata.
- To determine the safety and tolerability of eribulin in this population.
Main Methods:
- A multicenter ECOG trial treated patients with progressive metastatic CRPC.
- Patients received eribulin 1.4 mg/m² intravenously on days 1 and 8 of a 21-day cycle.
- The study stratified patients into chemotherapy-naive, prior-taxane, or two-prior-cytotoxic chemotherapy arms.
Main Results:
- Confirmed PSA response rates were 29% (chemotherapy-naive), 10% (prior-taxane), and 4% (two-prior-chemotherapy).
- Median progression-free survival ranged from 2.3 to 3.7 months across strata.
- Common toxicities included fatigue, neuropathy, alopecia, nausea, anorexia, and hematological changes.
Conclusions:
- Eribulin did not demonstrate adequate activity in chemotherapy-naive or pretreated metastatic CRPC patients.
- The study concluded that eribulin is not supported for further investigation in this setting.
- The observed efficacy did not meet prespecified study endpoints.
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