Cabazitaxel in mCRPC Patients With AR-V7 Positive Circulating Tumor Cells (CTCs) (CABA-V7)

A Single Arm Phase 2 Multicenter Study Determining the Response to Cabazitaxel in Metastatic Prostate Cancer (mCRPC) Patients With AR-V7 Positive Circulating Tumor Cells (CTCs)

After failure on docetaxel, which has been the standard first line therapy for patients with metastatic castration-resistant prostate cancer (mCRPC), several treatment options are currently available.

In retrospective studies, resistance has been described to two of the treatment options, enzalutamide and abiraterone, when a splice variant of the Androgen Receptor (AR-V7) is present on circulating tumor cells (CTCs). The investigators hypothesize that patients with AR-V7 positive CTCs do have a meaningful response to cabazitaxel.

Study Overview

• Status: Active, not recruiting
• Conditions: Metastatic Prostate Cancer; Circulating Tumor Cell
• Intervention / Treatment: Drug: Cabazitaxel; Other: Antihistamine; Other: Corticosteroid; Other: H2 antagonist; Other: Antiemetic

Detailed Description

After failure on docetaxel, which has been the standard first line therapy for patients with metastatic castration-resistant prostate cancer (mCRPC), several treatment options are currently available.

Two of the treatment options are directed against the androgen receptor (AR), enzalutamide and abiraterone. A third option is cabazitaxel, a next generation taxane. No head-to-head comparisons have been done for these three therapies in second-line mCRPC and as of yet, the optimal choice is unknown.

Resistance to the AR-targeted therapies is at least in part a consequence of signaling through constitutively active AR splice variants (AR-Vs). Because AR splice variants only occur after conversion to a castration-resistant tumor, and can be acquired during systemic therapy for mCRPC, analysis of the castration-naïve primary tumor is not informative in the setting of second-line treatment of mCRPC.

Circulating tumor cells (CTCs) can be analyzed repetitively and in real-time. Recently, AR-V7 messenger ribonucleid acid (mRNA) expression in CTCs was shown to be associated with lack of response to AR-targeted therapy (reference 1). AR-V7 mRNA expression does not seem to hinder response to cabazitaxel in our retrospective pilot study (reference 2) nor in two recently published retrospective studies (reference 3 and reference 4).

Therefore we hypothesize that the mRNA expression of AR-V7 in CTCs assessed before start of second-line treatment for mCRPC does not affect prostate-specific antigen (PSA) response to cabazitaxel in patients who have progressed to docetaxel.

Patients who are eligible to undergo second or third line treatment will be asked to undergo prescreening consisting of a CTC count and, in case ≥3 CTCs are detected, AR V7 determination. Patients with ≥3 CTCs with AR-V7 expression will be asked to sign a second informed consent to enter the treatment study. In this study they will receive Cabazitaxel 25 mg/m² every 3 weeks plus prednisone 10 mg daily, and undergo repeated blood sampling for biomarker sample collection.

During the prescreening in all patients, 2 x 10 mL blood will be drawn for enumeration and isolation of CTCs. All patients with ≥3 CTCs with AR-V7 expression will be asked to sign consent for the treatment study.

All patients included in the treatment study will be administrated cabazitaxel intravenously at a dose of 25 mg/m², during a one-hour infusion every 3 weeks, as well as continuous treatment with prednisone 5 mg orally twice daily, or 10 mg once daily. In the treatment study patients, an additional 2 x 10 mL blood will be drawn after the third cycle of treatment for CTC enumeration and isolation. An additional 10 mL blood will be drawn for storage of plasma at baseline and before start of every cycle (i.e., every 3 weeks) for analysis of cell-free DNA (cfDNA). Moreover, 4 x 5 mL blood (baseline; end of infusion, 2 and 6 hours after end of the first cabazitaxel infusion) will be drawn for pharmacokinetic studies, in order to explore a cabazitaxel exposure effect relation.

• Study Type: Interventional
• Enrollment (Anticipated): 140
• Phase: Phase 2

Contacts and Locations

Study Locations

• Netherlands
  • Delft, Netherlands
    • Reinier de Graaf Groep
  • Den Haag, Netherlands
    • Medisch Centrum Haaglanden
  • Gouda, Netherlands
    • Groene Hart Ziekenhuis
  • Nijmegen, Netherlands
    • Canisius Wilhelmina Ziekenhuis
  • Rotterdam, Netherlands
    • Maasstad Ziekenhuis
  • Rotterdam, Netherlands
    • Erasmus MC
  • Rotterdam, Netherlands
    • Franciscus Gasthuis en Vlietland
  • Tilburg, Netherlands
    • Tweesteden Ziekenhuid
  • Vlissingen, Netherlands
    • Admiraal de Ruyter Ziekenhuis

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Male

Description

Inclusion Criteria:

• Histologically or cytologically confirmed adenocarcinoma of the prostate without neuroendocrine differentiation or small cell features.
• Continued androgen deprivation therapy either by luteinizing hormone-releasing hormone (LHRH) agonists/antagonists or orchiectomy.
• Serum testosterone <50 ng/mL (1.7 nmol/L) within 21 days before prescreening.
• Age ≥18 years
• Received prior docetaxel, and experienced disease progression during or after treatment with docetaxel.
• Eastern Cooperative Oncology Group (ECOG) performance status 0-2 (appendix A)
• Written informed consent according to ICH-GCP (International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use - Good Clinical Practice) before study treatment and any study specific procedures

Exclusion Criteria:

• Geographical, psychological or other non-medical conditions interfering with follow-up
• Uncontrolled severe illness or medical condition (including uncontrolled diabetes mellitus or active systemic or local bacterial, viral, fungal - or yeast infection)
• Symptomatic central nervous system (CNS) metastases or history of psychiatric disorder that would prohibit the understanding and giving of informed consent.
• Chemotherapy or immunotherapy (other than LHRH analogues) within the last 4 weeks before study inclusion.
• Prior treatment with cabazitaxel
• Treatment with both abiraterone and enzalutamide in the post-docetaxel setting
• Radiotherapy to 40% or more of the bone marrow
• Known hypersensitivity to corticosteroids
• History of severe hypersensitivity reaction (≥grade 3) to docetaxel
• History of severe hypersensitivity reaction (≥grade 3) to polysorbate 80 containing drugs
• Concurrent or planned treatment with strong inhibitors or strong inducers of cytochrome P450 3A4/5 (a one week wash-out period is necessary for patients who are already on these treatments)
• Concomitant vaccination with yellow fever vaccine
• Abnormal liver functions
• Abnormal hematological blood counts

Study Plan

How is the study designed?

Design Details

• Primary Purpose: DIAGNOSTIC
• Allocation: NA
• Interventional Model: SINGLE_GROUP
• Masking: NONE

Number of Arms

1

Arms and Interventions

Participant Group / Arm

Intervention / Treatment

OTHER: Treatment; Treatment intervention with Cabazitaxel with premedication as necessary (antihistamine, corticosteroid, H2 antagonist, antiemetic prophylaxis)

Drug: Cabazitaxel; 25mg/m2 q3w; Other Names: Jevtana; Other: Antihistamine; As intravenous premedication (dexchlorpheniramine 5 mg, diphenhydramine 25 mg, or equivalent); Other: Corticosteroid; As intravenous premedication (dexamethasone 8 mg or equivalent); Other: H2 antagonist; As intravenous premedication (ranitidine or equivalent); Other Names: histamine H2 receptors blockers; Other: Antiemetic; Antiemetic prophylaxis is recommended and can be given orally or intravenously if necessary

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
PSA response	The primary endpoint is PSA response, defined as a ≥50% PSA decline from baseline during therapy.	12 weeks after start of treatment

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
CTC response	CTC response defined as a decrease from ≥5 CTCs per 7.5 mL blood at baseline to <5 CTCs per 7.5 mL blood	9-12 weeks after start of treatment
PSA change	PSA change from baseline at 12 weeks defined as the percent change in PSA from baseline at 12 weeks, according to PCWG2 criteria	12 weeks after start of treatment
PSA decrease	Maximum PSA decrease defined according to PCWG2 criteria	PSA will be assessed at baseline, every 3 weeks during study treatment (before every cycle), and in case of study treatment discontinuation without progression every 3 months until progression, death, whichever comes first
Progression free survival	Progression-free survival (PFS) defined as time from prescreening to the date of the first documentation of disease progression (PCWG2)	Until end of study, which is anticipated to be 4 years after inclusion of first patient. If progression is not observed during the study, data on PFS will be censored
Overall survival	Overall survival (OS) calculated from the date of prescreening to death due to any cause	Until end of study, which is anticipated to be 4 years after inclusion of first patient. If death is not observed during the study, data on OS will be censored at the date patient is known to be alive or at the cut-off date, whichever comes first
Adverse Events	Grade 3-4 adverse events (AEs) and serious adverse events (SAEs) during cabazitaxel according to CTCAE v4.03 in second and third-line treatment	Until 30 days after end of treatment, Cabazitaxel treatment will consist of a maximum 10 cycles Cabazitaxel (given once every 3 weeks if there are no delays)
Cumulative dose Cabazitaxel	Cumulative administered dose of cabazitaxel in second and third-line treatment	Until last day of administration of study medication (Cabazitaxel), Cabazitaxel treatment will consist of a maximum 10 cycles Cabazitaxel (given once every 3 weeks if there are no delays)
Splice variants	AR-V7 mRNA expression as well as mRNA expression of other splice variants in CTCs indicated as absent (-) or present (+)	Splice variant will be compared before and after cabazitaxel treatment in AR-V7 positive patients, as well as before start of enzalutamide or abiraterone and after disease progression to this treatment.
Total systemic exposure	Cabazitaxel concentration in the blood and total systemic exposure to cabazitaxel, measured by the calculated area under the curve (AUC)	After infusion of first cycle of study treatment (Cabazitaxel)
Value ctDNA quantification	To explore the value of ctDNA quantification during cabazitaxel treatment to predict tumor progression	Until end of study, which is anticipated to be 4 years after inclusion of first patient

Collaborators and Investigators

• Sponsor: Erasmus Medical Center
• Collaborators: Sanofi

Study record dates

Study Major Dates

• Study Start (ACTUAL): February 21, 2017
• Primary Completion (ANTICIPATED): January 1, 2022
• Study Completion (ANTICIPATED): August 19, 2022

Study Registration Dates

• First Submitted: February 7, 2017
• First Submitted That Met QC Criteria: February 8, 2017
• First Posted (ACTUAL): February 13, 2017

Study Record Updates

• Last Update Posted (ACTUAL): August 20, 2021
• Last Update Submitted That Met QC Criteria: August 19, 2021
• Last Verified: August 1, 2021

More Information

Terms related to this study

• Keywords: Androgen Receptor; AR-V7; Predictive Factor
• Additional Relevant MeSH Terms: Pathologic Processes; Neoplasms; Urogenital Neoplasms; Neoplasms by Site; Genital Neoplasms, Male; Prostatic Diseases; Neoplastic Processes; Neoplasm Metastasis; Prostatic Neoplasms; Neoplastic Cells, Circulating; Physiological Effects of Drugs; Neurotransmitter Agents; Molecular Mechanisms of Pharmacological Action; Autonomic Agents; Peripheral Nervous System Agents; Gastrointestinal Agents; Histamine Agents; Histamine Agonists; Histamine H1 Antagonists; Histamine Antagonists; Antiemetics; Histamine
• Other Study ID Numbers: NL58639.056.16

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: UNDECIDED
• IPD Plan Description: Information can be shared by importing it into another databases

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No