Oral Docetaxel (ModraDoc/r) in Combination With Hormonal Treatment and Radiation Therapy in High-risk Prostate Cancer (DOP)

Netherlands Cancer Institute (NKI)

Status and phase

Terminated

Phase 1

Conditions

Prostatic Neoplasms

Treatments

Radiation: high-dose intensity-modulated radiation therapy

Drug: androgen deprivation therapy

Drug: oral docetaxel (ModraDoc/r)

Study type

Interventional

Funder types

Other

Identifiers

NCT03066154

N15DOP

Details and patient eligibility

About

The optimal treatment for HRPC patients has not yet been established. Recent trials suggest a benefit from early treatment with docetaxel in the castration-sensitive setting, with an improvement in failure free survival in high risk and metastatic patients and increase in overall survival in the metastatic hormone-sensitive group. In these recent randomized controlled trials, patients were treated with hormonal therapy and radiotherapy and adjuvant docetaxel, assuming that early systemic treatment for high risk or metastatic disease could delay progression in patients with aggressive primary tumor characteristics.

With the fact that docetaxel is a known radiosensitizer, combined modality treatment with docetaxel during the radiotherapy could also lead to better local control and reduction of local recurrence. Several phase I and II studies have been done in HRPC patients, to evaluate the combination of high dose radiotherapy and concurrent weekly infusions with docetaxel.

Oral administration of docetaxel has many advantages above intravenously administered drugs for patients. Besides the higher patient convenience, possibly longer treatment duration can be achieved due to better safety. Frequently occurring toxicities of intravenously administered docetaxel, such as neutropenia, hypersensitivity reactions and peripheral polyneuropathy have rarely been observed with the oral docetaxel formulation ModraDoc006/r.

The primary aim of the N15DOP study is to determine the maximum tolerable dose (MTD) of ModraDoc006/r when given in a weekly bidaily schedule in combined modality with high dose intensity radiotherapy and hormonal therapy in castration-sensitive prostate cancer patients with high risk disease, including positive lymph nodes.

Full description

Phase IA part This is an open-label, dose-escalating, non-randomized, single centre phase I study of ModraDoc006/r combined with ADT and radiotherapy in patients with high risk prostate cancer, as defined by node positive prostate cancer with all of the following primary tumor characteristics: stage ≥cT2c, Gleason score ≥ 4+3, any PSA level.

Phase IB part After determination of the MTD of ModraDoc006/r in the combined treatment with radiotherapy and hormonal therapy and good tolerability of the treatment without unexpected adverse events during the radiotherapy until 6 weeks after the end of radiotherapy, the study will be further conducted to the phase IB part. This part will explore the feasibility and tolerability of long term treatment with ModraDoc006/r.

Enrollment

24 patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Histologically proven prostate cancer.
All eligible patients have hormone naïve non-metastatic node positive high risk prostate cancer. Node positive cancer will be defined as radiological demonstration of more than four pelvic lymph node(s) consisting of bean shaped lymph node(s) with a short axis of minimal 10 mm and/or round lymph node(s) with a minimal size of 8 mm on PSMA, MRI or CT scan.

PSMA-scans or PET-Choline scans may be used, but are not obligated. Since the use of the PSMA scan is significantly increased in current clinical practice and the chance of false positive results is considered very low in patients with more than 4 positive lymph nodes, histological confirmation of positive lymph nodes is not required for inclusion if more than 4 pathological nodes are seen with the PSMA, MRI or CT scan
High risk prostate cancer will be defined as node positive with all of the following primary tumour characteristics: Tumour stage ≥cT2c and Gleason score ≥4+3, any PSA
Age ≥ 18 years
No signs of metastatic disease on standard diagnostic scans.
Normal serum testosterone levels prior to treatment
Adequate haematological, renal and hepatic functions
1. Haemoglobin ≥ 6.0 mmol/l
2. ANC of ≥ 1.5 x 109 /L
3. Platelet count of ≥ 100 x 109 /L
4. Hepatic function as defined by serum bilirubin ≤ 1.5 x ULN, ALAT and ASAT ≤ 2.5 x ULN
5. Renal function as defined by serum creatinine ≤ 1.5 x ULN or creatinine clearance ≥ 50 ml/min (by Cockcroft-Gault formula).
WHO performance status of 0-2
Able and willing to undergo blood sampling for PK and PD analysis;
Life expectancy ≥ 3 months allowing adequate follow up of toxicity evaluation and antitumor activity;
Able and willing to swallow oral medication
Able and willing to give written informed consent;

Exclusion criteria

Any treatment with investigational drugs, chemotherapy or immunotherapy within 30 days prior to receiving the first dose of investigational treatment; Patients may be on ADT as long as this is has not been longer than 4 weeks prior the start of the radiotherapy.
Patients who have had prior pelvic radiation therapy
Patients who have had prior treatment with taxanes
TURP within 3 months before start of the study
Patients who have had a prostatectomy.
Any contra-indication for MRI
Major difficulties for marker implantation
Unreliable contraceptive methods. Men enrolled in this trial must agree to use a reliable contraceptive method throughout the study (adequate contraceptive methods are: condom, sterilization)
Unresolved (> grade 1) toxicities of previous chemotherapy, excluding alopecia.
Uncontrolled infectious disease or known Human Immunodeficiency Virus HIV-1 or HIV-2 type patients;
Patients with a known history of hepatitis B or C;
Bowel obstructions or motility disorders that may influence the resorption of drugs as judged by the treating physician
Concomitant use of MDR and CYP3A modulating drugs such as Ca+- entry blockers (verapamil, dihydropyridines), cyclosporine, quinidine, tamoxifen, megestrol and grapefruit juice, concomitant use of HIV medications, other protease inhibitors, (non) nucleoside analoga, or St. John's wort.
Pre-existing neuropathy greater than NCI-CTCAE v4.03 grade 1.
Patients with known alcoholism, drug addiction and/or psychiatric of physiological condition which in the opinion of the investigator would impair study compliance; Evidence of any other disease, neurological or metabolic dysfunction, physical examination finding or laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or puts the patient at high risk for treatment-related complications.
Legal incapacity