A PHASEII STUDY EVALUATING INTRAVENOUS MELPHALAN WITH AUTOLOGOUS WHOLE BLOOD STEM CELL TRANSPLANTATION (PBSCT)OVER THREE CYCLES IN PATIENTS WITH CASTRATION-RESISTANT PROSTATE CANCER (MEL-CAP).

• Status: Unknown status
• Trial end date: 2017-09-01
• Target enrollment: 0
• Participant gender: Male

Summary

The management of (castration-resistant) prostate cancer (CRPC) is becoming increasingly complex. The use of peripheral anti-androgens with gonadorelin analogues (maximum androgen blockade) is common place. Following the failure of such an approach, several strategies may be employed. Both corticosteroids and estrogens have a role and increasingly chemotherapy is being used. The demonstration of enhanced survival using 3 weekly docetaxel has meant that this is viewed by many as the standard of care for fit patients.

Melphalan is an established alkylating drug that has demonstrated some activity in CRPC, but to date, myelosuppression has prevented adequate dosing. We have recently conducted a phase I dose escalation study using melphalan and whole blood stem cell re-infusion and it shows that median overall survival is 22 months, which is higher than the median survival rate of 19 months for Docetaxel

Data from a previous phase I study has proved the successful administration of higher doses of IV Melphalan in combination with autologous blood infusion in patients with Castration-resistant prostate cancer.

Rapid falls in circulating tumour cells were seen within 2 weeks of starting Melphalan, however slow platelet recovery meant longer periods of platelet transfusion. For this study we intend to assess the efficacy of an intensified intravenous melphalan with autologous whole blood stem cell transplantation over three treatment cycles.

39 patients will be enrolled over a 3 year period and at least 17 patients need to survive progression free at least 6-months for this study to be considered positive.

Mel-CAP is a combination chemotherapy consisting of two chemotherapy drugs:

MELPHALAN and LENOGRASTIM for 3 cycles alternately.

• Phase: Phase 2/Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Barts & The London NHS Trust; Queen Mary University of London
• Treatments: Lenograstim; Melphalan

Criteria

Inclusion Criteria:

1. Men aged ≥18 years

2. Histological diagnosis of prostate cancer

3. Progressive Castration-resistant Prostate Cancer defined as:

• a rising PSA; or

• development of new sites of disease in the presence of a suppressed testosterone (<1.5 nmol/l); or

• if testosterone >1.5 nmol/l, maximum androgen blockade failure (MAB) (MAB = GnRH analogue and peripheral anti-androgen - flutamide 250 mg 3x/day or bicalutamide 50 mg/ day or cyproterone 100mg 3x/day)

4. ECOG performance status 0-2

5. Adequate haematological reserve:

• Unsupported Hb >9.0 g/l

• Platelets >100x109/l

• WBC >3x109/l

• Neutrophils >1.5x109/l

6. Renal sufficiency:

•Creatinine <200 µmol/l

7. Hepatic sufficiency:

• Bilirubin <30 µmol/l

• ALT <3xULN unless due to liver metastasis

8. Able to give written informed consent and comply with the protocol study procedures

Exclusion Criteria:

1. Patients who have suffered a previous hypersensitivity reaction to melphalan

2. Patients with known hypersensitivity to lenograstim or to any of the excipients

3. History of myeloid malignancy

4. Lenograstim should not be administered concurrently with cytotoxic chemotherapy (i.e. on the same day)

5. Previous invasive carcinoma <3 years prior to study entry

6. Cardiac condition contra-indicating large volume venesection (i.e., active angina or cardiac failure)

7. Current treatment with another investigational medicinal (chemotherapeutic) product or participation in another investigational therapeutic (chemotherapy)study, at any time during the treatment period and 30 days preceding study entry.

8. Life expectancy <12 weeks

9. Unwilling or unable to provide written informed consent