Feasibility of a Chemotherapy With Docetaxel-Prednisone for Castration-resistant Metastatic Prostate Cancer Elderly Patients

Prostate Cancer Clinical Trial

— GERICO10  

Official title:

Randomized Phase II Study Evaluating the Feasibility of a Chemotherapy With Docetaxel-Prednisone in a Weekly Schedule or Every 3 Weeks, for Castration-resistant Metastatic Prostate Cancer Elderly Patients (>=75), "Vulnerable" or "Frail" , as Defined by the Criteria of the International Society of Geriatric Oncology (SIOG)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01254513
• Other study ID #: GERICO10/0910 (GetugP03)
• Status: Completed
• Phase: Phase 2
• Start date: December 9, 2010
• Est. completion date: April 27, 2017

Study information

• Verified date: June 2021
• Source: UNICANCER
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The objective of this study is to evaluate the feasibility of two different chemotherapy protocols with adjusted doses for patients aged 75 and over who often have medical problems other than prostate cancer. Patient will receive Docetaxel either every 3 weeks or weekly. In both cases, chemotherapy is combined with prednisone. The protocol will be considered feasible when patient will receive 6 cycles of chemotherapy (1 cycle = 3 weeks).

Additionally to this primary objective, efficacy will also be evaluated for both protocols as well as tolerance to treatment, quality of life and evolution of geriatric data.

Description:

Standard management of castration-resistant metastatic prostate cancer is represented by chemotherapy with Docetaxel 75 mg/m² every 3 weeks combined with Prednisone since a symptomatic and overall survival benefit was demonstrated.

Although this benefit is independent of age in the study by Tannock (cut-off:69), it does not seem possible to extrapolate these results, obtained in a selected population, to the majority of patients we encounter in daily practice, >= 75 years old and / or unfit.

Retrospective studies have shown that chemotherapy was feasible, at standard or adapted doses in an unselected elderly population with good results in terms of tolerance and efficacy over symptoms.

Our study aims to evaluate prospectively the feasibility of a chemotherapy with Docetaxel/Prednisone administered every 3 weeks (60 mg / m² at D1C1 then 70 mg / m² at D1 for subsequent cycles if tolerance is good) or weekly (35mg / m² at D1 and D8 with Day 1 = Day 21) to patients >= 75 years old, evaluated by comprehensive geriatric assessment, belonging to group 2 "vulnerable" or to group 3 "frail" of the classification proposed by the International Society of Geriatric Oncology (SIOG).

Feasibility is defined as the possibility for a patient to receive 6 cycles of chemotherapy without withdrawal. Reasons for study withdrawal were defined by the GERICO Group and are the followings:

• stop or delay of chemotherapy > 2 weeks

• Necessity to reduce the dose of chemotherapy > 25 %

• febrile neutropenia or non-haematological grade 3 toxicity (except alopecia) according to NCI-CTCAE V4.0.

• Geriatric criterion (Activity of Daily Living (ADL) decrease >= 2 points)

The statistical methodology used is a double randomized phase II after stratification according to the SIOG criteria, based on a Simon Optimum plan.

A pharmacokinetic / pharmacodynamic study is associated to our project, based on a method of population pharmacokinetic. The aim is to highlight predictors of the haematological tolerance of this chemotherapy by evaluating clinical, geriatric and biological parameters.

The results of this study will support the terms of prescription of chemotherapy, in patients aged 75 and over, classified as "vulnerable" or "frail" regarding SIOG criteria, with defined geriatric assessment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 66
• Est. completion date: April 27, 2017
• Est. primary completion date: May 10, 2014
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 75 Years and older

Eligibility

Inclusion Criteria:

• Age >= 75

• Histologically proven prostate adenocarcinoma

• Metastatic disease, not pre-treated with chemotherapy refractory to castration

• Hormone refractory prostate cancer is defined as follows:

• Patients with documented testosterone castration (<0.50 ng / ml)

• Patient who received prior hormonal therapy (either orchidectomy or Luteinizing hormone-releasing hormone (LHRH) agonist alone or combined with an anti-androgen)

• Patients should continue primary androgen suppression by LHRH agonist (in case of non-surgical castration)

• For patients treated with anti-androgens prior to inclusion, a wash-out period is required (4 weeks for flutamide and nilutamide, 6 weeks for other products) as well as measured progression after anti-androgen discontinuation.

• Progressive disease under hormonotherapy, with progression defined by

Increase of PSA level (two consecutive increases of PSA compared to baseline with a minimum of one week between both measurements)

OR emergence of a new lesion

OR measurable progressive disease (increase of a previous measurable lesion >= 25% in cross section)

OR progressive bone metastases (defined only by the appearance of a new lesion on bone scan)

OR progressive symptoms (defined as cancer pain Grade 2 according to the NCI-CTC V4.0, despite level 2 analgesics intake).

• Patients of Groups 2 and 3 [ "vulnerable" and "frail"] of SIOG classification

• WHO Performance Status (PS) >= 3

• PSA >= 5 ng / ml

• Neutrophils >= 2.109 /L

• Platelets >= 100.109/L

• Haemoglobin = 9 g/dl

• Bilirubin and SGOT / SGPT <1.5 x ULN (<= 2.5 x ULN if hepatic metastasis)

• creatinine <= 2.5 x ULN

• In case of previous palliative or analgesic radiotherapy, a minimum of 14 days must have elapsed between end of radiotherapy and inclusion into the study

• Previous treatment with bisphosphonates should be continued without change during the study treatment and can not be initiated either within 28 days prior to study entry or during the study

• Signed informed consent by patients, according to local regulations

Exclusion Criteria:

• "healthy" or "terminal illness" Groups according to the recommendations of International Society of Geriatric Oncology (SIOG)

• Concomitant or previous malignancy within 5 years prior the study (except basal or squamous in situ cell skin carcinoma)

• Presence of brain metastasis symptoms

• Prior treatment by intravenous radiopharmaceutical agent (e.g. Strontium 89, Samarium lexidronam) within 2 months before study entry

• Initiation of a bisphosphonate therapy within 28 days prior to randomisation

• Any concomitant anticancer treatment (radiotherapy, radiopharmaceutical agent, chemotherapy)

• Patients with uncontrolled infection

• Patients with peripheral neuropathy of grade> 1

• Patients medically unstable (e.g. unstable diabetes, uncontrolled hypertension or decompensated heart failure or myocardial infarct within 3 months)

• Gastro duodenal active ulcer

• Hypersensitivity to study drugs

• Treatment with any experimental drug within 30 days prior to or during the study

• Psychological, familial, sociological or geographical location conditions which do not allow medical monitoring and compliance with study protocol.

• Patients protected by the law or patients placed under protective supervision of adults

Related Conditions & MeSH terms

• Prostate Cancer
• Prostatic Neoplasms

Intervention

Drug:
• Docetaxel every 3 weeks + Prednisone
Docetaxel IV 60 mg/m²/d then IV 70 mg/m²/d for subsequent cycles every 3 weeks Prednisone 10 mg/day continuously
• Docetaxel weekly+ Prednisone
Docetaxel weekly 35 mg/m²/day at day 1 and day 8 of each cycle (J1 = J21) Prednisone 10 mg/day continuously

Locations

Country	Name	City	State
France	Clinique Claude Bernard	Albi
France	CHI Annemasse-Bonneville	Ambilly
France	Centre Paul Papin	Angers
France	CH de Blois	Blois
France	Institut Bergonie	Bordeaux Cedex
France	Centre Francois Baclesse	Caen
France	CH Intercommunal	Castres
France	Centre Hospitalier de Chambery	Chambery
France	Centre Jean Perrin	Clermont-ferrand
France	Clinique Sainte Marguerite	Hyeres
France	Chd Vendee	La Roche Sur Yon
France	Clinique Hartmann	Levallois-perret
France	Centre Oscar Lambret	Lille
France	Hôpital Saint Vincent de Paul	Lille
France	Centre Leon Berard	Lyon
France	Institut Paoli Calmettes	Marseille
France	CHU Nimes	Nimes
France	Chr Orleans	Orleans
France	Institut Curie/Claudius Regaud	Paris
France	Polyclinique Francheville	Périgueux
France	Centre Hospitalier Lyon Sud	Pierre-benite
France	Centre Hospitalier de La Region D'Annecy	Pringy Cedex
France	Institut Curie - Centre Rene Huguenin	Saint-cloud
France	Ico - Centre Rene Gauducheau	Saint-herblain Cedex
France	CH de Senlis	Senlis
France	Centre Paul Strauss	Strasbourg
France	Hôpitaux du Léman	Thonon-les-bains
France	Clinique Pasteur	Toulouse
France	Clinique Saint Jean du Languedoc	Toulouse
France	Institut Claudius Regaud	Toulouse
France	Polyclinique Du Parc	Toulouse

Sponsors (1)

Lead Sponsor	Collaborator
UNICANCER

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Feasibility of 2 different protocols of Docetaxel chemotherapy	Main criteria is the rate of patients receiving 6 cycles of treatment without experiencing any of the following criteria: Stop or delay of chemotherapy > 2 weeks; Necessity to reduce the dose of chemotherapy > 25 %; Febrile neutropenia or non-haematological grade 3 toxicity (except alopecia)according to NCI-CTCAE V4.0; Geriatric criterion ( ADL decrease >= 2 points)	Up to 18 weeks (6 cycles of chemotherapy)
Secondary	Overall Survival	Overall Survival is defined as the time from randomization until death for any cause or last follow-up news (censored data).	From randomization until death for any cause or last follow-up news (censored data)
Secondary	Geriatric evaluation	The impact of the chemotherapy will be evaluated on Comprehensive Geriatric Assessment : Test de screening G8; Cumulative Illness Rating Scale(CIRSG); Folstein Mini Mental State (MMS); Activity of Daily Living (ADL); Instrumental Activity of Daily Living (IADL); Geriatric Depression Scale (GDS); Mini Nutritionnal Assessment (MNA)	At baseline, D1 of Cycle 1 and Cycle 4, at the end of treatment and at follow-up visits
Secondary	Number of patients with Adverse Events	Tolerance and safety will be assessed through recording of adverse events using NCI-CTCAE toxicity classification V4.0.	At baseline, D1 of each cycle , at the end of treatment and at the follow-up visits
Secondary	Quality of Life	The impact of the chemotherapy is evaluated on the European Organisation for Research and Treatment of Cancer (EORTC) Quality Of Life - Questionnaire - QLQ-C30	At baseline, D1 of the Cycle 4, at the end of the treatment and at the follow-up visits
Secondary	Vital signs measurement	Tolerance and safety will be assessed through vital signs measurement.	At baseline, D1 of each cycle , at the end of treatment and at the follow-up visits
Secondary	Prostate-specific antigen (PSA) measurements	Efficacy will be assessed through monitoring PSA values	At baseline, D1 of each cycle , at the end of treatment and at the follow-up visits