Skip to main content
OpenTrials
Completed

NCT Number: NCT01828736

Efficacy of Combination of Trastuzumab to Gemcitabine - Platinum Advanced or Metastatic Urothelial Carcinoma

A multicenter, randomized, Phase 2 trial to study the effectiveness and feasibility of association of trastuzumab with combination chemotherapy in advanced or metastatic bladder cancer patients. Combining monoclonal antibody therapy with combination chemotherapy may improve treatment efficacy on tumours overexpressed HER 2.

Completed

Looking for future studies?

Notify Me

Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Transitional cell carcinoma of the urothelium or bladder histologically proven stage IV AJCC [locally advanced (T4b and / or N + M0) unresectable or metastatic (M1)]
  • Tumor and / or metastasis overexpressing HER2 immunohistochemistry (IHC 3 +) or IHC 2 + and FISH +. Centralized analysis.
  • Measurable disease with at least one lesion with a diameter> 2 cm for conventional methods (clinical examination, CT or MRI) or> 1 cm for the helical scanner. In case of single metastasis, metastatic disease should be histologically proven
  • Age ≥ 18 years and ≤80 years
  • Life expectancy> 3 months,
  • Index performance status <2 according to ECOG PS,
  • No prior chemotherapy other than adjuvant and / or neoadjuvant chemotherapy, without Herceptin ® and complete for more than 6 months (naive to any previous chemotherapy in the metastatic setting)
  • No radiotherapy within 4 weeks prior to inclusion,
  • Normal cardiac function as measured by ejection fraction (LVEF> 50%),
  • Blood and liver satisfactory constants:

Hematological criteria: - Neutrophils> 1.5 x 109 / L, - Chips> 100 x 109 / L - Hemoglobin> 10 g / dL, Liver function: - Alkaline phosphatase (unless bone metastases) <2 x N - Total bilirubin <1.5 x N - transaminases (AST, ALT) <1.5 x N, renal Constants: - Creatinine clearance > 30 ml / min (Cockcroft and Gault, cf. Annex XV protocol)

  • Patient's written consent after full information.

Exclusion criteria

  • Concurrent treatment with an experimental drug, participation in another clinical trial within <30 days
  • Patients previously treated with Herceptin ®, or another treatment targeting growth factors EGF (eg Iressa ®, Tarceva ®)
  • Existence of a severe pulmonary disease, liver or kidney is likely to be exacerbated by the treatment,
  • Other medical conditions: congestive heart failure or angina pectoris even if medically controlled failure, history of myocardial infarction before entering the trial, hypertension or uncontrolled arrhythmias, significant valvular disease,
  • Patient with dyspnoea at rest or requiring oxygen therapy or with respiratory failure,
  • Presence of a severe infection requiring antibiotics,
  • Presence of CNS metastases or meningeal
  • History of another malignancy uncured or cured for less than 5 years (except basal cell carcinoma, papillary thyroid carcinoma in situ of the cervix treated)
  • Pregnant or lactating or not using effective contraception Women,
  • For Cisplatin only: carrying a serious neurological disease, current events devices> NCI grade 2 neuropathy, hearing loss, creatinine clearance <60 ml / min, the patient can not support a patient hydration.

Treatment and study plan

trastuzumab

Biological

Bottles of 150 mg; Charging dose: 8mg/kg then 6mg/kg every 21 days given IV

Other names: anti-c-erB-2, Herceptin, MOAB HER2

Gemcitabine

Drug

Given IV, 1000 mg/m² BSA on Day 1 and Day 8 every 21 days

Other names: dFdC, difluorodeoxycytidine hydrochloride, Gemzar, gemcitabin hydrochloride

carboplatin

Drug

Given IV: AUC 5 on Day 1 every 21 days

Other names: Carboplat, CBDCA, JM-8, Paraplat, Paraplatin

Cisplatin

Drug

Given IV, 70 mg/m² BSA on day 1 every 21 days

Other names: cis-Diamminedichloroplatinum(II), Platinum Diamminodichloride, Diamminodichloride, Platinum, cis-Platinum, cis Platinum, Dichlorodiammineplatinum, cis-Diamminedichloroplatinum, cis Diamminedichloroplatinum, cis-Dichlorodiammineplatinum(II), Platinol, Platidiam, Platino, NSC-119875, Biocisplatinum

Primary outcomes

  1. Progression Free survival

    Time frame: Participants will be followed from radomization until progression or death, up to 3 years

Secondary outcomes

  1. Objective response rate

    Time frame: Objective Response Rate will be assessed during treatment period, every 3 cycles, up to 7 months

  2. Number of participants with adverse events as a measure of safety and tolerability

    Time frame: Participants will be followed all along the study period, an expected average of 3 years

    Toxicity will be classify according to NCI-CTC criteria Version 2.0. Cardiac toxicity will be assessed according to the NYHA (New York Heart Association) criteria.

  3. Quality of life

    Time frame: Quality of Life will be assessed during the study period, every 3 cycles (Arm A patients) or every 3 months (Arm B patients), up to 3 years

    Quality of Life will be assessed according to the EORTC QLQ-C30 Version 3 questionnaire

  4. Overall survival

    Time frame: Participants will be followed from randomization until death or lost of follow-up, up to 3 years

Sponsors and collaborators

Lead sponsor

Association Pour La Recherche des Thérapeutiques Innovantes en Cancérologie

Other

Collaborators

  • Roche Pharma AG

Registry information

Official study title

Multicenter Randomized Phase 2 Trial of Gemcitabine - Platinum With or Without Trastuzumab in Advanced or Metastatic Urothelial Carcinoma With HER2 Overexpression

Acronym: CVH-CT02

Important dates

Study start
2004
Primary completion
2010
Study completion
2010
First posted
Apr 11, 2013
Registry last updated
Feb 6, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.