Urinary Bladder CancerPhase 2PURONCT01374789
PURO Panitumumab in Combination With Gemcitabine/Cisplatin in Advanced Urothelial Cancer
A Phase 2 study testing GemCis + Panitumumab and GemCis in people with Urinary Bladder Cancer, run by WiSP Wissenschaftlicher Service Pharma GmbH at 20 sites in Germany.
Trial summary
The primary objective of the study is to assess the efficacy of the combination consisting of gemcitabine/cisplatin and panitumumab in patients with urothelial carcinoma and wild-type HRAS (non-mutated status). Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Urinary Bladder Cancer
- What is being tested?
- GemCis + Panitumumab and GemCis
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 2 participants
- Where
- 20 sitesGermany
- Study dates
- Jul 2010to Mar 2012
- Phase
- Phase 2
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Histologically or cytologically confirmed, unresectable urothelial carcinoma of the bladder or the upper urinary tract
- Wild-type HRAS
- Male and female subjects > 18 years of age
- General condition ECOG 0-1
- Life expectancy at least 12 weeks
- Women of child-bearing potential: negative pregnancy test and use of effective contraception(oral contraceptive, coil); men: use of adequate male contraception (condom) for up to 3 months after discontinuation of panitumumab therapy
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- Locally advanced or metastatic disease (T3b,T4 and/or N+ and/or M+)
- At least one unidimensionally measurable lesion detectable in CT or MRI corresponding to the RECIST criteria
- Adequate haematological, hepatic, renal and metabolic function parameters:
- Leukocytes > 3000/mm³, ANC ≥ 1500/mm³, platelets ≥ 100,000/mm³, hemoglobin > 9 g/dl Creatinine clearance ≥ 50 ml/min and serum creatinine ≤ 1.5 x upper limit of normal Bilirubin ≤ 1.5 x upper limit of normal, GOT-GPT ≤ 2.5 x upper limit of normal in absence of liver metastases, or ≤ 5 x upper limit of normal in presence of liver metastases, AP ≤ 5 x upper limit of normal Magnesium ≥ lower limit of normal; calcium ≥ lower limit of normal INR and PTT < 1.5 x the upper limit of the normal reference range
Who cannot join
- HRAS mutation
- Absence of any of the above-listed inclusion criteria
- Dialysis-dependence following nephrectomy
- Patients with cerebral tumours and/or cerebral metastases
- Clinically significant cardiovascular disease in (incl. myocardial infarction, unstable angina, symptomatic congestive heart failure, serious uncontrolled cardiac arrhythmia) ≤ 1 year before enrolment.
- Patients with uncontrolled hypertension; systolic blood pressure > 150 mmHg or diastolic blood pressure > 90 mmHg despite optimal medical treatment
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- History of interstitial lung disease, e.g. pneumonitis or pulmonary fibrosis or evidence of interstitial lung disease on baseline chest CT scan.
- Patients with thrombotic or embolic events, such as stroke or pulmonary embolism
- Patients with recent or known history of haemorrhagic diathesis
- Known significant neurological or psychiatric disorders, including dementia and epileptic seizures
- Serious inflammatory eye conditions, hearing impairment
- Pulmonary (pO2 < 60 mmHg), haemopoietic (e.g. serious bone marrow aplasia), hepatic or renal disorders
- Patients with poorly controlled diabetes mellitus
- Serious bacterial or fungal infections (>grade 2 NCI CTC Version 3)
- Chronic hepatitis B or C; HIV infection
- Autoimmune disease
- Allergic reaction to one of the medications to be used
- Status post organ transplantation
- Status post autologous bone marrow transplantation or stem cell transplantation in the 4 months prior to study commencement
- Manifest secondary malignancy or other form of cancer in the previous 5 years (excluding basalioma, in situ cervical cancer, incidental prostatic cancer)
- Subject pregnant or breast feeding, or planning to become pregnant within 6 months after the end of treatment
- Subject (male or female) is not willing to use highly effective methods of contraception (per institutional standard) during treatment and for 3 months (male or female) after the end of treatment (adequate: oral contraceptives, intrauterine device or barrier method in conjunction with spermicidal jelly).
- Active participation in other clinical studies in the previous 4 weeks
- Prior systemic therapy with cytostatics or immunotherapeutic agents
- Concurrent use of other anticancer treatments after study commencement
- Intravesical chemotherapy in the previous 4 weeks
- Radiotherapy in the previous 4 weeks
- Previous radiotherapy in which all lesions to be used for the evaluation of tumour response were irradiated
- Patients in a closed institution according to an authority or court decision
Trial locations and contacts
20 sites in 1 country.
20 sites in 1 country
Germany20 sites
Bundeswehrkrankenhaus Berlin
Berlin, 10115
Krankenhaus am Urban
Berlin, 10967
Heilig-Geist-Krankenhaus
Cologne, 50737
St.-Josefs-Hospitals Dortmund
Dortmund, 44263
Universitätsklinikum Dresden
Dresden, 01307
Universitätsklinikum Düsseldorf
Düsseldorf, 40225
Universitätsklinikum Erlangen
Erlangen, 91054
Klinikum Fulda
Fulda, 36043
Universitätsklinikum Hamburg Eppendorf
Hamburg, 20246
Medizinische Hochschule Hannover, Urologie
Hanover, 30625
Universitätskllinikum Heidelberg
Heidelberg, 69121
Klinikum Kassel
Kassel, 34215
Klinikum Ludwigshafen
Ludwigshafen, 67063
Universitätsklinikum Mainz
Mainz, 55131
Uroloische Praxis
Markkleeberg, 04416
Universitätsklinikum Münster
Münster, 48149
Johanniter Krankenhaus
Stendal, 39576
Universitätsklinikum Ulm, Urologische Klinik
Ulm, 89075
Klinikum Weiden
Weiden, 92637
Gemeinschaftspraxis für Urologie DGU
Wuppertal, 742103
About this study
Official title: PURO - An Open-label, Randomised, Multicentre, Phase II Study to Evaluate the Efficacy of Chemotherapy With Gemcitabine and Cisplatin in Combination With the EGF Receptor Antibody Panitumumab (GemCisP) Versus GemCis in the First-line Therapy of Locally Advanced/Metastatic Urothelial Carcinoma in Patients With Wild-type HRAS
The primary objective of the study is to assess the efficacy of the combination consisting of gemcitabine/cisplatin and panitumumab in patients with urothelial carcinoma and wild-type HRAS (non-mutated status). The progression-free survival rate at 12 months will be compared to expectations derived from historical data, which are verified by a randomised control group without the antibody.
Read the detailed description
Mutation of ras oncogenes is frequently observed in human tumours and occurs in approximately 30% of all cancer types. Frequent mutation "hot spots" occur in codon 12 (glycine to valine), codon 13 (glycine to cysteine) and codon 61 (glutamine to arginine, lysine and leucine) (Bonner et al. 1993, Levesque et al. 1993). Point mutations in ras genes result in blockade of intrinsic GTPase activity, the physiological mechanism that switches off ras GTPases. The consequence is persistent up-regulation of the signal pathway and increased cell proliferation. The first HRAS mutation in association with bladder cancer was described during establishment of the human urinary bladder carcinoma cell line T24. In further studies, a research group led by Fitzgerald was able to demonstrate that HRAS gene mutations were present in the urine sediment of up to 44% of patients with urinary bladder cancer (Fitzgerald et al. 1995).
Viola et al. subsequently investigated whether an increased mutation rate is accompanied by increased expression of ras proteins in bladder cancer. It was shown that there is indeed increased expression of ras proteins in dedifferentiated tumours and carcinomas in situ, whereas highly differentiated tumours do not exhibit this rate of expression (Viola et al. 1985).
At present, there is no clinical evidence, that the findings of an obvious lack of activity of EGFR antibodies in colorectal cancer with RAS-related mutations, is likewise valid in urothelial carcinoma. However, as it is the aim of this study to detect a first signal of activity in this type of cancer, and the chance of missing such evidence in a phase II trial with limited patient numbers is high anyway, it seems sensible, not to miss this opportunity of "enrichment". In case of a clearly positive signal of efficacy in the present trial, a subsequent phase II study may focus on HRAS mutated tumors.
Overexpression of the EGF receptor in bladder cancer has been described by many research groups (Colquhuon \& Mellon, 2002) and is associated with an advanced stage of the tumour, progression of the tumour and a poor clinical prognosis. The EGFR antibody cetuximab (Erbitux®) has been investigated in a human urothelial carcinoma cell line and in a mouse model with human bladder carcinoma. Cetuximab was found to inhibit tumorigenesis and metastatic progression in vivo and in vitro by means of suppression of angiogenesis and simultaneous induction of apoptosis (Perotte et al., 1999; Inoue et al., 2000). Similar results have also been reported in urothelial carcinoma for the tyrosine kinase inhibitor gefitinib (Villares et al., 2007, Shrader et al., 2007).
There are currently two on-going studies of cetuximab in metastatic bladder cancer: a randomised phase II study of first-line treatment with Gemcitabine and Cisplatin +/- Erbitux (NCT00645593) and a randomised phase II study of second-line treatment with Erbitux +/- Paclitaxel (NCT00350025).
The HRAS mutation rate in urothelial carcinoma is approximately 40%. The primary objective of the study is to assess the efficacy of the combination consisting of gemcitabine/cisplatin and panitumumab in patients with wild-type HRAS (non-mutated status). The progression-free survival rate at 12 months will be compared to expectations derived from historical data, which are verified by a randomised control group without the antibody.
- Conditions
- Urinary Bladder Cancer
- Being tested
- GemCis + Panitumumab, GemCis
- Medical subject headings
- Urinary Bladder Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
GemCis + PanitumumabDrug
Also called Vectibix (Panitumumab)
Gemcitabine: 1250 mg/m², day 1 and 8, i.v., q3 Cisplatin: 70 mg/m², day 2, i.v., q3 Panitumumab 9 mg/kg/body weight, i.v., day 1,q3
GemCisDrug
Gemcitabine: 1250 mg/m², day 1 and 8, i.v., q3 Cisplatin: 70 mg/m², day 2, i.v., q3
| Study group | Role | What they receive |
|---|---|---|
| Arm A (GemCis + Panitumumab) | Experimental | gemcitabine + cisplatin + panitumumab Receives: Drug: GemCis + Panitumumab |
| Arm B (GemCis) | Active comparator | gemcitabine + cisplatin Receives: Drug: GemCis |
What is being measured
The primary outcome is the main question the study is designed to answer.
Primary end point: Progression-free survival rate after 12 months.
Measured: 12 months
Secondary outcomes (4)
Determination of best response (CR, PR and SD) rates in accordance with the RECIST criteria
Measured: up to 18 weeks
Duration of response, progression-free and overall survival time
Measured: 2 years
Documentation of adverse effects in accordance with the NCI CTC criteria
Measured: up to 18 weeks
Documentation of quality of life on the basis of the EORTC questionnaire
Measured: up to 18 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Jun 2011 (estimated)
- Study startJul 2010
- Primary completionMar 2012
- Study completionMar 2012
Why it stopped: The study was terminated due to insufficient recruitment.
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Urinary Bladder CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 2 participants (actual)
Sponsor and investigators
- Lead sponsor
- WiSP Wissenschaftlicher Service Pharma GmbH
- Sponsor type
- University, hospital or other
- Collaborators
- Gesellschaft fur Medizinische Innovation - Hamatologie und Onkologie mbH
- Responsible party
- Sponsor
- Investigators
- Kurt Miller, Prof. Dr., Principal investigator, Universitätsmedizin Charité Berlin, Klinik für Urologie
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01374789
- Sponsor's protocol ID
- WiSP_AG48
- Other IDs
- 2009-015119-42, GMIHO-007/2008, 2009
- Acronym
- PURO
- Status last verified
- Jun 2015
- First submitted
- 30 Mar 2011
- Last updated
- 3 Jun 2015
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 3 Jun 2015. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- PURO - An Open-label, Randomised, Multicentre, Phase II Study to Evaluate the Efficacy of Chemotherapy With Gemcitabine and Cisplatin in Combination With the EGF Receptor Antibody Panitumumab (GemCisP) Versus GemCis in the First-line Therapy of Locally Advanced/Metastatic Urothelial Carcinoma in Patients With Wild-type HRAS
- ClinicalTrials.gov ID
- NCT01374789
- Acronym / sponsor ID
- PURO / WiSP_AG48
- Conditions
- Urinary Bladder Cancer
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: The study was terminated due to insufficient recruitment.
- Enrolment
- 2 participants (actual)
- Lead sponsor
- WiSP Wissenschaftlicher Service Pharma GmbHUniversity, hospital or other
- Collaborators
- Gesellschaft fur Medizinische Innovation - Hamatologie und Onkologie mbH
- Study start
- Jul 2010
- Primary completion
- Mar 2012 (actual)
- Study completion
- Mar 2012 (actual)
- First posted
- 16 Jun 2011 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The primary objective of the study is to assess the efficacy of the combination consisting of gemcitabine/cisplatin and panitumumab in patients with urothelial carcinoma and wild-type HRAS (non-mutated status). The progression-free survival rate at 12 months will be compared to expectations derived from historical data, which are verified by a randomised control group without the antibody.
Detailed description
Mutation of ras oncogenes is frequently observed in human tumours and occurs in approximately 30% of all cancer types. Frequent mutation "hot spots" occur in codon 12 (glycine to valine), codon 13 (glycine to cysteine) and codon 61 (glutamine to arginine, lysine and leucine) (Bonner et al. 1993, Levesque et al. 1993). Point mutations in ras genes result in blockade of intrinsic GTPase activity, the physiological mechanism that switches off ras GTPases. The consequence is persistent up-regulation of the signal pathway and increased cell proliferation. The first HRAS mutation in association with bladder cancer was described during establishment of the human urinary bladder carcinoma cell line T24. In further studies, a research group led by Fitzgerald was able to demonstrate that HRAS gene mutations were present in the urine sediment of up to 44% of patients with urinary bladder cancer (Fitzgerald et al. 1995).
Viola et al. subsequently investigated whether an increased mutation rate is accompanied by increased expression of ras proteins in bladder cancer. It was shown that there is indeed increased expression of ras proteins in dedifferentiated tumours and carcinomas in situ, whereas highly differentiated tumours do not exhibit this rate of expression (Viola et al. 1985).
At present, there is no clinical evidence, that the findings of an obvious lack of activity of EGFR antibodies in colorectal cancer with RAS-related mutations, is likewise valid in urothelial carcinoma. However, as it is the aim of this study to detect a first signal of activity in this type of cancer, and the chance of missing such evidence in a phase II trial with limited patient numbers is high anyway, it seems sensible, not to miss this opportunity of "enrichment". In case of a clearly positive signal of efficacy in the present trial, a subsequent phase II study may focus on HRAS mutated tumors.
Overexpression of the EGF receptor in bladder cancer has been described by many research groups (Colquhuon \& Mellon, 2002) and is associated with an advanced stage of the tumour, progression of the tumour and a poor clinical prognosis. The EGFR antibody cetuximab (Erbitux®) has been investigated in a human urothelial carcinoma cell line and in a mouse model with human bladder carcinoma. Cetuximab was found to inhibit tumorigenesis and metastatic progression in vivo and in vitro by means of suppression of angiogenesis and simultaneous induction of apoptosis (Perotte et al., 1999; Inoue et al., 2000). Similar results have also been reported in urothelial carcinoma for the tyrosine kinase inhibitor gefitinib (Villares et al., 2007, Shrader et al., 2007).
There are currently two on-going studies of cetuximab in metastatic bladder cancer: a randomised phase II study of first-line treatment with Gemcitabine and Cisplatin +/- Erbitux (NCT00645593) and a randomised phase II study of second-line treatment with Erbitux +/- Paclitaxel (NCT00350025).
The HRAS mutation rate in urothelial carcinoma is approximately 40%. The primary objective of the study is to assess the efficacy of the combination consisting of gemcitabine/cisplatin and panitumumab in patients with wild-type HRAS (non-mutated status). The progression-free survival rate at 12 months will be compared to expectations derived from historical data, which are verified by a randomised control group without the antibody.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Arm A (GemCis + Panitumumab) | Experimental | Drug: GemCis + Panitumumabgemcitabine + cisplatin + panitumumab |
| Arm B (GemCis) | Active comparator | Drug: GemCisgemcitabine + cisplatin |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (10 listed)
- Histologically or cytologically confirmed, unresectable urothelial carcinoma of the bladder or the upper urinary tract
- Wild-type HRAS
- Male and female subjects > 18 years of age
- General condition ECOG 0-1
- Life expectancy at least 12 weeks
Key exclusion criteria (29 listed)
- HRAS mutation
- Absence of any of the above-listed inclusion criteria
- Dialysis-dependence following nephrectomy
- Patients with cerebral tumours and/or cerebral metastases
- Clinically significant cardiovascular disease in (incl. myocardial infarction, unstable angina, symptomatic congestive heart failure, serious uncontrolled cardiac arrhythmia) ≤ 1 year before enrolment.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| GemCis + PanitumumabAlso: Vectibix (Panitumumab)Gemcitabine: 1250 mg/m², day 1 and 8, i.v., q3 Cisplatin: 70 mg/m², day 2, i.v., q3 Panitumumab 9 mg/kg/body weight, i.v., day 1,q3 | Drug | Arm A (GemCis + Panitumumab) |
| GemCisGemcitabine: 1250 mg/m², day 1 and 8, i.v., q3 Cisplatin: 70 mg/m², day 2, i.v., q3 | Drug | Arm B (GemCis) |
Primary outcome
Primary end point: Progression-free survival rate after 12 months.
Time frame: 12 months
4 secondary outcomes
Determination of best response (CR, PR and SD) rates in accordance with the RECIST criteria
Time frame: up to 18 weeks
Duration of response, progression-free and overall survival time
Time frame: 2 years
Documentation of adverse effects in accordance with the NCI CTC criteria
Time frame: up to 18 weeks
Documentation of quality of life on the basis of the EORTC questionnaire
Time frame: up to 18 weeks
Results and safety
The study was stopped early (reason given: The study was terminated due to insufficient recruitment.). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Jun 2015.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Kurt Miller, Prof. Dr. principal investigator
Universitätsmedizin Charité Berlin, Klinik für Urologie
20 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing GemCis + Panitumumab and GemCis in people with Urinary Bladder Cancer, run by WiSP Wissenschaftlicher Service Pharma GmbH at 20 sites in Germany.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 10 inclusion and 29 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 3 Jun 2015. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 20 sites in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study was stopped early (reason given: The study was terminated due to insufficient recruitment.). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Primary end point: Progression-free survival rate after 12 months. (time frame: 12 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Jun 2015.