Anal Squamous Cell CarcinomaPhase 2VITALNCT01285778
Vectibix for the Treatment of Anal Cancer
A Phase 2 study testing panitumumab, mytomicin C, 5-FU, radiation in people with Anal Squamous Cell Carcinoma, run by Grupo Espanol Multidisciplinario del Cancer Digestivo at 20 sites in Spain.
Trial summary
Chemoradiation with 5-FU and Mitomycin C is the standard treatment in anal canal SCC. Panitumumab has shown efficacy in other tumors and anti-EGFR treatment has shown clinical activity in a single report of a refractory anal canal SCC patient. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Anal Squamous Cell Carcinoma
- What is being tested?
- panitumumab, mytomicin C, 5-FU, radiation
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 58 participants
- Where
- 20 sitesSpain
- Study dates
- Oct 2010to 24 Mar 2017
- 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
- Man or woman ≥ 18 years
- Competent to comprehend, sign, and date an IEC-approved informed consent form
- Histologically or cytologically-confirmed anal canal SCC
- T status 2-4 and any N status (pelvic or inguinal) radiologically defined by MRI
- De novo diagnosis of anal canal SCC not previously treated
- ECOG performance status of 0, 1 or 2
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- If a subject has prior history of cancer other than anal canal SCC, non-melanoma skin carcinoma, or in situ cervical carcinoma, then the subject should neither have received any treatment nor have shown any signs of active disease within the previous 5 years
- Adequate bone marrow function: neutrophils≥1.5 x109/ L; platelets≥100 x109/ L; hemoglobin≥ 9 g/ dL
- Hepatic function as follows: total bilirubin count ≤ 1.5 x ULN; ALT and AST ≤ 2.5 x ULN
- Calculated creatinine clearance or 24 hour creatinine clearance ≥ 50 mL/ min
- Magnesium≥ lower limit of normal
Who cannot join
- Metastatic anal canal SCC
- HIV infection (except patients with an undetectable viral load and CD4 cells count >400/mL which are eligible for the study)
- Known hypersensitivity to any of the study drugs
- Evidence of any other disease, 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
- Patients they have received prior systemic therapy or radiotherapy for the treatment of SCC anal carcinoma.
- Prior malignant tumor in the last 5 years, except a history of non-melanoma skin carcinoma, or in situ cervical carcinoma.
Show all 14Show fewer
- Clinically significant cardiovascular disease, for example myocardial infarction (< 6 months before treatment start), unstable angina, congestive heart failure, arrhythmia requiring medication, or uncontrolled hypertension
- Known positive test for, hepatitis C virus, chronic active hepatitis B infection
- Any kind of disorder that compromises the ability of the subject to give written informed consent and/or comply with the study procedures
- Any investigational agent within 30 days before enrolment
- Subject who is pregnant or breast feeding
- Surgery (excluding diagnostic biopsy or central venous catheter placement) and/or radiotherapy within 28 days prior to inclusion in the study.
- Woman or man of childbearing potential not consenting to use adequate contraceptive precautions i.e. double barrier contraceptive methods (eg diaphragm plus condom), or abstinence during the course of the study and for 6 months after the last study drug administration for women, and 3 month for men
- Psychological, familial, sociological, or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial.
Trial locations and contacts
20 sites in 1 country.
20 sites in 1 country
Spain20 sites
Centro Oncológico de Galicia
A Coruña, 15009
Hospital Universitario Germans Trias i Pujol. Institut Català Oncologia
Badalona, Barcelona, 08916
Hospital del Mar
Barcelona, 08003
Hospital Universitario Vall Hebron
Barcelona, 08035
Hospital Clínic i Provincial
Barcelona, 08036
Hospital Santa Creu i Sant Pau
Barcelona, 08041
Hospital Virgen Blanca
León, 24071
Hospital Universitario La Princesa
Madrid, 28006
Hospital Universitario Gregorio Marañón
Madrid, 28009
Fundación Jiménez Díaz
Madrid, 28040
Hospital Universitario La Paz
Madrid, 28046
Hospital Virgen de la Victoria
Málaga, 29010
Corporació Sanitaria Parc Taulí
Sabadell, Barcelona, 08208
Hospital Universitario de Salamanca
Salamanca, 37007
Hospital Infanta Sofía
San Sebastián de los Reyes, Madrid, 28702
Hospital Universitario Marqués de Valdecilla
Santander, 39008
Hospital Universitario Virgen del Rocío
Seville, 41013
Instituto Valenciano de Oncología
Valencia, 46009
Hospital General de Valencia
Valencia, 46014
Hospital Universitario Miguel Servet
Zaragoza, 50009
About this study
Official title: Phase 2 Trial to Assess the Efficacy and Safety of Chemoradiation With 5-fluorouracil, Mytomicin C and Panitumumab as a Treatment for Anal Squamous Cell Carcinoma
Chemoradiation with 5-FU and Mitomycin C is the standard treatment in anal canal SCC. Panitumumab has shown efficacy in other tumors and anti-EGFR treatment has shown clinical activity in a single report of a refractory anal canal SCC patient. Based on this background, we propose to conduct a phase II study to investigate the efficacy and toxicity of radiotherapy with the association:
- 5-FU 1000mg/m2 on days 1-4 and 29-32
- Mitomycin C 10mg/m2 on days 1 and 29
- Panitumumab 6 mg/kg on day 1, then every 2 weeks for 8 weeks
Read the detailed description
In the 1980s, the treatment of choice for anal cancer was abdominal-perineal amputation, which included the removal of the anus, rectum and lymphatic drainage areas and a permanent colostomy. With this treatment, 5-year survival rates were 40-70%. In the following years, however, it was shown that anal cancer was a tumor that was sensitive to chemotherapy and radiation, so surgery was not the first choice and was only reserved for resistant cases or relapses. Concomitant chemo and radiotherapy based on the Mitomycin C - 5-FU regimen is currently the standard treatment for localized (except T1N0) and locally advanced cases. This statement is supported by two randomized studies that showed that the administration of chemoradiation with Mitomycin C - 5FU was better than radiation in monotherapy. The trial conducted by the United Kingdom Coordinating Committee on Cancer Research (UKCCCR) randomized 585 patients to receive radiotherapy (45 Gy in 4-5 weeks) or the same radiotherapy regimen coupled with 5-FU (1000 mg/m2 x 4 days or 750 mg/m2 x 5 days), for the first and last week of radiotherapy and Mitomycin C 12 mg/m2 on day 1. The 3-year local failure rate was 39% in the combined arm versus 61% with radiotherapy alone. There were no differences in the 3-year overall survival rate. On the other hand, in the study conducted by EORTC, 110 patients were distributed to receive radiotherapy (45 Gy in 5 weeks, with an overimpression of 15 Gy in the patients with CR and 20 Gy if PR) or radiotherapy plus 5-FU (750 mg/m2 days 1-5 and 29-33) associated to Mitomycin C (15 mg/m2 on day 1). The CR rate was significantly greater in the group treated with chemoradiation (80% vs. 54%). After 5 years of follow-up, there was still an 18% increase in the local control rate in favor of the group treated with chemoradiation.
More recently, the results of a phase II CALGB trial, suggests that the administration of induction treatment with two cycles of cisplatin-5FU (cisplatin 100 mg/m2 on days 1 and 29 and 5FU 1000 mg/m2 days 1-4 and 29-32) followed by chemoradiotherapy with 5-FU and Mitomycin C was very promising, especially in patients with a poor prognosis, with 50% of patients remaining colostomy and disease-free at 48 months. However, in a randomized study by the RTOG group, which included 682 patients, this strategy was compared with the classic concomitant chemoradiation with 5-FU (1000 mg/m2 days 1-4 and 29-32) and Mitomycin C (10 mg/m2 days 1 and 29). No differences in survival were found, but it was also detected that the colostomy rate was greater in the patients treated with the regimen containing Cisplatin (HR, 1.68; 95% CI, 1.07-2.65; P=.02). The authors concluded that induction with cisplatin was not superior to the traditional administration of 5FU-Mitomycin C with RT.
Epidermoid anal cancer is a tumor that often expresses the EGFR receptor. In an initial study with 21 cases, it was reported that there was EGFR expression in all the biopsies. In another study with 38 cases, it was found that 55% of the tumors expressed EGFR. No study has been published, however, which has investigated the efficacy of Panitumumab in this tumor. There is only one report of a refractory case in which cetuximab was administered together with CPT-11 with an excellent response.
- Conditions
- Anal Squamous Cell Carcinoma
- Being tested
- panitumumab, mytomicin C, 5-FU, radiation
- Keywords
- Anal squamous cell carcinoma, panitumumab, chemoradiation, anal cancer, GEMCAD-09-02
- Medical subject headings
- Anus Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
panitumumab, mytomicin C, 5-FU, radiationDrug
Also called Vectibix
Radiation therapy will be administered concurrent with chemotherapy and Panitumumab treatment. It will start the day 1 of the systemic treatment. That is, the first day of radiation therapy will be the day of the administration of the first dose of Panitumumab and Mitomycin C, as well as the first day of the first 96-hours course of 5-FU continuous infusion. On day 1, drugs and radiation will be administered in the following order:
- First, Panitumumab. Panitumumab will be administered by IV infusion on day 1, and every 2 weeks during 8 weeks
- Then Mitomycin C, 10mg/m2 on days 1 and 29
- Then start the 5-FU continuous infusion, 1000mg/m2 on days 1-4 and 29-32
- Finally, no less than 2 hours after the start of the 5-FU infusion, first dose of radiation therapy.
| Study group | Role | What they receive |
|---|---|---|
| Panitumumab, mytomicin C, 5-FU, radiation | Experimental | Not described Receives: Drug: panitumumab, mytomicin C, 5-FU, radiation |
What is being measured
The primary outcome is the main question the study is designed to answer.
Three-year disease-free survival rate
To estimate the three-year disease-free survival rate in patients treated with 5-FU, mytomicin C and Panitumumab concurrently with radiation therapy as treatment for anal squamous cell carcinoma
Measured: 3 years
Secondary outcomes (7)
Disease free survival rate
To assess disease free survival in patients treated with 5-FU, Mytomicin C and Panitumumab concurrently with radiation therapy as treatment for anal squamous cell carcinoma.
Measured: 3 years
Three-year free local-regional failure rate
To assess three-year free local-regional failure rate in patients treated with 5-FU, Mytomicin C and Panitumumab concurrently with radiation therapy as treatment for anal squamous cell carcinoma.
Measured: 3 years
Overall survival
To assess overall survival in patients treated with 5-FU, Mytomicin C and Panitumumab concurrently with radiation therapy as treatment for anal squamous cell carcinoma.
Measured: 3 years
Colostomy-free survival rate
To assess two-year colostomy-free survival rate in patients treated with 5-FU, Mytomicin C and Panitumumab concurrently with radiation therapy as treatment for anal squamous cell carcinoma.
Measured: 2 years
Complete response rate
To assess complete response rate in patients treated with 5-FU, Mytomicin C and Panitumumab concurrently with radiation therapy as treatment for anal squamous cell carcinoma.
Measured: 3 years
Safety profile
- Incidence of adverse events (including all serious, grade 3, grade 4, and treatment related events)
- Changes in laboratory values.
Measured: 3 years
Predictive potential of different biomarkers
- To investigate the predictive potential of different biomarkers involved in different pathways on efficacy and/or safety endpoints:
- EGFR pathway
- DNA reparation mechanisms and apoptosis control
- Oxidative stress control mechanism
- Resistance mechanisms to alkylants (mitomycin C) and antimetabolits (5-FU)
- To describe the presence of HPV infection, isotype study and impact of the status on efficacy and/or safety.
- To evaluate the role of magnetic resonance imaging (MRI) in the determination of therapeutic efficacy and follow-up of these patients.
Measured: 3 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Jan 2011 (estimated)
- Study startOct 2010
- Primary completion24 Mar 2017
- Study completion24 Mar 2017
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Anal Squamous Cell CarcinomaStudies 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
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 58 participants (actual)
Sponsor and investigators
- Lead sponsor
- Grupo Espanol Multidisciplinario del Cancer Digestivo
- Sponsor type
- University, hospital or other
- Collaborators
- Amgen, Trial Form Support S.L.
- Responsible party
- Sponsor
- Investigators
- Jaime Feliu, MD, Study director, Hospital Universitario La PazVicente Alonso, MD, Principal investigator, Hospital Miguel ServetJaume Capdevila, MD, Principal investigator, Hospital Universitario Vall HebronRuth Vera, MD, Principal investigator, Hospital de NavarraMiriam Lopez, MD, Principal investigator, Hospital Infanta SofiaCarmen Castañon, MD, Principal investigator, Hospital Virgen Blanca (León)Carlos Fernández-Martos, MD, Principal investigator, Instituto Valenciano de OncologíaClara Montagut, MD, Principal investigator, Hospital del Mar
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01285778
- Sponsor's protocol ID
- GEMCAD-0902
- Acronym
- VITAL
- Status last verified
- May 2018
- First submitted
- 20 Jan 2011
- Last updated
- 16 May 2018
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 16 May 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Phase 2 Trial to Assess the Efficacy and Safety of Chemoradiation With 5-fluorouracil, Mytomicin C and Panitumumab as a Treatment for Anal Squamous Cell Carcinoma
- ClinicalTrials.gov ID
- NCT01285778
- Acronym / sponsor ID
- VITAL / GEMCAD-0902
- Conditions
- Anal Squamous Cell Carcinoma
- Keywords
- Anal squamous cell carcinoma, panitumumab, chemoradiation, anal cancer, GEMCAD-09-02
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 58 participants (actual)
- Lead sponsor
- Grupo Espanol Multidisciplinario del Cancer DigestivoUniversity, hospital or other
- Collaborators
- Amgen, Trial Form Support S.L.
- Study start
- Oct 2010 (actual)
- Primary completion
- 24 Mar 2017 (actual)
- Study completion
- 24 Mar 2017 (actual)
- First posted
- 28 Jan 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.
Chemoradiation with 5-FU and Mitomycin C is the standard treatment in anal canal SCC. Panitumumab has shown efficacy in other tumors and anti-EGFR treatment has shown clinical activity in a single report of a refractory anal canal SCC patient. Based on this background, we propose to conduct a phase II study to investigate the efficacy and toxicity of radiotherapy with the association:
- 5-FU 1000mg/m2 on days 1-4 and 29-32
- Mitomycin C 10mg/m2 on days 1 and 29
- Panitumumab 6 mg/kg on day 1, then every 2 weeks for 8 weeks
Detailed description
In the 1980s, the treatment of choice for anal cancer was abdominal-perineal amputation, which included the removal of the anus, rectum and lymphatic drainage areas and a permanent colostomy. With this treatment, 5-year survival rates were 40-70%. In the following years, however, it was shown that anal cancer was a tumor that was sensitive to chemotherapy and radiation, so surgery was not the first choice and was only reserved for resistant cases or relapses. Concomitant chemo and radiotherapy based on the Mitomycin C - 5-FU regimen is currently the standard treatment for localized (except T1N0) and locally advanced cases. This statement is supported by two randomized studies that showed that the administration of chemoradiation with Mitomycin C - 5FU was better than radiation in monotherapy. The trial conducted by the United Kingdom Coordinating Committee on Cancer Research (UKCCCR) randomized 585 patients to receive radiotherapy (45 Gy in 4-5 weeks) or the same radiotherapy regimen coupled with 5-FU (1000 mg/m2 x 4 days or 750 mg/m2 x 5 days), for the first and last week of radiotherapy and Mitomycin C 12 mg/m2 on day 1. The 3-year local failure rate was 39% in the combined arm versus 61% with radiotherapy alone. There were no differences in the 3-year overall survival rate. On the other hand, in the study conducted by EORTC, 110 patients were distributed to receive radiotherapy (45 Gy in 5 weeks, with an overimpression of 15 Gy in the patients with CR and 20 Gy if PR) or radiotherapy plus 5-FU (750 mg/m2 days 1-5 and 29-33) associated to Mitomycin C (15 mg/m2 on day 1). The CR rate was significantly greater in the group treated with chemoradiation (80% vs. 54%). After 5 years of follow-up, there was still an 18% increase in the local control rate in favor of the group treated with chemoradiation.
More recently, the results of a phase II CALGB trial, suggests that the administration of induction treatment with two cycles of cisplatin-5FU (cisplatin 100 mg/m2 on days 1 and 29 and 5FU 1000 mg/m2 days 1-4 and 29-32) followed by chemoradiotherapy with 5-FU and Mitomycin C was very promising, especially in patients with a poor prognosis, with 50% of patients remaining colostomy and disease-free at 48 months. However, in a randomized study by the RTOG group, which included 682 patients, this strategy was compared with the classic concomitant chemoradiation with 5-FU (1000 mg/m2 days 1-4 and 29-32) and Mitomycin C (10 mg/m2 days 1 and 29). No differences in survival were found, but it was also detected that the colostomy rate was greater in the patients treated with the regimen containing Cisplatin (HR, 1.68; 95% CI, 1.07-2.65; P=.02). The authors concluded that induction with cisplatin was not superior to the traditional administration of 5FU-Mitomycin C with RT.
Epidermoid anal cancer is a tumor that often expresses the EGFR receptor. In an initial study with 21 cases, it was reported that there was EGFR expression in all the biopsies. In another study with 38 cases, it was found that 55% of the tumors expressed EGFR. No study has been published, however, which has investigated the efficacy of Panitumumab in this tumor. There is only one report of a refractory case in which cetuximab was administered together with CPT-11 with an excellent response.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Panitumumab, mytomicin C, 5-FU, radiation | Experimental | Drug: panitumumab, mytomicin C, 5-FU, radiation |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (11 listed)
- Man or woman ≥ 18 years
- Competent to comprehend, sign, and date an IEC-approved informed consent form
- Histologically or cytologically-confirmed anal canal SCC
- T status 2-4 and any N status (pelvic or inguinal) radiologically defined by MRI
- De novo diagnosis of anal canal SCC not previously treated
Key exclusion criteria (14 listed)
- Metastatic anal canal SCC
- HIV infection (except patients with an undetectable viral load and CD4 cells count >400/mL which are eligible for the study)
- Known hypersensitivity to any of the study drugs
- Evidence of any other disease, 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
- Patients they have received prior systemic therapy or radiotherapy for the treatment of SCC anal carcinoma.
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 |
|---|---|---|
| panitumumab, mytomicin C, 5-FU, radiationAlso: VectibixRadiation therapy will be administered concurrent with chemotherapy and Panitumumab treatment. It will start the day 1 of the systemic treatment. That is, the first day of radiation therapy will be the day of the administration of the first dose of Panitumumab and Mitomycin C, as well as the first day of the first 96-hours course of 5-FU continuous infusion. On day 1, drugs and radiation will be administered in the following order: * First, Panitumumab. Panitumumab will be administered by IV infusion on day 1, and every 2 weeks during 8 weeks * Then Mitomycin C, 10mg/m2 on days 1 and 29 * Then start the 5-FU continuous infusion, 1000mg/m2 on days 1-4 and 29-32 * Finally, no less than 2 hours after the start of the 5-FU infusion, first dose of radiation therapy. | Drug | Panitumumab, mytomicin C, 5-FU, radiation |
Primary outcome
Three-year disease-free survival rate
Time frame: 3 years
To estimate the three-year disease-free survival rate in patients treated with 5-FU, mytomicin C and Panitumumab concurrently with radiation therapy as treatment for anal squamous cell carcinoma
7 secondary outcomes
Disease free survival rate
Time frame: 3 years
Three-year free local-regional failure rate
Time frame: 3 years
Overall survival
Time frame: 3 years
Colostomy-free survival rate
Time frame: 2 years
Complete response rate
Time frame: 3 years
Safety profile
Time frame: 3 years
Predictive potential of different biomarkers
Time frame: 3 years
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 May 2018.
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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.
Jaime Feliu, MD study director
Hospital Universitario La Paz
Vicente Alonso, MD principal investigator
Hospital Miguel Servet
Jaume Capdevila, MD principal investigator
Hospital Universitario Vall Hebron
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 panitumumab, mytomicin C, 5-FU, radiation in people with Anal Squamous Cell Carcinoma, run by Grupo Espanol Multidisciplinario del Cancer Digestivo at 20 sites in Spain.
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 11 inclusion and 14 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: finished, as of the sponsor's last update on 16 May 2018. 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 Spain. 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 is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Three-year disease-free survival rate (time frame: 3 years). 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 16 May 2018.