Follicular LymphomaPhase 3NCT01662102
Rituximab or Zevalin - Efficacy Trial of Therapeutic Alternatives (RoZetta)
A Phase 3 study testing Zevalin and Rituximab in people with Follicular Lymphoma, run by Spectrum Pharmaceuticals, Inc at 5 sites in United States.
Trial summary
The purpose of this study is to evaluate the effect of consolidation treatment Zevalin® versus maintenance treatment with Rituxan® on progression-free survival (PFS) following response induction with chemotherapy plus rituximab in previously untreated participants with follicular lymphoma. Read more about this study
- Who is it for?
- Ages 18 to 75 years
- Conditions the study is for
- Follicular Lymphoma
- What is being tested?
- Zevalin and Rituximab
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 1 participants
- Where
- 5 sitesUnited States
- Study dates
- 11 Dec 2012to 5 Mar 2013
- Phase
- Phase 3
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
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 to 75 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 18 to 75 years of age.
- Previously untreated with histologically confirmed grade 1, 2 or 3a cluster of differentiation-20 (CD20)-positive follicular lymphoma, with any of the GELF (Groupe d'Etude de Lymphomes Folliculaires) treatment criteria prior to induction.
- Achieved a response to induction treatment with either rituximab-cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) (6 cycles of R-CHOP21 or R-CHOP14), rituximab-cyclophosphamide, vincristine and prednisone (R-CVP) (6 cycles), or rituximab-bendamustine (R-B) (4 to 6 cycles).
- Must have completed all doses of the induction treatment, except for the modifications allowed in the protocol.
Who cannot join
- Transformation to high grade lymphoma (secondary to "low grade" follicular lymphoma [FL]).
- Grade 3b follicular lymphoma.
- Primary follicular lymphoma of the skin or gastrointestinal tract.
- Previous treatment of follicular lymphoma.
- Altered renal and hepatic function.
- Known human immunodeficiency virus (HIV) infection and/or active hepatitis B virus (HBV) and/or hepatitis C virus (HCV) infection
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- Serious co-morbid conditions (for example, ongoing infection, uncontrolled diabetes mellitus, gastric ulcers, active autoimmune disease).
- Life expectancy < 6.
- Must have:
- Platelet count ≥ 100x10^9/L.
- Bone marrow infiltration <25%.
Trial locations and contacts
5 sites in 1 country.
5 sites in 1 country
United States5 sites
Northeast Georgia Cancer Care
Athens, Georgia, 30607
Charleston Area Medical Center
Charleston, West Virginia, 25304
Illinois Cancer Specialists
Niles, Illinois, 60714
Park Nicollet Institute
Saint Louis Park, Minnesota, 55426
21st Century Oncology
Sun City, Arizona, 85351
About this study
Official title: An Open-Label, Multicenter, Randomized Study in Previously Untreated Follicular Lymphoma Patients to Evaluate the Efficacy of Consolidation With Zevalin® Versus Maintenance Treatment With Rituximab After Initial Therapeutic Response to Rituximab Plus Chemotherapy
The purpose of this study is to evaluate the effect of consolidation treatment Zevalin® versus maintenance treatment with Rituxan® on progression-free survival (PFS) following response induction with chemotherapy plus rituximab in previously untreated participants with follicular lymphoma.
Read the detailed description
This is an open-label, multicenter and randomized study. Participants registered after response induction (PR/CR) to R-chemotherapy. Participants achieving either a partial response (PR) or complete response (CR) following R-chemotherapy eligible for randomization to either consolidation with 90Y-ibritumumab tiuxetan followed by observation for 24 months, or rituximab maintenance for 24 months. After the observation/maintenance period, patients follow up for 5 years.
This study was terminated early for business reasons. (Maximum duration of study was up to approximately 2.7 months).
- Conditions
- Follicular Lymphoma
- Being tested
- Zevalin, Rituximab
- Medical subject headings
- Lymphoma, Follicular
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ZevalinDrug
Also called 90Y-ibritumomab tiuxetan
Zevalin administered intravenously.
RituximabDrug
Also called Rituxan
Rituximab administered intravenously.
| Study group | Role | What they receive |
|---|---|---|
| Zevalin Regimen Consolidation (Group A) | Experimental | 90Y-Ibritumomab tiuxetan administered 8 to 12 weeks after the last chemotherapy infusion. Each participant randomized to this treatment group was to receive a therapeutic dose of 14.8 MBq/kg (0.4 mCi/kg of total body weight) of 90Y ibritumomab tiuxetan (maximum 1,184 MBq or 32 mCi). Participants with a pre-treatment platelet count between 100 and 149 x10^9/L were to receive 0.3 mCi/Kg 90Y-ibritumomab tiuxetan. (Body weight ≤80 kg: 14.8 MBq [0.4 mCi] yttrium-90/kg and Body weight >80 kg: 1,184 MBq [32 mCi] maximum dose).
The 90Y ibritumomab tiuxetan regimen is as follows: Day 1 rituximab (250 mg/m^2); Day 7,8, or 9 rituximab (250 mg/m^2) followed by 90Y ibritumomab tiuxetan within 4 hours of the end of the rituximab infusion. (Maximum duration of study was up to approximately 2.7 months). Receives: Drug: Zevalin; Drug: Rituximab |
| Rituximab Maintenance (Group B) | Active comparator | Participants were to receive 375 mg/m^2 of rituximab, administered by intravenous (I.V.) infusion every 8 weeks, starting 8 to 12 weeks after the last R-chemotherapy cycle. (Maximum duration of study was up to approximately 2.7 months). Receives: Drug: Rituximab |
What is being measured
The primary outcome is the main question the study is designed to answer.
Progression Free Survival
Progression-free survival (PFS) is defined as the time from randomization until progression, relapse, death from any cause, or introduction of a new anti-lymphoma treatment (chemotherapy, radiation therapy or immunotherapy).
Measured: Up to approximately 2.7 months
Secondary outcomes (13)
Complete Response Rate
Measured: Up to approximately 2.7 months
Event Free Survival
EFS time is defined as the time from randomization to first documented progression, death from any cause, or introduction of a new anti-lymphoma treatment (chemotherapy, radiotherapy or immunotherapy).
Measured: Up to approximately 2.7 months
Time to Progression (TTP)
TTP is defined as the time from randomization to the first disease progression.
Measured: Up to approximately 2.7 months
Time to Next Anti-Lymphoma Treatment (TTNLT)
TTNLT is defined as the time from randomization to the first introduction of any new anti lymphoma regimen.
Measured: Up to approximately 2.7 months
Time to Next Chemotherapy (TTNCT)
TTNCT is defined as the time from randomization to the first introduction of any new chemotherapy (cytotoxic or radioimmunotherapy). The TTNCT may be the same as the TTNLT. Participants who respond to treatment and Participants who are lost to follow-up censored at the visit on which the dosing of a new medication was evaluated.
Measured: Up to approximately 2.7 months
Overall Response Rate (ORR)
Tumor response evaluated according to Cheson criteria at the time of randomization and at the end of the maintenance/observation, post randomization. ORR is defined as the percentage of Participants with a complete response (CR) or a partial response (PR), and compared between treatment groups. Participants with no response evaluation (for any reason) considered as not evaluable (NE).
Measured: Up to approximately 2.7 months
Overall Survival (OS)
OS is defined as the time from randomization to death from any cause. In living patients, survival time was censored on the last date participants were known to be alive.
Measured: Up to approximately 2.7 months
Transformation at First Progression
Transformation rate at first progression, defined as the appearance of diffuse areas of large lymphoma cells within a tumor site.
Measured: Up to approximately 2.7 months
Number of Participants With Toxicity
Toxicity graded according to the National Cancer Institute Common Toxicity Criteria for Adverse Events version 4.0.
Measured: Up to approximately 2.7 months
Number of Participants With Secondary Malignancies
Measured: Up to approximately 2.7 months
Functional Assessment of Cancer - General (FACT-G)
The FACT-G is a participant rated, 27-item compilation of general questions divided into 4 primary Quality of Life (QOL) sub-scales: physical well-being (PWB; 7-items, score range 0-28), social/family well-being (SWB; 7-items, score range 0-28), emotional well-being (EWB; 6-items, score range 0-24), and functional well-being (FWB; 7-items, score range 0-28). This tool represents the generic core questionnaire that are utilized in combination with cancer site-specific questionnaires, (FBrain, in this study) Overall score and four subscale scores with ranges and distributions that are sample-specific can be calculated.FACT-G is scored by summing the individual scale scores; higher scores indicate better quality of life. FACT-G uses 5-point rating scale ranging from (0) = Not at all; (1) = A little bit; (2) = Somewhat; (3) = Quite a bit; to (4) = Very much.The FACT-G total score is the sum of the four subscale scores (if least 80% completed) and has a possible range of 0-108 points.
Measured: Up to approximately 2.7 months
European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30)
EORTC-QLQ-C30 is a cancer-specific instrument with 30 questions for evaluation of new chemotherapy and provides an assessment of participant reported outcome dimensions. First 28 questions used 4-point scale (1=not at all,2=a little,3=quite a bit,4=very much) for evaluating 5 functional scales (physical,role,emotional,cognitive,social), 3 symptom scales (fatigue,nausea/vomiting,pain) \& other single items. For each item,high score represented high level of symptomatology/problem. Last 2 questions represented participant's assessment of overall health \& quality of life, coded on 7-point scale (1=very poor to 7=excellent).EORTC QLQ-C30 observed values and change from baseline for global health status (scoring of questions 29 \& 30) and 5 functional scales, 3 symptom scales and other single items (scoring of questions 1 to 28). Answers were converted into grading scale, with values between 0 and 100. High score represented a favourable outcome with a best quality of life for participant.
Measured: Up to approximately 2.7 months
Pharmacoeconomics (Cost Effectiveness Analysis)
A cost-effectiveness analysis done that compares the efficiency (cost/effectiveness unit) of consolidation treatment with 90Y-ibritumomab tiuxetan compared to maintenance treatment with rituximab. The analysis conducted according to a health economic analysis plan independent from this clinical study protocol.
Measured: Up to approximately 2.7 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Aug 2012 (estimated)
- Study start11 Dec 2012
- Primary completion5 Mar 2013
- Study completion5 Mar 2013
Why it stopped: Sponsor decision
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for Follicular LymphomaStudies 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 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 1 participants (actual)
Sponsor and investigators
- Lead sponsor
- Spectrum Pharmaceuticals, Inc
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Fernando Cabanillas, MD, Principal investigator, M.D. Anderson Cancer CenterThomas Witzig, MD, Principal investigator, The Mayo Clinic & FoundationSteven E Finkelstein, MD, Principal investigator, GenesisCare USALeonard Klein, MD, Principal investigator, Illinois Cancer Specialists - US OncologySteven Jubelirer, MD, Principal investigator, West Virginia UniversityPetros Nikolinakos, MD, Principal investigator, Northeast Georgia Cancer Care
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01662102
- Sponsor's protocol ID
- SPI-ZEV-12-302
- Status last verified
- Sep 2021
- First submitted
- 3 Aug 2012
- Last updated
- 4 Oct 2021
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 4 Oct 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- An Open-Label, Multicenter, Randomized Study in Previously Untreated Follicular Lymphoma Patients to Evaluate the Efficacy of Consolidation With Zevalin® Versus Maintenance Treatment With Rituximab After Initial Therapeutic Response to Rituximab Plus Chemotherapy
- ClinicalTrials.gov ID
- NCT01662102
- Acronym / sponsor ID
- SPI-ZEV-12-302
- Conditions
- Follicular Lymphoma
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Sponsor decision
- Enrolment
- 1 participants (actual)
- Lead sponsor
- Spectrum Pharmaceuticals, IncIndustry (pharma, biotech, devices)
- Study start
- 11 Dec 2012 (actual)
- Primary completion
- 5 Mar 2013 (actual)
- Study completion
- 5 Mar 2013 (actual)
- First posted
- 10 Aug 2012 (estimated)
- Results
- Posted 11 Jan 2016
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to evaluate the effect of consolidation treatment Zevalin® versus maintenance treatment with Rituxan® on progression-free survival (PFS) following response induction with chemotherapy plus rituximab in previously untreated participants with follicular lymphoma.
Detailed description
This is an open-label, multicenter and randomized study. Participants registered after response induction (PR/CR) to R-chemotherapy. Participants achieving either a partial response (PR) or complete response (CR) following R-chemotherapy eligible for randomization to either consolidation with 90Y-ibritumumab tiuxetan followed by observation for 24 months, or rituximab maintenance for 24 months. After the observation/maintenance period, patients follow up for 5 years.
This study was terminated early for business reasons. (Maximum duration of study was up to approximately 2.7 months).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Zevalin Regimen Consolidation (Group A) | Experimental | Drug: Zevalin, Drug: Rituximab90Y-Ibritumomab tiuxetan administered 8 to 12 weeks after the last chemotherapy infusion. Each participant randomized to this treatment group was to receive a therapeutic dose of 14.8 MBq/kg (0.4 mCi/kg of total body weight) of 90Y ibritumomab tiuxetan (maximum 1,184 MBq or 32 mCi). Participants with a pre-treatment platelet count between 100 and 149 x10^9/L were to receive 0.3 mCi/Kg 90Y-ibritumomab tiuxetan. (Body weight ≤80 kg: 14.8 MBq [0.4 mCi] yttrium-90/kg and Body weight >80 kg: 1,184 MBq [32 mCi] maximum dose). The 90Y ibritumomab tiuxetan regimen is as follows: Day 1 rituximab (250 mg/m^2); Day 7,8, or 9 rituximab (250 mg/m^2) followed by 90Y ibritumomab tiuxetan within 4 hours of the end of the rituximab infusion. (Maximum duration of study was up to approximately 2.7 months). |
| Rituximab Maintenance (Group B) | Active comparator | Drug: RituximabParticipants were to receive 375 mg/m^2 of rituximab, administered by intravenous (I.V.) infusion every 8 weeks, starting 8 to 12 weeks after the last R-chemotherapy cycle. (Maximum duration of study was up to approximately 2.7 months). |
Who may qualify
- Ages
- 18 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- 18 to 75 years of age.
- Previously untreated with histologically confirmed grade 1, 2 or 3a cluster of differentiation-20 (CD20)-positive follicular lymphoma, with any of the GELF (Groupe d'Etude de Lymphomes Folliculaires) treatment criteria prior to induction.
- Achieved a response to induction treatment with either rituximab-cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) (6 cycles of R-CHOP21 or R-CHOP14), rituximab-cyclophosphamide, vincristine and prednisone (R-CVP) (6 cycles), or rituximab-bendamustine (R-B) (4 to 6 cycles).
- Must have completed all doses of the induction treatment, except for the modifications allowed in the protocol.
Key exclusion criteria (11 listed)
- Transformation to high grade lymphoma (secondary to "low grade" follicular lymphoma [FL]).
- Grade 3b follicular lymphoma.
- Primary follicular lymphoma of the skin or gastrointestinal tract.
- Previous treatment of follicular lymphoma.
- Altered renal and hepatic function.
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 |
|---|---|---|
| ZevalinAlso: 90Y-ibritumomab tiuxetanZevalin administered intravenously. | Drug | Zevalin Regimen Consolidation (Group A) |
| RituximabAlso: RituxanRituximab administered intravenously. | Drug | Rituximab Maintenance (Group B), Zevalin Regimen Consolidation (Group A) |
Primary outcome
Progression Free Survival
Time frame: Up to approximately 2.7 months
Progression-free survival (PFS) is defined as the time from randomization until progression, relapse, death from any cause, or introduction of a new anti-lymphoma treatment (chemotherapy, radiation therapy or immunotherapy).
13 secondary outcomes
Complete Response Rate
Time frame: Up to approximately 2.7 months
Event Free Survival
Time frame: Up to approximately 2.7 months
Time to Progression (TTP)
Time frame: Up to approximately 2.7 months
Time to Next Anti-Lymphoma Treatment (TTNLT)
Time frame: Up to approximately 2.7 months
Time to Next Chemotherapy (TTNCT)
Time frame: Up to approximately 2.7 months
Overall Response Rate (ORR)
Time frame: Up to approximately 2.7 months
Overall Survival (OS)
Time frame: Up to approximately 2.7 months
Transformation at First Progression
Time frame: Up to approximately 2.7 months
Number of Participants With Toxicity
Time frame: Up to approximately 2.7 months
Number of Participants With Secondary Malignancies
Time frame: Up to approximately 2.7 months
Functional Assessment of Cancer - General (FACT-G)
Time frame: Up to approximately 2.7 months
European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30)
Time frame: Up to approximately 2.7 months
Pharmacoeconomics (Cost Effectiveness Analysis)
Time frame: Up to approximately 2.7 months
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Oct 2021.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
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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.
Fernando Cabanillas, MD principal investigator
M.D. Anderson Cancer Center
Thomas Witzig, MD principal investigator
The Mayo Clinic & Foundation
Steven E Finkelstein, MD principal investigator
GenesisCare USA
5 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Zevalin and Rituximab in people with Follicular Lymphoma, run by Spectrum Pharmaceuticals, Inc at 5 sites in United States.
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 4 inclusion and 11 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 4 Oct 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 5 sites in United States. 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 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 11 Jan 2016). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
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?
Progression Free Survival (time frame: Up to approximately 2.7 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 4 Oct 2021.