Follicular LymphomaPhase 3NCT02449252
Efficacy of Consolidative Involved-site Radiotherapy for Patients With Limited-stage Follicular Lymphoma
A Phase 3 study testing Consolidation involved-site radiotherapy (ISRT), Consolidation involved-field radiotherapy (IFRT) and cyclophosphamide in people with Follicular Lymphoma, run by Wuhan University at 1 site in China.
Trial summary
Radiotherapy (RT) is an important option for patients with limited stage FL. The recommended approach for patients with limited stage FL by The National Comprehensive Cancer Network (NCCN) is 24Gy~30Gy consolidation RT following effective systemic therapy. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Follicular Lymphoma
- What is being tested?
- Consolidation involved-site radiotherapy (ISRT), Consolidation involved-field radiotherapy (IFRT) and cyclophosphamide
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 120 participants
- Where
- 1 siteChina
- Study dates
- Oct 2015to Oct 2025
- Phase
- Phase 3
- 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 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Both male and female aged range from 18 years to 65 years.
- Eastern Cooperative Oncology Group(ECOG) performance status of 0 or 1.
- All patients had histologically confirmed Follicular lymphoma, grade 1 or 2.
- Limited-stage FL patients at newly diagnosed or recurrent without RT in initial management.
- Adequate organ function.
- Negative pregnancy test.
- Signed informed consent document on file.
Who cannot join
- Woman who were pregnant or lactating.
- With severe local infection or general infective disease.
- Primary lymphoma in special organ including cuticula, center never system, gastrointestinal tract, testicle, and lung.
- With other second primary malignancy except cutaneum carcinoma.
- Being or planning to participate in other study.
- Any patient who in the opinion of the investigator should not participate in the study.
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- Withdrawal Criteria:
- Patient are free to withdrawal completely from the study at any time upon request.
- Patient in the study may be stopped with the patient agreement at any time at the discretion of investigator.
- In-field progression on irradiation ongoing.
- Poor tolerability adverse events in the period of chemotherapy or irradiation after enrolled in the study.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Efficacy of Consolidative Involved-site Radiotherapy Following Effective Chemotherapy for Patients With Limited-stage Follicular Lymphoma: Wuhan University Cancer Center -NHL01 Trial
Radiotherapy (RT) is an important option for patients with limited stage FL. The recommended approach for patients with limited stage FL by The National Comprehensive Cancer Network (NCCN) is 24Gy~30Gy consolidation RT following effective systemic therapy. There is no universal consensus for a ''standard'' RT field size in the treatment of limited stage FL. The involved-site radiotherapy (ISRT) has been treated effectively for these patients. However, the certain target volumes of ISRT need to be defined for patients with limited stage FL after effective chemotherapy.
Read the detailed description
Follicular lymphoma (FL) is the second most common histology of non-Hodgkin's lymphoma and has significantly increased in incidence over the past three decades. FL, grade 1 or 2 has been recognized as having an indolent natural history with good long-term survival rates despite a high risk of recurrence. Approximately 25% of patients present with stage I or II disease (limited stage FL) at diagnosis, and their 10-year overall survival (OS) rate ranges from 52% to 79%. The treatment options include radiotherapy (RT) alone, immunotherapy ± chemotherapy, immunotherapy ± chemotherapy + RT, and even observation for selected patients. There were no differences in OS.
RT is an important option for patients with limited stage FL. Despite the evidence and these international guidelines' recommendation that primary RT has been considered the preferred treatment approach, RT alone remains worrisomely under used in the treatment of limited stage FL. The positive result that immediate RT was associated with improved disease-specific and overall survival (OS) in patients with stage I and II follicular lymphoma has been shown in SEER data. The OS and disease-free survival (DFS) at 15 years for limited stage FL treated with RT range from 40% to 66% and 40% to 49%, respectively. However, some controversies consider that the literature describing outcomes of early-stage follicular lymphoma treated with RT alone largely consists of retrospective accounts of selected patients from single institutions treated in an era before modern chemotherapy and staging procedures. For patients underwent rigorous staging with stage I FL, the results of The National LymphoCare Study show that progression-free survival (PFS) was significantly improved with either R-chemotherapy or systemic therapy + RT compared with patients receiving RT alone. The OS has no differences among the diverse treatment approaches in these patients. This result is also approved by several recent data both prospective study and retrospective analysis. So, it is questioned whether RT alone, which was the historical standard, is still the best choice for patients with limited stage FL. On combined-modality therapy (CMT) of limited stage FL, combined consolidation RT with brief modern CHOP or CHOP-like chemotherapy can improve the result of DFS though the OS failed to improvement. At the same time, a definitive radiation-dose study in indolent lymphoma from the British National Lymphoma Investigation shows that the 5-year freedom from local progression and OS have no difference either a radiation dose of 24 Gy or a dose of 40 to 45 Gy, respectively. Therefore, the recommended approach for patients with limited stage FL by the National Comprehensive Cancer Network (NCCN) is 24Gy~30Gy consolidation RT following effective systemic therapy. The main controversy focuses on the timing of RT, the combination between chemotherapy and RT and the ongoing reduction in radiation field size.
FL is generally considered an incurable disease and has a long-term outcomes of PFS and OS. Long-term complications related to RT among patients with early-stage FL should be focused as it emphasizes on Hodgkin's lymphoma (HL). In a British study of 2,456 patients with NHL, the relative risk (RR) of all malignancies were 1.3 per 10,000 person-years. The most common late non-neoplastic events were cardiac disease and infertility. In a study conducted by the European Organization for Research and Treatment of Cancer (EORTC), all late non-neoplastic events were observed in 46% of 757 patients at a median follow-up of 9.4 years after NHL treatment.
There is no universal consensus for a ''standard'' RT field size in the treatment of limited stage FL. The primary objective of reducing the RT field size is to lower rates of radiation-induced toxicity and radiation-induced second malignancy in long-term survivors without compromising disease control. Some previous studies show that involved-field RT (IFRT), involved regional RT (IRRT), and extended-field RT (EFRT) have similar survival outcomes. Even the radiotherapy field size is involved node RT (INRT). The retrospective results of Campbell et al show that the PFS was no significant difference for patients who received IRRT compared with patients who received INRT. Compared with the IRRT group, the smaller RT field size in the INRT group did not result in an increased risk of distant failure without infield or regional recurrence (38%vs 32%, respectively). However, the OS was inferior in the INRT group at 10 years (71% vs 59%). The underlying reason may relate to the absence of effective systemic therapy. Moreover, there is not the definition of CTV of RT in the research of Campbell et al. The planning target volume (PTV) of INRT in the research was also only added with physiologic movement and interfraction setup variation from gross target volume (GTV) which encompassed the sites of known disease.
It is necessary to design a prospective study with effective systemic therapy and the certain target volumes to evaluate the efficacy and adverse events of RT with smaller RT field size. Involved-site radiotherapy (ISRT), based on a modified involved field, aims to reduce the radiation volume treated and the probability of late effects. Its radiation targets include a gross tumor volume (GTV), a clinical target volume (CTV), and a planning target volume (PTV), which were defined in International Commission on Radiation Units and Measurements Report (ICRU) 50. This is based on defining the site of gross disease before chemotherapy, the GTV and using a CT-based volume with an expansion to form a CTV in the cranio-caudal direction.
Compared to the IFRT, the response rate and toxicities related to involved-site radiotherapy (ISRT) were to be evaluated for CR and PR patients with limited-stage FL after effective systemic treatment. The CTV of ISRT is defined as the region including the prechemotherapy volume of disease with 1.5 cm margin expanded cranio-caudally in the direction of potential lymphatic spread. The CTV should not extend into air in the transverse plane and should be limited in the involved lymph node region defined by the Cancer and Leukemia Group B (CALGB). The PTV is then extended from CTV by adding the necessary margin for setup error and organ motion.
- Conditions
- Follicular Lymphoma
- Being tested
- Consolidation involved-site radiotherapy (ISRT), Consolidation involved-field radiotherapy (IFRT), cyclophosphamide, doxorubicin, vincristine
- Keywords
- limited stage FL, Involved-site Radiotherapy, Chemotherapy
- Medical subject headings
- Lymphoma, Follicular
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Consolidation involved-site radiotherapy (ISRT)Radiation
six cycles modern CHOP chemotherapy. Involved-site radiotherapy (ISRT) is based on defining the site of gross disease before chemotherapy, the GTV and using a CT-based volume with an expansion to form a CTV in the cranio-caudal direction.
Involved-site radiotherapy (ISRT) is given in 24Gy~30Gy in 12~15 fractions of 2 Gy 5 days per week.
Consolidation involved-field radiotherapy (IFRT)Radiation
six cycles modern CHOP chemotherapy. Radiotherapy field of involved-field radiotherapy defined by CALGB is encompassed the prechemotherapy gross tumor.
Involved-field RT (IFRT) is given in 24Gy~30Gy in 12~15 fractions of 2 Gy 5 days per week.
cyclophosphamideDrug
patients in both arms will be given cyclophosphamide chemotherapy.
doxorubicinDrug
patients in both arms will be given cyclophosphamide chemotherapy.
vincristineDrug
patients in both arms will be given cyclophosphamide chemotherapy.
prednisoneDrug
patients in both arms will be given cyclophosphamide chemotherapy.
| Study group | Role | What they receive |
|---|---|---|
| ISRT group | Experimental | Six cycles chemotherapy (cyclophosphamide 750mg/square meter on day 1 + doxorubicin 50mg/square meter on day 1 + vincristine 1.4mg/square meter on day 1 (up to a maxomal dose of 2 mg) + prednisone 60mg/square meter on day 1 through 5, repeated at 21-day intervals).
Consolidation involved-site radiotherapy (ISRT) following in patients with complete or partial response beginning 1 month after the last cycle of chemotherapy. Receives: Radiation: Consolidation involved-site radiotherapy (ISRT); Drug: cyclophosphamide; Drug: doxorubicin; Drug: vincristine; Drug: prednisone |
| IFRT group | Active comparator | Six cycles chemotherapy (cyclophosphamide 750mg/square meter on day 1 + doxorubicin 50mg/square meter on day 1 + vincristine 1.4mg/square meter on day 1 (up to a maxomal dose of 2 mg) + prednisone 60mg/square meter on day 1 through 5, repeated at 21-day intervals).
Consolidation involved-field radiotherapy (IFRT) following in patients with complete or partial response beginning 1 month after the last cycle of chemotherapy. Receives: Radiation: Consolidation involved-field radiotherapy (IFRT); Drug: cyclophosphamide; Drug: doxorubicin; Drug: vincristine; Drug: prednisone |
What is being measured
The primary outcome is the main question the study is designed to answer.
Progression-free survival - PFS
Treatment failure was defined as any recurrence of non-Hodgkin lymphoma.
Measured: from the date of diagnosis to the date of treatment failure or death from any cause, whichever occurs first, Assessed up to 100 months.
Adverse events with grade 3 or 4 - AEs
Toxicity was scored according to the toxicity scale of the National Cancer Institute Common Terminology Criteria for Adverse Events 3.0.
Measured: The time from the day of treatment to the day of the first documented disease progression or death from any cause, Assessed up to 24 months.
Secondary outcomes (4)
Overall survival - OS
Measured: From the initial diagnosis of follicular lymphoma to death from any cause, Assessed up to 120 months.
Rate of in-field progression
Measured: From the start of RT to the first documented disease progression within the radiotherapy field, Assessed up to 120 months.
Rate of out-field progression
Measured: From the start of RT to the first documented disease progression outside the radiotherapy field, Assessed up to 120 months.
Rate of regional failure
Measured: From the start of RT to the first documented disease progression outside of ISRT field but within the involved region defined as CALGB, Assessed up to 120 months.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 May 2015 (estimated)
- Study startOct 2015
- Primary completionOct 2019 (estimated)
- Study completionOct 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- 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
- 120 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Wuhan University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Di Deng, Wuhan University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02449252
- Sponsor's protocol ID
- WUCC-NHL01 Trial
- Status last verified
- Dec 2015
- First submitted
- 7 May 2015
- Last updated
- 14 Dec 2015
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 14 Dec 2015. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Efficacy of Consolidative Involved-site Radiotherapy Following Effective Chemotherapy for Patients With Limited-stage Follicular Lymphoma: Wuhan University Cancer Center -NHL01 Trial
- ClinicalTrials.gov ID
- NCT02449252
- Acronym / sponsor ID
- WUCC-NHL01 Trial
- Conditions
- Follicular Lymphoma
- Keywords
- limited stage FL, Involved-site Radiotherapy, Chemotherapy
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 120 participants (estimated)
- Lead sponsor
- Wuhan UniversityUniversity, hospital or other
- Study start
- Oct 2015
- Primary completion
- Oct 2019 (estimated)
- Study completion
- Oct 2025 (estimated)
- First posted
- 20 May 2015 (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.
Radiotherapy (RT) is an important option for patients with limited stage FL. The recommended approach for patients with limited stage FL by The National Comprehensive Cancer Network (NCCN) is 24Gy~30Gy consolidation RT following effective systemic therapy. There is no universal consensus for a ''standard'' RT field size in the treatment of limited stage FL. The involved-site radiotherapy (ISRT) has been treated effectively for these patients. However, the certain target volumes of ISRT need to be defined for patients with limited stage FL after effective chemotherapy.
Detailed description
Follicular lymphoma (FL) is the second most common histology of non-Hodgkin's lymphoma and has significantly increased in incidence over the past three decades. FL, grade 1 or 2 has been recognized as having an indolent natural history with good long-term survival rates despite a high risk of recurrence. Approximately 25% of patients present with stage I or II disease (limited stage FL) at diagnosis, and their 10-year overall survival (OS) rate ranges from 52% to 79%. The treatment options include radiotherapy (RT) alone, immunotherapy ± chemotherapy, immunotherapy ± chemotherapy + RT, and even observation for selected patients. There were no differences in OS.
RT is an important option for patients with limited stage FL. Despite the evidence and these international guidelines' recommendation that primary RT has been considered the preferred treatment approach, RT alone remains worrisomely under used in the treatment of limited stage FL. The positive result that immediate RT was associated with improved disease-specific and overall survival (OS) in patients with stage I and II follicular lymphoma has been shown in SEER data. The OS and disease-free survival (DFS) at 15 years for limited stage FL treated with RT range from 40% to 66% and 40% to 49%, respectively. However, some controversies consider that the literature describing outcomes of early-stage follicular lymphoma treated with RT alone largely consists of retrospective accounts of selected patients from single institutions treated in an era before modern chemotherapy and staging procedures. For patients underwent rigorous staging with stage I FL, the results of The National LymphoCare Study show that progression-free survival (PFS) was significantly improved with either R-chemotherapy or systemic therapy + RT compared with patients receiving RT alone. The OS has no differences among the diverse treatment approaches in these patients. This result is also approved by several recent data both prospective study and retrospective analysis. So, it is questioned whether RT alone, which was the historical standard, is still the best choice for patients with limited stage FL. On combined-modality therapy (CMT) of limited stage FL, combined consolidation RT with brief modern CHOP or CHOP-like chemotherapy can improve the result of DFS though the OS failed to improvement. At the same time, a definitive radiation-dose study in indolent lymphoma from the British National Lymphoma Investigation shows that the 5-year freedom from local progression and OS have no difference either a radiation dose of 24 Gy or a dose of 40 to 45 Gy, respectively. Therefore, the recommended approach for patients with limited stage FL by the National Comprehensive Cancer Network (NCCN) is 24Gy~30Gy consolidation RT following effective systemic therapy. The main controversy focuses on the timing of RT, the combination between chemotherapy and RT and the ongoing reduction in radiation field size.
FL is generally considered an incurable disease and has a long-term outcomes of PFS and OS. Long-term complications related to RT among patients with early-stage FL should be focused as it emphasizes on Hodgkin's lymphoma (HL). In a British study of 2,456 patients with NHL, the relative risk (RR) of all malignancies were 1.3 per 10,000 person-years. The most common late non-neoplastic events were cardiac disease and infertility. In a study conducted by the European Organization for Research and Treatment of Cancer (EORTC), all late non-neoplastic events were observed in 46% of 757 patients at a median follow-up of 9.4 years after NHL treatment.
There is no universal consensus for a ''standard'' RT field size in the treatment of limited stage FL. The primary objective of reducing the RT field size is to lower rates of radiation-induced toxicity and radiation-induced second malignancy in long-term survivors without compromising disease control. Some previous studies show that involved-field RT (IFRT), involved regional RT (IRRT), and extended-field RT (EFRT) have similar survival outcomes. Even the radiotherapy field size is involved node RT (INRT). The retrospective results of Campbell et al show that the PFS was no significant difference for patients who received IRRT compared with patients who received INRT. Compared with the IRRT group, the smaller RT field size in the INRT group did not result in an increased risk of distant failure without infield or regional recurrence (38%vs 32%, respectively). However, the OS was inferior in the INRT group at 10 years (71% vs 59%). The underlying reason may relate to the absence of effective systemic therapy. Moreover, there is not the definition of CTV of RT in the research of Campbell et al. The planning target volume (PTV) of INRT in the research was also only added with physiologic movement and interfraction setup variation from gross target volume (GTV) which encompassed the sites of known disease.
It is necessary to design a prospective study with effective systemic therapy and the certain target volumes to evaluate the efficacy and adverse events of RT with smaller RT field size. Involved-site radiotherapy (ISRT), based on a modified involved field, aims to reduce the radiation volume treated and the probability of late effects. Its radiation targets include a gross tumor volume (GTV), a clinical target volume (CTV), and a planning target volume (PTV), which were defined in International Commission on Radiation Units and Measurements Report (ICRU) 50. This is based on defining the site of gross disease before chemotherapy, the GTV and using a CT-based volume with an expansion to form a CTV in the cranio-caudal direction.
Compared to the IFRT, the response rate and toxicities related to involved-site radiotherapy (ISRT) were to be evaluated for CR and PR patients with limited-stage FL after effective systemic treatment. The CTV of ISRT is defined as the region including the prechemotherapy volume of disease with 1.5 cm margin expanded cranio-caudally in the direction of potential lymphatic spread. The CTV should not extend into air in the transverse plane and should be limited in the involved lymph node region defined by the Cancer and Leukemia Group B (CALGB). The PTV is then extended from CTV by adding the necessary margin for setup error and organ motion.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| ISRT group | Experimental | Radiation: Consolidation involved-site radiotherapy (ISRT), Drug: cyclophosphamide, Drug: doxorubicin, Drug: vincristine, Drug: prednisoneSix cycles chemotherapy (cyclophosphamide 750mg/square meter on day 1 + doxorubicin 50mg/square meter on day 1 + vincristine 1.4mg/square meter on day 1 (up to a maxomal dose of 2 mg) + prednisone 60mg/square meter on day 1 through 5, repeated at 21-day intervals). Consolidation involved-site radiotherapy (ISRT) following in patients with complete or partial response beginning 1 month after the last cycle of chemotherapy. |
| IFRT group | Active comparator | Radiation: Consolidation involved-field radiotherapy (IFRT), Drug: cyclophosphamide, Drug: doxorubicin, Drug: vincristine, Drug: prednisoneSix cycles chemotherapy (cyclophosphamide 750mg/square meter on day 1 + doxorubicin 50mg/square meter on day 1 + vincristine 1.4mg/square meter on day 1 (up to a maxomal dose of 2 mg) + prednisone 60mg/square meter on day 1 through 5, repeated at 21-day intervals). Consolidation involved-field radiotherapy (IFRT) following in patients with complete or partial response beginning 1 month after the last cycle of chemotherapy. |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (7 listed)
- Both male and female aged range from 18 years to 65 years.
- Eastern Cooperative Oncology Group(ECOG) performance status of 0 or 1.
- All patients had histologically confirmed Follicular lymphoma, grade 1 or 2.
- Limited-stage FL patients at newly diagnosed or recurrent without RT in initial management.
- Adequate organ function.
Key exclusion criteria (11 listed)
- Woman who were pregnant or lactating.
- With severe local infection or general infective disease.
- Primary lymphoma in special organ including cuticula, center never system, gastrointestinal tract, testicle, and lung.
- With other second primary malignancy except cutaneum carcinoma.
- Being or planning to participate in other study.
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 |
|---|---|---|
| Consolidation involved-site radiotherapy (ISRT)six cycles modern CHOP chemotherapy. Involved-site radiotherapy (ISRT) is based on defining the site of gross disease before chemotherapy, the GTV and using a CT-based volume with an expansion to form a CTV in the cranio-caudal direction. Involved-site radiotherapy (ISRT) is given in 24Gy~30Gy in 12~15 fractions of 2 Gy 5 days per week. | Radiation | ISRT group |
| Consolidation involved-field radiotherapy (IFRT)six cycles modern CHOP chemotherapy. Radiotherapy field of involved-field radiotherapy defined by CALGB is encompassed the prechemotherapy gross tumor. Involved-field RT (IFRT) is given in 24Gy~30Gy in 12~15 fractions of 2 Gy 5 days per week. | Radiation | IFRT group |
| cyclophosphamidepatients in both arms will be given cyclophosphamide chemotherapy. | Drug | IFRT group, ISRT group |
| doxorubicinpatients in both arms will be given cyclophosphamide chemotherapy. | Drug | IFRT group, ISRT group |
| vincristinepatients in both arms will be given cyclophosphamide chemotherapy. | Drug | IFRT group, ISRT group |
| prednisonepatients in both arms will be given cyclophosphamide chemotherapy. | Drug | IFRT group, ISRT group |
Primary outcome
Progression-free survival - PFS
Time frame: from the date of diagnosis to the date of treatment failure or death from any cause, whichever occurs first, Assessed up to 100 months.
Treatment failure was defined as any recurrence of non-Hodgkin lymphoma.
Adverse events with grade 3 or 4 - AEs
Time frame: The time from the day of treatment to the day of the first documented disease progression or death from any cause, Assessed up to 24 months.
Toxicity was scored according to the toxicity scale of the National Cancer Institute Common Terminology Criteria for Adverse Events 3.0.
4 secondary outcomes
Overall survival - OS
Time frame: From the initial diagnosis of follicular lymphoma to death from any cause, Assessed up to 120 months.
Rate of in-field progression
Time frame: From the start of RT to the first documented disease progression within the radiotherapy field, Assessed up to 120 months.
Rate of out-field progression
Time frame: From the start of RT to the first documented disease progression outside the radiotherapy field, Assessed up to 120 months.
Rate of regional failure
Time frame: From the start of RT to the first documented disease progression outside of ISRT field but within the involved region defined as CALGB, Assessed up to 120 months.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Dec 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.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Consolidation involved-site radiotherapy (ISRT), Consolidation involved-field radiotherapy (IFRT) and cyclophosphamide in people with Follicular Lymphoma, run by Wuhan University at 1 site in China.
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 7 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: status not confirmed, as of the sponsor's last update on 14 Dec 2015. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Di Deng, MD (0086-27-67813153, dengdi69@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Progression-free survival - PFS (time frame: from the date of diagnosis to the date of treatment failure or death from any cause, whichever occurs first, Assessed up to 100 months.). The study lists 2 primary outcomes in all. 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 14 Dec 2015.