Follicular Lymphoma Clinical Trial
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.
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.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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