Prospective, multicenter, open label, phase III randomized clinical trial in previously untreated Follicular Lymphoma in early stage. Patients will be randomized to receive Radiotherapy or Radiotherapy plus Obinutuzumab.
Prospective, multicenter, open label, phase III randomized clinical trial in previously untreated Follicular Lymphoma in early stage (I-II non-bulky). Patients will be randomized to receive: \- Involved-Site Radiation Therapy at standard dose 24Gy - standard arm OR \- Involved-Site Radiation Therapy at standard dose 24Gy followed by Obinutuzumab 4 infusions weekly + 4 infusions every 3 weeks (8 total doses) - experimental arm
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
190
Involved-Site Radiation Therapy 24Gy
Involved-Site Radiation Therapy 24Gy followed by Obinutuzumab 1000mg flat dose 4 doses weekly plus addition 4 doses every 3 weeks
Progression-free survival (PFS)
Time between the randomization to first documentation of recurrence, progression or death from any cause at 2 years
Time frame: From treatment start up to 33 months (9 months treatment period and 24 months of follow-up)
Complete response rate (CRR)
Complete response (CR) rate according to the international criteria (Cheson 2014)
Time frame: From therapy start up to end of treatment (9 months)
Overall response rate (ORR)
ORR will be defined as the proportion of patients who have a partial or complete response at every treatment phase
Time frame: From therapy start up to end of treatment (9 months)
Disease Free Survival (DFS)
Time between the first documentation of Complete Response to any treatment failure, including disease progression, or discontinuation of treatment for any reason (e.g., disease progression, toxicity, patient preference, initiation of a new treatment without documented progression) or death from any cause
Time frame: From post radiotherapy assessment up to 45 months (9 months treatment phase plus 36 months of follow-up)
Event Free Survival (EFS)
Time between the randomization to any treatment failure, including disease progression, or discontinuation of treatment for any reason (e.g., disease progression, toxicity, patient preference, initiation of a new treatment without documented progression) or death from any cause
Time frame: From therapy start up to 45 months (9 months treatment phase plus 36 months of follow-up)
Number of patients with Molecular Response at end of treatment
MRD negativity at end of treatment for positive patients at baseline
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Nuovo Ospedale Civile di Sassuolo - Day Hospital Oncologico
Sassuolo, Modena (MO), Italy
RECRUITINGAzienda Ospedaliera Nazionale Ss Antonio E Biagio E C Arrigo, SCDU Ematologia
Alessandria, Italy
RECRUITINGAORN San Giuseppe Moscati Avellino, U.O.C. Ematologia e Trapianto Emopoietico
Avellino, Italy
RECRUITINGCentro Di Riferimento Oncologico Di Aviano, S.O.C. Oncologia Medica e dei Tumori Immunocorrelati
Aviano, Italy
RECRUITINGIstituto Tumori Bari Giovanni Paolo II, U.O. di Ematologia e Terapia Cellulare
Bari, Italy
RECRUITINGOspedale degli Infermi di Biella, SSD Ematologia
Biella, Italy
RECRUITINGAzienda Socio Sanitaria Territoriale Degli Spedali Civili Di Brescia, U.O. Ematologia
Brescia, Italy
RECRUITINGARNAS G. Brotzu, SC Ematologia e CTMO
Cagliari, Italy
NOT_YET_RECRUITINGIstituto Di Candiolo Fondazione Del Piemonte Per Loncologia IRCCS, Oncologia Medica
Candiolo, Italy
RECRUITINGIstituto Oncologico Veneto, U.O.C. Oncoematologia
Castelfranco Veneto, Italy
RECRUITING...and 39 more locations
Time frame: From therapy start up to end of treatment (9 months)
Rate of Adverse Events
Incidence and severity of AEs in both arms according to latest CTCAE criteria
Time frame: From therapy start up to 45 months (9 months treatment phase plus 36 months of follow-up)
Prognostic and predictive impact of presence/abscence of t(14;18) rearrangement measured by FISH
Prognostic and predictive impact on PFS in presence or absence of t(14;18) rearrangement measured by FISH
Time frame: From therapy start up to 45 months (9 months treatment phase plus 36 months of follow-up)
Prognostic role of Minimal Residual Disease by conventional (BCL2/IGH rearrangement by ddPCR) and ctDNA method
Prognostic role of conventional MRD (BCL2/IGH rearrangement by ddPCR) and of MRD on plasmatic circulating tumour deoxyribonucleic acid (ctDNA) at different time points for PFS and relapse
Time frame: From therapy start up to 45 months (9 months treatment phase plus 36 months of follow-up)
Prognostic and predictive value of different threshold of metabolic response expressed as SUVmax, MTV and TLG at baseline (PET-0);
Prognostic and predictive value of different threshold of metabolic response expressed as quantitative PET indexes (QPI) at baseline (PET-0), i.e. SUVmax, MTV and TLG;
Time frame: At baseline (before therapy start)
Prognostic and predictive role of liquid biopsy by DNA sequencing for lymphoma mutations
Prognostic and predictive role of liquid biopsy by DNA sequencing for lymphoma mutations at different time points on PFS and relapse
Time frame: From therapy start up to 45 months (9 months treatment phase plus 36 months of follow-up)
Prognostic and predictive value of radiological markers assessed by Machine Learning tools (pyRadiomics)
Prognostic and predictive value of radiomic analysis on PFS, assessed on both CT and PET scans by Machine Learning tools (pyRadiomics);
Time frame: From therapy start up to 45 months (9 months treatment phase plus 36 months of follow-up)
Correlation of MRD results with the radiomics results and clinical outcomes
Correlation of MRD results with the radiomics results and clinical outcomes
Time frame: From therapy start up to 45 months (9 months treatment phase plus 36 months of follow-up)
Comparison between genotype at diagnosis and at relapse assessed by RNA sequencing (CIBERSORTx)
Comparison between genotype at diagnosis and at relapse assessed by RNA sequencing (CIBERSORTx)
Time frame: From therapy start up to 45 months (9 months treatment phase plus 36 months of follow-up)
Evaluation of liquid biopsy as a tool to identity specific mutations predictive for clonal evolution of lymphoma
Evaluation of liquid biopsy as a tool to identity specific mutations predictive for clonal evolution of lymphoma
Time frame: From therapy start up to 45 months (9 months treatment phase plus 36 months of follow-up)