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Minimal residual disease after conventional treatment significantly impacts on progression-free survival of patients with follicular lymphoma: The FIL FOLL05 trial
- Publication Year :
- 2014
-
Abstract
- Purpose: The role of the minimal residual disease (MRD) in follicular lymphoma is still debated. In this study, we assessed whether the BCL2/IGH rearrangement could have a prognostic role in patients receiving R-CHOP, R-FM, or R-CVP. Experimental Design: DNAs from 415 patients among the 504 cases enrolled in the FOLL05 trial (NCT00774826) were centralized and assessed for the BCL2/IGH at diagnosis, at the end of treatment, and after 12 and 24 months. Results: At diagnosis, the molecular marker was detected in 53% of cases. Patients without molecular marker or with a low molecular tumor burden ( Conclusions: In this study, standardized molecular techniques have been adopted and applied on bone marrow samples from a large cohort. Data reported show that the MRD detection is a powerful independent predictor of PFS in patients with follicular lymphoma receiving conventional chemoimmunotherapy. Clin Cancer Res; 20(24); 6398–405. ©2014 AACR.
- Subjects :
- Male
Cancer Research
Neoplasm, Residual
Adolescent
Adult
Aged
Antineoplastic Combined Chemotherapy Protocols
Clinical Trials, Phase III as Topic
Female
Gene Dosage
Gene Rearrangement
Genes, bcl-2
Humans
Immunoglobulin Heavy Chains
Lymphoma, Follicular
Middle Aged
Prognosis
ROC Curve
Real-Time Polymerase Chain Reaction
Treatment Outcome
Young Adult
Oncology
Lymphoma
bcl-2
Follicular lymphoma
Gastroenterology
hemic and lymphatic diseases
Phase III as Topic
medicine.anatomical_structure
Residual
medicine.medical_specialty
MRD
FOLL05
Chemoimmunotherapy
Internal medicine
medicine
Follicular lymphoma, MRD
Clinical Trials
Progression-free survival
business.industry
Follicular
Cancer
Gene rearrangement
medicine.disease
Minimal residual disease
Surgery
Genes
Neoplasm
Bone marrow
business
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....b623aa8cdcc7130cbed9a3b0f7eb355b