The prognostic role of post-induction FDG-PET in patients with follicular lymphoma: a subset analysis from the FOLL05 trial of the Fondazione Italiana Linfomi (FIL)

被引:65
作者
Luminari, S. [1 ]
Biasoli, I. [2 ,3 ]
Versari, A. [4 ]
Rattotti, S. [5 ,6 ]
Bottelli, C. [7 ]
Rusconi, C. [8 ]
Merli, F. [9 ]
Spina, M. [10 ]
Ferreri, A. J. M. [11 ]
Zinzani, P. L. [12 ]
Gallamini, A. [13 ]
Franceschetto, A. [14 ]
Boccomini, C. [15 ]
Franceschetti, S. [16 ]
Salvi, F. [17 ]
Raimondo, F. D. [18 ]
Carella, A. M. [19 ]
Micol, Q. [1 ]
Balzarotti, M. [20 ]
Musto, P. [21 ]
Federico, M. [1 ]
机构
[1] Univ Modena & Reggio Emilia, Dept Diagnost Clin & Publ Hlth Med, Oncol Unit, I-41124 Modena, Italy
[2] Univ Fed Rio de Janeiro, Univ Hosp, Dept Med, BR-21941 Rio De Janeiro, Brazil
[3] Univ Fed Rio de Janeiro, Sch Med, BR-21941 Rio De Janeiro, Brazil
[4] Arcispedale S Maria Nuova Hosp IRCCS, Dept Nucl Med, Reggio Emilia, Italy
[5] Univ Pavia, Fdn IRCCS Policlin San Matteo, Dept Hematol Oncol, I-27100 Pavia, Italy
[6] Univ Pavia, Dept Mol Med, I-27100 Pavia, Italy
[7] Spedali Civil Brescia, Div Hematol, I-25125 Brescia, Italy
[8] Osped Niguarda Ca Granda, Dept Hematol & Oncol, Div Hematol, Milan, Italy
[9] Arcispedale S Maria Nuova Hosp IRCCS, Hematol Unit, Reggio Emilia, Italy
[10] Natl Canc Inst, Div Med Oncol A, Oncol Unit A, Aviano, Italy
[11] Ist Sci San Raffaele, Dept Oncohematol, Unit Lymphoid Malignancies, I-20132 Milan, Italy
[12] Inst Hematol & Med Oncol L&A Seragnoli, Bologna, Italy
[13] S Croce & Carle Hosp, Hematol Unit, Cuneo, Italy
[14] Univ Modena & Reggio Emilia, Dept Diagnost Clin & Publ Hlth Med, Nucl Med Unit, I-41124 Modena, Italy
[15] AO Citta Salute & Sci, SC Ematol 2, Turin, Italy
[16] Amedeo Avogadro Univ Eastern Piedmont, Dept Transalat Med, Div Hematol, Novara, Italy
[17] AO SS Antonio & Biagio & Cesare Arrigo, Hematol Unit, Alessandria, Italy
[18] Univ Catania, AOU Policlin OVE, Osped Ferrarotto, Div Hematol, Catania, Italy
[19] IRCCS San Martino IST, UOC Ematol 1, Genoa, Italy
[20] Humanitas Canc Ctr, Dept Oncol & Hematol, Rozzano, Italy
[21] IRCCS CROB, Dept Oncohematol, Potenza, Italy
关键词
FDG-PET; follicular lymphoma; prognosis; POSITRON-EMISSION-TOMOGRAPHY; RESPONSE CRITERIA; R-CVP; RITUXIMAB; CHEMOTHERAPY; CHOP; CYCLOPHOSPHAMIDE; MAINTENANCE; VINCRISTINE; INTERFERON;
D O I
10.1093/annonc/mdt562
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This subset analysis of the randomized FOLL05 trial demonstrated that post-induction PET can improve response assessment and is a strong independent prognostic tool in follicular lymphoma. Future studies should be designed to assess if a PET-driven approach could further improve outcome.[F-18]fluorodeoxyglucose-positron emission tomography (PET) is emerging as a strong diagnostic and prognostic tool in follicular lymphoma (FL) patients. In a subset analysis of the FOLL05 trial (NCT00774826), we investigated the prognostic role of post-induction PET (PI-PET) scan. Patients were eligible to this study if they had a PI-PET scan carried out within 3 months from the end of induction immunochemotherapy. Progression-free survival (PFS) was the primary study end point. A total of 202 patients were eligible and analysed for this study. The median age was 55 years (range 33-75). Overall, PI-PET was defined as positive in 49 (24%) patients. Conventional response assessment with CT scan was substantially modified by PET: 15% (22/145) of patients considered as having a complete response (CR) after CT were considered as having partial response (PR) after PI-PET and 53% (30/57) patients considered as having a PR after CT were considered as a CR after PI-PET. With a median follow-up of 34 months, the 3-year PFS was 66% and 35%, respectively, for patients with negative and positive PI-PET (P < 0.001). At multivariate analysis, PI-PET (hazard ratio 2.57, 95% confidence interval 1.52-4.34, P < 0.001) was independent of conventional response, FLIPI and treatment arm. Also, the prognostic role of PI-PET was maintained within each FLIPI risk group. In FL patients, PI-PET substantially modifies response assessment and is strongly predictive for the risk of progression. PET should be considered in further updates of response criteria.
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收藏
页码:442 / 447
页数:6
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