R-CHOP 14 with or without radiotherapy in nonbulky limited-stage diffuse large B-cell lymphoma

被引:151
|
作者
Lamy, Thierry [1 ]
Damaj, Gandhi [2 ]
Soubeyran, Pierre [3 ,4 ]
Gyan, Emmanuel [5 ]
Cartron, Guillaume [6 ]
Bouabdallah, Krimo [7 ]
Gressin, Remy [8 ]
Cornillon, Jerome [9 ]
Banos, Anne [10 ]
Le Du, Katell [11 ]
Benchalal, Mohamed [12 ]
Moles, Marie-Pierre [13 ]
Le Gouill, Steven [14 ]
Fleury, Joel [15 ]
Godmer, Pascal [16 ]
Maisonneuve, Herve [17 ]
Deconinck, Eric [18 ]
Houot, Roch [19 ]
Laribi, Kamel [20 ]
Marolleau, Jean Pierre [21 ]
Tournilhac, Olivier [22 ]
Branger, Bernard [23 ]
Devillers, Anne [24 ]
Vuillez, Jean Philippe [25 ,26 ]
Fest, Thierry [27 ,28 ]
Colombat, Philippe [29 ]
Costes, Valerie [30 ]
Szablewski, Vanessa [30 ]
Bene, Marie C. [31 ]
Delwail, Vincent [32 ,33 ]
机构
[1] Rennes Univ Hosp, INSERM Res Unit 1236, Hematol Dept, Rennes, France
[2] CHU Amiens, INSERM U1245, Hematol Dept, Amiens, France
[3] Bergonie Bordeaux Inst, Bordeaux, France
[4] Bordeaux Univ, Bordeaux, France
[5] Univ Tours, CHU Tours, INSERM U1415, Hematol & Cell Therapy Dept,CIC, Tours, France
[6] CHU Montpellier, CNRS, Unite Mixte Rech UMR 5235, Hematol Dept, Montpellier, France
[7] Univ Hosp Bordeaux, Hematol & Cell Therapy Dept, Bordeaux, France
[8] Univ Grenoble Alpes, Hosp Univ Grenoble, Onco Hematol Dept, INSERM U1209,CNRS UMR 5309, Site Sante, Grenoble, France
[9] Canc Inst Lucien Neuwirth, Hematol Dept, St Priest En Jarez, France
[10] Ctr Hosp Cote Basque, Hematol Dept, Bayonne, France
[11] Clin Victor Hugo, Hematol Dept, Le Mans, France
[12] Ctr Eugene Marquis, Radiotherapy Dept, Rennes, France
[13] CHU Angers, Hematol Dept, Angers, France
[14] Univ Nantes, CHU Nantes, Hematol Dept, Inst Rech Sante,CIC Hosp Hotel Dieu,INSERM Team 1, Nantes, France
[15] Med Pole Sante Republ, Oncol Dept, Clermont Ferrand, France
[16] Ctr Hosp Vannes, Hematol Dept, Vannes, France
[17] Ctr Hosp Dept Vendee, Hematol Dept, La Roche Sur Yon, France
[18] Univ Franche Comte, Ctr Hosp Reg Univ Besancon, Hematol Dept, INSERM UMR 1098, Besancon, France
[19] Rennes Univ Hosp, Hematol Dept, INSERM UMR 1236, Rennes, France
[20] Ctr Hosp Mans, Hematol Dept, Le Mans, France
[21] CHU Amiens, Dept EA4666, CIC U1415, Hematol & Cell Therapy Dept, Amiens, France
[22] CHU Clermont Ferrand, Hematol Dept, Clermont Ferrand, France
[23] Hlth Network Pays de Loire, Nantes, France
[24] Ctr Eugene Marquis, Nucl Med Dept, Rennes, France
[25] Grenoble Univ, INSERM U1039, CHU Grenoble, Imaging Nucl Med Dept, Grenoble, France
[26] Grenoble Univ, INSERM U1039, CHU Grenoble, Radiopharmaceut & Bioclin Dept, Grenoble, France
[27] Rennes Univ, Etab Francais du Sang, INSERM UMR 1236, Rennes, France
[28] CHU Rennes, Lab Hematol, Rennes, France
[29] Univ Tours, CHU Tours, CIC INSERM U1415, Hematol & Cell Therapy Dept, Tours, France
[30] CHU Montpellier, Pathol Dept, Montpellier, France
[31] Nantes Univ Hosp, Hematol Biol, Nantes, France
[32] Univ Poitiers, CHU Poitiers, CIC INSERM U1415, Hematol & Cell Therapy Dept, Poitiers, France
[33] Univ Poitiers, CIC INSERM 1402, Poitiers, France
关键词
SOUTHWEST-ONCOLOGY-GROUP; NON-HODGKIN-LYMPHOMA; PLUS RADIOTHERAPY; ELDERLY-PATIENTS; RADIATION-THERAPY; CHEMOTHERAPY; RITUXIMAB; MODALITY; SURVIVAL; DISEASE;
D O I
10.1182/blood-2017-07-793984
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The benefit of radiotherapy (RT) after chemotherapy in limited-stage diffuse large B-cell lymphoma (DLBCL) remains controversial. We conducted a randomized trial in patients with nonbulky limited-stage DLBCL to evaluate the benefit of RT after rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP). Patients were stratified according to the modified International Prognostic Index, including lactate dehydrogenase, Eastern Cooperative Oncology Group performance status, age, and disease stage. The patients received 4 or 6 consecutive cycles of R-CHOP delivered once every 2 weeks, followed or not by RT at 40 Gy delivered 4 weeks after the last R-CHOP cycle. All patients were evaluated by fluorodeoxyglucose-positron emission tomography scans performed at baseline, after 4 cycles of R-CHOP, and at the end of treatment. The primary objective of the trial was event-free survival (EFS) from randomization. The trial randomly assigned 165 patients in the R-CHOP arm and 169 in the R-CHOP plus RT arm. In an intent-to-treat analysis with a median follow-up of 64 months, 5-year EFS was not statistically significantly different between the 2 arms, with 89% +/- 2.9% in the R-CHOP arm vs 92% +/- 2.4% in the R-CHOP plus RT arm (hazard ratio, 0.61; 95% confidence interval [CI], 0.3-1.2; P = .18). Overall survival was also not different at 92% (95% CI, 89.5%-94.5%) for patients assigned to R-CHOP alone and 96%(95% CI, 94.3%-97.7%) for those assigned to R-CHOP plus RT (P = not significant). R-CHOP alone is not inferior to R-CHOP followed by RT in patients with nonbulky limited-stage DLBCL.
引用
收藏
页码:174 / 181
页数:8
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