Results of a lymphoblastic leukemia-like chemotherapy program with risk-adapted mediastinal irradiation and stem cell transplantation for adult patients with lymphoblastic lymphoma

被引:33
作者
Cortelazzo, Sergio [2 ]
Intermesoli, Tamara [3 ]
Oldani, Elena [3 ]
Ciceri, Fabio [4 ]
Rossi, Giuseppe [5 ]
Pogliani, Enrico M. [6 ]
Mattei, Daniele [7 ]
Romani, Claudio [8 ]
Cortelezzi, Agostino [9 ]
Borlenghi, Erika [5 ]
Corti, Consuelo [4 ]
Peruta, Barbara [3 ]
Spinelli, Orietta [3 ]
Rambaldi, Alessandro [3 ]
Bassan, Renato [1 ,3 ]
机构
[1] Osped Riuniti Bergamo, USC Ematol, I-24128 Bergamo, Italy
[2] Osped Civile, Div Hematol, Bolzano, Italy
[3] Osped Riuniti Bergamo, Div Hematol, Bergamo, Italy
[4] Hosp S Raffaele, Hematol Unit, Milan, Italy
[5] Spedali Civil Brescia, Div Hematol, I-25125 Brescia, Italy
[6] Univ Milano Bicocca, Dept Hematol, Hosp San Gerardo, Monza, Italy
[7] Hosp Santa Croce & Carle, Div Hematol, Cuneo, Italy
[8] Oncol Hosp A Businco, Hematol Unit, Cagliari, Italy
[9] Univ Milan, Osped Maggiore Policlin, Hematol Unit 1, Milan, Italy
关键词
Lymphoblastic lymphoma; Mediastinal irradiation; Minimal residual disease; Stem cell transplantation; BONE-MARROW-TRANSPLANTATION; B-LINEAGE; CLINICAL-FEATURES; T-LINEAGE; THERAPY; DISEASE; RADIOTHERAPY; CHILDHOOD; TRIALS; METHOTREXATE;
D O I
10.1007/s00277-011-1252-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The therapeutic role of mediastinal radiotherapy and stem cell transplantation (SCT) in lymphoblastic lymphoma (LL) remains controversial. In a risk-oriented design, we adopted a flexible treatment program in which (1) patients with persistent mediastinal abnormality, evaluated by post-induction computed chest tomography, received mediastinal irradiation; and (2) those with persistence of minimal residual disease (MRD), evaluated by MRD analysis of the bone marrow, underwent SCT. Twenty-eight out of 30 patients (T-lineage, n = 24; B-lineage, n = 6) achieved a complete response. Of 21 patients with mediastinal mass, 13 (62%) achieved a complete response after chemotherapy alone, while 6 (28.5%) required additional irradiation. Eleven patients were evaluated for MRD: 6 were negative and 5 positive. On the basis of MRD findings and clinical risk characteristics, 14 patients underwent SCT, 13 received maintenance chemotherapy, and 1 had local radiotherapy. Five patients relapsed. Among the 14 non-irradiated patients with T-LL, the mediastinal recurrence rate was only 7%. After a median follow-up of 3.9 years, 21 patients who responded were alive without recurrence (75%). The projected 5-year survival, disease-free survival, and relapse rate were 72%, 77%, and 18%, respectively. This program induced high remission and survival rates, indicating the feasibility and the benefits potentially associated with a selective, response-oriented policy of mediastinal irradiation and a concurrent MRD-based strategy to assign adult LL patients to SCT.
引用
收藏
页码:73 / 82
页数:10
相关论文
共 33 条
[1]  
Bassan R, 1999, HAEMATOLOGICA, V84, P1088
[2]   Improved risk classification for risk-specific therapy based on the molecular study of minimal residual disease (MRD) in adult acute lymphoblastic leukemia (ALL) [J].
Bassan, Renato ;
Spinelli, Orietta ;
Oldani, Elena ;
Intermesoli, Tamara ;
Tosi, Manuela ;
Peruta, Barbara ;
Rossi, Giuseppe ;
Borlenghi, Erika ;
Pogliani, Enrico M. ;
Terruzzi, Elisabetta ;
Fabris, Pietro ;
Cassibba, Vincenzo ;
Lambertenghi-Deliliers, Giorgio ;
Cortelezzi, Agostino ;
Bosi, Alberto ;
Gianfaldoni, Giacomo ;
Ciceri, Fabio ;
Bernardi, Massimo ;
Gallamini, Andrea ;
Mattei, Daniele ;
Di Bona, Eros ;
Romani, Claudio ;
Scattolin, Anna Maria ;
Barbui, Tiziano ;
Rambaldi, Alessandro .
BLOOD, 2009, 113 (18) :4153-4162
[3]   Role of induction chemotherapy and bone marrow transplantation in adult lymphoblastic lymphoma: A report on 62 patients from a single center [J].
Bouabdallah, R ;
Xerri, L ;
Bardou, VJ ;
Stoppa, AM ;
Blaise, D ;
Sainty, D ;
Maraninchi, D ;
Gastaut, JA .
ANNALS OF ONCOLOGY, 1998, 9 (06) :619-625
[4]   IMMUNOLOGICAL DETECTION OF COVERT LEUKEMIC SPREAD IN MEDIASTINAL T-CELL LYMPHOBLASTIC LYMPHOMA [J].
BRADSTOCK, KF ;
KERR, A .
LEUKEMIA RESEARCH, 1985, 9 (07) :905-&
[5]   Standardized MRD quantification in European ALL trials: Proceedings of the Second International Symposium on MRD assessment in Kiel, Germany, 18-20 September 2008 [J].
Brueggemann, M. ;
Schrauder, A. ;
Raff, T. ;
Pfeifer, H. ;
Dworzak, M. ;
Ottmann, O. G. ;
Asnafi, V. ;
Baruchel, A. ;
Bassan, R. ;
Benoit, Y. ;
Biondi, A. ;
Cave, H. ;
Dombret, H. ;
Fielding, A. K. ;
Foa, R. ;
Goekbuget, N. ;
Goldstone, A. H. ;
Goulden, N. ;
Henze, G. ;
Hoelzer, D. ;
Janka-Schaub, G. E. ;
Macintyre, E. A. ;
Pieters, R. ;
Rambaldi, A. ;
Ribera, J-M ;
Schmiegelow, K. ;
Spinelli, O. ;
Stary, J. ;
von Stackelberg, A. ;
Kneba, M. ;
Schrappe, M. ;
van Dongen, J. J. M. .
LEUKEMIA, 2010, 24 (03) :521-535
[6]  
Brunning RD, 2001, TUMOURS HAEMOTOPOIET, P111
[7]   Impact of cranial radiotherapy on central nervous system prophylaxis in children and adolescents with central nervous system-negative stage III or IV lymphoblastic lymphoma [J].
Burkhardt, B ;
Woessmann, W ;
Zimmermann, M ;
Kontny, U ;
Vormoor, J ;
Doerffel, W ;
Mann, G ;
Henze, G ;
Niggli, F ;
Ludwig, WD ;
Janssen, D ;
Riehm, H ;
Schrappe, M ;
Reiter, A .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (03) :491-499
[8]   Report of an international workshop to standardize response criteria for non-Hodgkin's lymphomas [J].
Cheson, BD ;
Horning, SJ ;
Coiffier, B ;
Shipp, MA ;
Fisher, RI ;
Connors, JM ;
Lister, TA ;
Vose, J ;
Grillo-López, A ;
Hagenbeek, A ;
Cabanillas, F ;
Klippensten, D ;
Hiddemann, W ;
Castellino, R ;
Harris, NL ;
Armitage, JO ;
Carter, W ;
Hoppe, R ;
Canellos, GP .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (04) :1244-1253
[9]   Minimal Disseminated Disease in Childhood T-Cell Lymphoblastic Lymphoma: A Report From the Children's Oncology Group [J].
Coustan-Smith, Elaine ;
Sandlund, John T. ;
Perkins, Sherrie L. ;
Chen, Helen ;
Chang, Myron ;
Abromowitch, Minnie ;
Campana, Dario .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (21) :3533-3539
[10]   Differences in folylpolyglutamate synthetase and dihydrofolate reductase expression in human B-lineage versus T-lineage leukemic lymphoblasts: Mechanisms for lineage differences in methotrexate polyglutamylation and cytotoxicity [J].
Galpin, AJ ;
Schuetz, JD ;
Masson, E ;
Yanishevski, Y ;
Synold, TW ;
Barredo, JC ;
Pui, CH ;
Relling, MV ;
Evans, WE .
MOLECULAR PHARMACOLOGY, 1997, 52 (01) :155-163