The predictive role of interim PET after the first chemotherapy cycle and sequential evaluation of response to ABVD in Hodgkin's lymphoma patients-the Polish Lymphoma Research Group (PLRG) Observational Study

被引:14
作者
Zaucha, J. M. [1 ,2 ,3 ]
Malkowski, B. [4 ,5 ]
Chauvie, S. [6 ]
Subocz, E. [7 ]
Tajer, J. [8 ]
Kulikowski, W. [9 ,10 ]
Fijolek-Warszewska, A. [11 ]
Biggi, A. [12 ]
Fallanca, F. [13 ]
Kobylecka, M. [14 ]
Dziuk, M. [15 ]
Woszczyk, D. [16 ]
Rybka, J. [17 ]
Kroll-Balcerzak, R. [18 ]
Bergesio, F. [6 ]
Romanowicz, A. [19 ]
Chamier-Cieminska, A. [20 ]
Kurczab, P. [21 ]
Giza, A. [22 ]
Lesniewski-Kmak, K. [1 ,2 ,3 ]
Zaucha, R. [23 ]
Swietlik, D. [24 ]
Wrobel, T. [17 ]
Knopinska-Posluszny, W. [9 ,10 ]
Walewski, J. [8 ]
Gallamini, A. [25 ]
机构
[1] Gdynia Oncol Ctr, Gdynia, Poland
[2] Med Univ Gdansk, Dept Oncol Propedeut, Gdansk, Poland
[3] Med Univ Gdansk, Dept Hematol & Transplantol, Gdansk, Poland
[4] Oncol Ctr, Dept Nucl Med, Bydgoszcz, Poland
[5] N Copernicus Univ, Coll Med, Positron Emiss Tomog & Mol Imagining Dept, Bydgoszcz, Poland
[6] Santa Croce & Carle Hosp, Med Phys Dept, Cuneo, Italy
[7] Mil Inst Med, Dept Hematol, Warsaw, Poland
[8] Maria Sklodowska Curie Mem Inst Oncol, Dept Lymphoproliferat Dis, Warsaw, Poland
[9] Interior Minist Hosp, Clin Dept Hematol, Warmia, Poland
[10] Mazury Med Univ, Olsztyn, Poland
[11] Affidea Mazovian PET CT Ctr, Warsaw, Poland
[12] Santa Croce & Carle Hosp, Dept Nucl Med, Cuneo, Italy
[13] Osped San Raffaele, Dept Nucl Med, Milan, Italy
[14] Warsaw Med Univ, Dept Nucl Med, Warsaw, Poland
[15] Mil Inst Med, Dept Nucl Med, Warsaw, Poland
[16] Reg Hosp, Hematol Unit, Opole, Poland
[17] Wroclaw Med Univ, Dept Hematol Blood Neoplasms & Bone Marrow Transp, Wroclaw, Poland
[18] Univ Med Sch, Dept Hematol, Poznan, Poland
[19] Cent Clin Hosp MSW, Dept Hematol, Warsaw, Poland
[20] Oncol Ctr, Dept Clin Oncol, Bydgoszcz, Poland
[21] Poradnia Onkol Oddzialem Chemioterapii Dziennej N, Rzeszow, Poland
[22] Jagiellonian Univ, Coll Med, Dept Hematol, Krakow, Poland
[23] Med Univ Gdansk, Dept Clin Oncol & Radiotherapy, Gdansk, Poland
[24] Med Univ Gdansk, Intrafac Coll Med Informat & Biostat, Gdansk, Poland
[25] A Lacassagne Canc Ctr, Dept Res Innovat & Stat, 33 Voie Romaine, F-06189 Nice 2, France
关键词
Hodgkin's lymphoma; interim PET; ABVD treatment; POSITRON-EMISSION-TOMOGRAPHY; FDG-PET; ADAPTED TREATMENT; PROGNOSTIC VALUE; CELL LYMPHOMA; THERAPY; SUPERIOR; CRITERIA; DISEASE; TRIAL;
D O I
10.1093/annonc/mdx524
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: Interim PET after two ABVD cycles (iPET2) predicts treatment outcome in classical Hodgkin's lymphoma. To test whether an earlier assessment of chemosensitivity would improve the prediction accuracy, we launched a prospective, multicenter observational study aimed at assessing the predictive value of iPET after one ABVD (iPET1) and the kinetics of response assessed by sequential PET scanning. Patients and methods: Consecutive patients with newly diagnosed classical Hodgkin's lymphoma underwent interim PET scan after one ABVD course (iPET1). PETs were interpreted according to the Deauville score (DS) as negative (-) (DS 1-3) and positive (+) (DS 4, 5). Patients with iPET1 DS 3-5 underwent iPET2. Results: About 106 early (I-IIA) and 204 advanced (IIB-IV) patients were enrolled between January 2008 and October 2014. iPET1 was (-) in 87/106 (82%) or (+) in 19/106 (18%) of early, and (-) in 133/204 (65%) or (+) in 71/204 (35%) of advanced stage patients, respectively. Twenty-four patients were excluded from response analysis due to treatment escalation. After a median follow-up of 38.2 (3.2-90.2) months, 9/102 (9%) early and 43/184 (23%) advanced patients experienced a progression-free survival event. At 36 months, negative and positive predictive value for iPET1 were 94% and 41% (early) and 84% and 43% (advanced), respectively. The kinetics of PET response was assessed in 198 patients with both iPETs. All 116 patients with iPET1(-) remained iPET2(-) (fast responders), 41/82 with IPET1(+) became iPET2(-) (slow responders), and the remaining 41 stayed iPET2(+) (non-responders); progression-free survival at 36 months for fast, slow and non-responders was 0.88, 0.79 and 0.34, respectively. Conclusion: The optimal tool to predict ABVD outcome in HL remains iPET2 because it distinguishes responders, whatever their time to response, from non- responders. However, iPET1 identified fast responders with the best outcome and might guide early treatment de-escalation in both early and advanced-stage HL.
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收藏
页码:3051 / 3057
页数:7
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