The impact of R-VACOP-B and interim FDG-PET/CT on outcome in primary mediastinal large B cell lymphoma

被引:47
作者
Avigdor, Abraham [1 ]
Sirotkin, Tsvi [4 ]
Kedmi, Meirav [1 ]
Ribakovsy, Elena [1 ]
Berkowicz, Miriam [1 ]
Davidovitz, Yaron [1 ]
Kneller, Abraham [1 ]
Merkel, Drorit [1 ]
Volchek, Yulia [1 ]
Davidson, Tima [2 ]
Goshen, Elinor [2 ]
Apter, Sara [3 ]
Shimoni, Avichai [1 ]
Ben-Bassat, Isaac [1 ]
Nagler, Arnon [1 ]
机构
[1] Chaim Sheba Med Ctr, Div Hematol & Bone Marrow Transplantat, IL-5265601 Ramat Gan, Israel
[2] Chaim Sheba Med Ctr, Dept Nucl Med, IL-5265601 Ramat Gan, Israel
[3] Chaim Sheba Med Ctr, Dept Diagnost Imaging, IL-5265601 Ramat Gan, Israel
[4] Tel Aviv Univ, Sackler Sch Med, IL-69978 Tel Aviv, Israel
关键词
Primary mediastinal B cell lymphoma; Chemotherapy; Prognosis; FDG-PET/CT scan; Rituximab; POSITRON-EMISSION-TOMOGRAPHY; CHOP-LIKE CHEMOTHERAPY; RADIOTHERAPY TECHNIQUES; INTERNATIONAL WORKSHOP; RESPONSE ASSESSMENT; RITUXIMAB; THERAPY; RADIATION; CRITERIA; TRIAL;
D O I
10.1007/s00277-014-2043-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The choice of a rituximab-based regimen and the prognostic significance of interim 2-[fluorine-18]fluoro-2-deoxy-d-glucose-positron emission tomography/computed tomography (FDG-PET/CT) in primary mediastinal large B cell lymphoma (PMBCL) are debatable. We evaluated the clinical features and outcomes of 95 consecutive patients with PMBCL who were treated between 1985 and 2009. Forty-three patients received rituximab-based chemotherapy, R-VACOP-B (N = 30) or R-CHOP21 (N = 13), whereas 52 patients were treated with VACOP-B (N = 47) or CHOP21 (N = 5). Radiotherapy was not given. Patients who received rituximab had a 5-year progression-free survival (PFS) of 79 % and overall survival (OS) of 97 % compared with 58 % (p = 0.06) and 88 % (p = 0.2), respectively, without rituximab. Five-year PFS in patients treated with R-VACOP-B, R-CHOP21, VACOP-B, and CHOP21 were 83, 69, 62, and 20 %, respectively (p = 0.039). However, direct comparison showed that the difference between PFS rates in patients receiving R-VACOP-B compared to R-CHOP21 was not statistically significant (p = 0.3). None of the standard clinical risk factors predicted for PFS and OS in patients receiving rituximab (R)-chemotherapy. Mid-interim FDG-PET/CT scans were performed in 30/43 patients who received R-chemotherapy. The negative predictive values of mid-PET activity were high (100 % for R-VACOP-B and 86 % for R-CHOP21) while the positive predictive values (PPV) were relatively low (30 and 75 %, respectively). Despite the low PPV, the 5-year PFS for mid-PET-negative patients (N = 16) was significantly higher (94 %) than that for mid-PET-positive (N = 14) patients (57 %, p = 0.015). This retrospective analysis demonstrates that the superiority of VACOP-B over CHOP21 for treatment of PMBCL disappeared once rituximab was added. The potential benefit of using interim PET activity as a guide for continuing therapy in patients with PMBCL remains unclear due to the relatively low PPV.
引用
收藏
页码:1297 / 1304
页数:8
相关论文
共 50 条
  • [21] The role of FDG-PET in the interim evaluation of therapy response in diffuse large B-cell lymphoma
    Ellmann, Annare
    [J]. TRANSFUSION AND APHERESIS SCIENCE, 2013, 49 (01) : 40 - 42
  • [22] Prognostic value of interim FDG-PET in R-CHOP-treated diffuse large B-cell lymphoma: Systematic review and meta-analysis
    Adams, Hugo J. A.
    Kwee, Thomas C.
    [J]. CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2016, 106 : 55 - 63
  • [23] Interim response in diffuse large B cell lymphoma on CT: what is the optimal size reduction (ΔSPD) for predicting outcome?
    Wei, Yun-Chen
    Ding, Chong-Yang
    Liang, Jin-Hua
    Wang, Li
    Zhu, Hua-Yuan
    Xia, Yi
    Wu, Jia-Zhu
    Fan, Lei
    Li, Tian-Nv
    Li, Jian-Yong
    Xu, Wei
    [J]. EUROPEAN RADIOLOGY, 2020, 30 (06) : 3094 - 3100
  • [24] Impact of FDG-PET/CT in the management of lymphoma
    Baba, Shingo
    Abe, Koichiro
    Isoda, Takuro
    Maruoka, Yasuhiro
    Sasaki, Masayuki
    Honda, Hiroshi
    [J]. ANNALS OF NUCLEAR MEDICINE, 2011, 25 (10) : 701 - 716
  • [25] Primary mediastinal B-cell lymphoma
    Coso, D.
    Rey, J.
    Bouabdallah, R.
    [J]. REVUE DE PNEUMOLOGIE CLINIQUE, 2010, 66 (01) : 32 - 35
  • [26] Interim FDG-PET/CT for therapy monitoring and prognostication in Hodgkin's Lymphoma
    Al-Ibraheem, Akram
    Anwer, Farah
    Juweid, Malik E.
    Shagera, Qaid Ahmed
    Khalaf, Aysar N.
    Obeidat, Shahed
    Mansour, Areen
    Ma'koseh, Mohammad
    Halahleh, Khalid
    Jaradat, Imad
    Almasri, Nidal
    Mansour, Asem
    [J]. SCIENTIFIC REPORTS, 2022, 12 (01)
  • [27] The treatment of primary mediastinal large B-cell lymphoma: a two decades monocentric experience with 98 patients
    Broccoli, Alessandro
    Casadei, Beatrice
    Stefoni, Vittorio
    Pellegrini, Cinzia
    Quirini, Federica
    Tonialini, Lorenzo
    Morigi, Alice
    Marangon, Miriam
    Argnani, Lisa
    Zinzani, Pier Luigi
    [J]. BMC CANCER, 2017, 17
  • [28] Role of radiotherapy in the treatment of primary mediastinal large B-cell lymphoma
    Wang, Jingjing
    Liu, Xianling
    Ma, Fang
    Huang, Ming
    Kallychurn, Yashpal Singh
    Hu, Chunhong
    [J]. Oncology Letters, 2015, 10 (05) : 2925 - 2930
  • [29] Interim 18-FDG-PET/CT failed to predict the outcome in diffuse large B-cell lymphoma patients treated at the diagnosis with rituximab-CHOP
    Pregno, Patrizia
    Chiappella, Annalisa
    Bello, Marilena
    Botto, Barbara
    Ferrero, Simone
    Franceschetti, Silvia
    Giunta, Francesca
    Ladetto, Marco
    Limerutti, Giorgio
    Menga, Massimo
    Nicolosi, Maura
    Priolo, Giorgio
    Puccini, Benedetta
    Rigacci, Luigi
    Salvi, Flavia
    Vaggelli, Luca
    Passera, Roberto
    Bisi, Gianni
    Vitolo, Umberto
    [J]. BLOOD, 2012, 119 (09) : 2066 - 2073
  • [30] Response to 'PET after response to R-CHOP in primary mediastinal large B-cell lymphoma'
    Vassilakopoulos, T. P.
    Papageorgiou, S.
    Pangalis, G. A.
    Chatziioannou, S.
    Angelopoulou, M. K.
    Panayiotidis, P.
    Konstantopoulos, K.
    Rondogianni, P.
    [J]. LEUKEMIA, 2016, 30 (08) : 1800 - 1801