Browsing by Author "Bomken, Simon (24401060100)"
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Publication Children and adolescents with marginal zone lymphoma have an excellent prognosis with limited chemotherapy or a watch-and-wait strategy after complete resection(2018) ;Ronceray, Leila (54911933000) ;Abla, Oussama (6506167666) ;Barzilai-Birenboim, Shlomit (57192254129) ;Bomken, Simon (24401060100) ;Chiang, Alan K. S. (7101623534) ;Jazbec, Janez (6602993382) ;Kabickova, Edita (6602305248) ;Lazic, Jelena (7004184322) ;Beishuizen, Auke (7003615260) ;Mellgren, Karin (6602767529) ;Tanaka, Fumiko (57205773592) ;Pillon, Marta (7006404245) ;Devalck, Christine (6701501578) ;Gouttenoire, Marina (57195222083) ;Makarova, Olga (57212714301) ;Burkhardt, Birgit (9248143700)Attarbaschi, Andishe (6602343033)Data on management of pediatric marginal zone lymphoma (MZL) are scarce. This retrospective study assessed characteristics and outcome in 66 patients who were <18 years old. Forty-four (67%) had an extranodal MZL (EMZL), 21 (32%) a nodal MZL (NMZL), and one patient a splenic MZL. Thirty-three patients (50%) received a variable combination of adjuvant chemotherapy/immunotherapy/radiotherapy, while the remainder, including 20 of 21 with NMZL, entered an active observation period. Overall survival was excellent (98 ± 2%), although 11 patients relapsed (17%; NMZL, n = 1; EMZL, n = 10), seven after any therapy and four after complete resection only. In conclusion, outcome of NZML, in particular, seems to be excellent after (in)complete resection and observation only. © 2017 Wiley Periodicals, Inc. - Some of the metrics are blocked by yourconsent settings
Publication Non-Hodgkin lymphoma and pre-existing conditions: Spectrum, clinical characteristics and outcome in 213 children and adolescents(2016) ;Attarbaschi, Andishe (6602343033) ;Carraro, Elisa (55834921600) ;Abla, Oussama (6506167666) ;Barzilai-Birenboim, Shlomit (57192254129) ;Bomken, Simon (24401060100) ;Brugieres, Laurence (7005615475) ;Bubanska, Eva (6603405979) ;Burkhardt, Birgit (9248143700) ;Chiang, Alan K. S. (7101623534) ;Csoka, Monika (22034152200) ;Fedorova, Alina (8710181800) ;Jazbec, Janez (6602993382) ;Kabickova, Edita (6602305248) ;Krenova, Zdenka (6507910356) ;Lazic, Jelena (7004184322) ;Loeffen, Jan (6602979459) ;Mann, Georg (7201974435) ;Niggli, Felix (7004026312) ;Miakova, Natalia (7801571393) ;Osumi, Tomoo (55965348200) ;Ronceray, Leila (54911933000) ;Uyttebroeck, Anne (6603028229) ;Williams, Denise (7407410786) ;Woessmann, Wilhelm (56006760500) ;Wrobel, Grazyna (7003317277)Pillon, Marta (7006404245)Children and adolescents with pre-existing conditions such as DNA repair defects or other primary immunodeficiencies have an increased risk of non-Hodgkin lymphoma. However, largescale data on patients with non-Hodgkin lymphoma and their entire spectrum of pre-existing conditions are scarce. A retrospective multinational study was conducted by means of questionnaires sent out to the national study groups or centers, by the two largest consortia in childhood non-Hodgkin lymphoma, the European Intergroup for Childhood non-Hodgkin Lymphoma, and the international Berlin-Frankfurt-Münster Study Group. The study identified 213 patients with non-Hodgkin lymphoma and a pre-existing condition. Four subcategories were established: a) cancer predisposition syndromes (n=124, 58%); b) primary immunodeficiencies not further specified (n=27, 13%); c) genetic diseases with no increased cancer risk (n=40, 19%); and d) non-classifiable conditions (n=22, 10%). Seventy-nine of 124 (64%) cancer predispositions were reported in groups with more than 20 patients: ataxia telangiectasia (n=32), Nijmegen breakage syndrome (n=26), constitutional mismatch repair deficiency (n=21). For the 151 patients with a known cancer risk, 5-year event-free survival and overall survival rates were 40%±4% and 51%±4%, respectively. Five-year cumulative incidences of progression/relapse and treatment-related death as a first event were 22%±4% and 24%±4%, respectively. Ten-year incidence of second malignancy was 24%±5% and 7-year overall survival of the 21 patients with a second malignancy was 41%±11%. Patients with non-Hodgkin lymphoma and pre-existing conditions have an inferior survival rate with a large proportion of therapy-related deaths compared to patients with non-Hodgkin lymphoma and no pre-existing conditions. They may require special vigilance when receiving standard or modified/reduced-intensity chemotherapy or when undergoing allogeneic stem cell transplantation. © 2016 Ferrata Storti Foundation. - Some of the metrics are blocked by yourconsent settings
Publication Primary central nervous system lymphoma: Initial features, outcome, and late effects in 75 children and adolescents(2019) ;Attarbaschi, Andishe (6602343033) ;Abla, Oussama (6506167666) ;Ronceray, Leila (54911933000) ;Bansil, Shweta (56845414400) ;Bomken, Simon (24401060100) ;Burkhardt, Birgit (9248143700) ;Ceppi, Francecso (35175592400) ;Chiang, Alan K.S. (7101623534) ;Dave, Hema (56441162600) ;Fedorova, Alina (8710181800) ;Henry, Michael (36893491900) ;Jazbec, Janez (6602993382) ;Kabickova, Edita (6602305248) ;Kotecha, Rishi S. (25932258900) ;Lazic, Jelena (7004184322) ;Loeffen, Jan (6602979459) ;Miakova, Natalia (7801571393) ;Osumi, Tomoo (55965348200) ;Pillon, Marta (7006404245) ;Pourtsidis, Apostolos (6602442628) ;Rigaud, Charlotte (55745198800) ;Tamamyan, Gevorg (55821557000) ;Tandon, Sneha (57211480939) ;Uyttebroeck, Anne (6603028229) ;Verdu-Amoros, Jamie (57219258587) ;Woessmann, Wilhelm (56006760500) ;Wrobel, Grazyna (7003317277)Giulino-Roth, Lisa (55535457700)[No abstract available]
