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Institute
Werner, Inge ; Aldrich, Annette ; Becker, Benjamin ; Becker, Dennis ; Brinkmann, Markus ; Burkhardt, Michael ; Caspers, Norbert ; Campiche, Sophie ; Chèvre, Nathalie ; Düring, Rolf‑Alexander ; Escher, Beate I. ; Fischer, Fabian ; Giebner, Sabrina ; Heye, Katharina ; Hollert, Henner ; Junghans, Marion ; Kienle, Cornelia ; Knauer, Katja ; Korkaric, Muris ; Märkl, Veronika ; Muncke, Jane ; Oehlmann, Jörg ; Reifferscheid, Georg ; Rensch, Daniel ; Schäffer, Andreas ; Schiwy, Sabrina ; Schwarz, Simon ; Segner, Helmut ; Simon, Eszter ; Triebskorn, Rita ; Vermeirssen, Etiënne L. M. ; Wintgens, Thomas ; Zennegg, Markus
This report provides a brief review of the 20th annual meeting of the German Language Branch of the Society of Environmental Toxicology and Chemistry (SETAC GLB) held from September 7th to 10th 2015 at ETH (Swiss Technical University) in Zurich, Switzerland. The event was chaired by Inge Werner, Director of the Swiss Centre for Applied Ecotoxicology (Ecotox Centre) Eawag-EPFL, and organized by a team from Ecotox Centre, Eawag, Federal Office of the Environment, Federal Office of Agriculture, and Mesocosm GmbH (Germany). Over 200 delegates from academia, public agencies and private industry of Germany, Switzerland and Austria attended and discussed the current state of science and its application presented in 75 talks and 83 posters. In addition, three invited keynote speakers provided new insights into scientific knowledge ‘brokering’, and—as it was the International Year of Soil—the important role of healthy soil ecosystems. Awards were presented to young scientists for best oral and poster presentations, and for best 2014 master and doctoral theses. Program and abstracts of the meeting (mostly in German) are provided as Additional file 1.
Aamodt, Kenneth ; Abel, N. ; Abeysekara, U. ; Abrahantes Quintana, A. ; Abramyan, A. ; Adamová, Dagmar ; Aggarwal, Madan Mohan ; Aglieri Rinella, Gianluca ; Agocs, A.G. ; Aguilar Salazar, S. ; Ahammed, Zubayer ; Ahmad, A. ; Ahmad, Nazeer ; Ahn, Sang Un ; Akimoto, R. ; Akindinov, Alexander ; Aleksandrov, Dmitry ; Alessandro, Bruno ; Alfaro Molina, Jose Ruben ; Alici, Andrea ; Almaráz Aviña, E. ; Alme, Johan ; Alt, Torsten ; Altini, V. ; Altinpinar, Sedat ; Andrei, Cristian ; Andronic, Anton ; Anelli, G. ; Angelov, V. ; Anson, Christopher Daniel ; Antičić, Tome ; Antinori, Federico ; Antinori, S. ; Antipin, K. ; Antończyk, Dariusz ; Antonioli, Pietro ; Anzo, A. ; Aphecetche, Laurent Bernard ; Appelshäuser, Harald ; Arcelli, Silvia ; Arceo, R. ; Arend, A. ; Armesto, Néstor ; Arnaldi, Roberta ; Aronsson, Tomas Robert ; Arsene, Ionut Cristian ; Asryan, A. ; Augustinus, Andre ; Averbeck, Ralf Peter ; Awes, T.C. ; Äystö, J. ; Azmi, Mohd Danish ; Bablok, Sebastian ; Bach, Matthias ; Badalà, Angela ; Baek, Yong Wook ; Bagnasco, Stefano ; Bailhache, Raphaëlle ; Bala, Remu ; Baldisseri, Alberto ; Baldit, A. ; Bán, J. ; Barbera, Roberto ; Barnaföldi, Gergely Gábor ; Barnby, L. ; Barret, Valerie ; Bartke, Jerzy ; Barile, Francesco ; Basile, Maurizio ; Basmanov, V. ; Bastid, Nicole ; Bathen, Bastian ; Batigne, Guillaume ; Batyunya, Boris ; Baumann, C. ; Bearden, Ian Gardner ; Becker, B. ; Belikov, Iouri ; Bellwied, Rene ; Belmont-Moreno, Ernesto ; Belogianni, A. ; Benhabib, L. ; Beolè, Stefania ; Berceanu, Ionela ; Bercuci, Alexandru ; Berdermann, E. ; Berdnikov, Yaroslav ; Betev, Latchezar ; Bhasin, Anju ; Bhati, Ashok Kumar ; Bianchi, Livio ; Bianchi, Nicola ; Bianchin, Chiara ; Bielčík, Jaroslav ; Bielčíková, Jana ; Bilandzic, Ante ; Bimbot, L. ; Biolcati, E. ; Blanc, A. ; Blanco, Fernando ; Blanco, Fernando ; Blau, Dmitry S. ; Blume, Christoph ; Boccioli, M. ; Bock, N. ; Bogdanov, Alexey A. ; Bøggild, Hans ; Bogolyubsky, M. ; Bohm, J. ; Boldizsár, László ; Bombara, Marek ; Bombonati, C. ; Bondila, M. ; Borel, Hervé ; Borisov, A. ; Bortolin, C. ; Bose, S. ; Bosisio, L. ; Bossú, Francesco ; Botje, Michiel ; Böttger, Stefan ; Bourdaud, G. ; Boyer, B. ; Braun, M. ; Braun-Munzinger, Peter ; Bravina, L. ; Bregant, Marco ; Breitner, Timo ; Bruckner, G. ; Brun, René ; Bruna, Elena ; Bruno, Giuseppe Eugenio ; Budnikov, Dmitry ; Büsching, Henner ; Bunčić, Predrag ; Busch, Oliver ; Buthelezi, Edith Zinhle ; Caffarri, Davide ; Cai, Xiao ; Caines, Helen Louise ; Calvo, E. ; Camacho, E. ; Camerini, Paolo ; Campbell, M. ; Canoa Roman, Veronica ; Capitani, G.P. ; Cara Romeo, G. ; Carena, Francesco ; Carena, Wisla ; Carminati, F. ; Casanova Díaz, A. ; Caselle, M. ; Castillo Castellanos, Javier Ernesto ; Castillo Hernandez, J.F. ; Catanescu, V. ; Cattaruzza, E. ; Cavicchioli, Costanza ; Cerello, Piergiorgio ; Chambert, V. ; Chang, B. ; Chapeland, Sylvain ; Charpy, A. ; Charvet, Jean-Luc Fernand ; Chattopadhyay, S. ; Chattopadhyay, S. ; Cherney, Michael Gerard ; Cheshkov, Cvetan Valeriev ; Cheynis, Brigitte ; Chiavassa, E. ; Chibante Barroso, Vasco Miguel ; Chinellato, David Dobrigkeit ; Chochula, Peter ; Choi, Kyungeon ; Chojnacki, Marek ; Christakoglou, Panagiotis ; Christensen, Christian Holm ; Christiansen, Peter L. ; Chujo, Tatsuya ; Chuman, F. ; Cicalò, Corrado ; Cifarelli, Luisa ; Cindolo, Federico ; Cleymans, Jean Willy Andre ; Cobanoglu, O. ; Coffin, J.-P. ; Coli, S. ; Colla, A. ; Conesa Balbastre, Gustavo ; Conesa del Valle, Zaida ; Conner, E.S. ; Constantin, P. ; Contin, Giacomo ; Contreras Nuno, Jesus Guillermo ; Corrales Morales, Yasser ; Cormier, Thomas Michael ; Cortese, Pietro ; Cortés Maldonado, Ismael ; Cosentino, Mauro Rogerio ; Costa, Filippo ; Cotallo, M.E. ; Crescio, E. ; Crochet, Philippe ; Cuautle Flores, Eleazar ; Cunqueiro Mendez, Leticia ; Cussonneau, J. ; Dainese, Andrea ; Dalsgaard, H.H. ; Danu, Andrea ; Das, Indranil ; Dash, Ajay Kumar ; Dash, Sadhana ; de Barros, G.O.V. ; De Caro, Annalisa ; De Cataldo, Giacinto ; Cuveland, Jan de ; De Falco, Alessandro ; De Gaspari, M. ; de Groot, J. ; De Gruttola, Daniele ; De Marco, Nora ; De Pasquale, Salvatore ; De Remigis, R. ; de Rooij, R. ; de Vaux, G. ; Delagrange, H. ; Delgado, Y. ; Dellacasa, G. ; Deloff, Andrzej ; Demanov, V. ; Dénes, Ervin Sandor ; Deppman, A. ; D’Erasmo, Ginevra ; Derkach, D. ; Devaux, A. ; Di Bari, Domenico ; Di Giglio, C. ; Di Liberto, S. ; Di Mauro, Antonio ; Di Nezza, Pasquale ; Dialinas, M. ; Díaz, L. ; Díaz, R. ; Dietel, Thomas ; Divià, Roberto ; Djuvsland, Øystein ; Dobretsov, V. ; Dobrin, Alexandru Florin ; Dobrowolski, Tadeusz Antoni ; Dönigus, Benjamin ; Domínguez, I. ; Don, D.M.M. ; Dordic, Olja ; Dubey, Anand Kumar ; Dubuisson, J. ; Ducroux, Laurent ; Dupieux, Pascal ; Dutta Majumdar, A.K. ; Dutta Majumdar, M.R. ; Elia, Domenico ; Emschermann, D. ; Enokizono, A. ; Espagnon, Bruno ; Estienne, Magali Danielle ; Esumi, ShinIchi ; Evans, David ; Evrard, S. ; Eyyubova, Gyulnara ; Fabjan, C.W. ; Fabris, Daniela ; Faivre, Julien ; Falchieri, D. ; Fantoni, Alessandra ; Fasel, Markus ; Fateev, O. ; Fearick, R. ; Fedunov, A. ; Fehlker, D. ; Fekete, V. ; Felea, Daniel ; Fenton-Olsen, B. ; Feofilov, Grigori A. ; Fernández Téllez, Arturo ; Gonzalez Ferreiro, Elena ; Ferretti, Alessandro ; Ferretti, R. ; Figueredo, Marcel Araujo Silva ; Filchagin, Sergey ; Fini, R. ; Fionda, Fiorella Maria Celeste ; Fiore, Enrichetta Maria ; Floris, Michele ; Fodor, Zoltán ; Foertsch, Siegfried Valentin ; Foka, Panagiota ; Fokin, Sergey ; Formenti, F. ; Fragiacomo, Enrico ; Fragkiadakis, M. ; Frankenfeld, Ulrich ; Frolov, A. ; Fuchs, Ulrich ; Furano, F. ; Furget, Christophe ; Fusco Girard, Mario ; Gaardhøje, Jens Jørgen ; Gadrat, S. ; Gagliardi, Martino ; Gago, A. ; Gallio, Mauro ; Ganoti, Paraskevi ; Ganti, Murthy S. ; Garabatos, Chilo ; García Trapaga, C. ; Gebelein, J. ; Gemme, R. ; Germain, Marie ; Gheata, Andrei George ; Gheata, Mihaela ; Ghidini, B. ; Ghosh, Premomoy ; Giraudo, G. ; Giubellino, Paolo ; Gładysz-Dziaduś, Ewa ; Glasow, R. ; Glässel, Peter ; Glenn, A. ; Gómez Jiménez, R. ; González Santos, H. ; González Trueba, Laura Helena ; González Zamora, Pedro ; Gorbunov, Sergey ; Gorbunov, Y. ; Gotovac, Sven ; Gottschlag, H. ; Grabski, Varlen ; Grajcarek, R. ; Grelli, Alessandro ; Grigoras, Alina Gabriela ; Grigoraș, Costin ; Grigoriev, Vladislav A. ; Grigoryan, Ara ; Grigoryan, Smbat ; Grinyov, Boris V. ; Grion, Nevio ; Gros, P. ; Große-Oetringhaus, Jan Fiete ; Grossiord, Jean-Yves ; Grosso, Raffaele ; Guber, Fedor ; Guernane, Rachid ; Guerra, C. ; Guerzoni, Barbara ; Gulbrandsen, Kristjan Herlache ; Gulkanyan, Hrant ; Gunji, Taku ; Gupta, Anik ; Gupta, Ramni ; Gustafsson, H.-A. ; Gutbrod, H. ; Haaland, Øystein Senneset ; Hadjidakis, Cynthia Marie ; Haiduc, Maria ; Hamagaki, Hideki ; Hamar, Gergö ; Hamblen, J. ; Han, B.H. ; Harris, John W. ; Hartig, M. ; Harutyunyan, A. ; Hasch, D. ; Hasegan, D. ; Hatzifotiadou, Despina ; Hayrapetyan, A. ; Heide, Markus ; Heinz, Mark Thomas ; Helstrup, Håvard ; Herghelegiu, Andrei Ionut ; Hernández, C. ; Herrera Corral, Gerardo Antonio ; Herrmann, Norbert ; Hetland, Kristin Fanebust ; Hicks, B. ; Hiei, A. ; Hille, P.T. ; Hippolyte, Boris ; Horaguchi, T. ; Hori, Y. ; Hristov, Peter ; Hřivnáčová, I. ; Hu, S. ; Huang, M. ; Huber, S. ; Humanic, Thomas J. ; Hutter, Dirk ; Hwang, D.S. ; Ichou, R. ; Ilkaev, Radiy ; Ilkiv, Iryna ; Inaba, Motoi ; Innocenti, P.G. ; Ippolitov, Mikhail ; Irfan, M. ; Ivan, C. ; Ivanov, A. ; Ivanov, Marian ; Ivanov, V. ; Iwasaki, T. ; Jacholkowski, Adam Wlodzimierz ; Jacobs, P. ; Jančurová, L. ; Jangal, S. ; Janik, R. ; Jena, Chitrasen ; Jena, Satyajit ; Jirden, L. ; Jones, Goronwy Tudor ; Jones, Peter Graham ; Jovanović, P. ; Jung, H. ; Jung, W. ; Jusko, Anton ; Kaidalov, A.B. ; Kalcher, S. ; Kaliňák, Peter ; Kalisky, M. ; Kalliokoski, T. ; Kalweit, Alexander Philipp ; Kamal, A. ; Kamermans, R. ; Kanaki, K. ; Kang, E. ; Kang, Ju Hwan ; Kapitan, J. ; Kaplin, Vladimir ; Kapusta, S. ; Karavichev, Oleg V. ; Karavicheva, Tatiana L. ; Karpechev, Evgeny ; Kazantsev, Andrey ; Kebschull, Udo ; Keidel, Ralf ; Khan, M.M. ; Khan, Shuaib Ahmad ; Khanzadeev, Alexei ; Kharlov, Yury ; Kikola, D. ; Kileng, Bjarte ; Kim, D.J. ; Kim, D.S. ; Kim, D.W. ; Kim, H.N. ; Kim, J. ; Kim, J.H. ; Kim, J.S. ; Kim, M. ; Kim, M. ; Kim, S.H. ; Kim, S. ; Kim, Y. ; Kirsch, Stefan ; Kisel, Ivan ; Kiselev, Sergej N. ; Kisiel, Adam Ryszard ; Klay, Jennifer Lynn ; Klein, Jochen ; Klein-Bösing, Christian ; Kliemant, Michael ; Klovning, A. ; Kluge, Alexander ; Knichel, Michael Linus ; Kniege, Stefan ; Koch, K. ; Kolevatov, R. ; Kolojvari, Anatoly ; Kondratiev, Valery P. ; Kondratyeva, Natalia ; Konevskih, A. ; Kornaś, Ewelina ; Kour, R. ; Kowalski, Marek ; Kox, Serge ; Kozlov, K. ; Kral, Jiří ; Králik, Ivan ; Kramer, F. ; Kraus, Ingrid ; Kravčáková, Adela ; Krawutschke, T. ; Krivda, Marian ; Krumbhorn, D. ; Krus, M. ; Kryshen, Evgeny ; Krzewicki, Mikolaj ; Kucheriaev, Yury ; Kuhn, Christian Claude ; Kuijer, Paulus Gerardus ; Kumar, Lokesh ; Kumar, N. ; Kupczak, R. ; Kurashvili, Podist ; Kurepin, Alexander ; Kurepin, A.N. ; Kuryakin, Alexey ; Kushpil, Svetlana ; Kushpil, V. ; Kutouski, M. ; Kvaerno, H. ; Kweon, Min Jung ; Kwon, Youngil ; La Rocca, Paola ; Lackner, F. ; Ladron de Guevara, Pedro ; Lafage, V. ; Lal, C. ; Lara Martinez, Camilo Ernesto ; Larsen, D.T. ; Laurenti, G. ; Lazzeroni, C. ; Le Bornec, Y. ; Le Bris, N. ; Lee, H. ; Lee, K.S. ; Lee, S.C. ; Lefèvre, F. ; Lenhardt, M. ; Leistam, L. ; Lehnert, Jörg ; Lenti, Vito ; León, H. ; León Monzón, Ildefonso ; León Vargas, H. ; Lévai, Péter ; Li, X. ; Li, Y. ; Lietava, Roman ; Lindal, Svein ; Lindenstruth, Volker ; Lippmann, Christian ; Lisa, Michael A. ; Liu, L. ; Loginov, Vitaly ; Lohn, S. ; Lopez, Xavier Bernard ; López Noriega, M. ; López-Ramírez, R. ; López Torres, Ernesto ; Løvhøiden, G. ; Lozea Feijo Soares, A. ; Lu, S. ; Lüttig, Philipp ; Lunardon, Marcello ; Luparello, Grazia ; Luquin, L. ; Lutz, Jean-Robert ; Ma, K. ; Ma, R. ; Madagodahettige-Don, D.M. ; Maevskaya, Alla ; Mager, Magnus ; Mahapatra, D.P. ; Maire, Antonin ; Makhlyueva, I. ; Mal’Kevich, Dmitry ; Malaev, Mikhail ; Malagalage, K.J. ; Maldonado Cervantes, Ivonne Alicia ; Malek, M. ; Malkiewicz, T. ; Malzacher, Peter ; Mamonov, Alexander ; Manceau, Loic Henri Antoine ; Mangotra, L. ; Manko, Vladislav ; Manso, Franck ; Manzari, Vito ; Mao, Yaxian ; Mareš, Jiří ; Margagliotti, Giacomo Vito ; Margotti, Anselmo ; Marín, Ana ; Martashvili, Irakli ; Martinengo, Paolo ; Martínez Hernández, M.I. ; Martínez Davalos, A. ; Martínez Garcia, Ginés ; Maruyama, Y. ; Marzari Chiesa, A. ; Masciocchi, Silvia ; Masera, Massimo ; Masetti, M. ; Masoni, Alberto ; Massacrier, Laure Marie ; Mastromarco, Mario ; Mastroserio, Annalisa ; Matthews, Z.L. ; Matyja, Adam Tomasz ; Mayani, D. ; Mazza, G. ; Mazzoni, Alessandra Maria ; Meddi, Franco ; Menchaca-Rocha, Arturo Alejandro ; Mendez Lorenzo, P. ; Meoni, M. ; Mercado Pérez, Jorge ; Mereu, P. ; Miake, Yasuo ; Michalon, A. ; Miftakhov, N. ; Milano, Leonardo ; Milošević, Jovan ; Minafra, F. ; Mischke, André ; Miśkowiec, Dariusz Czesław ; Mitu, C. ; Mizoguchi, K. ; Mlynarz, J. ; Mohanty, Bedangadas ; Molnar, Levente ; Mondal, Mriganka Mouli ; Montaño Zetina, Luis Manuel ; Monteno, M. ; Montes Prado, Esther ; Morando, Maurizio ; Moretto, Sandra ; Morsch, Andreas ; Moukhanova, T. ; Muccifora, Valeria ; Mudnic, Eugen ; Muhuri, Sanjib ; Müller, H. ; Munhoz, Marcelo Gameiro ; Munoz, J. ; Musa, Luciano ; Musso, A. ; Nandi, Basanta Kumar ; Nania, Rosario ; Nappi, Eugenio ; Navach, F. ; Navin, S. ; Nayak, Tapan Kumar ; Nazarenko, Sergey ; Nazarov, G. ; Nedosekin, Alexander ; Nendaz, F. ; Newby, J. ; Nianine, A. ; Nicassio, Maria ; Nielsen, Borge Svane ; Nikolaev, Sergey ; Nikolic, V. ; Nikulin, Sergey ; Nikulin, Vladimir ; Nilsen, B.S. ; Nilsson, M.S. ; Noferini, Francesco ; Nomokonov, Petr V. ; Nooren, Gerardus ; Novitzky, Norbert ; Nyatha, A. ; Nygaard, C. ; Nyiri, A. ; Nystrand, Joakim Ingemar ; Ochirov, A. ; Odyniec, G. ; Oeschler, Helmut ; Oinonen, M. ; Okada, K. ; Okada, Y. ; Oldenburg, Markus D. ; Oleniacz, Janusz ; Oppedisano, Chiara ; Orsini, F. ; 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Wagner, Boris ; Wagner, V. ; Wallet, L. ; Wan, R. ; Wang, D. ; Wang, Y. ; Wang, Y. ; Watanabe, K. ; Wen, Q. ; Wessels, J. ; Westerhoff, Uwe ; Wiechula, Jens ; Wikne, Jon ; Wilk, A. ; Wilk, Grzegorz Andrzej ; Williams, M. Crispin S. ; Willis, N. ; Windelband, Bernd ; Xu, C. ; Yang, C. ; Yang, H. ; Yasnopolskiy, S. ; Yermia, F. ; Yi, J. ; Yin, Zhongbao ; Yokoyama, Hiroki ; Yoo, In-Kwon ; Yuan, X. ; Yurevich, V. ; Yushmanov, Igor E. ; Zabrodin, E. ; Zagreev, B. ; Zalite, A. ; Zampolli, Chiara ; Zanevsky, Yuri V. ; Zaporozhets, Sergey ; Zarochentsev, Andrey ; Závada, Petr ; Zbroszczyk, Hanna Paulina ; Zelnicek, P. ; Zenin, A. ; Zepeda, A. ; Zgura, I. ; Zhalov, Mikhail ; Zhang, X. ; Zhou, D. ; Zhou, S. ; Zhu, J. ; Zichichi, Antonino ; Zinchenko, A. ; Zinovjev, Gennady M. ; Zoccarato, Y. ; Zycháček, V. ; Zynovyev, M.
The inclusive charged particle transverse momentum distribution is measured in proton–proton collisions at s=900 GeV at the LHC using the ALICE detector. The measurement is performed in the central pseudorapidity region (|η|<0.8) over the transverse momentum range 0.15<pT<10 GeV/c. The correlation between transverse momentum and particle multiplicity is also studied. Results are presented for inelastic (INEL) and non-single-diffractive (NSD) events. The average transverse momentum for |η|<0.8 is 〈pT〉INEL=0.483±0.001 (stat.)±0.007 (syst.) GeV/c and 〈pT〉NSD=0.489±0.001 (stat.)±0.007 (syst.) GeV/c, respectively. The data exhibit a slightly larger 〈pT〉 than measurements in wider pseudorapidity intervals. The results are compared to simulations with the Monte Carlo event generators PYTHIA and PHOJET.
Schimanski, Carl Christoph ; Möhler, Markus ; Schön, Michael ; Van Cutsem, Eric ; Greil, Richard ; Bechstein, Wolf Otto ; Hegewisch-Becker, Susanna ; Wichert, Götz Peter Lothar von ; Vöhringer, Matthias ; Heike, Michael ; Heinemann, Volker ; Peeters, Marc ; Kanzler, Stephan ; Kasper, Stefan ; Overkamp, Friedrich ; Schröder, Jan ; Seehofer, Daniel ; Kullmann, Frank ; Linz, Bernhard ; Schmidtmann, Irene ; Smith-Machnow, Victoria ; Gockel, Ines ; Lang, Hauke ; Galle, Peter R.
Background: 15-20% of all patients initially diagnosed with colorectal cancer develop metastatic disease and surgical resection remains the only potentially curative treatment available. Current 5-year survival following R0-resection of liver metastases is 28-39%, but recurrence eventually occurs in up to 70%. To date, adjuvant chemotherapy has not improved clinical outcomes significantly. The primary objective of the ongoing LICC trial (L-BLP25 In Colorectal Cancer) is to determine whether L-BLP25, an active cancer immunotherapy, extends recurrence-free survival (RFS) time over placebo in colorectal cancer patients following R0/R1 resection of hepatic metastases. L-BLP25 targets MUC1 glycoprotein, which is highly expressed in hepatic metastases from colorectal cancer. In a phase IIB trial, L-BLP25 has shown acceptable tolerability and a trend towards longer survival in patients with stage IIIB locoregional NSCLC.
Methods: This is a multinational, phase II, multicenter, randomized, double-blind, placebo-controlled trial with a sample size of 159 patients from 20 centers in 3 countries. Patients with stage IV colorectal adenocarcinoma limited to liver metastases are included. Following curative-intent complete resection of the primary tumor and of all synchronous/metachronous metastases, eligible patients are randomized 2:1 to receive either L-BLP25 or placebo. Those allocated to L-BLP25 receive a single dose of 300 mg/m2 cyclophosphamide (CP) 3 days before first L-BLP25 dose, then primary treatment with s.c. L-BLP25 930 mug once weekly for 8 weeks, followed by s.c. L-BLP25 930 mug maintenance doses at 6-week (years 1&2) and 12-week (year 3) intervals unless recurrence occurs. In the control arm, CP is replaced by saline solution and L-BLP25 by placebo. Primary endpoint is the comparison of recurrence-free survival (RFS) time between groups. Secondary endpoints are overall survival (OS) time, safety, tolerability, RFS/OS in MUC-1 positive cancers. Exploratory immune response analyses are planned. The primary endpoint will be assessed in Q3 2016. Follow-up will end Q3 2017. Interim analyses are not planned.
Discussion: The design and implementation of such a vaccination study in colorectal cancer is feasible. The study will provide recurrence-free and overall survival rates of groups in an unbiased fashion. Trial Registration EudraCT Number 2011-000218-20
Rödel, Franz ; Zhou, Shengtao ; Győrffy, Balász ; Raab, Monika ; Sanhaji, Mourad ; Mandal, Ranadip ; Martin, Daniel ; Becker, Sven ; Strebhardt, Klaus
Since type and duration of an appropriate adjuvant chemotherapy in early-stage ovarian cancer (OC) are still being debated, novel markers for a better stratification of these patients are of utmost importance for the design of an improved chemotherapeutical strategy. In contrast to numerous cancer studies on cellular proliferation based on the immunohistochemistry-driven evaluation of protein expression, we compared mRNA and protein expression of two independent markers of cellular proliferation, Ki-67 and Plk1, in a large cohort of 243 early-stage OC and their relationship with clinicopathological features and survival. Based on marker expression we demonstrate that early-stage OC patients (stages I/II, low-grade, serous) with high expression (Ki-67, Plk1) had a significantly shorter progression-free survival (PFS) and overall survival (OS) compared to patients with low expression (Ki-67, Plk1). Remarkably, based on mRNA expression this significant difference got lost in advanced stages (III/IV): At least for PFS, high levels of Ki-67 and Plk1 correlate with moderately better survival compared to patients with low expressing tumors. Our data suggest that in addition to Ki-67, Plk1 is a novel marker for the stratification of early-stage OC patients to maximize therapeutic efforts. Both, Ki-67 and Plk1, seem to be better suited in early-stages (I/II) as therapeutical targets compared to advanced-stages (III/IV) OC.
Köllermann, Jens ; Höh, Robert Benedikt ; Ruppel, Daniel ; Smith, Kevin ; Reis, Henning ; Wenzel, Mike ; Preißer, Felix Martin ; Kosiba, Marina ; Mandel, Philipp ; Karakiewicz, Pierre I. ; Becker, Andreas ; Chun, Felix ; Wild, Peter Johannes ; Kluth, Luis
The aim of this study is to investigate the incidental prostate cancer (iPCa) detection rates of different embedding methods in a large, contemporary cohort of patients with bladder outlet obstruction (BOO) treated with transurethral surgery. We relied on an institutional tertiary-care database to identify BOO patients who underwent either transurethral loop resection or laser (Holmium:yttrium–aluminium garnet) enucleation of the prostate (HoLEP) between 01/2012 and 12/2019. Embedding methods differed with regard to the extent of the additional prostate tissue submitted following the first ten cassettes of primary embedding (cohort A: one [additional] cassette/10 g residual tissue vs. cohort B: complete embedding of the residual tissue). Detection rates of iPCa among the different embedding methods were compared. Subsequently, subgroup analyses by embedding protocol were repeated in HoLEP-treated patients only. In the overall cohort, the iPCa detection rate was 11% (46/420). In cohort A (n = 299), tissue embedding resulted in a median of 8 cassettes/patient (range 1–38) vs. a median of 15 (range 2–74) in cohort B (n = 121) (p < .001). The iPCa detection rate was 8% (23/299) and 19% (23/121) in cohort A vs. cohort B, respectively (p < .001). Virtual reduction of the number of tissue cassettes to ten cassettes resulted in a iPCa detection rate of 96% in both cohorts, missing one stage T1a/ISUP grade 1 carcinoma. Increasing the number of cassettes by two and eight cassettes, respectively, resulted in a detection rate of 100% in both cohorts without revealing high-grade carcinomas. Subgroup analyses in HoLEP patients confirmed these findings, demonstrated by a 100 vs. 96% iPCa detection rate following examination of the first ten cassettes, missing one case of T1a/ISUP 1. Examination of 8 additional cassettes resulted in a 100% detection rate. The extent of embedding of material obtained from transurethral prostate resection correlates with the iPCa detection rate. However, the submission of 10 cassettes appears to be a reasonable threshold to reduce resource utilization while maintaining secure cancer detection.
Kaiser, Anna ; Aggensteiner, Pascal ; Holtmann, Martin ; Fallgatter, Andreas ; Romanos, Marcel ; Abenova, Karina ; Alm, Barbara ; Becker, Katja ; Döpfner, Manfred ; Ethofer, Thomas ; Freitag, Christine M. ; Geissler, Julia ; Hebebrand, Johannes ; Huss, Michael ; Jans, Thomas ; Jendreizik, Lea Teresa ; Ketter, Johanna ; Legenbauer, Tanja ; Philipsen, Alexandra ; Poustka, Luise ; Renner, Tobias ; Retz, Wolfgang ; Rösler, Michael ; Thome, Johannes ; Uebel-von Sandersleben, Henrik ; Wirth, Elena von ; Zinnow, Toivo ; Hohmann, Sarah ; Millenet, Sabina ; Holz, Nathalie E. ; Banaschewski, Tobias ; Brandeis, Daniel
Electroencephalography (EEG) represents a widely established method for assessing altered and typically developing brain function. However, systematic studies on EEG data quality, its correlates, and consequences are scarce. To address this research gap, the current study focused on the percentage of artifact-free segments after standard EEG pre-processing as a data quality index. We analyzed participant-related and methodological influences, and validity by replicating landmark EEG effects. Further, effects of data quality on spectral power analyses beyond participant-related characteristics were explored. EEG data from a multicenter ADHD-cohort (age range 6 to 45 years), and a non-ADHD school-age control group were analyzed (ntotal = 305). Resting-state data during eyes open, and eyes closed conditions, and task-related data during a cued Continuous Performance Task (CPT) were collected. After pre-processing, general linear models, and stepwise regression models were fitted to the data. We found that EEG data quality was strongly related to demographic characteristics, but not to methodological factors. We were able to replicate maturational, task, and ADHD effects reported in the EEG literature, establishing a link with EEG-landmark effects. Furthermore, we showed that poor data quality significantly increases spectral power beyond effects of maturation and symptom severity. Taken together, the current results indicate that with a careful design and systematic quality control, informative large-scale multicenter trials characterizing neurophysiological mechanisms in neurodevelopmental disorders across the lifespan are feasible. Nevertheless, results are restricted to the limitations reported. Future work will clarify predictive value.
Pérez-Palma, Eduardo ; Helbig, Ingo ; Klein, Karl Martin ; Anttila, Verneri ; Horn, Heiko ; Reinthaler, Eva Maria ; Gormley, Padhraig ; Ganna, Andrea ; Byrnes, Andrea ; Pernhorst, Katharina ; Toliat, Mohammad Reza ; Saarentaus, Elmo ; Howrigan, Daniel P. ; Hoffman, Per ; Miquel, Juan Francisco ; De Ferrari, Giancarlo V. ; Nürnberg, Peter ; Lerche, Holger ; Zimprich, Fritz ; Neubauer, Bern A. ; Becker, Albert John ; Rosenow, Felix ; Perucca, Emilio ; Zara, Federico ; Weber, Yvonne G. ; Lal, Dennis
Background: Microdeletions are known to confer risk to epilepsy, particularly at genomic rearrangement ‘hotspot’ loci. However, microdeletion burden not overlapping these regions or within different epilepsy subtypes has not been ascertained.
Objective: To decipher the role of microdeletions outside hotspots loci and risk assessment by epilepsy subtype.
Methods: We assessed the burden, frequency and genomic content of rare, large microdeletions found in a previously published cohort of 1366 patients with genetic generalised epilepsy (GGE) in addition to two sets of additional unpublished genome-wide microdeletions found in 281 patients with rolandic epilepsy (RE) and 807 patients with adult focal epilepsy (AFE), totalling 2454 cases. Microdeletions were assessed in a combined and subtype-specific approaches against 6746 controls.
Results: When hotspots are considered, we detected an enrichment of microdeletions in the combined epilepsy analysis (adjusted p=1.06×10−6,OR 1.89, 95% CI 1.51 to 2.35). Epilepsy subtype-specific analyses showed that hotspot microdeletions in the GGE subgroup contribute most of the overall signal (adjusted p=9.79×10−12, OR 7.45, 95% CI 4.20–13.5). Outside hotspots , microdeletions were enriched in the GGE cohort for neurodevelopmental genes (adjusted p=9.13×10−3,OR 2.85, 95% CI 1.62–4.94). No additional signal was observed for RE and AFE. Still, gene-content analysis identified known (NRXN1, RBFOX1 and PCDH7) and novel (LOC102723362) candidate genes across epilepsy subtypes that were not deleted in controls.
Conclusions: Our results show a heterogeneous effect of recurrent and non-recurrent microdeletions as part of the genetic architecture of GGE and a minor contribution in the aetiology of RE and AFE.
Pérez-Palma, Eduardo ; Helbig, Ingo ; Klein, Karl Martin ; Anttila, Verneri ; Horn, Heiko ; Maria Reinthaler, Eva ; Gormley, Padhraig ; Ganna, Andrea ; Byrnes, Andrea ; Pernhorst, Katharina ; Toliat, Mohammad Reza ; Saarentaus, Elmo ; Howrigan, Daniel P. ; Hoffman, Per ; Miquel, Juan Francisco ; De Ferrari, Giancarlo ; Nürnberg, Peter ; Lerche, Holger ; Zimprich, Fritz ; Neubauer, Bern A. ; Becker, Albert J. ; Rosenow, Felix ; Perucca, Emilio ; Zara, Federico ; Weber, Yvonne G. ; Lal, Dennis
Background Microdeletions are known to confer risk to epilepsy, particularly at genomic rearrangement “hotspot” loci. However, deciphering their role outside hotspots and risk assessment by epilepsy sub-type has not been conducted.
Methods We assessed the burden, frequency and genomic content of rare, large microdeletions found in a previously published cohort of 1,366 patients with Genetic Generalized Epilepsy (GGE) plus two sets of additional unpublished genome-wide microdeletions found in 281 Rolandic Epilepsy (RE) and 807 Adult Focal Epilepsy (AFE) patients, totaling 2,454 cases. These microdeletion sets were assessed in a combined analysis and in sub-type specific approaches against 6,746 ethnically matched controls.
Results When hotspots are considered, we detected an enrichment of microdeletions in the combined epilepsy analysis (adjusted-P= 2.00×10-7; OR = 1.89; 95%-CI: 1.51-2.35), where the implicated microdeletions overlapped with rarely deleted genes and those involved in neurodevelopmental processes. Sub-type specific analyses showed that hotspot deletions in the GGE subgroup contribute most of the signal (adjusted-P = 1.22×10-12; OR = 7.45; 95%-CI = 4.20-11.97). Outside hotspot loci, microdeletions were enriched in the GGE cohort for neurodevelopmental genes (adjusted-P = 4.78×10-3; OR = 2.30; 95%-CI = 1.42-3.70), whereas no additional signal was observed for RE and AFE. Still, gene content analysis was able to identify known (NRXN1, RBFOX1 and PCDH7) and novel (LOC102723362) candidate genes affected in more than one epilepsy sub-type but not in controls.
Conclusions Our results show a heterogeneous effect of recurrent and non-recurrent microdeletions as part of the genetic architecture of GGE and a minor to negligible contribution in the etiology of RE and AFE.