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  1. Article: Grade 3-4 Immune-Related Adverse Events Induced by Immune Checkpoint Inhibitors in Non-Small-Cell Lung Cancer (NSCLC) Patients Are Correlated with Better Outcome: A Real-Life Observational Study.

    Guezour, Nadia / Soussi, Ghassen / Brosseau, Solenn / Abbar, Baptiste / Naltet, Charles / Vauchier, Charles / Poté, Nicolas / Hachon, Lorry / Namour, Céline / Khalil, Antoine / Trédaniel, Jean / Zalcman, Gérard / Gounant, Valérie

    Cancers

    2022  Volume 14, Issue 16

    Abstract: Background: Immune checkpoint inhibitors (ICIs) have been a major advance in treating non-small-cell lung cancer (NSCLC). Programmed cell death protein-1/programmed death-ligand 1 blockade enhances immune function, mediating anti-tumor activity, yet ... ...

    Abstract Background: Immune checkpoint inhibitors (ICIs) have been a major advance in treating non-small-cell lung cancer (NSCLC). Programmed cell death protein-1/programmed death-ligand 1 blockade enhances immune function, mediating anti-tumor activity, yet causing immune-related adverse events (irAEs). We investigated the prognostic role of Grade 3−4 irAEs on overall survival (OS). Methods: This observational study recruited advanced NSCLC patients who received ICIs at Bichat-Claude Bernard University Hospital and in a community hospital, Saint-Joseph Foundation (Paris), between 1 January 2016 and 31 December 2019. Immunotherapy as a single-agent or double-drug combination was applied in the first and later lines. Univariable and multivariable analyses were instrumental in evaluating the prognostic impact of irAEs. Results: Overall, 201 consecutive ICI-treated patients were enrolled. High-grade irAEs (Grades 3−4) occurred in 36 patients (17.9%), including 11 (30.5%) cases of pneumonitis, 8 (22.2%) of colitis, 4 (11.1%) hepatic, 3 (8.3%) dermatological, 2 (5.5%) neurological events, and 2 cases (5.5%) of poly-arthralgia. The median OS was 10.4 ± 1.36 months (95% CI:7.7−13.1), being significantly higher in patients with high-grade irAEs than those without, 27.8 months vs. 8.1 months, respectively (HR = 2.5; p < 0.0001). Multivariable analysis revealed an independent association between high-grade irAEs and longer OS (HR = 0.29, 95% CI: 0.2−0.6, p < 0.0001). Conclusions: Our real-life study confirms that high-grade irAEs predict longer OS in advanced NSCLC.
    Language English
    Publishing date 2022-08-11
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2527080-1
    ISSN 2072-6694
    ISSN 2072-6694
    DOI 10.3390/cancers14163878
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Efficacy of Severe Acute Respiratory Syndrome Coronavirus-2 Vaccine in Patients With Thoracic Cancer: A Prospective Study Supporting a Third Dose in Patients With Minimal Serologic Response After Two Vaccine Doses.

    Gounant, Valérie / Ferré, Valentine Marie / Soussi, Ghassen / Charpentier, Charlotte / Flament, Héloïse / Fidouh, Nadhira / Collin, Gilles / Namour, Céline / Assoun, Sandra / Bizot, Alexandra / Brouk, Zohra / Vicaut, Eric / Teixeira, Luis / Descamps, Diane / Zalcman, Gérard

    Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer

    2021  Volume 17, Issue 2, Page(s) 239–251

    Abstract: Introduction: Coronavirus disease 2019 resulted in a 30% mortality rate in patients with thoracic cancer. Given that patients with cancer were excluded from serum antisevere acute respiratory syndrome coronavirus-2 (SARS-CoV-2) vaccine registration ... ...

    Abstract Introduction: Coronavirus disease 2019 resulted in a 30% mortality rate in patients with thoracic cancer. Given that patients with cancer were excluded from serum antisevere acute respiratory syndrome coronavirus-2 (SARS-CoV-2) vaccine registration trials, it is still unknown whether they would develop a protective antispike antibody response after vaccination. This prospective vaccine monitoring study primarily aimed to assess humoral responses to the SARS-CoV-2 vaccine in patients with thoracic cancer.
    Methods: SARS-CoV-2-spike antibodies were measured using the Abbot Architect SARS-CoV-2 immunoglobulin G immunoassay before the first injection of BNT162b2 mRNA vaccine, at week 4, and 2 to 16 weeks after the second vaccine dose administration. The factors associated with antibody response were analyzed.
    Results: Overall, 306 patients, with a median age of 67.0 years (interquartile range: 58-74), were vaccinated. Of these, 283 patients received two vaccine doses at 28-day intervals. After a 6.7-month median follow-up, eight patients (2.6%) contracted proven symptomatic SARS-CoV-2 infection, with rapid favorable evolution. Of the 269 serologic results available beyond day 14 after the second vaccine dose administration, 17 patients (6.3%) were still negative (<50 arbitrary units/mL, whereas 34 (11%) were less than 300 arbitrary units/mL (12.5th percentile). In multivariate analysis, only age (p < 0.01) and long-term corticosteroid treatment (p = 0.01) were significantly associated with a lack of immunization. A total of 30 patients received a third vaccine dose, with only three patients showing persistently negative serology thereafter, whereas the others exhibited clear seroconversion.
    Conclusions: SARS-CoV2 vaccines were found to be efficient in patients with thoracic cancer, most of them being immunized after two doses. A third shot given to 1% of patients with persistent low antibody titers resulted in an 88% immunization rate.
    MeSH term(s) Aged ; BNT162 Vaccine ; COVID-19 ; COVID-19 Vaccines ; Humans ; Lung Neoplasms ; Prospective Studies ; RNA, Viral ; SARS-CoV-2 ; Vaccines, Synthetic ; mRNA Vaccines
    Chemical Substances COVID-19 Vaccines ; RNA, Viral ; Vaccines, Synthetic ; mRNA Vaccines ; BNT162 Vaccine (N38TVC63NU)
    Language English
    Publishing date 2021-11-16
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2432037-7
    ISSN 1556-1380 ; 1556-0864
    ISSN (online) 1556-1380
    ISSN 1556-0864
    DOI 10.1016/j.jtho.2021.10.015
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Association of TP53 mutations with response and longer survival under immune checkpoint inhibitors in advanced non-small-cell lung cancer.

    Assoun, Sandra / Theou-Anton, Nathalie / Nguenang, Marina / Cazes, Aurélie / Danel, Claire / Abbar, Baptiste / Pluvy, Johan / Gounant, Valérie / Khalil, Antoine / Namour, Céline / Brosseau, Solenn / Zalcman, Gérard

    Lung cancer (Amsterdam, Netherlands)

    2019  Volume 132, Page(s) 65–71

    Abstract: Introduction: Tumor mutational burden (TMB) correlates with response to immune checkpoint inhibitors (ICI) in advanced non-small-cell lung cancer (aNSCLC). We hypothesized that TP53 mutations could reflect TMB and be associated with ICI benefit.: ... ...

    Abstract Introduction: Tumor mutational burden (TMB) correlates with response to immune checkpoint inhibitors (ICI) in advanced non-small-cell lung cancer (aNSCLC). We hypothesized that TP53 mutations could reflect TMB and be associated with ICI benefit.
    Methods: TP53 mutations were assessed by next-generation sequencing in aNSCLC patients treated with programmed death-1 (PD-1) blockers. Clinical data, tumor programmed death ligand-1 (PD-L1) expression, and KRAS mutational status were collected. The primary endpoint was overall survival (OS).
    Results: In total, 72 patients (median [interquartile range] age: 61 [33-83] years) were included; 52 (72%) were male; 39 (54%) had performance status 0-1; 53 (74%) had adenocarcinoma; 20 (28%) received first-line ICI, 52 (72%) second line or more. In 65 patients with available data, 36 (55%) expressed PD-L1 in ≥50% of tumor cells, 20 (31%) in 1-49% of cells, and nine (14%) were PD-L1-negative. Non-synonymous TP53 mutations were observed in 41 (57%) and 25 (35%) harbored KRAS-mutated tumors. After a median follow-up of 15.2 months (95% confidence interval [CI] 10.3-17.4 m), the median OS in the TP53-mutated group was 18.1 months (95% CI 6.6-not reached), vs. 8.1 months (95% CI 2.2-14.5, hazard ratio [HR] = 0.48; 95% CI 0.25-0.95, p = 0.04) in the TP53-wild-type group. Median progression-free survival was significantly longer in TP53-mutated patients (4.5 months, 95% CI 2.8-18.1 versus 1.4, 95% CI 1.1-3.5; p = 0.03), although TP53 mutation status failed to significantly influence PFS in the multivariate analysis (p = 0.32). Objective response rate (ORR) was higher in patients with TP53 mutation (51.2% vs. 20.7%; p = 0.01). In multivariate analysis, TP53 mutations independently associated with longer OS (HR = 0.35, 95% CI 0.16-0.77, p = 0.009).
    Conclusions: TP53-mutated status correlated with immunotherapy OS benefit in aNSCLC.
    MeSH term(s) Adult ; Aged ; Aged, 80 and over ; Antineoplastic Agents, Immunological/pharmacology ; Antineoplastic Agents, Immunological/therapeutic use ; B7-H1 Antigen/antagonists & inhibitors ; Biomarkers, Tumor/genetics ; Carcinoma, Non-Small-Cell Lung/drug therapy ; Carcinoma, Non-Small-Cell Lung/genetics ; Carcinoma, Non-Small-Cell Lung/mortality ; Female ; Follow-Up Studies ; High-Throughput Nucleotide Sequencing ; Humans ; Immunotherapy/methods ; Lung Neoplasms/drug therapy ; Lung Neoplasms/genetics ; Lung Neoplasms/mortality ; Male ; Middle Aged ; Mutation/genetics ; Neoplasm Staging ; Programmed Cell Death 1 Receptor/antagonists & inhibitors ; Proto-Oncogene Proteins p21(ras)/genetics ; Retrospective Studies ; Survival Analysis ; Tumor Suppressor Protein p53/genetics
    Chemical Substances Antineoplastic Agents, Immunological ; B7-H1 Antigen ; Biomarkers, Tumor ; CD274 protein, human ; KRAS protein, human ; PDCD1 protein, human ; Programmed Cell Death 1 Receptor ; TP53 protein, human ; Tumor Suppressor Protein p53 ; Proto-Oncogene Proteins p21(ras) (EC 3.6.5.2)
    Language English
    Publishing date 2019-04-08
    Publishing country Ireland
    Document type Journal Article
    ZDB-ID 632771-0
    ISSN 1872-8332 ; 0169-5002
    ISSN (online) 1872-8332
    ISSN 0169-5002
    DOI 10.1016/j.lungcan.2019.04.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Efficacy of SARS-CoV-2 vaccine in thoracic cancer patients: a prospective study supporting a third dose in patients with minimal serologic response after two vaccine doses

    GOUNANT, Valerie / FERRE, Valentine Marie / SOUSSI, Ghassen / charpentier, Charlotte / FLAMENT, Heloise / FIDOUH, Nadhira / COLLIN, Gilles / NAMOUR, Celine / ASSOUN, Sandra / BIZOT, Alexandra / BROUK, Zohra / VICAUT, Eric / TEXEIRA, Luis / DESCAMPS, Diane / ZALCMAN, Gerard

    medRxiv

    Abstract: Hypothesis Coronavirus disease 2019 (COVID-19) resulted in a 30% mortality rate in thoracic cancer patients. Given that cancer patients were excluded from serum anti-severe acute respiratory syndrome coronavirus 2 (SARS-CoV2) vaccine registration trials, ...

    Abstract Hypothesis Coronavirus disease 2019 (COVID-19) resulted in a 30% mortality rate in thoracic cancer patients. Given that cancer patients were excluded from serum anti-severe acute respiratory syndrome coronavirus 2 (SARS-CoV2) vaccine registration trials, it is still unknown whether they would develop a protective anti-spike antibody response following vaccination. This prospective vaccine monitoring study primarily aimed to assess humoral responses to SARS-CoV2 vaccine in thoracic cancer patients. Methods SARS-CoV2-spike antibodies were measured using Abbot ARCHITECT SARS-CoV-2 IgG immunoassay, prior to first injection of BNT162b2 mRNA vaccine, as well as at Week 4, and two-to-sixteen weeks after second vaccine dose. The factors associated with antibody response were analyzed. Results Overall, 306 patients, with a median age of 67.0 years (IQR=58-74), were vaccinated. Of these, 283 patients received two vaccine doses at 28-day intervals. After 4.7-month median follow-up, seven patients (2.3%) contracted proven symptomatic SARS-CoV-2 infection, with rapid favorable evolution. Of 269 serological results available beyond Day 14 post-second vaccine dose, 17 (6.3%) were still negative (<50 AU/mL) (arbitrary units/mL), while 34 (11%) were <300 AU/mL (12.5th percentile). In multivariate analysis, only age and chronic corticosteroid treatment were significantly associated with a lack of immunization. Thirty patients received a third vaccine dose, with only three patients showing persistent negative serology thereafter, whereas the others demonstrated clear seroconversion. Conclusion SARS-CoV2 vaccines were shown to be efficient in thoracic cancer patients, most of them being immunized after two doses. A third shot given to 11% of patients with persistent low antibody titers resulted in a 88% immunization rate.
    Keywords covid19
    Language English
    Publishing date 2021-08-13
    Publisher Cold Spring Harbor Laboratory Press
    Document type Article ; Online
    DOI 10.1101/2021.08.12.21261806
    Database COVID19

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  5. Article ; Online: Risk factors for Coronavirus Disease 2019 (COVID-19) severity and mortality among solid cancer patients and impact of the disease on anticancer treatment

    Lièvre, Astrid / Turpin, Anthony / Ray-Coquard, Isabelle / Le Malicot, Karine / Thariat, Juliette / Ahle, Guido / Neuzillet, Cindy / Paoletti, Xavier / Bouché, Olivier / Aldabbagh, Kais / Michel, Pierre / Debieuvre, Didier / Canellas, Anthony / Wislez, Marie / Laurent, Lucie / Mabro, May / Colle, Raphael / Hardy-Bessard, Anne-Claire / Mansi, Laura /
    Colomba, Emeline / Bourhis, Jean / Gorphe, Philippe / Pointreau, Yoann / Idbaih, Ahmed / Ursu, Renata / Di Stefano, Anna Luisa / Zalcman, Gérard / Aparicio, Thomas / Moulin, Solenne / Leleu, Olivier / Leparree, Sylvie / Goasdoue, Henri / Piprot, Christine / Tourneur, Gerald / Bayart, Vincent / Lignier, Delphine / Lachaier, Emma / Khamari, Marwa / Coutte, Alexandre / Siembida, Nicolas / Houessinon, Aline / Regimbeau, Jean Marc / Chauffert, Bruno / Moreira, Aurélie / Hautefeuille, Vincent / Hee, Christine / Boone, Mathieu / Bihan, Céline / Chive, Emilie / Poulet-Potriquier, Stéphane / Fahem, Rachida / Luet, Dominique / Roquin, Guillaume / Vitellius, Carole / Cornet-Trichereau, Nathanaëlle / Caroli-Bosc, François-Xavier / Thirot-Bidault, Anne / Ropert, Stanislas / Gachet - Masson, Julie / Dehais, Mélanie / L'helgoualc'h, Gwen-Ael / Ali-Mahamadou, Ibrahim / Talfi, Safia / Belmont, Laure / Kilendo, Dieudonné / Benrezzak, Nasro / Dubief, Emeline / Conroy, Guillaume / Delique, Laurence / Basso, Maud / Pons, Isabelle / Salignon, Karine / Villing, Anne-Laure / Mougenot, Emmanuelle / Porebski, Cassandra / Guiatni, Asma / Cloarec, Nicolas / Mineur, Laurent / Bouchaud, Marie / David, Céleste / Peytier, Annie / Greletty, Thomas / Audemar, Franck / Vignes, Emanuelle / Minne, Floriane / Goldzak, Guillaume / Huysman, Fabienne / Hocine, Fayçal / Lakkis, Zaher / Meynard, Guillaume / Almotlak, Hamadi / Klajer, Elodie / Sun, Xu-Shan / Wasselin, Julie / Catala, Pascale / Mazuy, Claire / Vandamme, Hélène / Prevost, Jean-Briac / Fadin, Aurélie / Basson, Laurent / Huguet, Jean-Baptiste / Dos Santos, Emmanuelle / Jany, Bérangère / Saad, Alain / Goutorbe, Frédéric / Oziol, Eric / Ramdani, Mohamed / Kadiri, Ouafae / Garbay, Delphine / Huet, Clotilde / Giroux Leprieur, Etienne / Teng, Wen / Monvoisin, Justine / Arnaud Coffin, Patrick / Roux, Sylvie / Orfeuvre, Hubert / Chagros, Mélanie / Pillon, Didier / Rassoul, Agathe / Poureau, Pierre Guillaume / Novello, Cécile / Ducray, François / Trouba, Cécile / Bastit, Vianney / Babin, Emmanuel / Leon, Vincent / Courtecuisse, Anne-Catherine / Vambre, Julie / Tack, Vincent / Desauw, Christophe / Meniai, Fatima / Peres, Christina / Esparcieux, Aurélie / Perrier, Hervé / Doux, Nathalie / Kaphan, Régis / Roques, Bertrand / Rebischung, Christine / Mille, Dominique / Fernandes, Gaëlle / Abdelli, Naceur / Jousset, Natacha / Combe, Pierre / Jonveaux, Eric / Dumont, Patrick / Kanaan, Marc / Berthelot Gras, Corinne / Panis, Valérie / Kaluzinski, Laure / Venant-Valery, Marjolène / Lam, You-Heng / Vallee, Laura / Riviere, Frédéric / Durand, Muriel / Benghadid, Dihya / Villeneuve, Emilie / Hentic Dhome, Olivia / Bounouar, Zedjiga / De Mestier, Louis / Dubois, Jacqueline / Eyriey, Magali / Moreau, Lionel / Baihas, Dib / Aldabbagh, Kaïs / Degriffolet, Dominique / Sebbagh, Virginie / Seghezzi, Jean-Christophe / Lozach-Brugirard, Marion / Mandrou, Julie / Mavier, Loubna / Hennetier, Florence / Wagner, Jean-Philippe / Carola, Elisabeth / Chandirakumaran, Karthiga / Loutski, Sandrine / Cojean-Zelek, Isabelle / Bouras, Amina / Lacour, Sandrine / Froura, Fahem / Ben Nadji, Hadjer / Cattelain, Sophie / Darloy, Franck / Jolimoy Boilleau, Geneviève / Maissiat, Cyrielle / Darut-Jouve, Ariane / Lorgis, Véronique / Charifi-Alaoui, Ikram / Ghiringhelli, François / Drouillard, Antoine / Chaix, Marie / Manfredi, Sylvain / Lepage, Côme / Gagnaire, Alice / Latournerie, Marianne / jourdan, Sofia / Perrot, Nora / folia, Mireille / Minello, Anne / Jouve, Jean-Louis / Fery, Marielle / Landau, Alain / Evrard, Diane / Valenza, Bruno / Paitel, Jean-François / Chablais, Laetitia / Kreitmann, Thomas / Lancry-Lecomte, Laurence / Monard, Adrien / Faugeras, Eve / Boucheret, Paul / Glommeau, Cécile / Tchikladze, Christine / Garnier Tixidre, Claire / Long, Jérôme / Zaidi, Manel / Delabarre, Véronique / Meyzenc, Juliette / Ferrand, Loïc / Moro-Sibilot, Denis / Bouheret, Paul / Leyronnas, Cécile / Herve, Camille / Thoor, Audrey / Jacquet, Emanuelle / Roth, Gaël / Madapathage-Senanyake, Videsheka / Chupeau, Peggy / Bieber, Elsa / Rosso, Maud / Lepage, Isabelle / Priou, Frank / Laly, Margot / Aprelon, Sylvie / Sobolak, Natacha / Homokos, Helen / Watelle, Fabienne / Pham-Becker, Alice / Lauridant, Géraldine / Dujardin, Charlotte / Lenglin, Etienne / Nienguet Tsota, Aimée / Dominguez, Sophie / Forestier, Alexandra / Nouvel, Franck / Lerooy, Justine / Ratajczak, Céline / Romano, Olivier / Brzyski, Dorothéee / Barriere, Aurélien / Genet, Dominique / Tisse, Julien / Zasadny, Xavier / Grelet, Adeline / Hennion-Imbault, Amélie / Haustraete, Eglantine / Louafi, Samy / Awad, Manal / Zekri, Younes / Cheneau, Caroline / Leissen, Nolwen / Egreteau, Joëlle / Breant, Alexandra / Sarabi, Matthieu / Labonne, Stéphanie / Forestier, Julien / Leclercq, Céline / Prunier-Bossion, Florence / Ray Coquard, Isabelle / Guillet, Marielle / Theillaumas, Aurélie / Prome, Emilie / Walter, Thomas / Philouze, Pierre / Lawo, Melody / De Talhouet, Solène / Beuvelot, Johanne / Molin, Yann / Bellecoste Martin, Marie / Saussereau, Maud / Agnelli, Lauren / Fakhry, Nicolas / Laplace, Christophe / Norguet Monnereau, Emmanuelle / Boucard, Céline / Djenad, Kahina / Fontaine, Catherine / Seitz, Jean-François / Dahan, Laétitia / Sigrand, Julie / Duluc, Muriel / Locher, Christophe / Fleury, Marjory / Brou Marie, Ange / Berkane, Ramdane / Poupblanc, Séverine / Auby, Dominique / Petran, Daniela / Texereau, Patrick / Guerineau, Elodie / Andre, Morgan / Mahjoubi, Linda / Sarrazin, Fanny / Jeanson, Sonia / Gschwend, Anthony / Birr, Virginie / Fore, Mathieu / Noirclerc, Monique / Dahou, Sihem / Spaeth, Dominique / Lambotin, Mélanie / Lelu, Thomas / Linot, Benjamin / Hugon, Nathalie / Rousseau, Dominique / Castanie, Hélène / Lenne, Carole / Lortholary, Alain / Cessot, Anatole / Merzoug, Messaouda / Naudin, Cécile / Vannetzel, Jean-Michel / Aziz, Ghina / Hadj Arab, Yacine / Pernes, Stéphanie / Roche-Lachaise, Isabelle / Fiteni, Frédéric / Yahiaoui, Hadjer / Marel Lopez, Gwendoline / Oddoz, Jeanne / Peira, Fabienne / Michel, Olivier / Meunier, Jérôme / Ouahrani, Brahim / Roger, Antoine / Branco, Sonia / Nguyen, Van / Gisselbrecht, Mathilde / Hammad, Ghania / Mordant, Pierre / Stroksztejn, Magda / Pocard, Marc / Nlo Meyengue, Luc / Sacco, Emmanuelle / Simon Anne, Sophie / Fabre-Guillevin, Elizabeth / Slim, Marine / Zaanan, Aziz / Cadranel, Jacques / Pluvy, Johan / Ursu, Rénata / Geraldo, Amyrath / Lihi, Rime / Vo, Maryline / Brouk, Zohra / Colle, Raphaël / Bennamoun, Mostefa / Lacan, Fabrice / Louvet, Christophe / Mebarki, Soraya / Veyri, Marianne / Paillaud, Elena / Lucas, Christelle / Dubreuil, Olivier / Lyamani, Jamila / Agguini, Hanane / Soularue, Emilie / Jourdaine, Clément / Verillaud, Benjamin / Herzine, Hakima / Raymond, Eric / Mathiot, Nathalie / Palmieri, Lola Jade / Epanya, Christian / Taieb, Julien / Bertrand, Eliane / Goujon, Gaël / Namour, Céline / Gazeau, Benoit / Zafirova, Biljana / Mirghani, Haitham / Belin, Catherine / Belkhir, Kahina / Gharib, Myriam / Vozy, Aurore / Amrane, Karim / Spano, Jean-Philippe / Wassermann, Johanna / Feuvret, Loic / Bachet, Jean-Baptiste / Philonenko, Sara / Guillot, Laetitia / Zabbe, Marion / Gibiat, Stéphanie / Baylot, Camille / Jouinot, Aude / Leduc, Nicolas / Vieillot, Sabine / James, Laurie / Ducerf, Camille / Blanc, Jean-Frédéric / Falandry Leger, Claire / Wautot, Virginie / Chauvenet, Marion / Vincent, Aude / Tougeron, David / Goulvent, Sandrine / Suc, Etienne / Laurenty, Anne-Pascale / Marquis, Eric / Bonnaire, Margaux / Dewolf, Maxime / Brenet, Esteban / Billard, Delphine / Litre, Claude-Fabien / Dumazet, Antoine / Botsen, Damien / Vazel, Marion / Carlier, Claire / Bonnerave, David / Marchand-Crety, Charles / Bouche, Olivier / Fosse, Patricia / Sefrioui, David / Watson, Sarah / Torche, Fatah / Muron, Thierry / Natur, Stéphane / Desgrippes, Romain / Bihel, Véronique / Ferrand, François-Régis / Leiterer, Caroline / Lavole, Julie / Moquet, Claire / Pressoir, Nathalie / Dziukala, Catherine / Ligeza Poisson, Catherine / Naji, Abdelhalim / Williet, Nicolas / Phelip, Jean-Marc / Di Palma, Fabrice / Kherrour Mehdi, Amina / Langrand-Escure, Julien / Fournel, Pierre / Pigne, Grégoire / Saban-Roche, Léa / Magne, Nicolas / Vassal, Cécile / Jacquin, Jean-Philippe / Ramirez, Carole / Vallard, Alexis / Collard, Olivier / Rivoirard, Romain / Graber, Ivan / Trager Maury, Stéphanie / Duboisset, Elodie / Ayllon Ugarte, Jorge / Rami, Dalilia / Saler, Christine / Reinbolt, Manon / Le Fevre, Clara / Ben Abdelghani, Meher / Dourthe, Louis-Marie / Perruisseau-Carrier, Joffrey / Nguimpi-Tambou, Marlène / Barret, Flavie / Di Stefano Anna, Luisa / Balthazard, Annie / Vassord-Dang, Camille / Le Marchand, Mathilde / Vergniol, Julien / Pripon, Iulia / Daemaegdt, Axelle / Latry, Vanessa / Larrieu, Muna / Landry, Gaëlle / Touihri Maximin, Laetitia / Del Piano, Francesco / Barlet, Agnès / Vernisse, Mylène / Lafond, Sophie / Genin, Charline / Sibertin-Blanc, Camille / Chabrillac, Emilien / Gregoire, Caroline / Vergez, Sébastien / Panouille, Quentin / Guimbaud, Rosine / Richa, Floriane / Lebellec, Loïc / Gounin, Sophie / Buiret, Guillaume / Baudin, Marine / Hamon, Hervé / Deshorgue, Anne-Claire / Barrascout, Eduardo / Legrand, Stéphanie / Houlze, Morgane / Cambula, Linda / Lopez, Anthony / Fouquet, Guillaume / Touabi, Kahina / GermaIn, Adeline / Godbert, Benoit / Voivret, Florence / Perrin, Julie / Da Silva, Rosa / Bernichon, Emilie

    European Journal of Cancer

    A French nationwide cohort study (GCO-002 CACOVID-19)

    2020  Volume 141, Page(s) 62–81

    Keywords Cancer Research ; Oncology ; covid19
    Language English
    Publisher Elsevier BV
    Publishing country us
    Document type Article ; Online
    ZDB-ID 82061-1
    ISSN 1879-0852 ; 0277-5379 ; 0959-8049 ; 0964-1947
    ISSN (online) 1879-0852
    ISSN 0277-5379 ; 0959-8049 ; 0964-1947
    DOI 10.1016/j.ejca.2020.09.035
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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