Joaquim Bosch-Barrera
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Bispecific immune-angiogenic blockade in extensive-stage small-cell lung cancer-positioning ivonescimab
Have a website account?Log In orRegister for exclusive website content. Home / Vol 15, No 1 (February 28, 2026) / Bispecific immune-angiogenic blockade in extensive-stage small-cell lung cancer—positioning ivonescimab PDF 15 views Full Text 1 views Peer Review File 10 views COI Form 11 views Session Timed Out Your session has expired. Please sign in again.
Induction chemo-immunotherapy followed by chemo-radiotherapy and immunotherapy maintenance in stage III NSCLC (APOLO): a phase 2 trial - Nature Communications
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Abstract Unresectable stage III NSCLC standard treatment is chemo-radiotherapy (CT-RT) followed by immunotherapy (IO) with durvalumab. We investigated adding an induction phase with chemo-immunotherapy (ChIO). APOLO was a multicentre, single-arm, phase 2 trial (NCT04776447). Non-resectable stage IIIA–IIIC NSCLC patients received induction ChIO (atezolizumab + carboplatin + paclitaxel, for 3 cycles), followed by concurrent CT-RT (3 cycles), and IO maintenance (atezolizumab for 16 cycles).
By Mariano Provencio, Begoña Campos, María Guirado, Laia Vilà, Rosario Garcia Campelo, Miriam Leandro Dorta, Sergio Vázquez Estévez, Asia Ferrández, M. Sala, Ana Ortega, Ana Blasco Verified, Amelia Insa, Maria Areses, Ivana Sullivan, Rafael Lopez, Virginia Calvo, Delvys Rodríguez-Abreu, Joaquim Bosch-Barrera, Ana López-Martín, Raquel Marsé, Laura A. Torrado, Julia Giner, Emilio Sánchez Saugar, Cristina Martinez-Toledo, Atocha Romero, Alberto Cruz-Bermúdez, Kirill Matskov, Manuel Fernández Bruno, Pilar Mediavilla
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Nature
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Mitochondrial priming and response to BH3 mimetics in “one-two punch” senogenic-senolytic strategies - Cell Death Discovery
Abstract A one-two punch sequential regimen of senescence-inducing agents followed by senolytic drugs has emerged as a novel therapeutic strategy in cancer. Unfortunately, cancer cells undergoing therapy-induced senescence (TIS) vary widely in their sensitivity to senotherapeutics, and companion diagnostics to predict the response of TIS cancer cells to a specific senolytic drug are lacking.
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