Lydia Gaba

ORCID: 0000-0002-6898-0557
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About
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Research Areas
  • Ovarian cancer diagnosis and treatment
  • Cancer Immunotherapy and Biomarkers
  • PARP inhibition in cancer therapy
  • Lung Cancer Treatments and Mutations
  • Endometrial and Cervical Cancer Treatments
  • Cancer Genomics and Diagnostics
  • Radiomics and Machine Learning in Medical Imaging
  • Cancer, Lipids, and Metabolism
  • Melanoma and MAPK Pathways
  • Renal cell carcinoma treatment
  • Prostate Cancer Treatment and Research
  • BRCA gene mutations in cancer
  • RNA modifications and cancer
  • Ferroptosis and cancer prognosis
  • Neuroendocrine Tumor Research Advances
  • Lymphoma Diagnosis and Treatment
  • Genetic factors in colorectal cancer
  • Reproductive Biology and Fertility
  • Peptidase Inhibition and Analysis
  • Colorectal Cancer Treatments and Studies
  • Radiopharmaceutical Chemistry and Applications
  • Intraperitoneal and Appendiceal Malignancies
  • Uterine Myomas and Treatments
  • PI3K/AKT/mTOR signaling in cancer
  • Immunotherapy and Immune Responses

Hospital Clínic de Barcelona
2016-2025

Consorci Institut D'Investigacions Biomediques August Pi I Sunyer
2015-2025

Universitat de Barcelona
2013-2025

Spanish Ovarian Cancer Research Group
2022-2024

Breast Cancer Research Foundation
2023

Target (United States)
2023

Barcelona Provincial Council
2020

Fundació Clínic per a la Recerca Biomèdica
2017

Antibody targeting of the immune checkpoint receptor PD1 produces therapeutic activity in a variety solid tumors, but most patients exhibit partial or complete resistance to treatment for reasons that are unclear. In this study, we evaluated tumor specimens from 65 with melanoma, lung nonsquamous, squamous cell head and neck cancers who were treated approved PD1-targeting antibodies pembrolizumab nivolumab. Tumor RNA before anti-PD1 therapy was analyzed on nCounter system using PanCancer...

10.1158/0008-5472.can-16-3556 article EN Cancer Research 2017-05-10
Ana Oaknin Laurence Gladieff Jerónimo Martínez-García Guillermo Villacampa Munetaka Takekuma and 95 more Ugo De Giorgi Kristina Lindemann Linn Woelber Nicoletta Colombo Linda Duska Alexandra Léary Ana Godoy-Ortiz Shin Nishio Antoine Angelergues María Jesús Rubio Lorena Fariñas-Madrid Satoshi Yamaguchi Domenica Lorusso Isabelle Ray‐Coquard Luís Manso Florence Joly Jesús Alarcón Philippe Follana Ignacio Romero Coriolan Lebreton José Alejandro Pérez Fidalgo Mayu Yunokawa Hanna Dahlstrand Véronique D’Hondt Leslie M. Randall Sophie Abadie‐Lacourtoisie Claudia Andreetta Nerea Anzizar Daiseuke Aoki Maria-Pilar Barretina-Ginesta Marco Johannes Battista Charlotte Bellier Anne Gry Bentzen Dominique Berton Bertrand Billemont Line Bjørge Maria Bjurberg Destin Black Alessandra Bologna Elena Ioana Braicu Cláudia Casanova Radoslav Chekerov Annick Chevalier Juan Cueva Bastian Czogalla Nicolas Delanoy Dominik Denschlag Oscar Derke Michael Eichbaum Takayuki Enomoto Carmen Esteban Michel Fabbro Tanja Fehm Annamaria Ferrero Markus C. Fleisch Anne Floquet Antonio Frassoldati Lydia Gaba Angiolo Gadducci Yolanda García García Elena Geuna Eva Guerra Lars Hanker Anne‐Claire Hardy‐Bessard Philipp Harter Kosei Hasegawa Kristina Hellman Ana Herrero Felix Hilpert Dionyssios Katsaros Matthias Koegel Anthoula Koliadi Jean‐Emmanuel Kurtz Bjoern Lampe Andrea Alberto Lissoni Alain Lortholary Giorgia Mangili Laura Mansi Frederik Marmé Cara Mathews William Mina Shinichiro Minobe Katherine Moxley Shoji Nagao Ornella Nicoletto Koji Nishino Hiroshi Nishio Shin Nishio Ana Oaknin Michaela Onstad Beatriz Pardo José Alejandro Pérez Fidalgo Carmela Pisano Andrés Poveda Julia Caroline Radosa

10.1016/s0140-6736(23)02405-4 article EN publisher-specific-oa The Lancet 2023-12-01

BackgroundWe hypothesized that the abundance of PD1 mRNA in tumor samples might explain differences overall response rates (ORR) observed following anti-PD1 monotherapy across cancer types.Patients and methodsRNASeqv2 data from 10078 representing 34 different types was analyzed TCGA. Eighteen immune-related gene signatures 547 genes, including PD1, were explored. Correlations between each gene/signature ORRs reported literature calculated. To translate silico findings to clinical setting, we...

10.1093/annonc/mdy335 article EN publisher-specific-oa Annals of Oncology 2018-08-23
Jean‐Emmanuel Kurtz Éric Pujade-Lauraine Ana Oaknin Lisa Belin Katharina Leitner and 95 more David Cibula Hannelore Denys Ora Rosengarten Manuel Rodrigues Nikolaus de Gregorio Jerónimo Martínez Edgar Petru Roman Kocián Ignace Vergote Patricia Pautier Barbara Schmalfeldt Lydia Gaba Stephan Polterauer Marie‐Ange Mouret‐Reynier Jalid Sehouli Cristina Churruca Frédèric Selle Florence Joly Véronique D’Hondt Émilie Bultot-Boissier Coriolan Lebreton Jean‐Pierre Lotz Rémy Largillier Pierre-Étienne Heudel Florian Heitz Jean‐Emmanuel Kurtz Sophie Abadie‐Lacourtoisie Cyril Abdeddaim J. Alexandre P. Augereau D. Avenin M. Azémar Nabil Baba-Hamed Olivia Bally Jérôme Barrière Fernando Bazán Dominique Berton Nathalie Bonichon-Lamichhane Nathalie Bonnin Elouen Boughalem R. Boustany Grenier Pierre-Emmanuel Brachet Fabien Brocard Émilie Bultot-Boissier Maria Cappiello-Bataller Hélène Castanie L. Chaigneau Camille Chakiba Dorothée Chocteau-Bouju Pierre Combe Aurélie Comte Elodie Coquan Cristina Costan P. Cottu L. Crouzet H. Curé Jérôme Dauba Hussain Dawood Laure De Cock T. De La Motte Rouge C. Debelleix Catherine Delbaldo Martin Demarchi Marion Deslandres Raymond Despax Véronique D’Hondt Anne Françoise DILLIES-LEGRAIN A Donnadieu C. Dubot Jean Marc Extra Michel Fabbro Claire Falandry F. Fiteni Anne Floquet Philippe Follana Jean‐Sébastien Frénel G. Freyer D. Garbay-Decoopman Céline Gavoille V. Girre Laurence Gladieff F. Goldwasser Alain Gratet Jean‐Christophe Grenier Anne‐Claire Hardy‐Bessard Pierre-Étienne Heudel Florence Joly A. Jouinot Emilie Kalbacher Marie‐Christine Kaminsky Laurence Lancry-Lecomte R. Largillier Fanny Le Du Alexandra Léary Coriolan Lebreton

PURPOSE Platinum-based doublets with concurrent and maintenance bevacizumab are standard therapy for ovarian cancer (OC) relapsing after a platinum-free interval (PFI) >6 months. Immunotherapy may be synergistic chemotherapy. PATIENTS AND METHODS ATALANTE/ENGOT-ov29 (ClinicalTrials.gov identifier: NCT02891824 ), placebo-controlled double-blinded randomized phase III trial, enrolled patients recurrent epithelial OC, one to two previous chemotherapy lines, PFI Eligible were randomly...

10.1200/jco.23.00529 article EN cc-by-nc-nd Journal of Clinical Oncology 2023-08-29
Ignace Vergote José Alejandro Pérez Fidalgo Erika Hamilton Giorgio Valabrega Toon Van Gorp and 95 more Jalid Sehouli David Cibula Tally Levy Stephen Welch Debra L. Richardson Eva Guerra Giovanni Scambia Stéphanie Henry Pauline Wimberger David S. Miller Jaroslav Klát Jerónimo Martínez Francesco Raspagliesi Bhavana Pothuri Ignacio Romero Alice Bergamini Brian M. Slomovitz Fabienne Schochter Estrid Høgdall Lorena Fariñas-Madrid Bradley J. Monk Dayana Michel Michael Kauffman Sharon Shacham Mansoor Raza Mirza Vicky Makker Ignace Vergote Toon Van Gorp Isabelle Cadron Annelore Barbeaux Nathalie Cornez Stéphanie Henry Joseph Kerger Debbie Debaere Hannelore Denys Mansoor Raza Mirza Amit M. Oza Lucy Gilbert Stephen Welch Michael Kolinsky Qi Zhou Jing Wang Yingjie Yang Kaijia Tu Li Wang Danbo Wang Ge Lou Xiaojian Yan Jiaxin Yang David Cibula Jaroslav Klát Bohuslav Melichar Michal Zikán Klaudia Reginacova Vít Weinberger Jalid Sehouli Pauline Wimberger Dirk Bauerschlag Fabian Trillsch Oliver Tomé Fabienne Schochter Marco Johannes Battista Bahriye Aktas Kristina Luebbe Mustafa Deryal George Fountzilas Athina Christopoulou Christos Papadimitriou Flora Zagouri Limor Helpman Tamar Safra Tally Levy Ilan Bruchim Ora Rosengarten Aviad Zick Giorgio Valabrega Giovanni Scambia Giorgia Mangili Francesco Raspagliesi Carmela Pisano Donata Sartori Ugo De Giorgi José Alejandro Pérez Fidalgo César Gómez-Raposo Ignacio Romero María Iglesias Ana Santaballa Nerea Ancizar Purificación Estévez Constanza Maximiano A. Yubero Ana Oaknin Eva Guerra Lydia Gaba Jerónimo Martínez

PURPOSE Selinexor inhibits exportin-1 (XPO1) resulting in nuclear accumulation of tumor suppressor proteins including p53 and has clinical activity endometrial cancer (EC). The primary end point was to assess progression-free survival (PFS) with once-weekly oral selinexor patients advanced or recurrent EC. PATIENTS AND METHODS ENGOT-EN5/GOG-3055/SIENDO a randomized, prospective, multicenter, double-blind, placebo-controlled, phase III study at 107 sites 10 countries. Patients 18 years older...

10.1200/jco.22.02906 article EN cc-by-nc-nd Journal of Clinical Oncology 2023-09-05

Most metastatic melanoma patients treated with BRAF inhibitors (BRAFi) ± MEK (MEKi) eventually progress on treatment. Along acquired resistance due to genetic changes, epigenetic mechanisms that could be reversed after BRAFi discontinuation have been described. The purpose of this study was analyse retrospectively outcomes for retreated BRAF-directed therapy.One hundred sixteen who received BRAFi-based therapy and, a break, were rechallenged MEKi at 14 centres in Europe, US and Australia...

10.1016/j.ejca.2017.12.007 article EN cc-by-nc-nd European Journal of Cancer 2018-01-19

Although chemotherapy is the cornerstone treatment for patients with metastatic colorectal cancer (mCRC), acquired chemoresistance common and constitutes main reason failure. Monoclonal antibodies against insulin-like growth factor-1 receptor (IGF-1R) have been tested in pre-treated mCRC patients, but results largely deceiving. We analysed time to progression, overall survival, mutational status of RAS, BRAF nuclear p-IGF-1R expression by immunohistochemistry, 470 CRC patients. The effect...

10.1038/bjc.2017.279 article EN cc-by-nc-sa British Journal of Cancer 2017-11-09

The PRIMA/ENGOT-OV26/GOG-3012 (NCT02655016) trial was amended to prospectively evaluate the safety and efficacy of an individualized starting dose (ISD) regimen niraparib for first-line maintenance therapy in patients with newly diagnosed advanced ovarian cancer.In phase 3 PRIMA trial, cancer a complete/partial response platinum-based chemotherapy (N = 733) were initially treated fixed (FSD) 300 mg once daily. Subsequently, protocol so enrolled received ISD: 200 daily baseline body weight <...

10.1002/cncr.34706 article EN cc-by-nc-nd Cancer 2023-04-14

ObjectiveTo assess patient-reported health-related quality of life (HRQoL) in patients with ovarian cancer (OC) who received niraparib as first-line maintenance therapy.MethodsPRIMA/ENGOT-OV26/GOG-3012 (NCT02655016) enrolled newly diagnosed advanced OC responded to platinum-based chemotherapy. Patients were randomized (2:1) or placebo once daily 28-day cycles until disease progression, intolerable toxicity, death. HRQoL was assessed a prespecified secondary end point using responses the...

10.1016/j.ygyno.2024.01.021 article EN cc-by Gynecologic Oncology 2024-02-06

Abstract Introduction Immune check-point inhibitors (ICI) were a major breakthrough in cancer care, but optimal patient selection remains elusive most tumors. Methods Overall 173 adult patients with metastatic solid tumors candidates to ICI clinical trials at our Institution prospectively recruited. Blood samples collected cycle 1 (C1D1) and 2 (C2D1) until the occurrence of progressive disease (PD). C1D1 LIPI, RMH, PMHI, NLR, dNLR, PIPO GRIm prognostic scores calculated. The primary endpoint...

10.1007/s00262-024-03933-w article EN cc-by Cancer Immunology Immunotherapy 2025-02-01

Abstract Purpose Sex influences chemotherapy-induced nausea and vomiting (CINV). However, in clinical practice, males females receive the same antiemetic prophylaxis. We compared CINV between sexes patients with different emetic risk schemes evaluated predisposing factors main adverse effects caused by antiemetics. Methods Prospective observational study conducted a tertiary-care hospital from February 2023 to May 2024 starting chemotherapy or new treatment line. was using MASCC tool, acute...

10.1007/s00520-025-09319-7 article EN cc-by Supportive Care in Cancer 2025-03-10

PURPOSE This phase IIb, single-arm, multicenter, global study (ADAGIO; ClinicalTrials.gov identifier: NCT04590248 ) assessed the efficacy and safety of adavosertib in patients with recurrent/persistent uterine serous carcinoma (USC) who had previously received platinum-based chemotherapy. METHODS Eligible were age 18 years older histologically confirmed USC, treated at least one chemotherapy regimen, evidence measurable disease. Adavosertib was administered orally 300 mg once daily on days...

10.1200/jco-24-01606 article EN Journal of Clinical Oncology 2025-04-22

(1) OBJECTIVE: To assess the performance of CA125, HE4, ROMA index and CPH-I to preoperatively identify epithelial ovarian cancer (EOC) or metastatic in ovary (MCO). (2) METHODS: single center retrospective study, including women with a diagnosis adnexal mass. We obtained AUC, sensitivity, specificity predictive values were for EOC MCO. Subgroup analysis harboring masses inconclusive malignancy by ultrasound features Stage I was performed. (3) RESULTS: 1071 patients included, 852 (79.6%)...

10.3390/diagnostics12010226 article EN cc-by Diagnostics 2022-01-17

Endometrial cancer (EC) is the second most common gynecological malignancy worldwide, first in developed countries [Sung et al. CA Cancer J Clin 71:209-249, 2021]. Although a majority diagnosed at an early stage with low risk of relapse, important proportion patients will relapse. Better knowledge molecular abnormalities crucial to identify high-risk groups stages as well for recurrent or metastatic disease whom adjuvant treatment must be personalized. The objective this guide summarize...

10.1007/s12094-022-02799-7 article EN cc-by Clinical & Translational Oncology 2022-03-21

Abstract In recent years, the incorporation of new strategies to therapeutic armamentarium has completely changed outcomes epithelial ovarian cancer (EOC). The identification predictive and prognostic biomarkers also enabled selection those patients more likely respond targeted agents. Nevertheless, EOC is still a highly lethal disease resistance many these agents common. objective this guideline summarize most relevant manage EOC, help clinician throughout challenging diagnostic processes...

10.1007/s12094-024-03531-3 article EN cc-by Clinical & Translational Oncology 2024-07-15

6050 Background: Niraparib is approved at a fixed starting dose (FSD) of 300 mg QD for maintenance treatment patients (pts) with recurrent ovarian cancer (OC) achieving complete or partial response to platinum-based chemotherapy based in the ENGOT-OV16/NOVA study. A post-hoc analysis NOVA showed baseline bodyweight (BW) and platelet count (PC) were predictive hematologic toxicities reductions. Following this analysis, PRIMA/ENGOT-OV26/GOG-3012 study was amended prospectively evaluate safety...

10.1200/jco.2020.38.15_suppl.6050 article EN Journal of Clinical Oncology 2020-05-20

Background: Despite impressive progression-free survival (PFS) results from PARP inhibitors (PARPi) in ovarian cancer, concerns about their effect on post-progression treatment outcomes have recently arisen, particularly when administered the relapsed setting. Overlapping mechanisms of resistance between PARPi and platinum been described, optimal therapies upon progression to are unknown. We communicate real-world data (RWD) subsequent chemotherapy used as maintenance cancer relapses,...

10.3390/cancers14184414 article EN Cancers 2022-09-11
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