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Antibiotic-exposed patients with non-small-cell lung cancer preserve efficacy outcomes following first-line chemo-immunotherapy.
Cortellini, A; Ricciuti, B; Facchinetti, F; Alessi, J V M; Venkatraman, D; Dall'Olio, F G; Cravero, P; Vaz, V R; Ottaviani, D; Majem, M; Piedra, A; Sullivan, I; Lee, K A; Lamberti, G; Hussain, N; Clark, J; Bolina, A; Barba, A; Benitez, J C; Gorría, T; Mezquita, L; Hoton, D; Aboubakar Nana, F; Besse, B; Awad, M M; Pinato, D J.
Afiliação
  • Cortellini A; Department of Biotechnology and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy; Division of Cancer, Department of Surgery and Cancer, Imperial College London, Hammersmith Hospital, London, UK. Electronic address: a.cortellini@imperial.ac.uk.
  • Ricciuti B; Lowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, USA.
  • Facchinetti F; Université Paris-Saclay, Institut Gustave Roussy, Inserm, Biomarqueurs Prédictifs et Nouvelles Stratégies Thérapeutiques en Oncologie, Villejuif, France.
  • Alessi JVM; Lowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, USA.
  • Venkatraman D; Lowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, USA.
  • Dall'Olio FG; Cancer Medicine Department, Gustave Roussy, Villejuif, France.
  • Cravero P; Lowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, USA.
  • Vaz VR; Lowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, USA.
  • Ottaviani D; Cancer Division, University College London Hospitals, London, UK.
  • Majem M; Medical Oncology Department, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.
  • Piedra A; Medical Oncology Department, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.
  • Sullivan I; Medical Oncology Department, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.
  • Lee KA; Department of Medical Oncology, Royal Marsden Hospital, London, UK; Department of Twin Research and Genetic Epidemiology, St Thomas's Hospital, King's College London, London, UK.
  • Lamberti G; Department of Experimental, Diagnostic and Specialty Medicine, S. Orsola-Malpighi University Hospital, Alma Mater Studiorum University of Bologna, Bologna, Italy.
  • Hussain N; Division of Cancer, Department of Surgery and Cancer, Imperial College London, Hammersmith Hospital, London, UK.
  • Clark J; Division of Cancer, Department of Surgery and Cancer, Imperial College London, Hammersmith Hospital, London, UK.
  • Bolina A; Division of Cancer, Department of Surgery and Cancer, Imperial College London, Hammersmith Hospital, London, UK.
  • Barba A; Medical Oncology Department, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.
  • Benitez JC; Cancer Medicine Department, Gustave Roussy, Villejuif, France.
  • Gorría T; Department of Medical Oncology, Hospital Clinic, Barcelona, Spain.
  • Mezquita L; Department of Medical Oncology, Hospital Clinic, Barcelona, Spain.
  • Hoton D; Department of Pathology, Cliniques universitaires Saint-Luc, Brussels, Belgium.
  • Aboubakar Nana F; Institut de Recherche Expérimentale et Clinique (IREC), Pôle de Pneumologie, ORL et Dermatologie (PNEU), Université catholique de Louvain (UCLouvain), Brussels, Belgium.
  • Besse B; Cancer Medicine Department, Gustave Roussy, Villejuif, France; University Paris-Saclay, School of Medicine, Villejuif, France.
  • Awad MM; Lowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, USA.
  • Pinato DJ; Division of Cancer, Department of Surgery and Cancer, Imperial College London, Hammersmith Hospital, London, UK; Division of Oncology, Department of Translational Medicine, University of Piemonte Orientale, Novara, Italy.
Ann Oncol ; 32(11): 1391-1399, 2021 11.
Article em En | MEDLINE | ID: mdl-34400292
ABSTRACT

BACKGROUND:

Prior antibiotic therapy (pATB) is known to impair efficacy of single-agent immune checkpoint inhibitors (ICIs), potentially through the induction of gut dysbiosis. Whether ATB also affects outcomes to chemo-immunotherapy combinations is still unknown. PATIENTS AND

METHODS:

In this international multicentre study, we evaluated the association between pATB, concurrent ATB (cATB) and overall survival (OS), progression-free survival (PFS) and objective response rate (ORR) in patients with non-small-cell lung cancer (NSCLC) treated with first-line chemo-immunotherapy at eight referral institutions.

RESULTS:

Among 302 patients with stage IV NSCLC, 216 (71.5%) and 61 (20.2%) patients were former and current smokers, respectively. Programmed death-ligand 1 tumour expression in assessable patients (274, 90.7%) was ≥50% in 76 (25.2%), 1%-49% in 84 (27.9%) and <1% in 113 (37.5%). Multivariable analysis showed pATB-exposed patients to have similar OS {hazard ratio (HR) = 1.42 [95% confidence interval (CI) 0.91-2.22]; P = 0.1207} and PFS [HR = 1.12 (95% CI 0.76-1.63); P = 0.5552], compared to unexposed patients, regardless of performance status. Similarly, no difference with respect to ORR was found across pATB exposure groups (42.6% versus 57.4%, P = 0.1794). No differential effect was found depending on pATB exposure duration (≥7 versus <7 days) and route of administration (intravenous versus oral). Similarly, cATB was not associated with OS [HR = 1.29 (95% CI 0.91-1.84); P = 0.149] and PFS [HR = 1.20 (95% CI 0.89-1.63); P = 0.222] when evaluated as time-varying covariate in multivariable analysis.

CONCLUSIONS:

In contrast to what has been reported in patients receiving single-agent ICIs, pATB does not impair clinical outcomes to first-line chemo-immunotherapy of patients with NSCLC. pATB status should integrate currently available clinico-pathologic factors for guiding first-line treatment decisions, whilst there should be no concern in offering cATB during chemo-immunotherapy when needed.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares / Antibacterianos Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares / Antibacterianos Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2021 Tipo de documento: Article