TY - JOUR
T1 - Effect of concomitant medications with immune-modulatory properties on the outcomes of patients with advanced cancer treated with immune checkpoint inhibitors
T2 - development and validation of a novel prognostic index
AU - Buti, Sebastiano
AU - Bersanelli, Melissa
AU - Perrone, Fabiana
AU - Tiseo, Marcello
AU - Tucci, Marco
AU - Adamo, Vincenzo
AU - Stucci, Luigia S.
AU - Russo, Alessandro
AU - Tanda, Enrica T.
AU - Spagnolo, Francesco
AU - Rastelli, Francesca
AU - Pergolesi, Federica
AU - Santini, Daniele
AU - Russano, Marco
AU - Anesi, Cecilia
AU - Giusti, Raffaele
AU - Filetti, Marco
AU - Marchetti, Paolo
AU - Botticelli, Andrea
AU - Gelibter, Alain
AU - Occhipinti, Mario Alberto
AU - Ferrari, Marco
AU - Vitale, Maria Giuseppa
AU - Nicolardi, Linda
AU - Chiari, Rita
AU - Rijavec, Erika
AU - Nigro, Olga
AU - Tuzi, Alessandro
AU - De Tursi, Michele
AU - Di Marino, Pietro
AU - Conforti, Fabio
AU - Queirolo, Paola
AU - Bracarda, Sergio
AU - Macrini, Serena
AU - Gori, Stefania
AU - Zoratto, Federica
AU - Veltri, Enzo
AU - Di Cocco, Barbara
AU - Mallardo, Domenico
AU - Vitale, Maria Grazia
AU - Santoni, Matteo
AU - Patruno, Leonardo
AU - Porzio, Giampiero
AU - Ficorella, Corrado
AU - Pinato, David J.
AU - Ascierto, Paolo A.
AU - Cortellini, Alessio
N1 - Publisher Copyright:
© 2020 Elsevier Ltd
PY - 2021/1
Y1 - 2021/1
N2 - Background: Concomitant medications are known to impact on clinical outcomes of patients treated with immune checkpoint inhibitors (ICIs). We aimed weighing the role of different concomitant baseline medications to create a drug-based prognostic score. Methods: We evaluated concomitant baseline medications at immunotherapy initiation for their impact on objective response rate (ORR), progression-free survival (PFS) and overall survival (OS) in a single-institution cohort of patients with advanced cancer treated with ICIs (training cohort, N = 217), and a drug-based prognostic score with the drugs resulting significantly impacting the OS was computed. Secondly, we externally validated the score in a large multicenter external cohort (n = 1012). Results: In the training cohort (n = 217), the median age was 69 years (range: 32–89), and the primary tumours were non–small-cell lung cancer (70%), melanoma (14.7%), renal cell carcinoma (9.2%) and others (6%). Among baseline medications, corticosteroids (hazard ratio [HR] = 2.3; 95% confidence interval [CI]: 1.60–3.30), systemic antibiotics (HR = 2.07; 95% CI: 1.31–3.25) and proton-pump inhibitors (PPIs) (HR = 1.57; 95% CI: 1.13–2.18) were significantly associated with OS. The prognostic score was calculated using these three drug classes, defining good, intermediate and poor prognosis patients. Within the training cohort, OS (p < 0.0001), PFS (p < 0.0001) and ORR (p = 0.0297) were significantly distinguished by the score stratification. The prognostic value of the score was also demonstrated in terms of OS (p < 0.0001), PFS (p < 0.0001) and ORR (p = 0.0006) within the external cohort. Conclusion: Cumulative exposure to corticosteroids, antibiotics and PPIs (three likely microbiota-modulating drugs) leads to progressively worse outcomes after ICI therapy. We propose a simple score that can help stratifying patients in routine practice and clinical trials of ICIs.
AB - Background: Concomitant medications are known to impact on clinical outcomes of patients treated with immune checkpoint inhibitors (ICIs). We aimed weighing the role of different concomitant baseline medications to create a drug-based prognostic score. Methods: We evaluated concomitant baseline medications at immunotherapy initiation for their impact on objective response rate (ORR), progression-free survival (PFS) and overall survival (OS) in a single-institution cohort of patients with advanced cancer treated with ICIs (training cohort, N = 217), and a drug-based prognostic score with the drugs resulting significantly impacting the OS was computed. Secondly, we externally validated the score in a large multicenter external cohort (n = 1012). Results: In the training cohort (n = 217), the median age was 69 years (range: 32–89), and the primary tumours were non–small-cell lung cancer (70%), melanoma (14.7%), renal cell carcinoma (9.2%) and others (6%). Among baseline medications, corticosteroids (hazard ratio [HR] = 2.3; 95% confidence interval [CI]: 1.60–3.30), systemic antibiotics (HR = 2.07; 95% CI: 1.31–3.25) and proton-pump inhibitors (PPIs) (HR = 1.57; 95% CI: 1.13–2.18) were significantly associated with OS. The prognostic score was calculated using these three drug classes, defining good, intermediate and poor prognosis patients. Within the training cohort, OS (p < 0.0001), PFS (p < 0.0001) and ORR (p = 0.0297) were significantly distinguished by the score stratification. The prognostic value of the score was also demonstrated in terms of OS (p < 0.0001), PFS (p < 0.0001) and ORR (p = 0.0006) within the external cohort. Conclusion: Cumulative exposure to corticosteroids, antibiotics and PPIs (three likely microbiota-modulating drugs) leads to progressively worse outcomes after ICI therapy. We propose a simple score that can help stratifying patients in routine practice and clinical trials of ICIs.
KW - Antibiotics
KW - Cancer patients
KW - Concomitant medications
KW - Corticosteroids
KW - Drugs
KW - Immune checkpoint inhibitors
KW - Immunotherapy
KW - Index
KW - Prognostic
KW - Proton-pump inhibitors
KW - Score
UR - http://www.scopus.com/inward/record.url?scp=85096157545&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2020.09.033
DO - 10.1016/j.ejca.2020.09.033
M3 - Article
SN - 0959-8049
VL - 142
SP - 18
EP - 28
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -