Inflammatory indices and clinical factors in metastatic renal cell carcinoma patients treated with nivolumab: the development of a novel prognostic score (Meet-URO 15 study).

biomarkers clinical factors immune checkpoint inhibitor immunotherapy prognostic score renal cell carcinoma

Journal

Therapeutic advances in medical oncology
ISSN: 1758-8340
Titre abrégé: Ther Adv Med Oncol
Pays: England
ID NLM: 101510808

Informations de publication

Date de publication:
2021
Historique:
received: 15 01 2021
accepted: 05 05 2021
entrez: 28 5 2021
pubmed: 29 5 2021
medline: 29 5 2021
Statut: epublish

Résumé

Despite the survival advantage, not all metastatic renal cell carcinoma (mRCC) patients achieve a long-term benefit from immunotherapy. Moreover, the identification of prognostic biomarkers is still an unmet clinical need. This multicenter retrospective study investigated the prognostic role of peripheral-blood inflammatory indices and clinical factors to develop a novel prognostic score in mRCC patients receiving at least second-line nivolumab. The complete blood count before the first cycle of therapy was assessed by calculating neutrophil-to-lymphocyte ratio (NLR), derived NLR (dNLR), lymphocyte-to-monocyte ratio (LMR), platelet-to-lymphocyte ratio (PLR), systemic inflammation index (SII), and systemic inflammation response index (SIRI). Clinical factors included pre-treatment International Metastatic RCC Database Consortium (IMDC) score, line of therapy, and metastatic sites. From October 2015 to November 2019, 571 mRCC patients received nivolumab as second- and further-line treatment in 69% and 31% of cases. In univariable and multivariable analyses all inflammatory indices, IMDC score, and bone metastases significantly correlated with overall survival (OS). The multivariable model with NLR, IMDC score, and bone metastases had the highest c-index (0.697) and was chosen for the developing of the score (Schneeweiss scoring system). After internal validation (bootstrap re-sampling), the final index (Meet-URO score) composed by NLR, IMDC score, and bone metastases had a c-index of 0.691. It identified five categories with distinctive OSs: group 1 (median OS - mOS = not reached), group 2 (mOS = 43.9 months), group 3 (mOS = 22.4 months), group 4 (mOS = 10.3 months), and group 5 (mOS = 3.2 months). Moreover, the Meet-URO score allowed for a fine risk-stratification across all three IMDC groups. The Meet-URO score allowed for the accurate stratification of pretreated mRCC patients receiving nivolumab and is easily applicable for clinical practice at no additional cost. Future steps include its external validation, the assessment of its predictivity, and its application to first-line combinations.

Sections du résumé

BACKGROUND BACKGROUND
Despite the survival advantage, not all metastatic renal cell carcinoma (mRCC) patients achieve a long-term benefit from immunotherapy. Moreover, the identification of prognostic biomarkers is still an unmet clinical need.
METHODS METHODS
This multicenter retrospective study investigated the prognostic role of peripheral-blood inflammatory indices and clinical factors to develop a novel prognostic score in mRCC patients receiving at least second-line nivolumab. The complete blood count before the first cycle of therapy was assessed by calculating neutrophil-to-lymphocyte ratio (NLR), derived NLR (dNLR), lymphocyte-to-monocyte ratio (LMR), platelet-to-lymphocyte ratio (PLR), systemic inflammation index (SII), and systemic inflammation response index (SIRI). Clinical factors included pre-treatment International Metastatic RCC Database Consortium (IMDC) score, line of therapy, and metastatic sites.
RESULTS RESULTS
From October 2015 to November 2019, 571 mRCC patients received nivolumab as second- and further-line treatment in 69% and 31% of cases. In univariable and multivariable analyses all inflammatory indices, IMDC score, and bone metastases significantly correlated with overall survival (OS). The multivariable model with NLR, IMDC score, and bone metastases had the highest c-index (0.697) and was chosen for the developing of the score (Schneeweiss scoring system). After internal validation (bootstrap re-sampling), the final index (Meet-URO score) composed by NLR, IMDC score, and bone metastases had a c-index of 0.691. It identified five categories with distinctive OSs: group 1 (median OS - mOS = not reached), group 2 (mOS = 43.9 months), group 3 (mOS = 22.4 months), group 4 (mOS = 10.3 months), and group 5 (mOS = 3.2 months). Moreover, the Meet-URO score allowed for a fine risk-stratification across all three IMDC groups.
CONCLUSION CONCLUSIONS
The Meet-URO score allowed for the accurate stratification of pretreated mRCC patients receiving nivolumab and is easily applicable for clinical practice at no additional cost. Future steps include its external validation, the assessment of its predictivity, and its application to first-line combinations.

Identifiants

pubmed: 34046089
doi: 10.1177/17588359211019642
pii: 10.1177_17588359211019642
pmc: PMC8135208
doi:

Types de publication

Journal Article

Langues

eng

Pagination

17588359211019642

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© The Author(s), 2021.

Déclaration de conflit d'intérêts

Conflict of interest statement: Dr Fornarini services advisory boards for Astellas, Janssen, Pfizer, Bayer, MSD, and Merck, and received travel accommodation from Astellas, Janssen, and Bayer. Dr Buti received honoraria as a speaker at scientific events and in an advisory role by BMS, Pfizer; MSD, Ipsen, Roche, Eli Lilly, AstraZeneca, Pierre-Fabre, Novartis. Dr Banna reports personal fees from AstraZeneca, Janssen-Cilag, Boehringer Ingelheim, Roche, and non-financial support from Bristol-Myers Squibb, AstraZeneca, MedImmune, Pierre Fabre, IPSEN, outside the submitted work. Dr De Giorgi services as an advisory/board member of Astellas, Bayer, Bristol-Myers Squibb, IPSEN, Janssen, Merck, Pfizer, and Sanofi, received research grant/funding to the institution from AstraZeneca, Roche, Sanofi, and travel/accommodations/expenses from Bristol-Myers Squibb, IPSEN, Janssen, and Pfizer. Dr Zucali services advisory boards/consulting for Pfizer, Bristol-Myers Squibb, MSD, IPSEN, Novartis, Roche, Amgen, AstraZeneca, Sanofi, Janssen, and Astellas. Dr Masini received personal fees as a speaker from Astellas, as a consultant from IPSEN, MSD, and Janssen, and for travel accommodation from BMS, Pfizer, Astellas, Janssen, and IPSEN. Dr Procopio services advisory boards/consulting for Astellas, AstraZeneca, Bayer, Bristol-Myers Squibb, Janssen, IPSEN, Merk, MSD, Novartis, and Pfizer. Dr Cortellini receives speaker fees/grant consultancies from Astrazeneca, BMS, MSD, Roche, Novartis, and Astellas. Dr Morelli received grants from MSD and Pfizer. Dr Bersanelli received research funding to the institution from Roche, Pfizer, Seqirus UK, AstraZeneca, Bristol-Myers Squibb, Novartis, and Sanofi, and received personal fees for advisory role, copyright transfer, consultancies, and as speaker at scientific events from Sciclone Pharmaceuticals, Bristol-Myers Squibb, AstraZeneca, Pierre-Fabre, Novartis, and Pfizer. The other authors have no conflicts of interest to disclose.

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Auteurs

Sara Elena Rebuzzi (SE)

Medical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino of Genova, Largo Rosanna Benzi 10, Genova, 16132, Italy.

Alessio Signori (A)

Department of Health Sciences, Section of Biostatistics, University of Genova, Genova, Italy.

Giuseppe Luigi Banna (GL)

Department of Oncology, Portsmouth Hospitals University NHS Trust, Portsmouth, UK Cannizzaro Hospital, Catania, Italy.

Marco Maruzzo (M)

Medical Oncology 1 Unit, Department of Oncology, Istituto Oncologico Veneto IOV IRCCS, Padova, Italy.

Ugo De Giorgi (U)

Department of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.

Paolo Pedrazzoli (P)

Medical Oncology Unit, IRCCS Policlinico San Matteo, Pavia, Italy.

Andrea Sbrana (A)

Medical Oncology Unit 2, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.

Paolo Andrea Zucali (PA)

Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milano, Italy.

Cristina Masini (C)

Medical Oncology Unit, AUSL-IRCCS of Reggio Emilia, Reggio Emilia, Italy.

Emanuele Naglieri (E)

Division of Medical Oncology, IRCCS Istituto Tumori "Giovanni Paolo II", Bari, Italy.

Giuseppe Procopio (G)

SS Oncologia Medica Genitourinaria, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.

Sara Merler (S)

Department of Oncology, Azienda Ospedaliera Universitaria Integrata di Verona, University of Verona,Verona, Italy.

Laura Tomasello (L)

Academic Unit of Medical Oncology, IRCCS Ospedale Policlinico San Martino of Genova, Genova, Italy.

Lucia Fratino (L)

Department of Medical Oncology, Centro di Riferimento Oncologico di Aviano CRO-IRCCS, Aviano, Italy.

Cinzia Baldessari (C)

Medical Oncology Unit, Department of Oncology and Hemathology, University Hospital of Modena, Modena, Italy.

Riccardo Ricotta (R)

Niguarda Cancer Center, Grande Ospedale Metropolitano Niguarda, Milano, Italy.

Stefano Panni (S)

Medical Oncology Unit, ASST - Istituti Ospitalieri Cremona Hospital, Cremona, Italy.

Veronica Mollica (V)

Oncologia Medica, Azienda Ospedaliero-Universitaria of Bologna, Bologna, Italy.

Maria Sorarù (M)

U.O. Oncologia, Ospedale di Camposampiero, Italy.

Matteo Santoni (M)

Oncology Unit, Macerata Hospital, Macerata, Italy.

Alessio Cortellini (A)

Department of Biotechnology and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.

Veronica Prati (V)

Medical Oncology Unit, ASL CN 2, Alba-Bra, Italy.

Hector Josè Soto Parra (HJ)

Department of Oncology, Medical Oncology, University Hospital Policlinico-San Marco, Catania, Italy.

Marco Stellato (M)

Department of Medical Oncology, Università Campus Bio-Medico of Roma, Rome, Italy.

Francesco Atzori (F)

Medical Oncology Department, University Hospital, University of Cagliari, Cagliari, Italy.

Sandro Pignata (S)

Department of Urology and Gynecology, Istituto Nazionale Tumori IRCCS Fondazione G. Pascale, Napoli, Italy.

Carlo Messina (C)

Medical Oncology Department, Santa Chiara Hospital, Trento, Italy.

Marco Messina (M)

UOC Oncologia Medica, Istituto Fondazione G. Giglio, Cefalù, Italy.

Franco Morelli (F)

Medical Oncology Department, Casa Sollievo Della Sofferenza Hospital, IRCCS, San Giovanni Rotondo, Italy.

Giuseppe Prati (G)

Department of oncology and advanced technologies AUSL - IRCCS Reggio Emilia, Reggio Emilia, Italy.

Franco Nolè (F)

Medical Oncology Division of Urogenital & Head & Neck Tumors, IEO, European Institute of Oncology IRCCS, Milano, Italy.

Francesca Vignani (F)

Division of Medical Oncology, Ordine Mauriziano Hospital, Torino, Italy.

Alessia Cavo (A)

Oncology Unit, Villa Scassi Hospital, Genova, Italy.

Giandomenico Roviello (G)

Department of Health Sciences, Section of Clinical Pharmacology and Oncology, University of Firenze, Firenze, Italy.

Francesco Pierantoni (F)

Medical Oncology 1 Unit, Department of Oncology, Istituto Oncologico Veneto IOV IRCCS, Padova, Italy.

Chiara Casadei (C)

Department of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.

Melissa Bersanelli (M)

Medical Oncology Unit, University Hospital of Parma, Parma, Italy.

Silvia Chiellino (S)

Medical Oncology Unit, IRCCS Policlinico San Matteo, Pavia, Italy.

Federico Paolieri (F)

Medical Oncology Unit 2, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.

Matteo Perrino (M)

Department of Oncology, IRCCS, Humanitas Clinical and Research Center, Rozzano, Milano, Italy.

Matteo Brunelli (M)

Department of Diagnostics and Public Health, Pathology Unit, University and Hospital Trust of Verona, Verona, Italy.

Roberto Iacovelli (R)

Medical Oncology Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Camillo Porta (C)

Chair of Oncology, Department of Biomedical Sciences and Human Oncology, University of Bari 'A. Moro', Bari, Italy.

Sebastiano Buti (S)

Medical Oncology Unit, University Hospital of Parma, Parma, Italy.

Giuseppe Fornarini (G)

Medical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino of Genova, Genova, Italy.

Classifications MeSH