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Time to strategy failure and treatment beyond progression in pretreated metastatic renal cell carcinoma patients receiving nivolumab: post-hoc analysis of the Meet-URO 15 study.
Murianni, Veronica; Signori, Alessio; Buti, Sebastiano; Rebuzzi, Sara Elena; Bimbatti, Davide; De Giorgi, Ugo; Chiellino, Silvia; Galli, Luca; Zucali, Paolo Andrea; Masini, Cristina; Naglieri, Emanuele; Procopio, Giuseppe; Milella, Michele; Fratino, Lucia; Baldessari, Cinzia; Ricotta, Riccardo; Mollica, Veronica; Sorarù, Mariella; Tudini, Marianna; Prati, Veronica; Malgeri, Andrea; Atzori, Francesco; Di Napoli, Marilena; Caffo, Orazio; Spada, Massimiliano; Morelli, Franco; Prati, Giuseppe; Nolè, Franco; Vignani, Francesca; Cavo, Alessia; Lipari, Helga; Roviello, Giandomenico; Catalano, Fabio; Damassi, Alessandra; Cremante, Malvina; Rescigno, Pasquale; Fornarini, Giuseppe; Banna, Giuseppe Luigi.
Afiliação
  • Murianni V; Medical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
  • Signori A; Department of Health Sciences (DISSAL), Section of Biostatistics, University of Genoa, Genoa, Italy.
  • Buti S; Medical Oncology Unit, University Hospital of Parma, Parma, Italy.
  • Rebuzzi SE; Department of Medicine and Surgery, University of Parma, Parma, Italy.
  • Bimbatti D; Medical Oncology Unit, Ospedale San Paolo, Savona, Italy.
  • De Giorgi U; Department of Internal Medicine and Medical Specialties (Di.M.I.), University of Genoa, Genoa, Italy.
  • Chiellino S; Oncologia 1, Istituto Oncologico Veneto, IOV - IRCCS, Padova, Italy.
  • Galli L; Medical Oncology Department, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
  • Zucali PA; Medical Oncology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Masini C; Medical Oncology 2, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.
  • Naglieri E; Department of Oncology, IRCCS, Humanitas Clinical and Research Center, Department of Biochemical Sciences, Humanitas University, Milano, Italy.
  • Procopio G; Medical Oncology, AUSL - IRCCS di Reggio Emilia, Reggio Emilia, Italy.
  • Milella M; U.O. Oncologia, IRCCS Istituto Tumori Giovanni Paolo II, Bari, Italy.
  • Fratino L; Medical Oncology, Fondazione IRCCS - Istituto Nazionale dei Tumori, Milano, Italy.
  • Baldessari C; Department of Medical Oncology, Azienda Ospedaliera Universitaria Integrata di Verona, Verona, Italy.
  • Ricotta R; Department of Medical Oncology, CRO Aviano - Centro di Riferimento Oncologico IRCCS, Aviano, Italy.
  • Mollica V; Department of Oncology and Hematology - Oncology Unit, Azienda Ospedaliera Universitaria di Modena, Modena, Italy.
  • Sorarù M; Oncology Unit, IRCCS MultiMedica, Sesto San Giovanni, Milano, Italy.
  • Tudini M; Medical Oncology, IRCCS - Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
  • Prati V; U.O.C. Medical Oncology, Ospedale Camposampiero, Padova, Italy.
  • Malgeri A; Medical Oncology, Osp. San Salvatore, ASL1 Avezzano Sulmona, L'Aquila, Italy.
  • Atzori F; Oncology Unit, Ospedale Michele e Pietro Ferrero, Verduno, Italy.
  • Di Napoli M; Medical Oncology Unit, Policlinico Universitario Campus Bio Medico, Roma, Italy.
  • Caffo O; Medical Oncology Department, University Hospital, University of Cagliari, Cagliari, Italy.
  • Spada M; Department of Urology and Gynecology, Istituto Nazionale Tumori IRCCS Fondazione G. Pascale, Napoli, Italy.
  • Morelli F; Medical Oncology, Ospedale S. Chiara, Trento, Italy.
  • Prati G; UOC Oncology, Fondazione Istituto San Raffaele Giglio di Cefalù, Cefalù, Italy.
  • Nolè F; Medical Oncology Department, Casa Sollievo Della Sofferenza Hospital, IRCCS, San Giovanni Rotondo, Italy.
  • Vignani F; Azienda Unità Sanitaria Locale - IRCCS di Reggio Emilia, Reggio Emilia, Italy.
  • Cavo A; Medical Oncology Division of Urogenital & Head & Neck Tumors, IEO, European Institute of Oncology IRCCS, Milano, Italy.
  • Lipari H; Division of Medical Oncology, Ordine Mauriziano Hospital, Torino, Italy.
  • Roviello G; Oncology Unit, Villa Scassi Hospital, Genoa, Italy.
  • Catalano F; Medical Oncology, Azienda Ospedaliera per l'Emergenza Cannizzaro, Catania, Italy.
  • Damassi A; Department of Health Sciences, Section of Clinical Pharmacology and Oncology, University of Firenze, Firenze, Italy.
  • Cremante M; Medical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
  • Rescigno P; Medical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
  • Fornarini G; Medical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
  • Banna GL; Translationsal and Clinical Research Institute, Centre for Cancer, Newcastle University, Newcastle Upon Tyne, United Kingdom.
Front Oncol ; 14: 1307635, 2024.
Article em En | MEDLINE | ID: mdl-38410103
ABSTRACT

Background:

Immunotherapies exhibit peculiar cancer response patterns in contrast to chemotherapy and targeted therapy. Some patients experience disease response after initial progression or durable responses after treatment interruption. In clinical practice, immune checkpoint inhibitors may be continued after radiological progression if clinical benefit is observed. As a result, estimating progression-free survival (PFS) based on the first disease progression may not accurately reflect the actual benefit of immunotherapy.

Methods:

The Meet-URO 15 study was a multicenter retrospective analysis of 571 pretreated metastatic renal cell carcinoma (mRCC) patients receiving nivolumab. Time to strategy failure (TSF) was defined as the interval from the start of immunotherapy to definitive disease progression or death. This post-hoc analysis compared TSF to PFS and assess the response and survival outcomes between patients treatated beyond progression (TBP) and non-TBP. Moreover, we evaluated the prognostic accuracy of the Meet-URO score versus the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) score based on TSF and PFS.

Results:

Overall, 571 mRCC patients were included in the analysis. Median TSF was 8.6 months (95% CI 7.0 - 10.1), while mPFS was 7.0 months (95% CI 5.7 - 8.5). TBP patients (N = 93) had significantly longer TSF (16.3 vs 5.5 months; p < 0.001) and overall survival (OS) (34.8 vs 17.9 months; p < 0.001) but similar PFS compared to non-TBP patients. In TBP patients, a median delay of 9.6 months (range 6.7-16.3) from the first to the definitive disease progression was observed, whereas non-TBP patients had overlapped median TSF and PFS (5.5 months). Moreover, TBP patients had a trend toward a higher overall response rate (33.3% vs 24.3%; p = 0.075) and disease control rate (61.3% vs 55.5%; p = 0.31). Finally, in the whole population the Meet-URO score outperformed the IMDC score in predicting both TSF (c-index 0.63 vs 0.59) and PFS (0.62 vs 0.59).

Conclusion:

We found a 2-month difference between mTSF and mPFS in mRCC patients receiving nivolumab. However, TBP patients had better outcomes, including significantly longer TSF and OS than non-TBP patients. The Meet-URO score is a reliable predictor of TSF and PFS.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália