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ePoster Display

696P - Is it possible to improve the prognostic ability of the IMDC score? Validation of the Meet-URO score in metastatic renal cell carcinoma (mRCC) patients (pts) receiving first-line nivolumab plus ipilimumab in the Italian Expanded Access Program (EAP)

Date

16 Sep 2021

Session

ePoster Display

Topics

Clinical Research;  Targeted Therapy;  Immunotherapy

Tumour Site

Renal Cell Cancer

Presenters

Sara Elena Rebuzzi

Citation

Annals of Oncology (2021) 32 (suppl_5): S678-S724. 10.1016/annonc/annonc675

Authors

S.E. Rebuzzi1, A. Signori2, M. Maruzzo3, G. Tortora4, L. Galli5, M. Rizzo6, U. De Giorgi7, L. Antonuzzo8, S. Bracarda9, G. Cartenì10, F. Atzori11, S. Tamberi12, G. Procopio13, L. Fratino14, M. Santoni15, C. Baldessari16, A. Astone17, F. Calabro'18, S. Buti19, G. Fornarini20

Author affiliations

  • 1 Department Of Internal Medicine And Medical Specialties (di.m.i.), University Of Genova, IRCCS Ospedale Policlinico San Martino, Medical Oncology Unit 1, 16132 - Genova/IT
  • 2 Department Of Health Sciences, Section Of Biostatistics, University of Genova, Genova/IT
  • 3 Medical Oncology Unit 1, Department Of Oncology, Istituto Oncologico Veneto IOV IRCCS, Padua/IT
  • 4 Medical Oncology, Fondazione Policlinico Universitario A. Gemelli, IRCCS, Università Cattolica Del Sacro Cuore, Rome/IT
  • 5 Medical Oncology Unit 2, Azienda Ospedaliera Universitaria Pisana, Pisa/IT
  • 6 Division Of Translational Oncology I, IRCCS Istituti Clinici Scientifici Maugeri, Pavia/IT
  • 7 Department Of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori" - IRST, Meldola/IT
  • 8 Clinical Oncology Unit, Careggi University Hospital, Firenze/IT
  • 9 Medical And Translational Oncology, Department Of Oncology, Azienda Ospedaliera Santa Maria, Terni/IT
  • 10 Division Of Oncology, Azienda Ospedaliera di Rilievo Nazionale A. Cardarelli, Napoli/IT
  • 11 Medical Oncology Department, University Hospital, University of Cagliari, Monserrato/IT
  • 12 Oncology Unit, Ospedale "degli Infermi", Faenza/IT
  • 13 Ss Oncologia Medica Genitourinaria, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano/IT
  • 14 Department Of Medical Oncology, Centro di Riferimento Oncologico di Aviano CRO-IRCCS, Aviano/IT
  • 15 Oncology Unit, Macerata Hospital, Macerata/IT
  • 16 Medical Oncology Unit, Department Of Oncology And Hemathology, University Hospital of Modena, Modena/IT
  • 17 Division Of Medical Oncology, Fatebenefratelli San Pietro Hospital, Rome/IT
  • 18 Division Of Medical Oncology B, San Camillo Forlanini Hospital, Rome/IT
  • 19 Medical Oncology Unit, University Hospital of Parma, Parma/IT
  • 20 Medical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genova/IT

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Abstract 696P

Background

The combination of neutrophil-to-lymphocyte ratio (NLR), IMDC score and bone metastases ini the Meet-URO score has shown to better stratify mRCC pts receiving ≥2nd line nivolumab compared with the IMDC score identifying five distinctive prognostic groups [Ther Adv Med Oncol 2021, available at: http://bit.ly/Meet-URO15_score]. This score is an easy tool for clinical practice at no additional costs and its application on first-line immune-combination therapies is highly awaited.

Methods

The real-world series of IMDC intermediate-poor risk mRCC pts receiving first-line nivolumab plus ipilimumab in the Italian EAP was analysed. Baseline NLR, IMDC score and the presence of bone metastases were assessed. The primary endpoint was overall survival (OS). The Harrell’s c-index was calculated to compare accuracy of Meet-URO and IMDC scores, as the capability of the prognostic score to be predictive of OS.

Results

306 mRCC pts were analysed with mOS not reached, OS at 1 year (1y-OS) of 66.8% and median progression-free survival (mPFS) of 8.4 months (mo). Median follow-up was 12.7 mo. According to the IMDC score, intermediate (67.3%) and poor-risk (32.7%) pts had an 1y-OS of 77.3% and 42.2% (p<0.001) and a mPFS of 10.4 and 3.3 mo (p<0.001), respectively. Applying the Meet-URO score to the population, two prognostic groups showed overlapping survival curves (probably due to the absence of the favorable-risk group) so that the original five groups of the Meet URO score were merged in four prognostic groups: group 1-2 (29.1%), group 3 (28.8%), group 4 (33.0%) and group 5 (9.1%) characterised by distinctive 1y-OS: 91.6%, 71.8%, 50% and 21.2%, respectively (p < 0.001). These groups had also distinctive mPFS: 16.6, 7.5, 4.9 and 1.8 mo respectively (p<0.001). The Meet-URO score had a higher discriminative ability compared with the IMDC score alone (c-index of 0.72 vs 0.65) in terms of OS.

Conclusions

This analysis showed the prognostic role of the Meet-URO score also in mRCC pts treated with first-line immune-combination and its higher accuracy in survival stratification compared with the standard IMDC score.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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