Efficacy and Safety of Pembrolizumab plus Axitinib combination for Metastatic Renal Cell Carcinoma in a Real-World Scenario: Data From the Prospective ProPAXI Study.

Axitinib First-line combination Pembrolizumab Prospective study Real world Renal cell carcinoma

Journal

Clinical genitourinary cancer
ISSN: 1938-0682
Titre abrégé: Clin Genitourin Cancer
Pays: United States
ID NLM: 101260955

Informations de publication

Date de publication:
14 Sep 2024
Historique:
received: 24 07 2024
revised: 01 09 2024
accepted: 07 09 2024
medline: 16 10 2024
pubmed: 16 10 2024
entrez: 15 10 2024
Statut: aheadofprint

Résumé

Pembrolizumab/Axitinib combination is approved as first-line therapy in mRCC. The aim of this study is to evaluate outcomes of PAXI combo in the real-world in Italy. This is a prospective study including patients diagnosed with mRCC who received combination as first-line therapy in recruiting Italian Centers. Data about patient characteristics, safety and outcome were collected. 170 pts have been treated from December 2020 to September 2023. The majority had clear-cell histology (83%). Sarcomatoid feature was present in 33%of available cases. About one half of patients (55%) had synchronous metastasis. In 58% of cases nephrectomy was performed, of which 27% were cytoreductive and 4% were deferred nephrectomies. Lung metastases were identified in 106 patients (62%), bone and liver involvement in 66 and 29 patients (38.8% and 17.1%) respectively. Stratifying by IMDC criteria, 32 patients (18.8%) were at favorable-risk, 106 (62.4%) at intermediate-risk, and 32 (18.8%) at poor-risk. At time of analysis, treatment was ongoing in 49% of patients. Progression occurred in 45% of patients. Median PFS was 19.2 months (95% CI: 15-NR). With a median follow-up of 19.3 months (range 1.3-34.5), at 24-months and 36-months landmark analysis 62% (95% CI, 53-70) and 58% (95% CI, 47-69) of treated patients are still alive respectively. Disease control rate was achieved in 84.6% of patients: 4.3% reached a complete response, 52% had a partial response and 28.8% a stable disease. Primary progression was observed in 15.3% of patients. In the multivariate analysis, the prognostic significance of age ≥ 65 years, non-clear cell histology, IMDC score, and adverse events and gender interaction as predictors of worse OS were confirmed. This is the first available prospective study on first-line Pembrolizumab/Axitinib combination in real world scenario. Our findings support the effectiveness and safety of first-line this combination in mRCC and reveal that gender emerged as a prognostic factor in relation to the occurrence of adverse events.

Sections du résumé

BACKGROUND BACKGROUND
Pembrolizumab/Axitinib combination is approved as first-line therapy in mRCC. The aim of this study is to evaluate outcomes of PAXI combo in the real-world in Italy.
METHODS METHODS
This is a prospective study including patients diagnosed with mRCC who received combination as first-line therapy in recruiting Italian Centers. Data about patient characteristics, safety and outcome were collected.
RESULTS RESULTS
170 pts have been treated from December 2020 to September 2023. The majority had clear-cell histology (83%). Sarcomatoid feature was present in 33%of available cases. About one half of patients (55%) had synchronous metastasis. In 58% of cases nephrectomy was performed, of which 27% were cytoreductive and 4% were deferred nephrectomies. Lung metastases were identified in 106 patients (62%), bone and liver involvement in 66 and 29 patients (38.8% and 17.1%) respectively. Stratifying by IMDC criteria, 32 patients (18.8%) were at favorable-risk, 106 (62.4%) at intermediate-risk, and 32 (18.8%) at poor-risk. At time of analysis, treatment was ongoing in 49% of patients. Progression occurred in 45% of patients. Median PFS was 19.2 months (95% CI: 15-NR). With a median follow-up of 19.3 months (range 1.3-34.5), at 24-months and 36-months landmark analysis 62% (95% CI, 53-70) and 58% (95% CI, 47-69) of treated patients are still alive respectively. Disease control rate was achieved in 84.6% of patients: 4.3% reached a complete response, 52% had a partial response and 28.8% a stable disease. Primary progression was observed in 15.3% of patients. In the multivariate analysis, the prognostic significance of age ≥ 65 years, non-clear cell histology, IMDC score, and adverse events and gender interaction as predictors of worse OS were confirmed.
CONCLUSION CONCLUSIONS
This is the first available prospective study on first-line Pembrolizumab/Axitinib combination in real world scenario. Our findings support the effectiveness and safety of first-line this combination in mRCC and reveal that gender emerged as a prognostic factor in relation to the occurrence of adverse events.

Identifiants

pubmed: 39405768
pii: S1558-7673(24)00195-2
doi: 10.1016/j.clgc.2024.102225
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

102225

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Disclosure The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Annalisa Guida (A)

Dipartimento di Oncologia, Azienda Ospedaliera Santa Maria of Terni, Terni, Italy; Dipartimento di Oncologia, Oncology 1 Unit, Istituto Oncologico Veneto IOV - IRCCS, Padova, Italy. Electronic address: guida.annalisa@hotmail.it.

Alessio Gili (A)

Department of Life Sciences, Health and Health Professions, link campus university Rome, Italy.

Claudia Mosillo (C)

Dipartimento di Oncologia, Azienda Ospedaliera Santa Maria of Terni, Terni, Italy.

Marco Maruzzo (M)

Dipartimento di Oncologia, Oncology 1 Unit, Istituto Oncologico Veneto IOV - IRCCS, Padova, Italy.

Eleonora Lai (E)

Dipartimento di Oncologia, Oncology 3 Unit, Istituto Oncologico Veneto IOV - IRCCS, Castelfranco Veneto, Italy.

Francesco Pierantoni (F)

Dipartimento di Oncologia, Oncology 3 Unit, Istituto Oncologico Veneto IOV - IRCCS, Castelfranco Veneto, Italy.

Davide Bimbatti (D)

Dipartimento di Oncologia, Oncology 1 Unit, Istituto Oncologico Veneto IOV - IRCCS, Padova, Italy.

Umberto Basso (U)

Dipartimento di Oncologia, Oncology 1 Unit, Istituto Oncologico Veneto IOV - IRCCS, Padova, Italy.

Giuseppe Fornarini (G)

Dipartimento di Oncologia, Medical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Sara Elena Rebuzzi (SE)

Dipartimento di Oncologia, Medical Oncology Unit, Ospedale San Paolo, Savona, Italy; Department of Internal Medicine and Medical Specialties, University of Genoa, Genoa, Italy.

Fabio Calabrò (F)

Department of Oncology, San Camillo Forlanini Hospital, Rome, Italy.

Linda Cerbone (L)

Department of Oncology, San Camillo Forlanini Hospital, Rome, Italy.

Claudia Caserta (C)

Dipartimento di Oncologia, Azienda Ospedaliera Santa Maria of Terni, Terni, Italy.

Grazia Sirgiovanni (G)

Dipartimento di Oncologia, Azienda Ospedaliera Santa Maria of Terni, Terni, Italy.

Debora Serafin (D)

Unit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Santa Chiara Hospital, Pisa, Italy.

Orazio Caffo (O)

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

Sarah Scagliarini (S)

Dipartimento integrato oncoematologico e toraco-polmonare, UOC di Oncologia, Azienda Ospedaliera di Rilievo Nazionale Cardarelli di Napoli, Naples, Italy.

Sergio Bracarda (S)

Dipartimento di Oncologia, Azienda Ospedaliera Santa Maria of Terni, Terni, Italy.

Classifications MeSH