Prognostic role of hematologic parameters of metastatic renal cell carcinoma treated with sunitinib

Author:

Bolzacchini Elena12ORCID,Giordano Monica1,Bertù Lorenza2,Bregni Marco3,Nigro Olga4,Galli Luca5,Antonuzzo Andrea5,Artale Salvatore6,Barzaghi Sabrina6,Danova Marco7,Torchio Martina7,Pinotti Graziella4,Dentali Francesco2

Affiliation:

1. U.O. Oncologia, Ospedale Sant’Anna, ASST-Lariana, Como, Italy

2. Dipartimento di Medicina e Chirurgia, Università degli Studi dell'Insubria di Varese, Varese, Italy

3. U.O. Oncologia,Ospedale di Circolo di Busto Arsizio, ASST della Valle Olona, Busto Arsizio, Italy

4. U.O. Oncologia,Ospedale di Circolo e Fondazione Macchi, ASST Sette Laghi, Varese, Italy

5. U.O. Oncologia, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy

6. U.O. Oncologia, Ospedale S.Antonio Abate, ASST della Valle Olona, Gallarate, Italy

7. U.O. Medicina Interna od Indirizzo Oncologico, Ospedale Civile, ASST di Pavia, Vigevano, Italy

Abstract

Background: Hemochrome parameters at the diagnosis of metastatic renal cell carcinoma (mRCC) and the development of macrocytosis during sunitinib therapy are considered prognostic. Objective: To evaluate the prognostic role of hematologic parameters and macrocytosis in mRCC treated with sunitinib. Methods: We analyzed clinical data of 100 patients with mRCC treated with sunitinib as first-line therapy in a retrospective multicenter study. We calculated neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and lymphocyte-to-monocyte ratio (LMR) at baseline and erythrocyte mean corpuscular volume (MCV) during therapy. We considered the following cutoffs: NLR >3, PLR >150, LMR <3, and MCV >100 fl. Clinical data histology, prior nephrectomy, Fuhrman grading, metastatic sites, Memorial Sloan-Kettering Cancer Center score, and Heng score were collected. Overall survival (OS) and progression-free survival (PFS) were calculated. Univariate and multivariate analysis using Cox regression model with time-dependent (macrocytosis) covariate were applied. Results: At the univariate analysis, low LMR was associated with shorter PFS and OS ( p = 0.02 and p = 0.06, respectively). High PLR was associated with worse PFS ( p = 0.005); median OS was 23 vs 28 months ( p = 0.13). At the multivariate analysis, poor risk (Heng score), low LMR, and high PLR were associated with shorter PFS (hazard ratio 7.1, 1.5, and 2, respectively); poor PS and poor risk (Heng score) were related to worst OS. Macrocytosis was observed in 26 patients and was not prognostic of survival. Conclusions: In our cohort of patients with mRCC treated with sunitinib, low LMR (>3) and high PLR (>150) were associated with shorter PFS. Macrocytosis was not prognostic.

Publisher

SAGE Publications

Subject

Cancer Research,Oncology,General Medicine

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