Immune checkpoint inhibitors (ICIs) and platinum-based chemotherapy (CT) are effective therapeutic agents for the palliative treatment of metastatic non-small-cell lung cancer (NSCLC); the aim of our study was to investigate the acute and chronic renal toxicities in this setting. We collected data on 292 patients who received cisplatin (35%), carboplatin-based regimens (25%), or ICI monotherapy (40%). The primary and secondary outcomes were compared to the acute kidney injury (AKI) rate and the mean estimated GFR (eGFR) decay between groups, respectively, over a mean follow-up duration of 15 weeks. We observed 26 AKI events (8.9%), mostly stage I AKI (80.7%); 15% were stage II AKI, 3.8% were stage III, and none required renal replacement therapy or ICU admission. The AKI rates were 10.9%, 6.8%, and 8.9% for the cisplatin, carboplatin, and ICI groups, respectively, and no significant differences were observed between the groups (p = 0.3). A global mean eGFR decay of 2.2 mL/min was observed, while for the cisplatin, carboplatin, and ICI groups, the eGFR decay values were 2.3 mL/min, 1.1 mL/min, and 3.5 mL/min, respectively. No significant differences were observed between the groups. Cisplatin/carboplatin-based CT and ICIs resulted in a similar incidence of AKI and eGFR decay, suggesting the safety of their cautious use, even in CKD patients.

Renal function outcomes in metastatic non-small-cell lung carcinoma patients treated with chemotherapy or immune checkpoint inhibitors: an unexpected scenario / Trevisani, F; Di Marco, F; Floris, M; Pani, A; Minnei, R; Scartozzi, M; Cirillo, A; Gelibter, A; Botticelli, A; Rijavec, E; Cattaneo, M; Garrone, O; Ghidini, M.. - In: VACCINES. - ISSN 2076-393X. - 10:5(2022). [10.3390/vaccines10050679]

Renal function outcomes in metastatic non-small-cell lung carcinoma patients treated with chemotherapy or immune checkpoint inhibitors: an unexpected scenario

Trevisani F
Primo
Conceptualization
;
Floris M
Methodology
;
Scartozzi M
Project Administration
;
Cirillo A
Data Curation
;
Gelibter A
Investigation
;
Botticelli A
Investigation
;
2022

Abstract

Immune checkpoint inhibitors (ICIs) and platinum-based chemotherapy (CT) are effective therapeutic agents for the palliative treatment of metastatic non-small-cell lung cancer (NSCLC); the aim of our study was to investigate the acute and chronic renal toxicities in this setting. We collected data on 292 patients who received cisplatin (35%), carboplatin-based regimens (25%), or ICI monotherapy (40%). The primary and secondary outcomes were compared to the acute kidney injury (AKI) rate and the mean estimated GFR (eGFR) decay between groups, respectively, over a mean follow-up duration of 15 weeks. We observed 26 AKI events (8.9%), mostly stage I AKI (80.7%); 15% were stage II AKI, 3.8% were stage III, and none required renal replacement therapy or ICU admission. The AKI rates were 10.9%, 6.8%, and 8.9% for the cisplatin, carboplatin, and ICI groups, respectively, and no significant differences were observed between the groups (p = 0.3). A global mean eGFR decay of 2.2 mL/min was observed, while for the cisplatin, carboplatin, and ICI groups, the eGFR decay values were 2.3 mL/min, 1.1 mL/min, and 3.5 mL/min, respectively. No significant differences were observed between the groups. Cisplatin/carboplatin-based CT and ICIs resulted in a similar incidence of AKI and eGFR decay, suggesting the safety of their cautious use, even in CKD patients.
2022
acute kidney injury (AKI); carboplatin; chronic kidney disease (CKD); cisplatin; immune checkpoint inhibitors; immunotherapy; multidisciplinary care; onconephrology; renal toxicity.
01 Pubblicazione su rivista::01a Articolo in rivista
Renal function outcomes in metastatic non-small-cell lung carcinoma patients treated with chemotherapy or immune checkpoint inhibitors: an unexpected scenario / Trevisani, F; Di Marco, F; Floris, M; Pani, A; Minnei, R; Scartozzi, M; Cirillo, A; Gelibter, A; Botticelli, A; Rijavec, E; Cattaneo, M; Garrone, O; Ghidini, M.. - In: VACCINES. - ISSN 2076-393X. - 10:5(2022). [10.3390/vaccines10050679]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1645553
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