TY - JOUR
T1 - Exploratory analysis of the effect of a dexamethasone-sparing regimen for prophylaxis of cisplatin-induced emesis on food intake (LUNG-NEPA study)
AU - Celio, Luigi
AU - Cortinovis, Diego
AU - Cogoni, Alessio Aligi
AU - Cavanna, Luigi
AU - Martelli, Olga
AU - Carnio, Simona
AU - Collovà, Elena
AU - Bertolini, Federica
AU - Petrelli, Fausto
AU - Cassano, Alessandra
AU - Chiari, Rita
AU - Zanelli, Francesca
AU - Pisconti, Salvatore
AU - Vittimberga, Isabella
AU - Letizia, Antonietta
AU - Misino, Andrea
AU - Gernone, Angela
AU - Bonizzoni, Erminio
AU - Pilotto, Sara
AU - De Placido, Sabino
AU - Bria, Emilio
PY - 2023
Y1 - 2023
N2 - We demonstrated the non-inferiority of a dexamethasone (DEX)-sparing (single-dose) regimen with NEPA, a netupitant/palonosetron fixed combination, for preventing chemotherapy-induced nausea and vomiting (CINV) caused by cisplatin. This pre-planned exploratory analysis assessed the effect of the DEX-sparing regimen on a patient's food intake. Chemotherapy-naive patients undergoing cisplatin (>= 70 mg/m(2)) were given NEPA and DEX (12 mg) on day 1 and randomized to receive either no further DEX (DEX1), or oral DEX (4 mg BID) on days 2-4 (DEX4). Patient-reported endpoint maintenance of usual daily food intake was assessed during the 5-days post-chemotherapy. The relationship between usual daily food intake and CINV control, pre-chemotherapy self-rated food intake and BMI-adjusted weight loss (WL) were evaluated. One-hundred fifty-two patients (76/group) were assessable. The proportion of patients reporting maintenance of usual daily food intake was similar in both groups: 69.7% (95% CI, 58.6-78.9) for DEX1 vs. 72.4% (95% CI, 61.4-81.2) for DEX4. Only CINV control was significantly associated with maintenance of usual daily food intake (P <= 0.001) during the overall phase. The DEX-sparing regimen does not adversely affect patient-reported daily food intake post-chemotherapy. The current analysis adds further insights into antiemetic efficacy of DEX sparing beyond day 1 in the challenging setting of cisplatin.Trial registration: The parent study was registered on ClinicalTrials.gov (NCT04201769).
AB - We demonstrated the non-inferiority of a dexamethasone (DEX)-sparing (single-dose) regimen with NEPA, a netupitant/palonosetron fixed combination, for preventing chemotherapy-induced nausea and vomiting (CINV) caused by cisplatin. This pre-planned exploratory analysis assessed the effect of the DEX-sparing regimen on a patient's food intake. Chemotherapy-naive patients undergoing cisplatin (>= 70 mg/m(2)) were given NEPA and DEX (12 mg) on day 1 and randomized to receive either no further DEX (DEX1), or oral DEX (4 mg BID) on days 2-4 (DEX4). Patient-reported endpoint maintenance of usual daily food intake was assessed during the 5-days post-chemotherapy. The relationship between usual daily food intake and CINV control, pre-chemotherapy self-rated food intake and BMI-adjusted weight loss (WL) were evaluated. One-hundred fifty-two patients (76/group) were assessable. The proportion of patients reporting maintenance of usual daily food intake was similar in both groups: 69.7% (95% CI, 58.6-78.9) for DEX1 vs. 72.4% (95% CI, 61.4-81.2) for DEX4. Only CINV control was significantly associated with maintenance of usual daily food intake (P <= 0.001) during the overall phase. The DEX-sparing regimen does not adversely affect patient-reported daily food intake post-chemotherapy. The current analysis adds further insights into antiemetic efficacy of DEX sparing beyond day 1 in the challenging setting of cisplatin.Trial registration: The parent study was registered on ClinicalTrials.gov (NCT04201769).
KW - Antineoplastic Agents/ therapeutic use
KW - Antineoplastic Agents/ therapeutic use
UR - https://publicatt.unicatt.it/handle/10807/273491
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85146767086&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85146767086&origin=inward
U2 - 10.1038/s41598-023-28464-9
DO - 10.1038/s41598-023-28464-9
M3 - Article
SN - 2045-2322
VL - 13
SP - N/A-N/A
JO - Scientific Reports
JF - Scientific Reports
IS - 1
ER -