TY - JOUR
T1 - Health-related quality of life in patients with RAS wild-type metastatic colorectal cancer treated with panitumumab-based first-line treatment strategy: A pre-specified secondary analysis of the Valentino study
AU - Raimondi, Alessandra
AU - Di Maio, Massimo
AU - Morano, Federica
AU - Corallo, Salvatore
AU - Lonardi, Sara
AU - Antoniotti, Carlotta
AU - Rimassa, Lorenza
AU - Sartore-Bianchi, Andrea
AU - Tampellini, Marco
AU - Ritorto, Giuliana
AU - Murialdo, Roberto
AU - Clavarezza, Matteo
AU - Zaniboni, Alberto
AU - Adamo, Vincenzo
AU - Tomasello, Gianluca
AU - Petrelli, Fausto
AU - Antonuzzo, Lorenzo
AU - Giordano, Monica
AU - Cinieri, Saverio
AU - Longarini, Raffaella
AU - Bergamo, Francesca
AU - Niger, Monica
AU - Antista, Maria
AU - Peverelli, Giorgia
AU - de Braud, Filippo
AU - Di Bartolomeo, Maria
AU - Pietrantonio, Filippo
N1 - Copyright © 2020 Elsevier Ltd. All rights reserved.
PY - 2020/8
Y1 - 2020/8
N2 - BACKGROUND: Quality of life (QoL) patient-reported outcomes (PROs) data from pivotal first-line trials in metastatic colorectal cancer (mCRC) are poor. The Valentino study showed that de-escalation to single-agent panitumumab after 4-month induction with panitumumab-FOLFOX is inferior to panitumumab-5-FU/LV in patients with RAS wild-type mCRC, although slightly reducing toxicity. We report QoL, a secondary end-point.METHODS: PROs were assessed by European Organisation for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire - Core 30 (QLQ-C30), EORTC QLQ-CR29, EuroQol EQ-5D questionnaires, at baseline and every 8 weeks until disease progression. First two evaluations correspond to induction treatment (identical in both arms), while subsequent to maintenance. To describe QoL changes over time, mean changes from baseline at each time point were calculated in overall population. To compare maintenance between two arms, mean changes and proportion of improved/stable/worse patients versus baseline were compared for each item.RESULTS: In arm A/B, 91.5%/92.0% of enrolled patients completed questionnaires at baseline. No significant differences in the two arms were reported in compliance, baseline scores and mean changes versus baseline for the three questionnaires during maintenance (24/32/40 weeks). Overall, mean changes versus baseline showed an early deterioration during induction with partial recovering during maintenance for global QoL, functional scales and several symptoms/items of QLQ-C30 (fatigue, nausea/vomiting, appetite loss, diarrhoea) and QLQ-CR29 (body image, dry mouth, hair loss, taste, faecal incontinence, sore skin), and EQ-5D Visual Analogue Scale (VAS) score.CONCLUSION: In patients with RAS wild-type mCRC, induction with oxaliplatin-containing chemotherapy plus anti-EGFRs induces a transient significant QoL deterioration. After induction phase, treatment deintensification determines an overall recovery of health-related QoL, besides the expected prevention of oxaliplatin-related neurotoxicity.
AB - BACKGROUND: Quality of life (QoL) patient-reported outcomes (PROs) data from pivotal first-line trials in metastatic colorectal cancer (mCRC) are poor. The Valentino study showed that de-escalation to single-agent panitumumab after 4-month induction with panitumumab-FOLFOX is inferior to panitumumab-5-FU/LV in patients with RAS wild-type mCRC, although slightly reducing toxicity. We report QoL, a secondary end-point.METHODS: PROs were assessed by European Organisation for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire - Core 30 (QLQ-C30), EORTC QLQ-CR29, EuroQol EQ-5D questionnaires, at baseline and every 8 weeks until disease progression. First two evaluations correspond to induction treatment (identical in both arms), while subsequent to maintenance. To describe QoL changes over time, mean changes from baseline at each time point were calculated in overall population. To compare maintenance between two arms, mean changes and proportion of improved/stable/worse patients versus baseline were compared for each item.RESULTS: In arm A/B, 91.5%/92.0% of enrolled patients completed questionnaires at baseline. No significant differences in the two arms were reported in compliance, baseline scores and mean changes versus baseline for the three questionnaires during maintenance (24/32/40 weeks). Overall, mean changes versus baseline showed an early deterioration during induction with partial recovering during maintenance for global QoL, functional scales and several symptoms/items of QLQ-C30 (fatigue, nausea/vomiting, appetite loss, diarrhoea) and QLQ-CR29 (body image, dry mouth, hair loss, taste, faecal incontinence, sore skin), and EQ-5D Visual Analogue Scale (VAS) score.CONCLUSION: In patients with RAS wild-type mCRC, induction with oxaliplatin-containing chemotherapy plus anti-EGFRs induces a transient significant QoL deterioration. After induction phase, treatment deintensification determines an overall recovery of health-related QoL, besides the expected prevention of oxaliplatin-related neurotoxicity.
KW - Aged
KW - Antineoplastic Agents, Immunological/administration & dosage
KW - Antineoplastic Combined Chemotherapy Protocols/administration & dosage
KW - Biomarkers, Tumor/genetics
KW - Colorectal Neoplasms/drug therapy
KW - Female
KW - Fluorouracil/administration & dosage
KW - Genes, ras
KW - Humans
KW - Italy
KW - Leucovorin/administration & dosage
KW - Male
KW - Middle Aged
KW - Mutation
KW - Neoplasm Metastasis
KW - Organoplatinum Compounds/administration & dosage
KW - Panitumumab/administration & dosage
KW - Patient Reported Outcome Measures
KW - Progression-Free Survival
KW - Quality of Life
KW - Time Factors
U2 - 10.1016/j.ejca.2020.04.048
DO - 10.1016/j.ejca.2020.04.048
M3 - Article
VL - 135
SP - 230
EP - 239
JO - Eur. J. Cancer
JF - Eur. J. Cancer
SN - 0959-8049
ER -