TY - JOUR
T1 - Adjuvant pembrolizumab versus placebo in resected high-risk stage II melanoma
T2 - Health-related quality of life from the randomized phase 3 KEYNOTE-716 study
AU - Khattak, Muhammad A.
AU - Luke, Jason J.
AU - Long, Georgina V.
AU - Ascierto, Paolo A.
AU - Rutkowski, Piotr
AU - Schadendorf, Dirk
AU - Robert, Caroline
AU - Grob, Jean Jacques
AU - de la Cruz Merino, Luis
AU - Del Vecchio, Michele
AU - Spagnolo, Francesco
AU - Mackiewicz, Jacek
AU - Chiarion-Sileni, Vanna
AU - Carlino, Matteo S.
AU - Mohr, Peter
AU - De Galitiis, Federica
AU - Ross, Merrick I.
AU - Eroglu, Zeynep
AU - Chen, Ke
AU - Jiang, Ruixuan
AU - Fukunaga-Kalabis, Mizuho
AU - Krepler, Clemens
AU - Eggermont, Alexander M.M.
AU - Kirkwood, John M.
N1 - Publisher Copyright:
© 2022 The Author(s), Merck Sharp & Dohme LLC., a subsidiary of Merck & Co., Inc.,
PY - 2022/11/1
Y1 - 2022/11/1
N2 - Background: Adjuvant pembrolizumab significantly improved recurrence-free survival (RFS) versus placebo in resected stage IIB and IIC melanoma in the phase 3 KEYNOTE-716 study. Health-related quality of life (HRQoL) results are reported. Methods: Patients were randomly assigned 1:1 to pembrolizumab 200 mg (2 mg/kg, patients ≥12 to <18 years) Q3W or placebo for ≤17 cycles or until disease recurrence, unacceptable toxicity, or withdrawal. Change from baseline in EORTC QLQ-C30 global health status (GHS)/quality of life (QoL) was a prespecified exploratory end point. Change in EORTC QLQ-C30 functioning, symptom, and single-item scales, and EQ-5D-5L visual analog scale (VAS) were also summarized. Primary analyses were performed at week 48 to ensure adequate completion/compliance. The HRQoL population comprised patients who received ≥1 dose of treatment and completed ≥1 assessment. Results: The HRQoL population included 969 patients (pembrolizumab, n = 483; placebo, n = 486). Compliance at week 48 was ≥80% for both instruments. EORTC QLQ-C30 GHS/QoL, physical functioning, role functioning, and EQ-5D-5L VAS scores were stable from baseline to week 48 in both arms, with no clinically meaningful decline observed. Scores did not differ significantly between pembrolizumab and placebo. EORTC QLQ-C30 GHS/QoL, physical functioning, role functioning, and EQ-5D-5L VAS scores remained stable through week 96 in both arms. Conclusions: HRQoL was stable with adjuvant pembrolizumab, with no clinically meaningful decline observed. Change from baseline in HRQoL was similar between arms. These results, in conjunction with the improved RFS and manageable safety previously reported, support the use of adjuvant pembrolizumab for high-risk stage II melanoma.
AB - Background: Adjuvant pembrolizumab significantly improved recurrence-free survival (RFS) versus placebo in resected stage IIB and IIC melanoma in the phase 3 KEYNOTE-716 study. Health-related quality of life (HRQoL) results are reported. Methods: Patients were randomly assigned 1:1 to pembrolizumab 200 mg (2 mg/kg, patients ≥12 to <18 years) Q3W or placebo for ≤17 cycles or until disease recurrence, unacceptable toxicity, or withdrawal. Change from baseline in EORTC QLQ-C30 global health status (GHS)/quality of life (QoL) was a prespecified exploratory end point. Change in EORTC QLQ-C30 functioning, symptom, and single-item scales, and EQ-5D-5L visual analog scale (VAS) were also summarized. Primary analyses were performed at week 48 to ensure adequate completion/compliance. The HRQoL population comprised patients who received ≥1 dose of treatment and completed ≥1 assessment. Results: The HRQoL population included 969 patients (pembrolizumab, n = 483; placebo, n = 486). Compliance at week 48 was ≥80% for both instruments. EORTC QLQ-C30 GHS/QoL, physical functioning, role functioning, and EQ-5D-5L VAS scores were stable from baseline to week 48 in both arms, with no clinically meaningful decline observed. Scores did not differ significantly between pembrolizumab and placebo. EORTC QLQ-C30 GHS/QoL, physical functioning, role functioning, and EQ-5D-5L VAS scores remained stable through week 96 in both arms. Conclusions: HRQoL was stable with adjuvant pembrolizumab, with no clinically meaningful decline observed. Change from baseline in HRQoL was similar between arms. These results, in conjunction with the improved RFS and manageable safety previously reported, support the use of adjuvant pembrolizumab for high-risk stage II melanoma.
KW - Adjuvant
KW - Immunotherapy
KW - Melanoma
KW - Patient-reported outcomes
KW - Pembrolizumab
UR - http://www.scopus.com/inward/record.url?scp=85139288504&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2022.08.004
DO - 10.1016/j.ejca.2022.08.004
M3 - Article
C2 - 36202690
AN - SCOPUS:85139288504
SN - 0959-8049
VL - 176
SP - 207
EP - 217
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -