Your browser doesn't support javascript.
loading
Pembrolizumab versus ipilimumab for advanced melanoma: 10-year follow-up of the phase III KEYNOTE-006 study.
Long, G V; Carlino, M S; McNeil, C; Ribas, A; Gaudy-Marqueste, C; Schachter, J; Nyakas, M; Kee, D; Petrella, T M; Blaustein, A; Lotem, M; Arance, A M; Daud, A I; Hamid, O; Larkin, J; Yao, L; Singh, R; Lal, R; Robert, C.
Afiliación
  • Long GV; Melanoma Institute Australia, The University of Sydney, Sydney, Australia; Faculty of Medicine & Health, The University of Sydney, Sydney, Australia; Charles Perkins Centre, The University of Sydney, Sydney, Australia; Royal North Shore and Mater Hospitals, Sydney, Australia. Electronic address:
  • Carlino MS; Melanoma Institute Australia, The University of Sydney, Sydney, Australia; Faculty of Medicine & Health, The University of Sydney, Sydney, Australia; Westmead and Blacktown Hospitals, Sydney, Australia.
  • McNeil C; Chris O'Brien Lifehouse, Camperdown, Australia.
  • Ribas A; Jonsson Comprehensive Cancer Center at The University of California Los Angeles (UCLA), Los Angeles, USA.
  • Gaudy-Marqueste C; Aix-Marseille University, Assistance Publique-Hôpitaux de Marseille, CRCM La Timone Hospital, Dermatology and Skin Cancer Department, Marseille, France.
  • Schachter J; Sheba Medical Center-Tel HaShomer, Ramat Gan, Israel.
  • Nyakas M; Oslo University Hospital, Oslo, Norway.
  • Kee D; Austin Health, Heidelberg, Australia.
  • Petrella TM; Sunnybrook Health Sciences Centre, Toronto, Canada.
  • Blaustein A; Mount Sinai Medical Center Comprehensive Cancer Center, Miami Beach, USA.
  • Lotem M; Sharett Institute of Oncology, Hadassah University Hospital Ein Kerem, Jerusalem, Israel.
  • Arance AM; Hospital Clinic Barcelona and IDIBAPS, Barcelona, Spain.
  • Daud AI; Melanoma & Skin Cancer Center, University of California San Francisco, San Francisco.
  • Hamid O; The Angeles Clinic and Research Institute, a Cedars-Sinai Affiliate, Los Angeles, USA.
  • Larkin J; The Royal Marsden NHS Foundation Trust, London, UK.
  • Yao L; Merck & Co., Inc., Rahway, USA.
  • Singh R; Merck & Co., Inc., Rahway, USA.
  • Lal R; Merck & Co., Inc., Rahway, USA.
  • Robert C; Gustave Roussy and Paris-Saclay University, Villejuif, France. Electronic address: caroline.robert@gustaveroussy.fr.
Ann Oncol ; 2024 Sep 15.
Article en En | MEDLINE | ID: mdl-39306585
ABSTRACT

BACKGROUND:

Pembrolizumab significantly improved overall survival (OS) versus ipilimumab for unresectable advanced melanoma in KEYNOTE-006 (NCT01866319); 10-year follow-up data are presented. PATIENTS AND

METHODS:

Patients with unresectable stage III or IV melanoma were randomly assigned (111) to pembrolizumab 10 mg/kg i.v. every 2 weeks or every 3 weeks for ≤2 years (pooled), or ipilimumab 3 mg/kg i.v. every 3 weeks for four cycles. After KEYNOTE-006, patients could transition to KEYNOTE-587 (NCT03486873) for long-term follow-up. Eligible patients could receive second-course pembrolizumab. The primary endpoint was OS; modified progression-free survival (PFS; censored at date last known alive), modified PFS on second-course pembrolizumab, and melanoma-specific survival were exploratory.

RESULTS:

Of 834 patients randomly assigned in KEYNOTE-006 (pembrolizumab, n = 556; ipilimumab, n = 278), 333 (39.9%) were eligible for KEYNOTE-587; 211/333 patients (25.3%) transitioned to KEYNOTE-587 (pembrolizumab, n = 159; ipilimumab, n = 52) and 122 (14.6%) did not. For patients who transitioned to KEYNOTE-587 (n = 211), median time from randomization in KEYNOTE-006 to data cut-off for KEYNOTE-587 (1 May 2024) was 123.7 months (range, 122.0-127.3 months). Median OS was 32.7 months [95% confidence interval (CI) 24.5-41.6 months] for pembrolizumab and 15.9 months (95% CI 13.3-22.0 months) for ipilimumab [hazard ratio (HR), 0.71 (95% CI 0.60-0.85)]; 10-year OS was 34.0% and 23.6%, respectively. Among patients who completed ≥94 weeks of pembrolizumab, median OS from week 94 was not reached (NR; 95% CI NR-NR); 8-year OS rate was 80.8%. Median modified PFS was 9.4 months (95% CI 6.7-11.6 months) for pembrolizumab and 3.8 months (2.9-4.3 months) for ipilimumab [HR, 0.64 (95% CI 0.54-0.75)]. Among patients who received second-course pembrolizumab, median modified PFS from start of second course was 51.8 months (95% CI 11.0 months-NR); 6-year modified PFS was 49.2%. Median melanoma-specific survival was 51.9 months (95% CI 30.0-114.7 months) for pembrolizumab and 17.2 months (13.9-25.9 months) for ipilimumab [HR, 0.66 (95% CI 0.55-0.81)].

CONCLUSIONS:

These results confirm that pembrolizumab provides long-term survival benefits in advanced melanoma, supporting it as a standard of care in this setting.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Ann Oncol Asunto de la revista: NEOPLASIAS Año: 2024 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Ann Oncol Asunto de la revista: NEOPLASIAS Año: 2024 Tipo del documento: Article Pais de publicación: Reino Unido