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Nivolumab as Second-Line Therapy Improves Survival in Patients with Unresectable Hepatocellular Carcinoma.
Sanai, Faisal M; Odah, Hassan O; Alshammari, Kanan; Alzanbagi, Adnan; Alsubhi, Murooj; Tamim, Hani; Alolayan, Ashwaq; Alshehri, Ahmed; Alqahtani, Saleh A.
Afiliación
  • Sanai FM; Gastroenterology Section, Department of Medicine, King Abdulaziz Medical City, Ministry of the National Guard-Health Affairs, Jeddah 21423, Saudi Arabia.
  • Odah HO; King Abdullah International Medical Research Center, Jeddah 22384, Saudi Arabia.
  • Alshammari K; King Saud bin Abdulaziz University for Health Sciences, Jeddah 22384, Saudi Arabia.
  • Alzanbagi A; Gastroenterology Section, Department of Medicine, King Abdulaziz Medical City, Ministry of the National Guard-Health Affairs, Jeddah 21423, Saudi Arabia.
  • Alsubhi M; Oncology Department, King Abdulaziz Medical City, King Abdullah International Medical Research Center, Ministry of National Guard Health Affairs, Riyadh 11481, Saudi Arabia.
  • Tamim H; Gastroenterology and Hepatology Department, King Abdullah Medical City, Makkah 57657, Saudi Arabia.
  • Alolayan A; Department of Medical Imaging, King Abdulaziz Medical City, Riyadh 11426, Saudi Arabia.
  • Alshehri A; College of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.
  • Alqahtani SA; Department of Internal Medicine, American University of Beirut Medical Center, Beirut 1107, Lebanon.
Cancers (Basel) ; 16(12)2024 Jun 11.
Article en En | MEDLINE | ID: mdl-38927902
ABSTRACT

BACKGROUND:

Limited data exists for the efficacy and outcomes of nivolumab as a second-line treatment for unresectable hepatocellular carcinoma (uHCC). We aimed to assess the efficacy and safety of nivolumab in patients with uHCC who experienced disease progression during sorafenib treatment.

METHODS:

In this retrospective, observational, multicenter study, adult Child-Turcotte-Pugh A/7B patients with uHCC who tolerated sorafenib therapy but showed disease progression switched to second-line intravenous nivolumab (n = 42). A similar number of consecutive, unselected patients who were maintained on sorafenib therapy, regardless of tumoral response or progression, served as historical controls (n = 38). The primary endpoint was overall survival (OS, defined as the time from starting sorafenib in either group up to death due to any cause) and analyzed by intention-to-treat.

RESULTS:

The mean age of the overall cohort was 72.4 ± 10.1 years, of whom 87.5% were males and 58.8% had underlying viral etiology. Patients in the two cohorts were similar, except those who received nivolumab had more co-morbidities (70.0% vs. 15.4%), ECOG-2 status (21.4% vs. 15.8%), BCLC stage C (81.0% vs. 47.4%), and extravascular invasion (54.4% vs. 21.8%) (p < 0.05 for all). More patients in the nivolumab arm were Child-Turcotte-Pugh B (35.7% vs. 21.1%, p = 0.15). Median OS was 22.2 months (95% CI 8.9-49.8) on second-line nivolumab and 11.0 months (95% CI 3.6-18.4) on sorafenib alone (HR 1.93; 95% CI 1.1-3.3, p = 0.014). Median OS after starting nivolumab was 10.2 months, and time-to-progression was 4.9 months (95% CI 3.2-6.3).

CONCLUSION:

Nivolumab is an effective second-line treatment option in patients with uHCC who progress on sorafenib, with significantly improved OS. These early real-life data offer encouraging results, similar to those shown in Phase I/IIa clinical trials. Further investigations are warranted for the use of nivolumab as a monotherapy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cancers (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Arabia Saudita Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cancers (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Arabia Saudita Pais de publicación: Suiza