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Phase II Trial of FOLFIRINOX in Advanced Biliary Tract Cancer.
Bazarbashi, Shouki; Aseafan, Mohamed; Elshenawy, Mahmoud; Alzahrani, Ahmed; Aljubran, Ali H; Almugbel, Fahad; Alzannan, Noura; Elhassan, Tusneem.
Afiliação
  • Bazarbashi S; Oncology, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Centre, Riyadh, SAU.
  • Aseafan M; Medical Oncology, Security Forces Hospital Program, Riyadh, SAU.
  • Elshenawy M; Oncology, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Centre, Riyadh, SAU.
  • Alzahrani A; Clinical Oncology and Nuclear Medicine, Menoufia University, Menoufia, EGY.
  • Aljubran AH; Oncology, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Centre, Riyadh, SAU.
  • Almugbel F; Oncology, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Centre, Riyadh, SAU.
  • Alzannan N; Oncology, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Centre, Riyadh, SAU.
  • Elhassan T; Oncology Research, Cancer Centre of Excellence, King Faisal Specialist Hospital and Research Centre, Riyadh, SAU.
Cureus ; 16(1): e52656, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38380191
ABSTRACT

INTRODUCTION:

Biliary tract cancers (BTCs), characterized by poor prognosis and limited treatment options, are increasingly prevalent malignancies with a five-year survival rate of less than 20% for advanced-stage disease. The standard first-line chemotherapy combining gemcitabine and cisplatin offers modest survival benefits, necessitating the exploration of more effective therapies. This study reports the results of a single-arm, open-label, phase 2 trial assessing the efficacy and safety of fluorouracil, leucovorin, oxaliplatin, and irinotecan (FOLFIRINOX) as a first-line treatment for metastatic or locally advanced unresectable BTC.

METHODS:

Patients aged ≥18 with measurable disease and adequate organ function were enrolled, receiving biweekly FOLFIRINOX for up to 12 cycles with follow-up imaging every four cycles. The primary endpoint was the overall response rate (ORR), with progression-free survival (PFS), overall survival (OS), and safety as secondary endpoints.

RESULTS:

Thirteen patients were enrolled from December 2016 to September 2021 before early termination due to slow accrual and the emergence of immunotherapy. The ORR was 54%, with a disease control rate of 77%. Median PFS and OS were 6.8 and 19.25 months, respectively. Grade 3/4 toxicities were predominantly hematologic, with neutropenia being the most common severe adverse event.

CONCLUSION:

The trial suggests that FOLFIRINOX is a potentially effective first-line therapy for unresectable or metastatic BTC with a manageable safety profile. However, the early termination of the study and the introduction of immunotherapy warrant further research to confirm these findings.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cureus Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cureus Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos