Long-Term Outcomes and Exploratory Analyses of the Randomized Phase III BILCAP Study.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
20 06 2022
Historique:
pubmed: 23 3 2022
medline: 18 6 2022
entrez: 22 3 2022
Statut: ppublish

Résumé

The BILCAP study described a modest benefit for capecitabine as adjuvant therapy for curatively resected biliary tract cancer (BTC), and capecitabine has become the standard of care. We present the long-term data and novel exploratory subgroup analyses. This randomized, controlled, multicenter, phase III study recruited patients age 18 years or older with histologically confirmed cholangiocarcinoma or muscle-invasive gallbladder cancer after resection with curative intent and an Eastern Cooperative Oncology Group performance status of < 2. Patients were randomly assigned 1:1 to receive oral capecitabine (1,250 mg/m Between March 15, 2006, and December 4, 2014, 447 patients were enrolled; 223 patients with BTC resected with curative intent were randomly assigned to the capecitabine group and 224 to the observation group. At the data cutoff of January 21, 2021, the median follow-up for all patients was 106 months (95% CI, 98 to 108). In the intention-to-treat analysis, the median OS was 49.6 months (95% CI, 35.1 to 59.1) in the capecitabine group compared with 36.1 months (95% CI, 29.7 to 44.2) in the observation group (adjusted hazard ratio 0.84; 95% CI, 0.67 to 1.06). In a protocol-specified sensitivity analysis, adjusting for minimization factors, nodal status, grade, and sex, the OS hazard ratio was 0.74 (95% CI, 0.59 to 0.94). We further describe the prognostic impact of R status, grade, nodal status, and sex. This long-term analysis supports the previous analysis, suggesting that capecitabine can improve OS in patients with resected BTC when used as adjuvant chemotherapy after surgery and should be considered as the standard of care.

Identifiants

pubmed: 35316080
doi: 10.1200/JCO.21.02568
doi:

Substances chimiques

Capecitabine 6804DJ8Z9U

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2048-2057

Subventions

Organisme : Cancer Research UK
ID : 4273
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Auteurs

John Bridgewater (J)

UCL Cancer Institute, London, United Kingdom.

Peter Fletcher (P)

Cancer Clinical Trials Unit, Birmingham, United Kingdom.

Daniel H Palmer (DH)

Molecular and Clinical Cancer Medicine, Liverpool, United Kingdom.

Hassan Z Malik (HZ)

University Hospital Aintree, Liverpool, United Kingdom.

Raj Prasad (R)

Leeds Teaching Hospital NHS Trust, Leeds, United Kingdom.

Darius Mirza (D)

Birmingham Woman's and Children's NHS Trust, Birmingham, United Kingdom.

Alan Anthony (A)

Leeds Teaching Hospital NHS Trust, Leeds, United Kingdom.

Pippa Corrie (P)

Cambridge University Hospitals NHS Trust, Cambridge, United Kingdom.

Stephen Falk (S)

University Hospitals Bristol NHS Trust, Bristol, United Kingdom.

Meg Finch-Jones (M)

University Hospitals Bristol NHS Trust, Bristol, United Kingdom.

Harpreet Wasan (H)

Imperial College Healthcare NHS Trust, London, United Kingdom.

Paul Ross (P)

Guys and St Thomas's NHS Trust, London, United Kingdom.

Lucy Wall (L)

Western General Hospital, Edinburgh, United Kingdom.

Jonathan Wadsley (J)

Weston Park Cancer Centre, Sheffield, United Kingdom.

Thomas R Evans (TR)

University of Glasgow, Glasgow, United Kingdom.

Deborah Stocken (D)

Leeds Institute of Clinical Trials Research, Leeds, United Kingdom.

Clive Stubbs (C)

Cancer Clinical Trials Unit, Birmingham, United Kingdom.

Raaj Praseedom (R)

Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.

Yuk Ting Ma (YT)

Institute of Immunology and Immunotherapy, Birmingham, United Kingdom.

Brian Davidson (B)

Royal Free Hospital NHS Trust, London, United Kingdom.

John Neoptolemos (J)

University of Heidelberg, Heidelberg, Germany.

Tim Iveson (T)

University Hospital Southampton NHS Trust, Southampton, United Kingdom.

David Cunningham (D)

Royal Marsden Hospital, London, United Kingdom.

O James Garden (OJ)

University of Edinburgh, Edinburgh, United Kingdom.

Juan W Valle (JW)

University of Manchester, Manchester, United Kingdom.

John Primrose (J)

University of Southampton, Southampton, United Kingdom.

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Classifications MeSH