Prospective validation of a lymphocyte infiltration prognostic test in stage III colon cancer patients treated with adjuvant FOLFOX
Publikation: Beitrag in Fachzeitschrift › Forschungsartikel › Beigetragen › Begutachtung
Beitragende
- Université de Versailles Saint-Quentin-en-Yvelines
- Hôpital Ambroise Paré
- Fédération Francophone de Cancérologie Digestive (FFCD)
- Université de Bourgogne
- INSERM - Institut national de la santé et de la recherche médicale
- Autonomous University of Barcelona
- Università degli Studi di Firenze
- Université libre de Bruxelles (ULB)
- Centre Hospitalier Départemental Vendée
- CHU de Reims
- Centre Jean Perrin
- Centre Georges-François Leclerc
- Université Paris Cité
- Hopital Europeen Georges-Pompidou
- Klinikum Wels - Grieskirchen GmbH
- Universitätskliniken Salzburg
- Landeskrankenhaus Hall Tirol
- Medizinische Universität Innsbruck
- Krankenhaus der Barmherzigen Brüder St. Veit/Glan
- Landeskrankenhaus Hochsteiermark, Standort Leoben
- LKH-Universitätsklinikum Graz
- Bezirkskrankenhaus Kufstein
- Landeskrankenhaus Bregenz
- Medizinische Universität Wien
- Landeskrankenhaus-Universitätsklinikum Graz
- Pyhrn-Eisenwurzen Klinikum Steyr
- Krankenhaus Barmherzige Schwestern Ried
- Landeskrankenhaus Rankweil
- Kepler Universitätsklinikum
- Landeskrankenhaus Oberpullendorf
- Krankenhaus St. Vinzenz Zams
- Klinikum Klagenfurt am Wörthersee
- Landesklinikum Wiener Neustadt
- Oberwart AÖ KH
- Imeldaziekenhuis
- Clinique St-Jospeh
- University Hospital of Mont-Godinne
- AZ Damiaan
- AZ Delta Hospital
- Centre hospitalier universitaire de Liège
- KU Leuven
- C.H. Peltzer-La Tourelle
- Centre Hospitalier de Jolimont-Lobbes
- Centre Hospitalier Universitaire UCL Namur
- Ghent University
- AZ Groeninge
- Centre Médical de L'Avenue
Abstract
Background The prognostic value of lymphocyte infiltration (LI) of colorectal carcinoma (CC) has been demonstrated by several groups. However, no validated test is currently available for clinical practice. We previously described an automated and reproducible method for testing LI and aimed to validate it for clinical use. Patients and methods According to National Institutes of Health criteria, we designed a prospective validation of this biomarker in patients included in the PETACC8 phase III study. Primary objective was to compare percentage of patients alive and without recurrence at 2 years in patients with high versus low LI (#NCT02364024). Associations of LI with patient recurrence and survival were analysed, and multivariable models were adjusted for treatment and relevant factors. Automated testing of LI was performed on virtual slides without access to clinical data. Results Among the 1220 CC patients enrolled, LI was high, low and not evaluable in 241 (19.8%), 790 (64.8%) and 189 (15.5%), respectively. Primary objective was met with a 2-year recurrence rate of 14.4% versus 21.1% in patients with high and low LI, respectively (p = 0.02). Patients with high LI also had better disease free survival (DFS) and overall survival (OS). Tumour stage, grade, RAS status and BRAF status were with LI the only prognostic markers in multivariable analysis for OS. Subgroup analyses revealed that high LI had better DFS and OS in mismatch repair (MMR) proficient patients, and in patients without RAS mutation, but not in MMR deficient and RAS mutated patients. Conclusion Although this is the first validation with high level of evidence (IIB) of the prognostic value of a LI test in colon cancers, it still needs to be confirmed in independent series of colon cancer patients.
Details
Originalsprache | Englisch |
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Seiten (von - bis) | 16-24 |
Seitenumfang | 9 |
Fachzeitschrift | European journal of cancer |
Jahrgang | 82 |
Publikationsstatus | Veröffentlicht - 1 Sept. 2017 |
Peer-Review-Status | Ja |
Externe IDs
PubMed | 28651158 |
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ORCID | /0000-0002-9321-9911/work/164199011 |
Schlagworte
Ziele für nachhaltige Entwicklung
ASJC Scopus Sachgebiete
Schlagwörter
- Biomarker, Colorectal carcinoma, Immune response, Prospective cohort study