Consensus molecular subgroups (CMS) of colorectal cancer (CRC) and first-line efficacy of FOLFIRI plus cetuximab or bevacizumab in the FIRE3 (AIO KRK-0306) trial.


Journal

Annals of oncology : official journal of the European Society for Medical Oncology
ISSN: 1569-8041
Titre abrégé: Ann Oncol
Pays: England
ID NLM: 9007735

Informations de publication

Date de publication:
01 11 2019
Historique:
entrez: 24 12 2019
pubmed: 24 12 2019
medline: 4 8 2020
Statut: ppublish

Résumé

FIRE-3 compared first-line therapy with FOLFIRI plus either cetuximab or bevacizumab in 592 KRAS exon 2 wild-type metastatic colorectal cancer (mCRC) patients. The consensus molecular subgroups (CMS) are grouping CRC samples according to their gene-signature in four different subtypes. Relevance of CMS for the treatment of mCRC has yet to be defined. In this exploratory analysis, patients were grouped according to the previously published tumor CRC-CMSs. Objective response rates (ORR) were compared using chi-square test. Overall survival (OS) and progression-free survival (PFS) times were compared using Kaplan-Meier estimation, log-rank tests. Hazard ratios (HR) were estimated according to the Cox proportional hazard method. CMS classification could be determined in 438 out of 514 specimens available from the intent-to-treat (ITT) population (n = 592). Frequencies for the remaining 438 samples were as follows: CMS1 (14%), CMS2 (37%), CMS3 (15%), CMS4 (34%). For the 315 RAS wild-type tumors, frequencies were as follows: CMS1 (12%), CMS2 (41%), CMS3 (11%), CMS4 (34%). CMS distribution in right- versus (vs) left-sided primary tumors was as follows: CMS1 (27% versus 11%), CMS2 (28% versus 45%), CMS3 (10% versus 12%), CMS4 (35% versus 32%). Independent of the treatment, CMS was a strong prognostic factor for ORR (P = 0.051), PFS (P < 0.001), and OS (P < 0.001). Within the RAS wild-type population, OS observed in CMS4 significantly favored FOLFIRI cetuximab over FOLFIRI bevacizumab. In CMS3, OS showed a trend in favor of the cetuximab arm, while OS was comparable in CMS1 and CMS2, independent of targeted therapy. CMS classification is prognostic for mCRC. Prolonged OS induced by FOLFIRI plus cetuximab versus FOLFIRI plus bevacizumab in the FIRE-3 study appears to be driven by CMS3 and CMS4. CMS classification provides deeper insights into the biology to CRC, but at present time has no direct impact on clinical decision-making.The FIRE-3 (AIO KRK-0306) study had been registered at ClinicalTrials.gov: NCT00433927.

Sections du résumé

BACKGROUND
FIRE-3 compared first-line therapy with FOLFIRI plus either cetuximab or bevacizumab in 592 KRAS exon 2 wild-type metastatic colorectal cancer (mCRC) patients. The consensus molecular subgroups (CMS) are grouping CRC samples according to their gene-signature in four different subtypes. Relevance of CMS for the treatment of mCRC has yet to be defined.
PATIENTS AND METHODS
In this exploratory analysis, patients were grouped according to the previously published tumor CRC-CMSs. Objective response rates (ORR) were compared using chi-square test. Overall survival (OS) and progression-free survival (PFS) times were compared using Kaplan-Meier estimation, log-rank tests. Hazard ratios (HR) were estimated according to the Cox proportional hazard method.
RESULTS
CMS classification could be determined in 438 out of 514 specimens available from the intent-to-treat (ITT) population (n = 592). Frequencies for the remaining 438 samples were as follows: CMS1 (14%), CMS2 (37%), CMS3 (15%), CMS4 (34%). For the 315 RAS wild-type tumors, frequencies were as follows: CMS1 (12%), CMS2 (41%), CMS3 (11%), CMS4 (34%). CMS distribution in right- versus (vs) left-sided primary tumors was as follows: CMS1 (27% versus 11%), CMS2 (28% versus 45%), CMS3 (10% versus 12%), CMS4 (35% versus 32%). Independent of the treatment, CMS was a strong prognostic factor for ORR (P = 0.051), PFS (P < 0.001), and OS (P < 0.001). Within the RAS wild-type population, OS observed in CMS4 significantly favored FOLFIRI cetuximab over FOLFIRI bevacizumab. In CMS3, OS showed a trend in favor of the cetuximab arm, while OS was comparable in CMS1 and CMS2, independent of targeted therapy.
CONCLUSIONS
CMS classification is prognostic for mCRC. Prolonged OS induced by FOLFIRI plus cetuximab versus FOLFIRI plus bevacizumab in the FIRE-3 study appears to be driven by CMS3 and CMS4. CMS classification provides deeper insights into the biology to CRC, but at present time has no direct impact on clinical decision-making.The FIRE-3 (AIO KRK-0306) study had been registered at ClinicalTrials.gov: NCT00433927.

Identifiants

pubmed: 31868905
pii: S0923-7534(20)32595-3
doi: 10.1093/annonc/mdz387
pmc: PMC6927316
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
Bevacizumab 2S9ZZM9Q9V
Cetuximab PQX0D8J21J
Leucovorin Q573I9DVLP
Fluorouracil U3P01618RT
Camptothecin XT3Z54Z28A

Banques de données

ClinicalTrials.gov
['NCT00433927']

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

1796-1803

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of the European Society for Medical Oncology.

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Auteurs

S Stintzing (S)

Department of Medicine, Division of Hematology, Oncology, and Tumor Immunology (CCM), Charité Universitaetsmedizin Berlin, Berlin, Germany. Electronic address: sebastian.stintzing@charite.de.

P Wirapati (P)

SIB Swiss Institute of Bioinformatics, Bioinformatic Core Facility, Lausanne, Switzerland.

H-J Lenz (HJ)

USC Norris Comprehensive Cancer Center, Los Angeles, USA.

D Neureiter (D)

Institute of Pathology, Paracelsus Medical University/Salzburger Landeskliniken (SALK), Salzburg, Austria.

L Fischer von Weikersthal (L)

Gesundheitszentrum St. Marien, Amberg.

T Decker (T)

Oncological Practice, Ravensburg.

A Kiani (A)

Medizinische Klinik IV, Klinikum Bayreuth, Bayreuth.

F Kaiser (F)

VK&K Studien GbR, Landshut.

S Al-Batran (S)

Department of Hematology and Oncology, Krankenhaus Nordwest, Frankfurt/Main.

T Heintges (T)

Department of Medicine II, Städtisches Klinikum Neuss, Neuss.

C Lerchenmüller (C)

Oncological Practice, Münster.

C Kahl (C)

Haematology and Oncology, Staedtisches Klinikum Magdeburg, Magdeburg.

G Seipelt (G)

Oncological Practice, Bad Soden.

F Kullmann (F)

Department of Medicine I, Klinikum Weiden, Weiden.

M Moehler (M)

University Hospital Mainz, Mainz, Germany.

W Scheithauer (W)

Department of Internal Medicine I & Comprehensive Cancer Center, Medical University Vienna, Vienna, Austria.

S Held (S)

ClinAssess GmbH, Leverkusen.

D P Modest (DP)

Department of Medicine III, University Hospital, LMU Munich, Munich.

A Jung (A)

Institute of Pathology University of Munich, Munich, Germany.

T Kirchner (T)

Institute of Pathology University of Munich, Munich, Germany.

D Aderka (D)

Department of Gastrointestinal Oncology, Chaim Sheba Medical Center, Ramat Gan, Israel.

S Tejpar (S)

Molecular Digestive Oncology, UZ Leuven, Belgium.

V Heinemann (V)

Department of Medicine III, University Hospital, LMU Munich, Munich.

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Classifications MeSH