Efficacy of FOLFIRI plus cetuximab vs FOLFIRI plus bevacizumab in 1st-line treatment of older patients with RAS wild-type metastatic colorectal cancer: an analysis of the randomised trial FIRE-3.


Journal

British journal of cancer
ISSN: 1532-1827
Titre abrégé: Br J Cancer
Pays: England
ID NLM: 0370635

Informations de publication

Date de publication:
09 2022
Historique:
received: 26 04 2021
accepted: 09 05 2022
revised: 14 04 2022
pubmed: 1 6 2022
medline: 3 9 2022
entrez: 31 5 2022
Statut: ppublish

Résumé

The evidence on the efficacy of anticancer therapy is limited in older patients with metastatic colorectal cancer (mCRC). This retrospective analysis of phase III FIRE-3 trial assesses the efficacy of FOLFIRI plus either cetuximab or bevacizumab according to the patients' age and sidedness of primary tumour. The study endpoints overall response rate (ORR), progression-free survival (PFS) and overall survival (OS) were compared between younger (<65 years) and older (≥65 years) patients, followed by stratification according to primary tumour sidedness. ORR was compared using Fisher´s exact test, OS and PFS were estimated by the Kaplan-Meier method and compared using the log-rank test. Univariate Cox regression analyses assessed hazard ratios and 95% confidence intervals for OS and PFS. Overall, older patients with RAS WT tumours had a significantly shorter OS when compared to younger patients (25.9 months vs 29.3 months, HR 1.29; P = 0.02). Also the proportion of right-sided tumours was significantly greater in older patients (27.1% vs 17.9%; P = 0.029). Secondary resection rates were numerically higher in younger patients (25.4% vs. 17.6%, P = 0.068) than in older patients. This was primarily seen in the Cetuximab arm, where older patients underwent less likely resection (13.1% vs. 26%; P = 0.02). Older patients with left-sided tumours showed only a trend towards greater efficacy of cetuximab (HR 0.86; P = 0.38). In patients with right-sided primary tumours, older patients did not appear to benefit from cetuximab in contrast to younger patients (≥65 years: 16.6 months vs 23.6 months, HR 1.1; P = 0.87; <65 years: 21.9 months vs 16.4 months HR 1.5; P = 0.31). In FIRE-3, OS was generally shorter in older patients in comparison to younger patients. This could be explained by the overrepresentation of right-sided tumours and a lower secondary resection rate in older patients. The efficacy of targeted therapy was dependent on tumour sidedness in older patients with RAS WT mCRC. FIRE-3 (NCT00433927).

Sections du résumé

BACKGROUND
The evidence on the efficacy of anticancer therapy is limited in older patients with metastatic colorectal cancer (mCRC). This retrospective analysis of phase III FIRE-3 trial assesses the efficacy of FOLFIRI plus either cetuximab or bevacizumab according to the patients' age and sidedness of primary tumour.
METHODS
The study endpoints overall response rate (ORR), progression-free survival (PFS) and overall survival (OS) were compared between younger (<65 years) and older (≥65 years) patients, followed by stratification according to primary tumour sidedness. ORR was compared using Fisher´s exact test, OS and PFS were estimated by the Kaplan-Meier method and compared using the log-rank test. Univariate Cox regression analyses assessed hazard ratios and 95% confidence intervals for OS and PFS.
RESULTS
Overall, older patients with RAS WT tumours had a significantly shorter OS when compared to younger patients (25.9 months vs 29.3 months, HR 1.29; P = 0.02). Also the proportion of right-sided tumours was significantly greater in older patients (27.1% vs 17.9%; P = 0.029). Secondary resection rates were numerically higher in younger patients (25.4% vs. 17.6%, P = 0.068) than in older patients. This was primarily seen in the Cetuximab arm, where older patients underwent less likely resection (13.1% vs. 26%; P = 0.02). Older patients with left-sided tumours showed only a trend towards greater efficacy of cetuximab (HR 0.86; P = 0.38). In patients with right-sided primary tumours, older patients did not appear to benefit from cetuximab in contrast to younger patients (≥65 years: 16.6 months vs 23.6 months, HR 1.1; P = 0.87; <65 years: 21.9 months vs 16.4 months HR 1.5; P = 0.31).
CONCLUSIONS
In FIRE-3, OS was generally shorter in older patients in comparison to younger patients. This could be explained by the overrepresentation of right-sided tumours and a lower secondary resection rate in older patients. The efficacy of targeted therapy was dependent on tumour sidedness in older patients with RAS WT mCRC.
CLINICAL TRIAL
FIRE-3 (NCT00433927).

Identifiants

pubmed: 35637412
doi: 10.1038/s41416-022-01854-y
pii: 10.1038/s41416-022-01854-y
pmc: PMC9427779
doi:

Substances chimiques

Bevacizumab 2S9ZZM9Q9V
Cetuximab PQX0D8J21J
Leucovorin Q573I9DVLP
Fluorouracil U3P01618RT
Camptothecin XT3Z54Z28A

Banques de données

ClinicalTrials.gov
['NCT00433927']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

836-843

Informations de copyright

© 2022. The Author(s).

Références

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pubmed: 26111811

Auteurs

Laura E Fischer (LE)

Department of Medicine III, LMU University Hospital Munich, München, Germany. laura.fischer@med.uni-muenchen.de.

Sebastian Stintzing (S)

Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Hematology, Oncology and Cancer Immunology, Campus Mitte, Berlin, Germany.

Ludwig Fischer von Weikersthal (LF)

Gesundheitszentrum St. Marien, Amberg, Germany.

Dominik P Modest (DP)

Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Hematology, Oncology and Cancer Immunology, Campus Mitte, Berlin, Germany.

Thomas Decker (T)

Oncological Practice, Ravensburg, Germany.

Alexander Kiani (A)

Klinikum Bayreuth GmbH, Bayreuth, Germany.

Florian Kaiser (F)

Oncological Praxis, Landshut, Germany.

Salah-Eddin Al-Batran (SE)

Institute of Clinical Cancer Research at Krankenhaus Nordwest University Cancer Center, Frankfurt, Germany.

Tobias Heintges (T)

Rheinlandklinikum Neuss, Lukaskrankenhaus, Neuss, Germany.

Christian Lerchenmüller (C)

Oncological Practice, Münster, Germany.

Christoph Kahl (C)

Department of Hematology, Oncology and Palliative Care, Klinikum Magdeburg gGmbH, Magdeburg, Germany.
Department of Internal Medicine, Clinic III-Hematology, Oncology and Palliative Care, Rostock University Medical Center, Rostock, Germany.

Gernot Seipelt (G)

Oncological Practice, Bad Soden, Germany.

Frank Kullmann (F)

Department of Medicine I, Klinikum Weiden, Weiden, Germany.

Martina Stauch (M)

Oncological Practice, Kronach, Germany.

Werner Scheithauer (W)

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

Clemens Giessen-Jung (C)

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

Jens Uhlig (J)

Oncological Practice, Naunhof, Germany.

Bettina Peuser (B)

Onkologische Praxis am Diakonissenhaus, Leipzig, Germany.

Claudio Denzlinger (C)

Marienhospital, Stuttgart, Germany.

Arndt Stahler (A)

Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Hematology, Oncology and Cancer Immunology, Campus Mitte, Berlin, Germany.

Lena Weiss (L)

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

Kathrin Heinrich (K)

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

Swantje Held (S)

linAssess GmbH, Leverkusen, Germany.

Andreas Jung (A)

Institut für Pathologie, Ludwig-Maximilians-Universität, München, Germany.

Thomas Kirchner (T)

Institut für Pathologie, Ludwig-Maximilians-Universität, München, Germany.

Volker Heinemann (V)

Department of Medicine III, LMU University Hospital Munich, München, Germany.
Comprehensive Cancer Center (CCC Munich LMU), LMU University Hospital Munich, Munich, Germany.

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