Tumour location and efficacy of first-line EGFR inhibitors in KRAS/RAS wild-type metastatic colorectal cancer: retrospective analyses of two phase II randomised Spanish TTD trials. Issue 6 (1st December 2019)
- Record Type:
- Journal Article
- Title:
- Tumour location and efficacy of first-line EGFR inhibitors in KRAS/RAS wild-type metastatic colorectal cancer: retrospective analyses of two phase II randomised Spanish TTD trials. Issue 6 (1st December 2019)
- Main Title:
- Tumour location and efficacy of first-line EGFR inhibitors in KRAS/RAS wild-type metastatic colorectal cancer: retrospective analyses of two phase II randomised Spanish TTD trials
- Authors:
- Benavides, Manuel
Díaz-Rubio, Eduardo
Carrato, Alfredo
Abad, Albert
Guillén, Carmen
Garcia-Alfonso, Pilar
Gil, Silvia
Cano, María Teresa
Safont, María José
Gravalos, Cristina
Manzano, José Luis
Sánchez, Antonio
Alcaide, Julia
López, Rafael
Massutí, Bartomeu
Sastre, Javier
Martínez, Eva
Escudero, Pilar
Méndez, Miguel
Aranda, Enrique - Abstract:
- Abstract : Purpose: Metastatic colorectal cancer (mCRC) is a group of distinct diseases, with clinical and molecular differences between right-sided and left-sided tumours driving varying prognosis. Methods: Patients with KRAS / RAS -wild type (wt) mCRC treated in first line with epidermal growth factor receptor inhibitors (EGFR-Is) (cetuximab or panitumumab) plus oxaliplatin or irinotecan-based chemotherapy from two phase II randomised trials conducted by the Spanish Cooperative for the Treatment of Digestive Tumours group were included in this retrospective study. The main objective was to analyse the prognostic effect of primary tumour location on objective response rate (ORR), progression-free survival (PFS) and overall survival (OS). Results: Patients with KRAS -wt right-sided tumours (n=52) had significantly lower efficacy as compared with patients with KRAS -wt left-sided tumours (n=209); confirmed ORR (25% vs 47%, respectively; OR 0.4, 95% CI 0.2 to 0.8, p=0.004); and shorter median PFS (7.2 vs 9.9 months; HR 0.6, 95% CI 0.4 to 0.9, p=0.0157) and OS (13.6 vs 27.7 months; HR 0.5, 95% CI 0.3 to 0.7, p<0.0001). Similar results were observed in the RAS -wt populations. The further classification of left-sided tumours as colon or rectum delivered similar survival outcomes, as well as a tendency to diminished ORR in patients with rectum tumours. Conclusion: We observed significantly improved efficacy outcomes in patients with KRAS / RAS -wt mCRC treated with first-lineAbstract : Purpose: Metastatic colorectal cancer (mCRC) is a group of distinct diseases, with clinical and molecular differences between right-sided and left-sided tumours driving varying prognosis. Methods: Patients with KRAS / RAS -wild type (wt) mCRC treated in first line with epidermal growth factor receptor inhibitors (EGFR-Is) (cetuximab or panitumumab) plus oxaliplatin or irinotecan-based chemotherapy from two phase II randomised trials conducted by the Spanish Cooperative for the Treatment of Digestive Tumours group were included in this retrospective study. The main objective was to analyse the prognostic effect of primary tumour location on objective response rate (ORR), progression-free survival (PFS) and overall survival (OS). Results: Patients with KRAS -wt right-sided tumours (n=52) had significantly lower efficacy as compared with patients with KRAS -wt left-sided tumours (n=209); confirmed ORR (25% vs 47%, respectively; OR 0.4, 95% CI 0.2 to 0.8, p=0.004); and shorter median PFS (7.2 vs 9.9 months; HR 0.6, 95% CI 0.4 to 0.9, p=0.0157) and OS (13.6 vs 27.7 months; HR 0.5, 95% CI 0.3 to 0.7, p<0.0001). Similar results were observed in the RAS -wt populations. The further classification of left-sided tumours as colon or rectum delivered similar survival outcomes, as well as a tendency to diminished ORR in patients with rectum tumours. Conclusion: We observed significantly improved efficacy outcomes in patients with KRAS / RAS -wt mCRC treated with first-line EGFR-I plus chemotherapy in left-sided primary tumours as compared with right-sided primary tumours. Trial registration numbers: NCT01161316 and NCT00885885 . … (more)
- Is Part Of:
- ESMO open. Volume 4:Issue 6(2019)
- Journal:
- ESMO open
- Issue:
- Volume 4:Issue 6(2019)
- Issue Display:
- Volume 4, Issue 6 (2019)
- Year:
- 2019
- Volume:
- 4
- Issue:
- 6
- Issue Sort Value:
- 2019-0004-0006-0000
- Page Start:
- Page End:
- Publication Date:
- 2019-12-01
- Subjects:
- panitumumab -- cetuximab -- metastatic colorectal cancer -- primary tumour location -- sidedness
Cancer -- Periodicals
616.994005 - Journal URLs:
- http://esmoopen.bmj.com/ ↗
https://www.esmoopen.com/current ↗
https://www.sciencedirect.com/journal/esmo-open ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/esmoopen-2019-000599 ↗
- Languages:
- English
- ISSNs:
- 2059-7029
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 17106.xml