Utilisation of systemic therapy options in routine treatment of metastatic colorectal cancer in Australia
- Author(s)
- Delahunty, R; Lee, M; Wong, H; Johns, J; McKendrick, J; Lee, B; Kosmider, S; Cooray, P; Ananda, S; Desai, J; Tran, B; Tie, J; Gibbs, P; Wong, R;
- Details
- Publication Year 2020-02,Volume 50,Issue #2,Page 165-172
- Journal Title
- Internal Medicine Journal
- Publication Type
- Journal Article
- Abstract
- BACKGROUND/AIM: In the treatment of metastatic colorectal cancer (mCRC), exposure to all three active cytotoxic agents; 5-fluorouracil/capecitabine, irinotecan and oxaliplatin improves overall survival. The addition of biologic agents (bevacizumab and cetuximab/panitumumab) further improves survival. The uptake of available systemic agents for mCRC in routine practice in Australia is poorly described. METHODS: The ACCORD database was interrogated to determine demographics, treatments and outcomes for patients diagnosed with mCRC between 1/01/2011 and 1/01/2016 at 6 Melbourne centres. RESULTS: 1130 mCRC patients were identified: median age was 69 years (range 26-105), 61% had synchronous disease. KRAS status was known in 62%, of whom 49% were KRAS wild-type. At the time of analysis, 67% of all patients had commenced systemic treatment, 50% had received two or more lines of therapy and 19% of KRAS wild-type patients had received all five active drugs. Of KRAS-mutated patients, 35% had received all four PBS-reimbursed active drugs. Patients who had not received chemotherapy included 72 patients who underwent metastatectomy alone. At a median follow-up of 34 months, median overall survival was 25 months for all patients and 69 months for those who underwent metastatectomy. CONCLUSION: In this community-based cohort 33% of patients had not received any systemic therapy for mCRC and few patients had received all available active systemic agents. As many patients remain alive these figures will likely increase over time. The overall survival of patients with mCRC in this community-based cohort was 25 months and not dissimilar to that achieved in recent clinical trials. This article is protected by copyright. All rights reserved.
- Publisher
- Wiley
- Research Division(s)
- Personalised Oncology
- PubMed ID
- 30887616
- Publisher's Version
- https://doi.org/10.1111/imj.14288
- Terms of Use/Rights Notice
- Refer to copyright notice on published article.
Creation Date: 2019-03-27 08:18:48
Last Modified: 2020-04-02 10:04:36