Phase II Study of Preoperative Capecitabine and Oxaliplatin-based Intensified Chemoradiotherapy With or Without Induction Chemotherapy in Patients With Locally Advanced Rectal Cancer and Synchronous Liver-limited Resectable Metastases. (December 2016)
- Record Type:
- Journal Article
- Title:
- Phase II Study of Preoperative Capecitabine and Oxaliplatin-based Intensified Chemoradiotherapy With or Without Induction Chemotherapy in Patients With Locally Advanced Rectal Cancer and Synchronous Liver-limited Resectable Metastases. (December 2016)
- Main Title:
- Phase II Study of Preoperative Capecitabine and Oxaliplatin-based Intensified Chemoradiotherapy With or Without Induction Chemotherapy in Patients With Locally Advanced Rectal Cancer and Synchronous Liver-limited Resectable Metastases
- Authors:
- Cho, Hyungwoo
Kim, Jeong Eun
Kim, Kyu-pyo
Yu, Chang Sik
Kim, Jin Cheon
Kim, Jong Hoon
Lee, Myung Ah
Jang, Hong Seok
Oh, Seong Taek
Kim, Sun Young
Oh, Jae Hwan
Kim, Dae Yong
Hong, Yong Sang
Kim, Tae Won - Abstract:
- Abstract : Objectives: Controversy surrounds the management of patients with locally advanced rectal cancer with synchronous resectable liver metastases (LMs). This study was designed to improve both systemic and local control in these patients. Methods: Patients with locally advanced rectal cancer (cT3-4N0 or cTanyN1-2) and synchronous resectable liver-limited metastases (cM1a) were randomly assigned to receive either preoperative treatments of induction CapeOx, followed by chemoradiotherapy with CapeOx (CapeOx-RT) (arm A) or CapeOx-RT alone (arm B). Induction CapeOx consisted of oxaliplatin 130 mg/m 2 on day 1 and capecitabine 1000 mg/m 2 twice daily on days 1 to 14, every 3 weeks for 2 cycles; CapeOx-RT consisted of radiotherapy with 45 Gy/25 daily fractions±5.4 Gy/3 fractions, oxaliplatin 50 mg/m 2 weekly for 5 weeks, and capecitabine 825 mg/m 2 twice daily on days 1 to 38. Total mesorectal excision and simultaneous liver metastasectomy were planned within 6 weeks after completion of preoperative treatments. The primary endpoint was R0 resection rate of both the primary tumor and LMs. Results: Thirty-eight patients were randomly assigned to the present study, 18 to arm A and 20 to arm B. The overall R0 resection rate for both the primary tumor and LMs was 77.8% in arm A and 70.0% in arm B ( P =0.72). The median progression-free survival was 14.2 versus 15.1 months ( P =0.422) and the 3-year overall survival rate was 75.0% versus 88.8% ( P =0.29), respectively.Abstract : Objectives: Controversy surrounds the management of patients with locally advanced rectal cancer with synchronous resectable liver metastases (LMs). This study was designed to improve both systemic and local control in these patients. Methods: Patients with locally advanced rectal cancer (cT3-4N0 or cTanyN1-2) and synchronous resectable liver-limited metastases (cM1a) were randomly assigned to receive either preoperative treatments of induction CapeOx, followed by chemoradiotherapy with CapeOx (CapeOx-RT) (arm A) or CapeOx-RT alone (arm B). Induction CapeOx consisted of oxaliplatin 130 mg/m 2 on day 1 and capecitabine 1000 mg/m 2 twice daily on days 1 to 14, every 3 weeks for 2 cycles; CapeOx-RT consisted of radiotherapy with 45 Gy/25 daily fractions±5.4 Gy/3 fractions, oxaliplatin 50 mg/m 2 weekly for 5 weeks, and capecitabine 825 mg/m 2 twice daily on days 1 to 38. Total mesorectal excision and simultaneous liver metastasectomy were planned within 6 weeks after completion of preoperative treatments. The primary endpoint was R0 resection rate of both the primary tumor and LMs. Results: Thirty-eight patients were randomly assigned to the present study, 18 to arm A and 20 to arm B. The overall R0 resection rate for both the primary tumor and LMs was 77.8% in arm A and 70.0% in arm B ( P =0.72). The median progression-free survival was 14.2 versus 15.1 months ( P =0.422) and the 3-year overall survival rate was 75.0% versus 88.8% ( P =0.29), respectively. Conclusions: Both treatment strategies showed considerable R0 resection rates; however, further study will be warranted to apply these intensified strategies in clinical practice. Abstract : Supplemental Digital Content is available in the text. … (more)
- Is Part Of:
- American journal of clinical oncology. Volume 39:Number 6(2016)
- Journal:
- American journal of clinical oncology
- Issue:
- Volume 39:Number 6(2016)
- Issue Display:
- Volume 39, Issue 6 (2016)
- Year:
- 2016
- Volume:
- 39
- Issue:
- 6
- Issue Sort Value:
- 2016-0039-0006-0000
- Page Start:
- Page End:
- Publication Date:
- 2016-12
- Subjects:
- rectal cancer -- liver metastasis -- chemoradiotherapy
Cancer -- Treatment -- Periodicals
Oncology -- Periodicals
Tumors -- Periodicals
616.994005 - Journal URLs:
- http://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=toc&D=yrovft&AN=00000421-000000000-00000 ↗
http://www.amjclinicaloncology.com ↗
http://journals.lww.com ↗ - DOI:
- 10.1097/COC.0000000000000315 ↗
- Languages:
- English
- ISSNs:
- 0277-3732
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0823.500000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 244.xml