Radical Chemo-Radiotherapy for Oesophageal Cancer: An audit of dose-fractionation schedules and timeliness of treatment

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Transcription:

Radical Chemo-Radiotherapy for Oesophageal Cancer: An audit of dose-fractionation schedules and timeliness of treatment Dr L Dixon and Dr J Wadsley Department of Clinical Oncology, Weston Park Hospital, Sheffield, UK.

Background Chemo-radiotherapy is a radical treatment option for patients with oesophageal cancer. RCR guidelines 1, include both squamous cell carcinoma and adenocarcinoma of the oesophagus as Category 1 tumour types.

Background Category 1 tumour types no prolongation of overall treatment time in excess of two days. Within any audit this should be met for 95% patient group. RCR Dose Fractionation Guidelines 2006 50.4Gy in 28 fractions, or 50Gy in 25 fractions. Current local guidelines 50Gy in 25 fractions.

Aims Primary aim - to audit the timeliness and dose fractionation schedule of radical chemoradiotherapy for oesophageal cancer from Sept 2004 Jan 2013. Secondary aim - to assess the survival following treatment: median survival 1-year and 2-year overall survival

Standards 1. Most patients should have dose fractionation schedules which comply with RCR guidelines 2 2. At least 95% of patients should not have a prolongation of overall treatment time in excess of two days 1 3. There is no possible standard for survival figures.

Methods Retrospective audit Electronic search identified patients treated between Sept 2004 and Jan 2013. 52 patients included Analysis was performed using MS Excel and Kaplan-Meier survival was generated GraphPad Prism.

Age Demographics Number Percent 40-49 3 5.7 50-59 11 21.1 60-69 23 44.2 70-79 15 28.8 Sex Male 27 51.9 Female 25 48.1 Histology Squamous 46 88.5 Adenocarcinoma 6 11.5

Results 1 94% (49) received a dose fractionation schedules in accordance with RCR guidelines 2. These patients received 50Gy in 25#

Discussion 1 Target Achieved Most patients received the recommended dose fractionation schedule. Three (6%) patients received alternative doses Two received 54Gy in 30# One received 54Gy in 27#

Results 2 85% (44) completed treatment without a prolongation of treatment in excess of 2 days.

Discussion 2 Not Achieved Only 85% did not have excessive prolongation to treatment 8 (15%) patients had excessive prolongations 7 patients - not treated on bank holidays 1 patient - 5 day gap due to oesophageal stent insertion; gap calculation was performed to compensate (54Gy in 27#)

Discussion 2 RCR guidance 1 published December 2008 32 patients treated subsequently to this Of these - 94% (30/32) had no prolongation in excess of two days 2 patients - not treated bank holidays 1 adenocarcinoma (3 days) 1 squamous cell (2 days) Both patients identified as Category 2 by clinician

Results 3 Median survival: 26.1 months (range 4.1-101) Overall 1-year survival: 69.2% Overall 2-year survival: 56% 100 Percent survival 50 0 0 50 100 Time (months)

Discussion 3 Survival comparable with the results of the SCOPE-1 trial 3 - radical chemo-radiotherapy +/- Cetuximab. Chemo-radiotherapy alone Median survival 25 months 2-year survival of 56%.

Action Plan Results presented locally and nationally Ensure patients correctly identified as Category 1, and treated appropriately Review local guidelines to ensure compliance with RCR guidelines regarding timeliness of treatment.

Future Plans Re-audit to review progress and ensure standards are being maintained. Comparison with radical radiotherapy alone Review survival disease related or other causes Review tolerability of treatment Toxicity and long term effects

References 1. The timely delivery of radical radiotherapy: standards and guidelines for the management of unscheduled treatment interruptions, Third edition, 01 December 2008. RCR Guidelines. 2. RCR Dose Fractionation Guidelines, June 2006. 3. Chemoradiotherapy with or without Cetuximab in patients with oesophageal cancer (SCOPE1): a multicentre, phase 2/3 randomised trial. Crosby T, Hurt CN, Falk S, Gollins S, Mukherjee S, Staffurth J, Ray R, Bashir N, Bridgewater JA, Geh JI, Cunningham D, Blazeby J, Roy R, Maughan T, Griffiths G. Lancet Oncol. 2013 Jun;14(7):627-37. doi: 10.1016/S1470-2045(13)70136-0. Epub 2013 Apr 25.

Thank you