Impaired postoperative leucocyte counts after preoperative radiotherapy for rectal cancer in the Stockholm III Trial

Author:

Pettersson D1,Glimelius B23,Iversen H1,Johansson H2,Holm T1,Martling A1

Affiliation:

1. Department of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden

2. Department of Oncology and Pathology, Karolinska Institute, Stockholm, Sweden

3. Department of Radiology, Oncology and Radiation Science, Uppsala University, Uppsala, Sweden

Abstract

Abstract Background Radiotherapy (RT) in rectal cancer increases postoperative morbidity. A suggested reason is RT-induced bone marrow depression resulting in impaired leucocyte counts. The ongoing Stockholm III Trial randomizes patients with operable rectal cancers to short-course RT with immediate surgery (SRT), short-course RT with surgery delayed for 4–8 weeks (SRT-delay) and long-course RT with surgery delayed for 4–8 weeks (LRT-delay). This study examined differences between the randomization arms regarding leucocyte response and postoperative complications. Methods Patients randomized in the Stockholm III Trial between October 1998 and November 2010 were included. Data were collected in a prospective register. Additional data were obtained by retrospective review of clinical records. Results Of 657 randomized patients, 585 had data on leucocytes. The SRT arm had the highest proportion of postoperative complications (SRT, 52·5 per cent; SRT-delay, 39·4 per cent; LRT-delay, 41 per cent; P = 0·010). There was no association between low preoperative leucocyte count and postoperative complications (P = 0·238). Irrespective of randomization arm, patients with an impaired postoperative to preoperative leucocyte ratio had the highest rate of complications (low ratio, 56·6 per cent; intermediate ratio, 46·9 per cent; high ratio, 36·3 per cent; P = 0·010). The SRT arm had the highest proportion of low ratios (SRT, 48·9 per cent; SRT-delay, 22·8 per cent; LRT-delay, 22 per cent; P < 0·001). Conclusion An impaired postoperative leucocyte response is associated with postoperative complications. The highest risk is with immediate surgery following short-course radiotherapy. Registration number: NCT 00904813 (http://www.clinicaltrials.gov).

Publisher

Oxford University Press (OUP)

Subject

Surgery

Reference12 articles.

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2. Cavallin-Ståhl E. A systematic overview of radiation therapy effects in rectal cancer;Glimelius;Acta Oncol,2003

3. Randomized study on preoperative radiotherapy in rectal carcinoma [see comments];Stockholm Colorectal Cancer Study Group;Ann Surg Oncol,1996

4. Long-term results of a randomised trial of short-course low-dose adjuvant pre-operative radiotherapy for rectal cancer: reduction in local treatment failure [see comments];Goldberg;Eur J Cancer,1994

5. Interval between preoperative radiotherapy and surgery influences postoperative mortality in rectal cancer patients: the sooner the better;Marijnen;Eur J Cancer,2001

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