Effect of radiotherapy for rectal cancer on ovarian androgen production

Author:

Segelman J12ORCID,Buchli C13,Svanström Röjvall A14,Matthiessen P5,Arver S67,Bottai M8,Ahlberg M13,Jasuja R9,Flöter-Rådestad A1011,Martling A13

Affiliation:

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

2. Department of Surgery, Ersta Hospital, Stockholm, Sweden

3. Division of Coloproctology, Karolinska University Hospital, Stockholm, Sweden

4. Department of Surgery, St Göran Hospital, Stockholm, Sweden

5. Department of Surgery, School of Health and Medical Sciences, Örebro University, Örebro, Sweden

6. Department of Medicine, Karolinska Institutet, Stockholm, Sweden

7. Centre for Andrology and Sexual Medicine, Karolinska University Hospital, Stockholm, Sweden

8. Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden

9. Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, and Function Promoting Therapies, Weston, Massachusetts, USA

10. Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden

11. Division of Obstetrics and Gynaecology, Karolinska University Hospital, Stockholm, Sweden

Abstract

Abstract Background The impact of radiotherapy (RT) for rectal cancer on ovarian androgen production is unknown. The aim was to examine the effect of RT for rectal cancer on androgen levels in non-oophorectomized women and the association with female sexual desire. Methods This prospective cohort study included women who had surgery for rectal cancer with or without RT. Serum testosterone, free testosterone, androstenedione and dehydroepiandrosterone sulphate (DHEA-S) levels were assessed at baseline, after RT and 1 year after surgery. Sexual desire was assessed by means of the Female Sexual Function Index. Results Twenty-seven participants had surgery alone (RT– group) and 98 had preoperative RT and surgery (RT+ group). During the first year after surgery, median serum testosterone and free testosterone levels decreased from 0·6 (range 0·1–3·6) to 0·5 (0·1–2·3) nmol/l (P < 0·001) and from 9·1 (1·6–45·8) to 7·9 (1·4–22·7) pmol/l (P < 0·001) respectively in the RT+ group, but did not change in the RT– group. Longitudinal regression analysis confirmed a decrease in testosterone and free testosterone after RT. The adjusted change in androstenedione and DHEA-S was not significant in any group. The mean change in testosterone (odds ratio (OR) 2·74, 95 per cent c.i. 1·06 to 7·11; P = 0·038), free testosterone (OR 1·08, 1·02 to 1·15; P = 0·011), androstenedione (OR 1·52, 1·07 to 2·16; P = 0·019) and DHEA-S (OR 0·49, 0·27 to 0·89; P = 0·019) was related to change in sexual desire. Conclusion RT decreased levels of androgens predominantly derived from the ovaries, whereas androgens of mainly adrenal origin remained unchanged. Reduction in ovarian androgens may be associated with reduced sexual desire.

Funder

Swedish Cancer Society

Stockholm Cancer Society

Stockholm County Council

Karolinska Institutet

Bengt Ihre Foundation

National Institutes of Health

Cancerfonden

Stockholms Läns Landsting

Publisher

Oxford University Press (OUP)

Subject

Surgery

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