Patient age predicts the delay before survivors of cancer utilise their cryopreserved sperm for assisted reproductive technology.
Author(s)
Type
Journal Article
Abstract
Objective: Sperm cryopreservation (sperm banking) is the recommended standard of care for fertility preservation for men with cancer. Men can utilise their sperm for assisted reproductive technology (ART) when they are ready to become fathers. However, the duration of sperm cryopreservation that should be offered to men is unknown. We hypothesised that younger men with cancer require a longer duration of sperm storage before readiness to utilise their samples for ART, compared with older patients. To test this hypothesis, we investigated whether age at sperm harvest predicts the time of sperm storage necessary before ART.
Design: A retrospectively analysed cohort study spanning 37 years using prospectively acquired routine clinical data.
Setting: A specialist andrology facility in the UK, that provides unlimited storage of sperm as part of NHS treatment free-of-charge to the patient.
Participants: Adolescent boys and men with a confirmed diagnosis of cancer were identified by cross-referencing and verifying patient records: Human Fertility & Embryology Authority (HEFA), Department of Andrology, and the NHS Spine Services Portal database, part of the Health and Social Care Information Centre.
Main outcome measures: The primary outcome measures were the effect of age on the time from sperm cryopreservation to use for ART, and the specificity and sensitivity of age at predicting the requirement of >10 years sperm storage.
Results: 4305 men harvested and cryopreserved their sperm between 1976 and 2013. Men with cancer comprised 3191 and were included in the study. The cancer types that indicated sperm cryopreservation comprised testicular (1130, 35.4%), lymphoma (762, 23.9%), leukaemia (462, 14.5%), and others (838, 26.3%). At sperm harvesting, their median age was 30.3 years (IQR 24.6 to 36.2). Sperm from 217 (6.8%) patients with a median age of 31.3 (IQR 26.5 to 36.7) were utilized for ART after a median of 7.8 years (interquartile range (IQR) 3.5 to 14.3).
Increasing age (HR=1.02, 95% CI 1.01 to 1.04, P=0.001), or age decile compared to ≤20 years (P=0.003), was associated with a reduced time interval to sperm utilisation. Age at harvest (P=0.006) was robust to multivariate Cox models (including cancer diagnosis, survival, and year of harvest) and sensitivity analyses. Age ≤30 years at sperm harvest was highly specific (86.1%) and sensitive (65.0%) at predicting the requirement for over ten years of sperm storage prior to ART (AUC 0.82, 95% CI 0.74 to 0.90, P<0.0001).
Conclusions: Age at sperm cryopreservation is a key predictor for the likely storage duration necessary prior to ART in men with cancer. A policy of fixed duration of sperm storage may disproportionately deny young patients with cancer access to ART. Policies on sperm storage duration in this population should be reviewed.
Design: A retrospectively analysed cohort study spanning 37 years using prospectively acquired routine clinical data.
Setting: A specialist andrology facility in the UK, that provides unlimited storage of sperm as part of NHS treatment free-of-charge to the patient.
Participants: Adolescent boys and men with a confirmed diagnosis of cancer were identified by cross-referencing and verifying patient records: Human Fertility & Embryology Authority (HEFA), Department of Andrology, and the NHS Spine Services Portal database, part of the Health and Social Care Information Centre.
Main outcome measures: The primary outcome measures were the effect of age on the time from sperm cryopreservation to use for ART, and the specificity and sensitivity of age at predicting the requirement of >10 years sperm storage.
Results: 4305 men harvested and cryopreserved their sperm between 1976 and 2013. Men with cancer comprised 3191 and were included in the study. The cancer types that indicated sperm cryopreservation comprised testicular (1130, 35.4%), lymphoma (762, 23.9%), leukaemia (462, 14.5%), and others (838, 26.3%). At sperm harvesting, their median age was 30.3 years (IQR 24.6 to 36.2). Sperm from 217 (6.8%) patients with a median age of 31.3 (IQR 26.5 to 36.7) were utilized for ART after a median of 7.8 years (interquartile range (IQR) 3.5 to 14.3).
Increasing age (HR=1.02, 95% CI 1.01 to 1.04, P=0.001), or age decile compared to ≤20 years (P=0.003), was associated with a reduced time interval to sperm utilisation. Age at harvest (P=0.006) was robust to multivariate Cox models (including cancer diagnosis, survival, and year of harvest) and sensitivity analyses. Age ≤30 years at sperm harvest was highly specific (86.1%) and sensitive (65.0%) at predicting the requirement for over ten years of sperm storage prior to ART (AUC 0.82, 95% CI 0.74 to 0.90, P<0.0001).
Conclusions: Age at sperm cryopreservation is a key predictor for the likely storage duration necessary prior to ART in men with cancer. A policy of fixed duration of sperm storage may disproportionately deny young patients with cancer access to ART. Policies on sperm storage duration in this population should be reviewed.
Date Issued
2015-12-03
Date Acceptance
2015-10-01
Citation
Blood, 2015, 126 (23), pp.4481-4481
ISSN
0006-4971
Publisher
American Society of Hematology
Start Page
4481
End Page
4481
Journal / Book Title
Blood
Volume
126
Issue
23
Copyright Statement
This research was originally published in Blood. Patel A, Stroud T, Breen D, Taifoor A, Bradshaw A, Szydlo R, Ramsay JWA, Bloom SR, Dhillo WS, Jayasena CN. Patient age predicts the delay before survivors of cancer utilise their cryopreserved sperm for assisted reproductive technology. Blood. 2015; 126:4481-4481. © the American Society of Hematology
Sponsor
The Academy of Medical Sciences
Identifier
https://ash.confex.com/ash/2015/webprogram/Paper86303.html
Subjects
Science & Technology
Life Sciences & Biomedicine
Hematology
Immunology
1102 Cardiovascular Medicine And Haematology
1103 Clinical Sciences
1114 Paediatrics And Reproductive Medicine
Publication Status
Published
Coverage Spatial
Orlando, FL, USA