1977
DOI: 10.1016/s0022-3476(77)81305-x
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Postpubertal evaluation of gonadal function following cyclophosphamide therapy before and during puberty

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Cited by 101 publications
(30 citation statements)
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“…This can be explained by the lower total radiation dose used in single-fraction TBI, but there is also evidence that fractionation of one dose may lead to longer sterile periods in man [1]. Variations in the exposure to alkylating agents prior to BMT could be responsible for this absence of testicular recovery, as the cumulative dosage rather than the daily dosage is the most important factor determining gonadotoxicity of cyclophosphamide, also used in the preparative regimens [14,22,26]. In view of the known vulnerability of germinal epithelium to irradiation and the elevated FSH levels, we expect most of the male patients to be infertile.…”
Section: Discussionmentioning
confidence: 99%
“…This can be explained by the lower total radiation dose used in single-fraction TBI, but there is also evidence that fractionation of one dose may lead to longer sterile periods in man [1]. Variations in the exposure to alkylating agents prior to BMT could be responsible for this absence of testicular recovery, as the cumulative dosage rather than the daily dosage is the most important factor determining gonadotoxicity of cyclophosphamide, also used in the preparative regimens [14,22,26]. In view of the known vulnerability of germinal epithelium to irradiation and the elevated FSH levels, we expect most of the male patients to be infertile.…”
Section: Discussionmentioning
confidence: 99%
“…However, the long-term ability to suppress a relapse is likely only for cyclophosphamide. Among the three immunosuppressants, cyclophosphamide and chlorambucil have gonadal toxicity which seems to be dose dependent [20,21]. Further administration of these drugs should be avoided, especially in pubertal boys, in view of the cumulative toxicity.…”
Section: Discussionmentioning
confidence: 99%
“…This effect may to some extent be dose related and has been observed in males treated before as well as during and after puberty [3, 38,[40][41][42][43]. The concept that the prepubertal testis may be less susceptible remains to be proven in humans; some studies suggest a higher risk in the sexually more mature patients [33], others show no age relationship [35,39,42].…”
Section: Discussionmentioning
confidence: 99%