St. Clark et al., GONADAL-FUNCTION FOLLOWING CHEMOTHERAPY FOR HODGKINS-DISEASE - A COMPARATIVE-STUDY OF MVPP AND A 7-DRUG HYBRID REGIMEN, Journal of clinical oncology, 13(1), 1995, pp. 134-139
Purpose and Methods: Gonadal function was assessed in 89 patients afte
r chemotherapy for Hodgkin's disease (HD). Thirty-seven patients had r
eceived mechlorethamine, vinblastine, prednisolone, and procarbazine (
MVPP) and 52 patients, a hybrid combination of chlorambucil, vinblasti
ne, prednisolone, procarbazine, doxorubicin, vincristine, and etoposid
e (ChlVPP/EVA). Fifty men (MVPP, n = 21; ChlVPP/EVA, n = 29) with a me
dian age of 26 years (range, 16 to 54) and 39 women (MVPP, n = 16; Chl
VPP/EVA, n = 23) with a median age of 30 years (range, 15 to 47) were
studied at a median of 30 months (range, 4 to 83) following chemothera
py. Results: Semen analysis showed azoospermia in 35 of 37 men, and in
creased serum follicle-stimulating hormone (FSH) levels in this group
confirmed severe germinal epithelial damage. Analysis of pretreatment
semen in 28 men showed azoospermia in one, oligospermia in four (sperm
count < 20 x 10(6)/mL), and a normal sperm count in the remaining 23.
In the women, 26 of 34 (76%) with a regular menstrual cycle before co
mmencing chemotherapy become amenorrheic following treatment. Menses r
eturned in 10 women, who had a median age of 25 years (range, 21 to 34
), and there were two pregnancies in this group. In the other 16, with
a median age of 36 years (range, 27 to 47), amenorrhea persisted and
premature ovarian failure was confirmed by increased serum gonadotroph
ins and reduced estradiol (E(2)) concentrations. Of the original eight
women in whom menses were maintained following treatment, two subsequ
ently developed amenorrhea and the clinical and biochemical features o
f an early menopause. In total, 18 of 34 women (53%) required hormone
replacement therapy for chemotherapy-induced ovarian failure. Conclusi
on: There was no statistically significant difference in the frequency
or severity of gonadal dysfunction between MVPP- and ChlVPP/EVA-treat
ed patients. We conclude that both of these chemotherapy schedules cau
se substantial damage to gonadal function in both sexes.