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1.
Placenta ; 132: 27-31, 2023 02.
Article in English | MEDLINE | ID: mdl-36623416

ABSTRACT

INTRODUCTION: hematopoietic stem cells transplantation (HSCT) is a treatment option for malignant and non-malignant haematological diseases. Because of the improved survival rates and the more widespread use of reproductive technologies in the last two decades, the number of patients who conceive is increasing while the pathogenesis of some obstetrical complications observed is not yet fully clarified. METHODS: we present complete data about two pregnancies in women who had previously undergone HSTC, with conditioning regimen including total body irradiation. One pregnancy is spontaneous and one after oocytes donation. RESULTS: In both pregnancies we observed relevant intrauterine growth retardation, attributable to a deficit in implantation and placentation. Ultrasound and histological data point to a defective placenta development, possibly sustained by uterine vessel damage caused by irradiation. A deeper understanding of factors influencing placentation post total body irradiation and HSCT, including the possible role of donor's sex and graft versus host disease, is pivotal to improve pregnancy outcomes in this specific population.


Subject(s)
Graft vs Host Disease , Hematopoietic Stem Cell Transplantation , Pregnancy Complications , Female , Pregnancy , Humans , Graft vs Host Disease/pathology , Graft vs Host Disease/therapy , Hematopoietic Stem Cell Transplantation/adverse effects , Placenta/pathology , Hematopoietic Stem Cells , Whole-Body Irradiation
2.
J Obstet Gynaecol ; 36(6): 783-788, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27153290

ABSTRACT

Two-hundred and sixty-nine females aged ≤42 and undergoing an allogeneic stem cell transplant were retrospectively studied to assess the effect of age, conditioning regimen and chronic graft-versus-host disease (cGVHD) on resumption of stable menstrual cyclicity. Overall, a stable menstrual cyclicity was observed in 22% of cases. The cumulative probability of menses resumption was significantly age and conditioning regimen related. A statistically significant inverse correlation between cGVHD severity and menses resumption was observed only in univariate analysis. In patients with residual ovarian function, infertility was found in 43% and early menopause in 45%. An increased incidence of prematurity and low birth weight (LBW) was observed among the single spontaneous pregnancies. Follicle-stimulating hormone (FSH) and 17 beta-oestradiol levels were found to be inadequate to detect both early signs of menses resumption and menstrual stability. Our study confirms the crucial role of full dose total body irradiation (TBI) and age on menses recovery and fertility after haematopoietic stem cell transplantation (HSCT). The impact of severe cGVHD remains unclear.


Subject(s)
Fertility , Hematopoietic Stem Cell Transplantation/adverse effects , Menstrual Cycle , Menstruation Disturbances/etiology , Transplantation Conditioning/adverse effects , Adult , Age Factors , Estradiol/blood , Female , Follicle Stimulating Hormone/blood , Graft vs Host Disease/etiology , Hematopoietic Stem Cell Transplantation/methods , Humans , Infertility/etiology , Menstruation Disturbances/blood , Pregnancy , Pregnancy Outcome , Retrospective Studies , Transplantation Conditioning/methods
3.
Haematologica ; 98(3): 339-45, 2013 Mar.
Article in English | MEDLINE | ID: mdl-22929982

ABSTRACT

The aim of this study was to assess the degree of spermatogenesis defects in sperm analysis in long-term male survivors after allogeneic hematopoietic stem cell transplantation in order to identify the risk factors related to potential infertility after hematopoietic stem cell transplantation and to provide data on longitudinal sperm recovery after hematopoietic stem cell transplantation. Here, the Late Effects Working Party of the European Group for Blood and Marrow Transplantation reports data of sperm analysis from 224 males who underwent hematopoietic stem cell transplantation. Median time between transplantation and sperm analysis was 63 months (8-275 months). At last sperm analysis, presence of any degree of spermatozoa was reported in 70 (31%) and complete azoospermia in 154 (69%) patients. In multivariate analysis, being conditioned with total body irradiation (RR 7.1; 95% CI: 3.4-14.8) and age over 25 years at transplantation (RR 2.4; 95% CI: 1.09-5.2) were significantly associated with higher risk for azoospermia. In patients not conditioned with total body irradiation, ongoing chronic graft-versus-host disease is the main adverse factor for sperm recovery (RR of 3.11; 95% CI: 1.02-9.47; P=0.045). Already established risk factors, such as total body irradiation and age older than 25 years at hematopoietic stem cell transplantation, were seen to be the most relevant adverse risk factor for sperm production after hematopoietic stem cell transplantation. Furthermore, for the first time, ongoing graft-versus-host disease has been shown to be the most relevant adverse factor for sperm recovery, particularly in patients conditioned without total body irradiation. We also introduce a useful scoring system to predict the probability of male long-term survivors' azoospermia.


Subject(s)
Azoospermia/etiology , Graft vs Host Disease/complications , Adult , Graft vs Host Disease/etiology , Health Surveys , Hematopoietic Stem Cell Transplantation/adverse effects , Humans , Male , Middle Aged , Retrospective Studies , Risk Factors , Semen Analysis , Survivors , Transplantation Conditioning/adverse effects , Transplantation, Homologous , Young Adult
4.
Haematologica ; 88(10): 1163-8, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14555313

ABSTRACT

BACKGROUND AND OBJECTIVES: Graft-versus-host disease (GVHD) is a complex syndrome observed after bone marrow transplantation (BMT) affecting several organs including the lower genital female tract. We tried to evaluate the incidence of genital tract involvement and whether there are specific risk factors. DESIGN AND METHODS: A retrospective study was conducted in order to describe genital manifestations of GVHD and evaluate its incidence, severity and remission among 213 females who underwent BMT. The risk factors studied were previous pregnancies, vaginal cultures just before BMT and hormonal replacement therapy (HRT). RESULTS: Genital lesions considered as expression of GVHD were found in 53 patients (24.9%). They appeared in the first 100 days after BMT in 12 women and beyond in 41 cases. Seventy-three percent of patients with such lesions showed some evidence of chronic GVHD elsewhere. The proposed grading, the first attempt of its kind, showed that genital chronic GVHD was minimal in 66%, moderate in 22% and severe in 12% of patients. Vaginal fibrosis, sometimes with complete obstruction, was seen in this last form. This occurred in 86.8% of patients after 2-157 months (median 22) while persistent GVHD was observed in 7 of them. In our sample no significant association was found between genital GVHD and previous pregnancies or vaginal infections at BMT, while HRT seems poorly associated with gynecological manifestations of GVHD (p=0.049). INTERPRETATION AND CONCLUSIONS: Genital GVHD is not unusual after BMT. It can seriously affect female sexuality and the overall quality of life. We suggest stressing the importance of early detection of genital involvement in order to prevent the most serious lesions. Further studies are needed to identify the triggering factors associated with the development of genital GVHD.


Subject(s)
Bone Marrow Transplantation/adverse effects , Genital Diseases, Female/epidemiology , Genitalia, Female/pathology , Graft vs Host Disease/epidemiology , Adolescent , Adult , Aged , Anemia, Aplastic/surgery , Anemia, Aplastic/therapy , Bone Marrow Transplantation/methods , Child , Female , Genital Diseases, Female/pathology , Graft vs Host Disease/pathology , Humans , Incidence , Leukemia/surgery , Leukemia/therapy , Middle Aged , Remission Induction/methods , Retrospective Studies , Risk Factors , Time , Transplantation, Homologous
5.
Ann N Y Acad Sci ; 966: 187-92, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12114271

ABSTRACT

Several lines of experimental evidence suggest that sex hormones may influence the development and activity of chronic graft-versus-host disease (cGVHD), which frequently occurs in patients undergoing allogeneic bone marrow transplantation (ABMT). Following ABMT, young women are commonly treated with hormone replacement therapy (HRT) because of irreversible gonadal failure. It seemed therefore worthwhile to investigate the effects of this therapy on the activity of cGVHD. Premenopausal women treated with ABMT for hematological malignancies between January 1997 and December 2000 were evaluated for cGVHD activity. They were divided into two groups, depending on whether or not they were treated with HRT. Seventy-one women qualified for the present study: 39 received HRT (treated group), while 32 did not (controls). In both groups of patients, cGVHD activity score was comparable before the start of HRT. No differences were observed in cGVHD activity score between the HRT group and controls after 3, 6, 12, and 24 months from the start of HRT. Furthermore, HRT did not induce any increase in the cGVHD activity score in the treated group of patients at any time from the start of HRT. According to present data, HRT did not appear to influence the activity of cGVHD in young women who underwent ABMT for hematological malignancies. Therefore, we can safely propose this therapy for women with gonadal failure after ABMT.


Subject(s)
Bone Marrow Transplantation/adverse effects , Estrogen Replacement Therapy , Graft vs Host Disease , Hematologic Neoplasms/therapy , Primary Ovarian Insufficiency/drug therapy , Adult , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Estrogen Replacement Therapy/adverse effects , Female , Graft vs Host Disease/etiology , Humans , Middle Aged , Primary Ovarian Insufficiency/etiology , Retrospective Studies , Safety , Severity of Illness Index , Transplantation Conditioning/adverse effects , Transplantation, Homologous/adverse effects , Whole-Body Irradiation/adverse effects
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