Source:http://linkedlifedata.com/resource/pubmed/id/19136393
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2009-5-27
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pubmed:abstractText |
Our objective was to investigate the impact of methotrexate, paclitaxel, ifosfamide, and cisplatin (M-TIP) on long-term fertility in poor-risk nonseminomatous germ cell tumors (NSGCT). Thirty patients with poor-risk NSGCT (median age, 29 years; range, 17-62 years) were treated with methotrexate 250 mg/m(2) with folinic acid rescue (day 1) and paclitaxel 175 mg/m(2) (day 1), followed by ifosfamide 1.2 g/m(2) and cisplatin 20 mg/m(2) (days 2-6). Treatment consisted of 4 cycles of M-TIP administered every 3 weeks. Twenty-one patients were continuously disease-free at a median follow-up of 5.3 years (range, 0.9-8.4 years). Sperm count and hormonal analyses were examined prechemotherapy (30 patients) and postchemotherapy (21 patients). Counts were classified as follows: lower than 1 x 10(6)/mL, azoospermia; 1-20 x 10(6)/mL, oligospermia (OS); higher than 20 x 10(6)/mL, normospermia (NS). Patients were followed for a median of 2.3 years (range, 0.9-3.8 years) postchemotherapy. The prechemotherapy median luteinizing hormone (LH) serum levels were slightly above the upper normal limit, whereas the serum levels of follicle-stimulating hormone (FSH) and testosterone (T) were within the reference interval. Eleven (52.3%) patients had NS prechemotherapy. Among the patients with NS, 72.7% still had NS following chemotherapy. Overall, 17 of 21 (80.9%; 33.3% OS and 47.6% NS) patients had recovery of spermatogenesis after treatment. The median FSH serum levels were significantly elevated at least 1 year postchemotherapy when compared with the pretreatment levels. Eighteen months after the completion of chemotherapy the median FSH levels had returned to the reference limits. Serum LH and T levels were unaffected by chemotherapy. Prior to chemotherapy 4 of 30 patients had fathered 5 children. Since completion of chemotherapy, 5 patients have fathered 5 children. The majority of men with poor-risk germ cell tumors who were treated with the M-TIP regimen demonstrated recovery spermatogenesis after treatment, and Leydig cell function was unaffected.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cisplatin,
http://linkedlifedata.com/resource/pubmed/chemical/Follicle Stimulating Hormone,
http://linkedlifedata.com/resource/pubmed/chemical/Ifosfamide,
http://linkedlifedata.com/resource/pubmed/chemical/Luteinizing Hormone,
http://linkedlifedata.com/resource/pubmed/chemical/Methotrexate,
http://linkedlifedata.com/resource/pubmed/chemical/Paclitaxel,
http://linkedlifedata.com/resource/pubmed/chemical/Testosterone
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pubmed:status |
MEDLINE
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pubmed:issn |
1939-4640
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pubmed:author |
pubmed-author:EconomopoulosTT,
pubmed-author:GerostathouMM,
pubmed-author:KamposiorasCC,
pubmed-author:KarageorgopoulouSS,
pubmed-author:KoumarianouAA,
pubmed-author:MacherasAA,
pubmed-author:PapaxoinisGG,
pubmed-author:PectasidesDD,
pubmed-author:PectasidesEE,
pubmed-author:PsyrriAA,
pubmed-author:SkondraMM,
pubmed-author:TountasNN
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pubmed:issnType |
Electronic
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pubmed:volume |
30
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
280-6
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pubmed:meshHeading |
pubmed-meshheading:19136393-Adolescent,
pubmed-meshheading:19136393-Adult,
pubmed-meshheading:19136393-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:19136393-Cisplatin,
pubmed-meshheading:19136393-Fertility,
pubmed-meshheading:19136393-Follicle Stimulating Hormone,
pubmed-meshheading:19136393-Humans,
pubmed-meshheading:19136393-Ifosfamide,
pubmed-meshheading:19136393-Luteinizing Hormone,
pubmed-meshheading:19136393-Male,
pubmed-meshheading:19136393-Mediastinal Neoplasms,
pubmed-meshheading:19136393-Methotrexate,
pubmed-meshheading:19136393-Middle Aged,
pubmed-meshheading:19136393-Neoplasms, Germ Cell and Embryonal,
pubmed-meshheading:19136393-Paclitaxel,
pubmed-meshheading:19136393-Risk Factors,
pubmed-meshheading:19136393-Spermatogenesis,
pubmed-meshheading:19136393-Spermatozoa,
pubmed-meshheading:19136393-Testicular Neoplasms,
pubmed-meshheading:19136393-Testis,
pubmed-meshheading:19136393-Testosterone,
pubmed-meshheading:19136393-Young Adult
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pubmed:articleTitle |
Testicular function in poor-risk nonseminomatous germ cell tumors treated with methotrexate, paclitaxel, ifosfamide, and cisplatin combination chemotherapy.
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pubmed:affiliation |
Second Department of Internal Medicine, Propaedeutic, Oncology Section, University of Athens, Attikon University Hospital, Rimini 1, Haidari, Athens, Greece. pectasid@otenet.gr
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pubmed:publicationType |
Journal Article,
Clinical Trial
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