Prognostic significance of an early decline in serum alpha-fetoprotein during chemotherapy for ovarian yolk sac tumors

2016 ◽  
Vol 142 (3) ◽  
pp. 452-457 ◽  
Author(s):  
Thibault de la Motte Rouge ◽  
Patricia Pautier ◽  
Catherine Genestie ◽  
Annie Rey ◽  
Sébastien Gouy ◽  
...  
Tumor Biology ◽  
1999 ◽  
Vol 20 (4) ◽  
pp. 212-217 ◽  
Author(s):  
Ritsu Yamamoto ◽  
Yukio Wakui ◽  
Kazuhisa Taketa ◽  
Hiroshi Ishikura ◽  
Noriaki Sakuragi ◽  
...  

1999 ◽  
Vol 162 (3 Part 1) ◽  
pp. 959-959
Author(s):  
R. de Wit ◽  
L. Collette ◽  
R. Sylvester ◽  
P.H.M. de Mulder ◽  
D.T. Sleijfer ◽  
...  

2018 ◽  
Vol 28 (1) ◽  
pp. 77-84 ◽  
Author(s):  
Cecile Faure Conter ◽  
Caihong Xia ◽  
David Gershenson ◽  
Jean Hurteau ◽  
Al Covens ◽  
...  

BackgroundWhereas among pediatric oncologists, ovarian yolk sac tumor (O-YST) is considered a chemosensitive tumor, it is often cited as an adverse prognostic factor in adult women with ovarian germ cell tumors.MethodsThe Malignant Germ Cell International Consortium data set included 6 pediatric clinical trials (United States, United Kingdom, and France) and 2 adult gynecology clinical trials (United States). Any patient with an O-YST that was International Federation of Gynecology and Obstetrics stage IC or higher and treated with a platinum-based chemotherapy was eligible. Age was modeled as a continuous and a categorical variable (children, 0-10 years; adolescents, 11–17 years; and adults, ≥18 years). In addition, analyses to establish the optimal cut point for age were conducted. Tumors were coded as pure YST (YST +/− teratoma), mixed YST (YST + other malignant germ cell component), or putative YST (“mixed” germ cell tumor + alpha-fetoprotein >1000 ng/mL). Histology, stage (II/III vs IV), preoperative alpha-fetoprotein levels (<1000; 1000–10,000, or >10,000 ng/mL), and chemotherapeutic regimen (carboplatin vs cisplatin) were analyzed as covariates.ResultsTwo hundred fifty-one patients (median age, 13 years; range, 0–38 years) were identified (78 children, 139 adolescents, and 34 adults). Histology was pure, mixed, and putative in 129, 56, and 66 cases, respectively. Twenty-six patients had stage IV disease, similarly distributed in the 3 age groups. Median follow-up was 5.8 years. The overall 5-year event-free survival and overall survival was 91% (95% confidence interval, 87%–94%) and 96% (92%–98%), respectively. Age did not affect risk of event or death, modeled either as a categorical or continuous variable. Analysis failed to identify an age cut point that affected risk. None of the other covariates investigated had a prognostic impact on event-free survival or overall survival.ConclusionsOvarian yolk sac tumors have an excellent outcome across all age-groups. Age has no apparent impact on the probability of event or death, allowing pediatric and gynecologic oncologists to enroll patients onto joint pediatric and adult trials.


Urology ◽  
1993 ◽  
Vol 42 (1) ◽  
pp. 79-80 ◽  
Author(s):  
Jack A. Brewer ◽  
Edward S. Tank

2020 ◽  
Vol 26 (1) ◽  
Author(s):  
Archika Gupta ◽  
Shiv Narain Kureel ◽  
Shalini Bhalla ◽  
Anand Pandey ◽  
Gurmeet Singh ◽  
...  

Abstract Background Intraabdominal testicular tumors are rare in prepubertal children, and most of the cases reported are intraabdominal testicular teratoma. The present study reports the first case of intraabdominal testicular yolk sac tumor (YST) with normal preoperative serum alpha-fetoprotein levels and diagnosis confirmed on histopathology and immunohistochemistry. Case Presentation A 2-year-old boy presented with bilateral nonpalpable undescended testes (UDT) and abdominal mass. Preoperative serum alpha-fetoprotein was normal. Contrast-enhanced computed tomography (CECT) scan of whole abdomen revealed a heterogeneous mildly enhancing space-occupying lesion in midline and left side of pelvis, left intraabdominal testis and nonvisualization of right testis. During surgery, the mass was found to involve right testis with one turn of torsion of its pedicle. Derotation of testis was performed, and right radical orchiectomy was performed. Left orchiopexy was also performed at the same time. Histopathology and immunohistochemistry confirmed diagnosis of intraabdominal testicular YST. There was no recurrence or distant metastasis at 12-month follow-up after surgery. Conclusion In a case of nonpalpable UDT and abdominal mass/pain, one should always consider possibility of intraabdominal testicular tumor and should investigate the case with serum tumor markers and ultrasound/CECT abdomen. Further, histology of tumor helps in guiding treatment of condition.


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