scholarly journals High-Dose Chemotherapy with Stem Cell Rescue in Desmoplastic Small Round Cell Tumor: A Single-Institution Experience and Review of the Literature

Sarcoma ◽  
2018 ◽  
Vol 2018 ◽  
pp. 1-10
Author(s):  
Kayleen Bailey ◽  
Michael Roth ◽  
Daniel Weiser ◽  
Jonathan Gill

Purpose. Desmoplastic small round cell tumor (DSRCT) is a rare cancer that predominantly affects males averaging 21 years of age at the time of diagnosis. We describe four cases from our institution and place them within the context of a comprehensive review of the literature. Patients and Methods. Study population included any patient who received treatment at Children’s Hospital at Montefiore (CHAM) with histologic diagnosis of DSRCT. A search of the electronic databases PubMed, Cochrane Central Register of Controlled Trials, MEDLINE, and EMBASE for the terms “desmoplastic” AND “small” AND “round” AND “cell” AND “tumor” was performed. Results. One CHAM patient died of disease at 39 months, one patient has relapsed disease at 40 months, and two patients have no evidence of disease at 60 and 91 months. In the literature review, the 3-year OS was 36% and 5-year OS was 13%. There was a statistically significant difference in OS between no transplant and SCT in remission (p=0.004); however, there was no difference between no transplant and SCT not in remission (p=0.23). Conclusion. Given the poor prognosis in DSRCT, this study supports further prospective research into the possible benefit of consolidation of autologous SCT in patients with DSRCT who are in remission, with the alternative inference that these patients in remission may fare well without SCT. Our retrospective review of the literature does not support SCT for patients who are not in remission.

2014 ◽  
Vol 2014 ◽  
pp. 1-5 ◽  
Author(s):  
Christina K. Lettieri ◽  
Pamela Garcia-Filion ◽  
Pooja Hingorani

Desmoplastic small round cell tumor (DSRCT) is a rare but highly fatal malignancy. Due to the rarity of this neoplasm, no large population based studies exist.Procedure. This is a retrospective cohort analysis. Incidence rates were calculated based on sex and ethnicity and compared statistically. Gender-, ethnicity-, and treatment- based survival were calculated using the Kaplan-Meier method.Results. A total of 192 cases of DSRCT were identified. Peak incidence age was between 20 and 24 years. Age-adjusted incidence rate for blacks was 0.5 cases/million and for whites was 0.2 cases/million (P=0.037). There was no statistically significant difference in survival based on gender or ethnicity. When adjusted for age, there was no statistically significant difference in survival amongst patients who received radiation therapy compared to those who did not (HRadj = 0.73; 95% CI 0.49, 1.11). There was a statistically significant survival advantage for patients who received radiation after surgery compared to those who did not (HR 0.49; 95% CI 0.30, 0.79).Conclusion. DSRCT is more common in males and in people of African-American descent. Although overall survival remains poor, radiation therapy following surgery seems to improve outcome in these patients.


2015 ◽  
Vol 2 (1) ◽  
pp. 9-15 ◽  
Author(s):  
Vadim Khachaturov ◽  
Roth W. Christopher ◽  
Jacob R. Hodge ◽  
John Joseph Doyle ◽  
Darren J. Leitao ◽  
...  

2014 ◽  
Vol 12 (1) ◽  
pp. 9 ◽  
Author(s):  
Xiang Li ◽  
Jing Yu ◽  
Shibao Fang ◽  
Xiaoming Xing ◽  
Jie Zhao

2015 ◽  
Vol 10 (2) ◽  
pp. 1103-1108 ◽  
Author(s):  
DIEGO CEZAR DA SILVA PECHUTTI ◽  
PEDRO LUIZ DE ARRUDA LOURENÇAO ◽  
BONIFACIO KATSUNORI TAKEGAWA ◽  
CRISTIANO CLAUDINO OLIVEIRA ◽  
ALEXANDRE NETO

2021 ◽  
Vol 11 ◽  
Author(s):  
Guixia Wei ◽  
Xinyao Shu ◽  
Yuwen Zhou ◽  
Xia Liu ◽  
Xiaorong Chen ◽  
...  

Intra-abdominal desmoplastic small round cell tumor (IDSRCT) is a rare and highly malignant soft tissue neoplasm, which is characterized by rapid progression and poor prognosis. The mechanism underlying the development of this neoplasm remains elusive, but all cases are characterized by the chromosomal translocation t (11;22) (p13; q12), which results in a formation of EWSR1-WT1 gene fusion. The diagnosis of IDSRCT is often made with core-needle tissue biopsy specimens or laparoscopy or laparotomy. Immunohistochemical analyses have shown the co-expression of epithelial, neuronal, myogenic, and mesenchymal differentiation markers. FISH or reverse transcription polymerase chain reaction detecting EWS-WT1 fusion can be performed to assist in molecular confirmation. There is no standard of care for patients with IDSRCT currently, and majority of newly diagnosed patients received the aggressive therapy, which includes >90% resection of surgical debulking, high-dose alkylator-based chemotherapy, and radiotherapy. More recently, targeted therapy has been increasingly administered to recurrent IDSRCT patients and has been associated with improved survival in clinical conditions. Immunotherapy as a possible therapeutic strategy is being explored in patients with IDSRCT. In this review, we summarize currently available knowledge regarding the epidemiology, potential mechanisms, clinical manifestations, diagnosis, treatment, and prognosis of IDSRCT to assist oncologists in comprehensively recognizing and accurately treating this malignancy.


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