Literature DB >> 9241501

Markedly improved survival in malignant sacro-coccygeal teratomas--16 years, experience.

D Misra1, J Pritchard, D P Drake, E M Kiely, L Spitz.   

Abstract

AIM OF STUDY: To see the impact of cisplatin- and carboplatin-based protocols on survival in malignant sacrococcygeal teratomas (SCT).
METHODS: Twenty infants and children with malignant SCT were treated at the Hospital for Sick Children, Great Ormond Street, London, over a 16-year period from 1979 to 1994. There were 5 males and 15 females, age ranged from 1 day to 3.5 years (mean 18 months).
RESULTS: Twelve patients (60%) had distant metastasis: 9 lung metastasis, 2 liver involvement, 2 bony metastases, 1 cerebral metastasis and 1 bilateral inguinal lymph node deposits. From 1982 to 1986, patients received the BEP chemotherapy protocol which included cis-platinum, bleomycin and etoposide (VP 16). After 1986, cis-platinum was replaced with carboplatin in the new JEB protocol. Patient 1 did not receive any chemotherapy, Patients 2-4 received varying protocols (2 deaths), Patients 5-8 received the BEP regime (1 death) and Patients 9-20 received JEB (1 death). The first three deaths were due to uncontrolled local disease and/or metastasis, while the latter death was due to bleomycin toxicity. Overall, 9 of 12 (75%) patients with distant metastasis survived as opposed to 7 of 8 (88%) patients with localised disease. Of the 12 patients who received the JEB protocol, 11 (92%) survived, including 7 patients with metastatic disease and 2 with local recurrence. Seven patients (35%) had relapse while on treatment or follow-up, 4 of these are disease-free with further therapy. In 6 of these children, serum AFP rose before there was clinical or radiological evidence of relapse. In 2 other patients, further chemotherapy was recommenced solely on the basis of rising serum AFP, these patients did not subsequently develop overt metastasis.
CONCLUSIONS: We conclude that the treatment of choice for malignant SCT is the JEB regime, to be given for 4 courses or to be continued for 2 courses beyond documented Complete Response (CR). Excision of the primary tumour and coccyx should be done in all cases even if a CR has been documented. Metastases not responding to chemotherapy would need appropriate surgery, radiotherapy is hardly ever needed. An overall cure rate exceeding 90% can be expected.

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Year:  1997        PMID: 9241501     DOI: 10.1055/s-2008-1071078

Source DB:  PubMed          Journal:  Eur J Pediatr Surg        ISSN: 0939-7248            Impact factor:   2.191


  4 in total

1.  Somatic malignant transformation in a sacrococcygeal teratoma in a child and the use of F18FDG PET imaging.

Authors:  R Howman-Giles; A J A Holland; D Mihm; J M Montfort; S Arbuckle; S Kellie
Journal:  Pediatr Surg Int       Date:  2007-09-09       Impact factor: 1.827

2.  Long-term outcomes of surgery for malignant sacrococcygeal teratoma: 20-year experience of a regional UK centre.

Authors:  Basem A Khalil; Asher Aziz; Pierina Kapur; Gill Humphrey; Antonino Morabito; James Bruce
Journal:  Pediatr Surg Int       Date:  2009-01-28       Impact factor: 1.827

3.  Sacrococcygeal Teratoma with Yolk Sac Component in a Neonate.

Authors:  Ashwini Chandrasekhar Khanolkar; Nirali Chirag Thakkar; Yogesh Kumar Sarin
Journal:  J Neonatal Surg       Date:  2015-07-01

4.  Long-Term Outcomes of Sacrococcygeal Germ Cell Tumors in Infancy and Childhood.

Authors:  Rangsan Niramis; Maitree Anuntkosol; Veera Buranakitjaroen; Achariya Tongsin; Varaporn Mahatharadol; Wannisa Poocharoen; Suranetr La-Orwong; Kulsiri Tiansri
Journal:  Surg Res Pract       Date:  2015-10-04
  4 in total

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