Outcome and late effects of patients treated for childhood vaginal malignant germ cell tumors

Author:

Coppin Robin1ORCID,Martelli Helene2,Chargari Cyrus3,Sudour‐Bonnange Helene4ORCID,Orbach Daniel5ORCID,Vérité Cecile6,Pasquet Marlene7,Saumet Laure8,Piguet Christophe9,Patte Catherine1,Guérin Florent2ORCID,Faure‐Conter Cecile10ORCID,Fresneau Brice111ORCID

Affiliation:

1. Department of Children and Adolescents Oncology Gustave Roussy Paris‐Saclay University Villejuif France

2. Department of Pediatric Surgery Bicêtre Hospital ‐ Assistance Publique‐Hôpitaux de Paris ‐ Université Paris Saclay Le Kremlin‐Bicêtre France

3. Department of Radiation Therapy Gustave Roussy Paris‐Saclay University Villejuif France

4. Department of Pediatric Oncology and AYA Unit Centre Oscar Lambret Lille France

5. SIREDO Oncology Center (Care Innovation and Research for Children Adolescents and Young Adults with Cancer) Institut Curie PSL University Paris France

6. Department of Pediatric Onco‐Hematology Centre Hospitalier Universitaire Bordeaux France

7. Department of Pediatric Onco‐Hematology Centre Hospitalier Universitaire Toulouse France

8. Department of Pediatric Onco‐Hematology Centre Hospitalier Universitaire Montpellier France

9. Department of Pediatric Onco‐Hematology Centre Hospitalier Universitaire Limoges France

10. Department of Pediatric Oncology Institut d'Hemato‐Oncologie Pediatrique Lyon France

11. Paris‐Saclay University Paris‐Sud University Epidemiology of Radiation CESP INSERM Villejuif France

Abstract

AbstractPurposeVaginal malignant germ cell tumors (MGCT) are rare, occurring in children less than 2 years old and raise the question of the optimal local treatment.MethodsWe included children treated for vaginal MGCT according to the French TGM‐95/2013 regimen. Patients were classified as standard risk (SR: localized disease and alpha‐fetoprotein (AFP) < 10,000 ng/mL) or high risk (HiR: metastatic and/or AFP > 10,000 ng/mL) and were treated, respectively, with three to five VBP (vinblastine–bleomycin–cisplatin) or four to six VIP (etoposide–ifosfamide–cisplatin), followed by conservative surgery and/or brachytherapy in case of post‐chemotherapy residuum.ResultsFourteen patients were included (median age = 12 months), of which six (43%) were classified as HiR. AFP levels were normalized after first‐line chemotherapy in all cases but one. A vaginal post‐chemotherapy residuum (median size = 8 mm, range: 1–24 mm) was observed in 13/14 patients, treated by complete resection in seven of 13 (viable cells in three of seven), incomplete resection in four of 13 (viable cells in two of four), with adjuvant brachytherapy in two of 13, and exclusive brachytherapy in two of 13 (viable cells in one of six). Among the six patients with viable disease, four patients received adjuvant chemotherapy. One patient (SR) experienced immediate postoperative relapse despite presenting no viable residual cells and was treated with four VIP cycles and brachytherapy. At last follow‐up (median = 4.6 years, range: 0.5–16), all patients were alive in complete remission. Five patients suffered from vaginal sequelae with synechiae and/or stenosis (of whom four had undergone brachytherapy).ConclusionChildhood vaginal MGCTs show a highly favorable prognosis with risk‐adapted chemotherapy and local treatment of post‐chemotherapy residuum (preferably by conservative surgery with partial vaginectomy). Brachytherapy could be an alternative when conservative surgery is not deemed possible or in cases of incomplete resection with residual viable cells.

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference26 articles.

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4. Pediatric germ cell tumors

5. Clear Cell Adenocarcinoma of the Female Genital Tract: Long-Term Outcome and Fertility Aspects After Brachytherapy Aimed at a Conservative Treatment

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