[Diagnosis of uterine sarcomas and rare uterine mesenchymal tumours with malignant potential. Guidelines of the French Sarcoma Group and Rare Gynaecological Tumours]

Bull Cancer. 2024 Jan;111(1):97-116. doi: 10.1016/j.bulcan.2023.08.002. Epub 2023 Oct 6.
[Article in French]

Abstract

The landscape of uterine sarcomas is becoming more complex with the description of new entities associated with recurrent driver molecular alterations. Uterine sarcomas, in analogy with soft tissue sarcomas, are distinguished into complex genomic and simple genomic sarcomas. Leiomyosarcomas and undifferentiated uterine sarcomas belong to complex genomic sarcomas group. Low-grade and high-grade endometrial stromal sarcomas, other rare tumors associated with fusion transcripts (such as NTRK, PDGFB, ALK, RET ROS1) and SMARCA4-deficient uterine sarcoma are considered simple genomic sarcomas. The most common uterine sarcoma are first leiomyosarcoma and secondly endometrial stromal sarcomas. Three different histological subtypes of leiomyosarcoma (fusiform, myxoid, epithelioid) are identified, myxoid and epithelioid leiomyosarcoma being more aggressive than fusiform leiomyosarcoma. The distinction between low-grade and high-grade endometrial stromal sarcoma is primarily morphological and immunohistochemical and the detection of fusion transcripts can help the diagnosis. Uterine PEComa is a rare tumor, which is distinguished into borderline and malignant, according to a risk assessment algorithm. Embryonal rhabdomyosarcoma of the uterine cervix is more common in children but can also occur in adult women. Embryonal rhabdomyosarcoma of the uterine cervix is almost always DICER1 mutated, unlike that of the vagina which is wild-type DICER1, and adenosarcoma which can be DICER1 mutated but with less frequency. Among the emerging entities, sarcomas associated with fusion transcripts involving the NTRK, ALK, PDGFB genes benefit from targeted therapy. The integration of molecular data with histology and clinical data allows better identification of uterine sarcomas in order to better treat them.

Keywords: ALK; Adenosarcoma; Adénosarcome; Endometrial stromal sarcoma; Leiomyosarcoma; Léiomyosarcome; NTRK; PDGFB; PEComa; PECome; Rhabdomyosarcome; SMARCA4; Sarcome du stroma endométrial; Sarcome utérin; Sarcome utérin indifférencié; Translocations; Undifferentiated uterine sarcoma; Uterine sarcoma.

Publication types

  • English Abstract

MeSH terms

  • Adult
  • Child
  • DEAD-box RNA Helicases*
  • DNA Helicases
  • Endometrial Neoplasms*
  • Female
  • Genital Neoplasms, Female*
  • Humans
  • Leiomyosarcoma* / diagnosis
  • Leiomyosarcoma* / genetics
  • Leiomyosarcoma* / therapy
  • Nuclear Proteins
  • Protein-Tyrosine Kinases
  • Proto-Oncogene Proteins
  • Receptor Protein-Tyrosine Kinases
  • Rhabdomyosarcoma, Embryonal* / diagnosis
  • Rhabdomyosarcoma, Embryonal* / genetics
  • Rhabdomyosarcoma, Embryonal* / therapy
  • Ribonuclease III*
  • Sarcoma, Endometrial Stromal* / diagnosis
  • Sarcoma, Endometrial Stromal* / genetics
  • Sarcoma, Endometrial Stromal* / therapy
  • Soft Tissue Neoplasms*
  • Transcription Factors
  • Uterine Cervical Neoplasms*
  • Uterine Neoplasms* / diagnosis
  • Uterine Neoplasms* / genetics
  • Uterine Neoplasms* / therapy

Substances

  • Protein-Tyrosine Kinases
  • Proto-Oncogene Proteins
  • Receptor Protein-Tyrosine Kinases
  • SMARCA4 protein, human
  • DNA Helicases
  • Nuclear Proteins
  • Transcription Factors
  • DICER1 protein, human
  • Ribonuclease III
  • DEAD-box RNA Helicases