CA-125 in Disease Progression and Treatment of Lymphangioleiomyomatosis

Chest. 2018 Feb;153(2):339-348. doi: 10.1016/j.chest.2017.05.018. Epub 2017 May 30.

Abstract

Background: Lymphangioleiomyomatosis (LAM) is a destructive lung disease of women caused by proliferation of neoplastic-like LAM cells, with mutations in the TSC1/2 tumor suppressor genes. Based on case reports, levels of cancer antigen 125 (CA-125), an ovarian cancer biomarker, can be elevated in patients with LAM. We hypothesized that elevated serum CA-125 levels seen in some patients with LAM were due to LAM, not other malignancies, and might respond to sirolimus treatment.

Methods: Serum CA-125 levels were measured for 241 patients at each visit. Medical records were reviewed for co-morbidities, disease progression, and response to sirolimus treatment. CA-125 expression in LAM cells was determined by using immunohistochemical analysis.

Results: Almost 25% of patients with LAM had at least one elevated serum CA-125 measurement. Higher serum CA-125 levels correlated with lower FEV1, premenopausal status, and pleural effusion in a multivariate model (each P < .001). Serum CA-125 levels decreased following sirolimus treatment (P = .002). CA-125 and α-smooth muscle actin were co-expressed in LAM lung nodules.

Conclusions: Higher serum CA-125 levels were associated with pleural effusions and reduced pulmonary function and were decreased with sirolimus therapy. LAM cells express CA-125. Some elevated serum CA-125 levels may reflect serosal membrane involvement.

Keywords: CA-125; lymphangioleiomyomatosis; mTOR; pleural effusion; tuberous sclerosis.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Analysis of Variance
  • Biomarkers / blood
  • CA-125 Antigen / blood*
  • CA-125 Antigen / metabolism
  • Disease Progression
  • Female
  • Humans
  • Immunohistochemistry
  • Immunosuppressive Agents / therapeutic use*
  • Lymphangioleiomyomatosis / blood*
  • Lymphangioleiomyomatosis / drug therapy*
  • Lymphangioleiomyomatosis / metabolism
  • Middle Aged
  • Pleural Effusion / blood
  • Respiratory Function Tests
  • Sirolimus / therapeutic use*
  • Young Adult

Substances

  • Biomarkers
  • CA-125 Antigen
  • Immunosuppressive Agents
  • Sirolimus