Metastatic Breast Cancer With Bone and Liver Progression After Multiple Therapies

This breast cancer diagnosis at a glance

Stage at diagnosis
Stage IV
Subtype
Invasive Ductal Carcinoma
Biomarkers
Initial tumor: ER 80%, PgR 60%, HER2 negative, Ki67 18%. Liver metastasis: ER 75%, PgR 55%, HER2 FISH negative, Ki67 22%.
Sex
female
Spread to
bone, liver
Treatment
surgery, chemotherapy, radiation and hormone therapy
Outcome
In Memory

Treatment course, step by step

  1. She underwent lumpectomy with axillary dissection in 2006.
  2. She then received adjuvant chemotherapy.
  3. Radiation followed.
  4. Tamoxifen followed.
  5. Bone metastases in 2009 were treated with aromatase inhibitors and an LH-RH analogue.
  6. Capecitabine was used after further bone progression.
  7. Fulvestrant plus an LH-RH analogue followed.
  8. Oral vinorelbine was used after another progression.
  9. Radiation was also given for bone disease.
  10. Liver progression in 2013 was treated with docetaxel.
  11. Eribulin was given for 10 cycles in 2014.
  12. Weekly liposomal epirubicin followed.
  13. Chemotherapy was stopped when massive liver progression and hepatic failure developed.

What happened, in summary

A 37-year-old woman underwent lumpectomy and axillary dissection in 2006 for grade 2 invasive ductal breast carcinoma. The tumor was ER 80%, PgR 60% and HER2 negative. She received epirubicin/cyclophosphamide followed by paclitaxel, radiation and tamoxifen. In 2009, vertebral metastases were detected. Hormone treatment with aromatase inhibitors and an LH-RH analogue produced a partial response, but bone disease progressed in 2011. She then received 8 cycles of capecitabine. Fulvestrant plus an LH-RH analogue later produced a complete response before another bone progression. Oral vinorelbine, short-course radiation and bone-directed therapy produced another temporary response. By October 2013, the cancer had reached the liver. A liver biopsy remained hormone-receptor positive and HER2 FISH negative. Docetaxel produced a partial response after 4 cycles, followed by progression after 9 cycles. Eribulin was started in July 2014 and continued for 10 cycles, with improved quality of life and no major toxicity, before the liver disease progressed again. Weekly liposomal epirubicin produced another partial response. By December 2015, however, she developed ascites and jaundice, and CT showed massive hepatic involvement with liver failure. Chemotherapy was stopped, and she died on January 31, 2016.

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This is a lay summary of an account first published by PMC / PubMed Central. Read the original in full

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