Stage IV ERBB2-Mutated Lung Cancer With Extensive Bone Metastases

This lung cancer diagnosis at a glance

Stage at diagnosis
Stage IV
Biomarkers
ERBB2 exon 20 insertion (A775_G776 insYVMA). A PIK3CA R425L mutation was later detected at progression and considered a possible resistance mechanism.
Sex
female
Spread to
bone
Treatment
surgery, chemotherapy, targeted therapy and radiation
Outcome
Setback / Progression

Treatment course, step by step

  1. She underwent urgent stabilization of a right femur lesion.
  2. She then received carboplatin, paclitaxel, bevacizumab and an investigational anti-MET therapy, with initial improvement followed by slow progression over 14 months.
  3. Vinorelbine plus trastuzumab followed for 7 months.
  4. Docetaxel plus trastuzumab was then given.
  5. Focal palliative radiation was also delivered to bone metastases, with stable disease for 5 additional months.
  6. Pemetrexed followed after progression.
  7. The cancer progressed again and she transitioned to hospice care.

What happened, in summary

A 61-year-old woman with a 10-pack-year smoking history was diagnosed with Stage IV lung carcinoma after presenting with extensive bone disease, including a destructive lesion in the right femur, together with a mass in the left lower lung. The femur required urgent surgical stabilization, and pathology confirmed metastatic carcinoma from a lung primary. Molecular testing identified an ERBB2 exon 20 insertion. She received carboplatin, paclitaxel, bevacizumab and an investigational anti-MET treatment. The lung lesions initially decreased slightly, followed by slow progression over the next 14 months. She then received vinorelbine plus trastuzumab for 7 months. A later combination of docetaxel plus trastuzumab, together with focal palliative radiation for bone metastases, produced stable disease for about 5 more months. After another progression, she was treated with pemetrexed. The cancer continued to progress, and she transitioned to hospice care. Additional molecular testing at progression identified a PIK3CA R425L alteration that was considered a possible mechanism of resistance to prior HER2-directed treatment.

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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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