Stage IV METex14 lung adenocarcinoma: responding well to capmatinib and SBRT

This lung cancer diagnosis at a glance

Stage at diagnosis
Stage IV
Subtype
Adenocarcinoma
Biomarkers
MET exon 14 skipping mutation; PD-L1 >80%. EGFR/RAS/MEK wild type; lung-origin markers present.
Sex
Male
Spread to
brain; bone (thoracic/lumbar vertebrae, right iliac crest, and additional suspicious C3/T4 lesions)
Treatment
targeted therapy and radiation
Outcome
Responding Well

Treatment course, step by step

  1. Capmatinib 800 mg/day with denosumab 120 mg every 3 weeks
  2. SBRT to vertebral metastases 30 Gy/3 fractions [prompt pain relief]
  3. 3-month PET/CT partial metabolic and volumetric regression with resolution of bone hypermetabolism
  4. SBRT to primary lung lesion 50 Gy/5 fractions with capmatinib held 5 days before and after
  5. brain lesion resolved on MRI
  6. isolated right iliac crest oligoprogression treated with pelvic SBRT 30 Gy/3 fractions
  7. no progression at 24 months on continuous capmatinib.

What happened, in summary

This 73-year-old man had well-controlled type 2 diabetes, a 25 pack-year smoking history, productive cough, coughing blood, 3 kg of weight loss, and worsening general health. Chest CT showed a large right upper-lobe lung mass measuring 9 x 7.5 x 5 cm, intertracheobronchial lymph nodes, and a lytic lesion in the D7 vertebral body. CT-guided biopsy confirmed moderately differentiated lung adenocarcinoma. Staging showed a small 3 mm enhancing brain focus and bone disease involving thoracic and lumbar vertebrae, with additional suspicious cervical and thoracic lesions. PET/CT also showed mediastinal lymph-node involvement. The cancer was diagnosed as oligometastatic lung adenocarcinoma with limited brain and bone involvement. Immunohistochemistry showed CK7-positive, CK20-positive, TTF-1-positive, P40-negative disease, with PD-L1 expression above 80%. Next-generation sequencing identified a MET exon 14 skipping mutation and no EGFR, RAS, or MEK alterations. A multidisciplinary tumor board recommended capmatinib 800 mg/day with denosumab. He first received SBRT to vertebral metastases, 30 Gy in 3 fractions, which quickly relieved pain. The asymptomatic brain lesion was not irradiated. After 3 months on capmatinib, PET/CT showed partial metabolic and volume regression of the primary lung cancer and resolution of bone hypermetabolism. At 10 months, imaging showed further tumor regression and complete resolution of mediastinal uptake, allowing SBRT to the primary lung lesion, 50 Gy in 5 fractions. Brain MRI later showed complete resolution of the enhancing lesion. At 18 months, isolated right iliac crest oligoprogression was treated with pelvic SBRT. At 24 months, he was alive, asymptomatic, still taking capmatinib, and had no evidence of disease progression.

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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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