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. Author manuscript; available in PMC: 2019 Jun 1.
Published in final edited form as: Cancer Immunol Res. 2018 Apr 5;6(6):630–635. doi: 10.1158/2326-6066.CIR-17-0715

Table 1.

Clinical characteristics of the patients and the imaging and histologic findings of sarcoid-like granulomatosis of the lung

Baseline Patient Characteristics
Patient 1 Patient 2 Patient 3 Patient 4
Age/Sex 61/Female 29/Male 65/Female 74/Male
Tumor type Lung adenocarcinoma Hodgkin lymphoma Melanoma Melanoma
Prior therapy Carboplatin, pemetrexed, plus bevacizumab ABVD; ICE; GND; autologous stem cell transplant with BEAM; brentuximab Ipilimumab plus nivolumab Carboplatin plus etoposide; ipilimumab; temozolomide;
Immunotherapy agent Pembrolizumab Nivolumab and Lirilumab Pembrolizumab Pembrolizumab
Treatment regimen 200 mg every 3 weeks Nivolumab: 3mg/kg every 2 weeks; Lirilumab: 3mg/kg, every 4 weeks 2mg/kg every 3 weeks 2mg/kg every 3 weeks
Clinical Characteristics of Sarcoid-like Granulomatosis of the Lung
Onset since therapy initiation 8.0 months 20.7 months 11.3 months 14.3 months
New or worsening respiratory symptom None None None None
Treatment for sarcoid-like granulomatosis Hold pembrolizumab Hold nivolumab and lirilumab Hold pembrolizumab Hold pembrolizumab
Imaging Features of Sarcoid-like Granulomatosis of the Lung (Fig. 1)
Patient 1 Patient 2 Patient 3 Patient 4
Lung
  • Focal nodular consolidation (2.1×1.5 cm) with GGO halo in the right lower lobe

  • FDG-avid on PET

  • Focal nodular opacity (1.5×1.4 cm) with GGO halo in the right lower lobe

  • Increased to a focal consolidation (3.3×2.0 cm) and new bilateral small nodular opacities after 2 months

  • FDG-avid on PET

  • Focal round consolidation (2.5×1.8 cm) with GGO halo in the left upper lobe

  • Focal area of small centrilobular nodular opacities

  • Gradually increased to a focal consolidation (3.9×2.8 cm) over 16 months in the right lower lobe

New or enlarging lymph nodes None None None None
Follow-up imaging
  • Consolidation markedly decreased on follow-up CT scans performed 2 and 4 months after holding pembrolizumab

  • Consolidation markedly decreased on follow-up CT performed 2 months later while on another immune-checkpoint inhibitor regimen

  • Consolidation resolved on follow-up CT performed 1 month after holding pembrolizumab

  • Consolidation markedly decreased on follow-up CT performed 4 months after holding pembrolizumab

Histologic Findings of Sarcoid-like Granulomatosis of the Lung (Fig. 2)
Patient 1 Patient 2* Patient 3 Patient 4
  • Diffuse replacement of the lung parenchyma by large aggregates of epithelioid histiocytes forming non-necrotizing granulomas

  • Alveolar spaces filled by organizing fibroblasts, alveolar macrophages, numerous lymphocytes focally forming aggregates, scattered eosinophils, and rare epithelioid giant cells

  • N/A (Biopsy not performed)

  • Interstitial non-necrotizing granulomas with associated lymphocytic infiltrates and peri-airway granulomas with prominent giant cells

*

The patient also underwent biopsy of supraclavicular node that has been involved by lymphoma, which showed distorted architecture by nodules containing loose aggregates of histiocytes and giant cells with admixed lymphocytes rimmed by circumferential fibrosis, representing a pattern reminiscent of sarcoidosis.

ABVD: Doxorubicin Hydrochloride, Bleomycin, Vincristine Sulfate, Dacarbazine

ICE: Ifosfamide, Carboplatin, and Etoposide

GND: Gemcitabine, Navelbine, and Doxorubicin

BEAM: Carmustine, Etoposide, Cytarabine, and Melphalan

GGO: ground glass opacity

FDG: fluorodeoxyglucose

PET: positron emission tomography