Sustained complete response to TMEp-CI-M platform in refractory small-cell lung cancer with brainstem metastasis: a case report with over 20 months of disease-free survival - Report - MDSpire

Sustained complete response to TMEp-CI-M platform in refractory small-cell lung cancer with brainstem metastasis: a case report with over 20 months of disease-free survival

  • By

  • Yating Wu

  • Hang Li

  • Yonghai Peng

  • Weiqiang Fan

  • June 1, 2026

  • 0 min

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Long-term Complete Remission Achieved with TMEp-CI-M Treatment in Refractory Small-Cell Lung Cancer with Brainstem Metastasis

Overview

This case study reports a 60-year-old male with extensive-stage small-cell lung cancer (ES-SCLC) and brainstem metastasis who achieved over 20 months of disease-free survival following treatment with the TMEp-CI-M platform. The regimen included stereotactic body radiotherapy, low-dose etoposide, anlotinib, and a bispecific antibody, resulting in normalization of ProGRP levels.

Background

Brainstem metastasis from small-cell lung cancer is rare and typically associated with poor prognosis. Standard treatment options for extensive-stage SCLC have limited efficacy, highlighting the need for innovative therapeutic strategies. The TMEp-CI-M platform aims to enhance immunotherapy responses in patients with challenging tumor microenvironments.

Data Highlights

No numerical data or trial data presented in the article.

Key Findings

  • The patient achieved no evidence of disease (NED) for over 20 months.
  • Treatment included stereotactic body radiotherapy, low-dose etoposide, and anlotinib.
  • The bispecific antibody cadonilimab was used for checkpoint inhibition.
  • ProGRP levels normalized from 1803 pg/mL to 23.71 pg/mL after the first treatment cycle.
  • Only Grade 1 hypothyroidism was reported as an adverse event.

Clinical Implications

The TMEp-CI-M platform may provide a novel approach for treating refractory ES-SCLC, particularly in patients with brainstem metastases. This case suggests that innovative treatment strategies could lead to prolonged disease-free survival in challenging cases.

Conclusion

The successful application of the TMEp-CI-M platform in this case indicates its potential for enhancing immunotherapy efficacy in ES-SCLC. Further studies are needed to validate these findings across larger populations.

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