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Network Pharmacology Prediction and Experimental Validation of Trichosanthes-Fritillaria thunbergii Action Mechanism Against Lung Adenocarcinoma
Published on: March 3, 2023
A case of osimertinib-resistant lung adenocarcinoma responded effectively to alternating therapy
Haruki Hirakawa1, Kazutoshi Komiya1, Chiho Nakashima1
1Division of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Saga University, Saga, Japan.
Abstract:
We report a case of initial lung adenocarcinoma in which transformation to small cell lung carcinoma (SCLC) was observed after acquired resistance to the 3rd generation epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) osimertinib and alternating treatment between chemotherapy and osimertinib was effective. A 61-year-old woman with EGFR mutation positive stage IV lung adenocarcinoma was administered 1st generation EGFR-TKI for 8 months as the first line therapy, then chemotherapy and 2nd generation EGFR-TKI after progressive disease (PD). Four years after initial diagnosis, EGFR T790M was detected in a metastatic lesion of the right thoracic wall and osimertinib was prescribed. Although partial response (PR) was achieved, a new metastatic lesion appeared in the right pleurum near the diaphragm, in which SCLC characteristics were observed with elevation of pro-gastrin-releasing peptide (pro-GRP) at the time of PD under osimertinib. Osimertinib was discontinued and carboplatin plus irinotecan chemotherapy was chosen as the next treatment, leading to PR after 2 cycles. Subsequently, the right thoracic wall tumor harboring T790M and the right pleural tumor near the diaphragm showing transformation to SCLC exhibited opposite responses to therapy alternating between osimertinib and chemotherapy. It is concluded that extended disease control can be achieved by combining appropriate treatments according to the mechanisms of resistance inferred from precise genetic and pathological examination in real time.
Insights
This case study shows small cell lung cancer (SCLC) transformation in lung adenocarcinoma resistant to osimertinib. Alternating chemotherapy and osimertinib effectively controlled both tumor types, extending disease control.
Area of Science:
- Oncology
- Genetics
- Pharmacology
Background:
- Lung adenocarcinoma with EGFR mutations often treated with EGFR tyrosine kinase inhibitors (EGFR-TKIs).
- Acquired resistance to EGFR-TKIs, including osimertinib, is a clinical challenge.
- Transformation to small cell lung carcinoma (SCLC) is a known resistance mechanism.
Observation:
- A patient with stage IV EGFR-mutant lung adenocarcinoma developed resistance to osimertinib.
- A metastatic lesion transformed into small cell lung carcinoma (SCLC) with elevated pro-gastrin-releasing peptide (pro-GRP).
- Tumors with EGFR T790M and SCLC characteristics showed differential responses to osimertinib and chemotherapy.
Findings:
- Alternating treatment with chemotherapy (carboplatin plus irinotecan) and osimertinib achieved partial response in both resistant lung adenocarcinoma and SCLC.
- The T790M-harboring tumor responded to osimertinib, while the SCLC transformed tumor responded to chemotherapy.
- Real-time genetic and pathological examination guided treatment selection.
Implications:
- This case highlights the potential for SCLC transformation as an acquired resistance mechanism to osimertinib.
- Sequential and alternating treatment strategies tailored to specific resistance mechanisms can achieve extended disease control.
- Precise molecular and pathological profiling is crucial for optimizing treatment in advanced lung cancer.
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