Efficacy of Disitamab Vedotin in Treating HER2 2+/FISH- Gastric Cancer
Li Dai1, Xiangren Jin1, Liuxing Wang1
1Department of Gastrointestinal Surgery, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, 550001, People's Republic of China.
Abstract:
Currently, effective therapies for advanced gastric cancer with systemic metastasis are lacking. Pharmacological research has been slowly progressing over the past decades. Here, we report the case of a 56-year-old female with human epidermal growth factor receptor 2 (HER2) expression (IHC 2+/FISH-) in gastric cancer with systemic metastasis. The first-line therapeutic regime consisted of systemic administration of camrelizumab, local arterial infusion of oxaliplatin and arterial embolization, oral apatinib, and PS scheme (oral tegafur-gimeracil-oteracil (S-1) and paclitaxel (PTX), which was administered both intraperitoneally and systemically). After the treatment, a 3-month progression-free survival (PFS) was observed. Due to the occurrence of CTCAE grade 4 adverse reactions, the patient could not tolerate chemotherapy. In the second line of treatment, we replaced the PS scheme with disitamab vedotin and continued the use of carrilizumab and apatinib. After four cycles, efficacy evaluation showed that it was stable disease (SD), only CTCAE 1/2 grade adverse reactions occurred, and endoscopy examination showed local tumor control with a reduction in the ulcer lesion. At the time of submission of the current manuscript, a 6-month PFS was achieved and the treatment was continued. Due to the safety and efficacy of disitamab vedotin observed in our case, we propose that disitamab vedotin could be a promising drug for the treatment of advanced gastric cancer patients with HER2 expression.
Insights
A novel treatment combining camrelizumab, apatinib, and disitamab vedotin shows promise for advanced gastric cancer with HER2 expression, achieving 6-month progression-free survival with manageable side effects.
Area of Science:
- Oncology
- Pharmacology
- Medical Case Study
Background:
- Advanced gastric cancer with systemic metastasis presents significant therapeutic challenges.
- Human epidermal growth factor receptor 2 (HER2) expression is a key factor in gastric cancer treatment strategies.
- Current therapies for metastatic gastric cancer have limited efficacy and progression-free survival.
Observation:
- A 56-year-old female patient with HER2-expressing metastatic gastric cancer received a complex first-line regimen including camrelizumab, oxaliplatin, apatinib, and a PS scheme (S-1 and paclitaxel).
- The patient experienced severe adverse reactions, necessitating a change in treatment.
- Second-line therapy involved replacing the PS scheme with disitamab vedotin, continuing camrelizumab and apatinib, which resulted in stable disease and improved tolerability.
Findings:
- The initial multi-agent therapy provided 3-month progression-free survival but was limited by severe toxicity.
- Disitamab vedotin, in combination with camrelizumab and apatinib, demonstrated efficacy in achieving stable disease and local tumor control.
- The patient achieved a 6-month progression-free survival with the second-line regimen, with only grade 1/2 adverse events.
Implications:
- Disitamab vedotin shows potential as a safe and effective therapeutic option for advanced gastric cancer patients with HER2 expression.
- Combination therapy including disitamab vedotin may offer a viable strategy for managing metastatic gastric cancer.
- Further clinical investigation is warranted to confirm the role of disitamab vedotin in HER2-positive gastric cancer treatment.
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