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S-1 plus apatinib as first-line palliative treatment for stage IVB gastroesophageal junction adenocarcinoma: A case report and review of the literature.

AbstractRATIONALE:
Apatinib has been proven to significantly prolong the survival of the patients with advanced chemotherapy-refractory gastric cancer. To date, studies on apatinib plus S-1 as first-line palliative therapy for metastatic gastroesophageal junction (GEJ) cancer are rare.
PATIENT CONCERNS:
A 61-year-old female patient was admitted with dysphagia, significant loss of body weight, and poor performance status.
DIAGNOSES:
Endoscopic biopsy revealed the diagnosis of poorly-differentiated GEJ adenocarcinoma, and the patient was clinically staged as T3NxM1G3 (IVB).
INTERVENTIONS:
She had received 4 cycles of palliative therapy using oral apatinib (425 mg daily) plus S-1 (40 mg twice daily for 4 weeks, with a 2-week drug-free interval), followed by maintenance low-dose apatinib (250 mg daily) plus S-1 at the same dosage thereafter.
OUTCOMES:
Her progression-free survival was nearly 5 months, and the overall survival was >11 months up to now. The adverse events were tolerable.
LESSONS:
Apatinib plus S-1 might be an alternative option for late-stage GEJ cancer. However, high-quality trials are warranted before the recommendation of this therapeutic regimen.
AuthorsChu Zhang, Guang-Mao Yu, Miao Zhang, Dong Liu
JournalMedicine (Medicine (Baltimore)) Vol. 99 Issue 1 Pg. e18691 (Jan 2020) ISSN: 1536-5964 [Electronic] United States
PMID31895837 (Publication Type: Case Reports, Journal Article, Review)
Chemical References
  • Antineoplastic Agents
  • Drug Combinations
  • Pyridines
  • S 1 (combination)
  • Tegafur
  • apatinib
  • Oxonic Acid
Topics
  • Adenocarcinoma (drug therapy)
  • Antineoplastic Agents (administration & dosage)
  • Drug Combinations
  • Esophageal Neoplasms (drug therapy)
  • Esophagogastric Junction
  • Female
  • Humans
  • Middle Aged
  • Oxonic Acid
  • Pyridines (administration & dosage)
  • Stomach Neoplasms (drug therapy)
  • Tegafur

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