This trial is a single-arm, prospective clinical study aimed at evaluating the efficacy and safety of hetrombopag in preventing chemotherapy-induced thrombocytopenia (CIT) in patients with gastrointestinal tumors. The study plans to enroll 40 patients with gastrointestinal tumors who develop thrombocytopenia due to chemotherapy. Patients who meet the inclusion and exclusion criteria will maintain the same treatment regimen and dosage as the previous cycle (N-1 cycle). On the day of chemotherapy in the current cycle (N cycle), they will take hetrombopag (D1) at 7.5 mg/day orally for 14 consecutive days on an empty stomach, and may eat two hours after administration, avoiding taking it with meals.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
40
Hetrombopag 7.5 mg/day orally starting on Day 1 for up to 14 days.
Shanghai Changhai Hospital
Shanghai, China
RECRUITINGThe proportion of patients with a platelet count >75×10⁹/L on day 14 (D14)
Time frame: From enrollment to the end of treatment at 2 weeks
The proportion of patients whose next chemotherapy cycle is delayed (≥4 days)
Time frame: From enrollment up to Day 25
The proportion of patients with platelet count >75×10⁹/L on day 21 (D21)
Time frame: From enrollment up to Day 21
The proportion with platelet count >100×10⁹/L on day 21 (D21)
Time frame: From enrollment up to Day 21
The proportion of patients with platelet count <50×10⁹/L
Time frame: From enrollment up to Day 21
The proportion of patients requiring platelet rescue therapy
Time frame: From enrollment up to Day 21
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.