To Evaluate Thrombosis Risk in Chemotherapy Patients With Solid Tumors Who Receiving Thrombocytopenia Treatment

Sponsor
Liaoning Tumor Hospital & Institute (Other)
Overall Status
Completed
CT.gov ID
NCT05688306
Collaborator
(none)
3,494
1
20.4
171.3

Study Details

Study Description

Brief Summary

Chemotherapy-induced thrombocytopenia (CIT) is a common hematological toxicity in patients with solid tumors undergo chemotherapy, which can increase the risk of bleeding, prolong hospital stay, increase medical costs, and even lead to death in severe cases. The incidence and severity of CIT varies among different chemotherapy regimens. Recombinant human interleukin-11 (rhIL-11) and recombinant human thrombopoietin (rhTPO) have been approved for the treatment of chemotherapy-induced thrombocytopenia.

Tumor patients are at high risk for venous thromboembolism (VTE). In the clinical study of rhIL-11, it was found that the administration of rhIL-11 in healthy subjects caused an increase in the plasma concentration of vWF factor in the form of normal mults. The application of rhIL-11 in patients with myeloid leukemia can increase the concentration of α2 globulin, fibrinogen and prothrombin time. However, there have been no large-scale clinical studies at home and abroad to evaluate whether platelet raising therapy will increase the risk of thrombosis in chemotherapy patients with solid tumor. This study is aimed to evaluate the efficacy and safety of platelet upwelling therapy in patients with solid tumors undergoing chemotherapy.

Condition or Disease Intervention/Treatment Phase
  • Drug: Recombinant Human Interleukin-11 for Injection

Study Design

Study Type:
Observational
Actual Enrollment :
3494 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
A Real World Observational Study to Evaluate Thrombosis Risk in Chemotherapy Patients With Solid Tumors Who Receiving Platelet-raising Therapy
Actual Study Start Date :
Sep 2, 2020
Actual Primary Completion Date :
May 16, 2022
Actual Study Completion Date :
May 16, 2022

Outcome Measures

Primary Outcome Measures

  1. To assess the incidence of thrombosis. [1 month after treatment.]

Secondary Outcome Measures

  1. To evaluate the absolute count of platelets. [1 month after treatment.]

  2. To evaluate the level D-dimer. [1 month after treatment.]

  3. To examine the coagulation function index. [1 month after treatment.]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with pathological diagnosis of solid tumors or lymphomas.

  • Have received chemotherapy.

  • Diagnosed of CIT.

  • Continuous use of platelet raising drugs for at least 5 days.

Exclusion Criteria:
  • Thrombocytopenia caused other than chemotherapy, including but not limited to: traditional Chinese medicine, congenital platelet disease, etc.

  • The basic value of platelet count is continuously higher than 300×10^9/L.

  • Those without blood routine or coagulation function data.

  • Those who received non-chemotherapy drugs that may cause thrombocytopenia, such as sulfonamides.

  • Pseudothrombocytopenia due to Ethylenediamine tetraacetic acid (EDTA) as an anticoagulant in test samples.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Xing Xiaojing Shenyang Liaoning China 110000

Sponsors and Collaborators

  • Liaoning Tumor Hospital & Institute

Investigators

  • Principal Investigator: Xiaojing Xing, Liaoning Tumor Hospital & Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Liaoning Tumor Hospital & Institute
ClinicalTrials.gov Identifier:
NCT05688306
Other Study ID Numbers:
  • IL-11xs
First Posted:
Jan 18, 2023
Last Update Posted:
Jan 18, 2023
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 18, 2023