Hematopoietic Stem Cell-containing Autologous Blood Reinfusion for Bone Marrow Protection in Cervical Cancer Patients

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-60
SponsorChongqing University Cancer Hospital

About this trial

The aim of this project is to promote the reconstruction of haematopoietic function after chemoradiotherapy for cervical cancer with the innovative use of autologous haematopoietic containing stem cell blood transfusion support.To explore the effect of stored hemopoietic stem cell support therapy on bone marrow protection after concurrent chemoradiotherapy, in order to promote its clinical application.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Autologous blood transfusion with haematopoietic stem cells

    Other intervention

    Transfusion of autologous blood containing haematopoietic stem cells for haematopoietic reconstruction after chemoradiotherapy.Blood tests were performed weekly, if the patient's neutrophils were less than 1.0 × 109 / L during chemoradiotherapy, G-CSF was given as a remedial treatment. If fever occurs, antibiotics were given promptly.Monitor peripheral blood after transfusion. If peripheral blood leukocyte count does not reach 1.0 x 109/L, administer G-CSF 150 μg subcutaneously daily until peripheral blood leukocyte count reaches 1.0 x 109/L.Patients were tested monthly for peripheral blood cells for 6 months after the end of treatment.

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Autologous blood transfusion support therapy groupExperimental treatment 1 intervention
Group B: Conventional treatment groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Incidence of Grade 3-4 neutropenia

Incidence of Grade 3-4 neutropenia

Time frame
6 months
2

Time to reconstruct haematopoietic function

Time to reconstruct haematopoietic function

Time frame
6 months

Secondary outcomes

1

the rate of postponement of the course of chemoradiotherapy

the rate of postponement of the course of chemoradiotherapy

Time frame
3 months
2

reduction in chemotherapy dose

reduction in chemotherapy dose

Time frame
3 months
3

Incidence of febrile neutropenia (FN)

Incidence of febrile neutropenia (FN)

Time frame
3 months
4

Incidence of hematopoietic stem cell reinfusion treatment Adverse Events [Safety and Tolerability])

Incidence of hematopoietic stem cell reinfusion treatment Adverse Events \[Safety and Tolerability\])

Time frame
1 months

Other outcomes

Sponsors and contacts

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