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Clinical application of pelvic tumor concurrent radiotherapy and chemotherapy for I degree thrombocytopenia

Clinical application of pelvic tumor concurrent radiotherapy and chemotherapy for I degree thrombocytopenia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026588
Enrollment
Unknown
Registered
2019-10-15
Start date
2020-01-01
Completion date
Unknown
Last updated
2019-10-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tumor

Interventions

experimental group + control group:Synchronous chemoradiotherapy + TPO versus Synchronous chemoradiotherapy

Sponsors

Xiangya Boai Rehabilitation Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) All patients were diagnosed as cervical cancer or rectal cancer by pathology, clinical stage was performed according to the staging criteria, and patients with platelet decline with concurrent radiotherapy and chemotherapy according to the CSCO 2019 version of the principle of diagnosis and treatment; (2) diagnostic criteria that met the level 1 decrease of platelet count, that is, all selected All cases showed 75×10^9/L = 70 points, PS score < 2 points; (5) normal liver and kidney function; (6) aged 18-70 years; (7) standardized radiotherapy and chemotherapy for cervical cancer or rectal cancer.

Exclusion criteria

Exclusion criteria: (1) those with bone marrow metastasis; (2) patients with reduced PLT due to non-chemotherapy or radiotherapy and chemotherapy, such as with idiopathic PLT reduction; (3) those with a history of active bleeding; (4) those with a history of thromboembolism; (5) patients with severe uncontrollable Infection; (6) poor patient compliance; (7) pregnancy or other patients with untreated cancer; (8) with contraindications for radiotherapy and chemotherapy; (9) serious medical diseases; (10) the investigator believes that continuing the trial does not meet scientific or ethical principles.

Design outcomes

Primary

MeasureTime frame
Platelet;

Countries

China

Contacts

Public ContactLong Bin

Xiangya Boai Rehabilitation Hospital

15173116467@qq.com+86 15173116467

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026