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The study of relationship between pelvic functional bone marrow's dose volume parameters of pelvic malignant tumors intensity-modulated radiotherapy plans and acute hematological toxicities during concurrent chemoradiotherapy

The study of relationship between pelvic functional bone marrow's dose volume parameters of pelvic malignant tumors intensity-modulated radiotherapy plans and acute hematological toxicities during concurrent chemoradiotherapy

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OIN-17011113
Enrollment
Unknown
Registered
2017-04-11
Start date
2017-05-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Gynecological tumor and rectum cancer

Interventions

Rectum cancer group:pelvic functional bone marrow's dose-volume parameter's limits
gynecological cancer group:pelvic functional bone marrow's dose-volume parameter's limits

Sponsors

Jiangmen Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for rectum cancer: 1) pathological confirmation, clinical stage II and III,patients needing preoperative chemoradiotherapy or postoperative chemoradiotherapy but without pretreatment radiotherapy; 2) aged 18 to 80 years, PS 0-2; 3) normal liver and kidney function; 4) normal bone marrow function: Hb >10 g/dl, neutrophil cells= 2000/ul, WBC = 4000/ul,PLT = 100,000/ul; 5) all patients signed the informed consent of chemoradiotherapy. Inclusion criteria for cervical cancer/endometrial cancer: 1) pathological confirmation, clinical stage IB to IVa, patients needing radical chemoradiotherapy or those who have some bad prognostic factors and need postoperative chemoradiotherapy; 2) All patients should not have any pretreatment radiotherapy before concurrent chemoradiotherapy; 3) aged 18 to 80 years, PS 0-2; 4) normal liver and kidney function; 5) normal bone marrow function: Hb >10 g/dL,neutrophil cells= 2000/ul, WBC = 4000/ul, PLT = 100,000/ul; 6) all patients signed the informed consent of radiotherapy.

Exclusion criteria

Exclusion criteria: Exclusion criteria for rectum cancer: 1) Patients once received pelvic pretreatment radiotherapy before concurrent chemoradiotherapy; 2) Patients with severe comorbidities which make them not tolerate any chemoradiotherapy; 3) Patients with severe obstructive disease. Exclusion criteria for cervical cancer/endometrial cancer: 1) Patients need para-aortic radiotherapy; 2) Patients once received pelvic pretreatment radiotherapy before concurrent chemoradiotherapy; 3) Patients with severe comorbidities which make them not tolerate any chemoradiotherapy; 4) Patients with severe obstructive disease.

Design outcomes

Primary

MeasureTime frame
functional bone marrow 1 and functional bone marrow 2's parameters of dose and volume;hematological toxicity during chemoradiotherapy;

Countries

China

Contacts

Public ContactXiao Lin

Jiangmen Central Hospital

xiaolin7966165@126.com+86 13929058809

Outcome results

None listed

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