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Effects of Chemotherapy on Circulating Tumor Cells and Recurrences in Cervical Cancer Patients

Effects of Chemotherapy on Circulating Tumor Cells and Recurrences in IB-IIA Cervical Cancer Patients With Intermediate Risk Factors After Radical Surgery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01063296
Enrollment
400
Registered
2010-02-05
Start date
2010-03-31
Completion date
2014-01-31
Last updated
2010-02-09

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

Conditions

Cervical Cancer

Keywords

cervical cancer

Brief summary

Cervical cancer is a major health problem for Chinese women. It is estimated that nearly 100,000 new cervical cancer cases occur in China every year, which accounts for about 20 percent of global new cases. Surgery and radiotherapy are two major radical treatment methods for IB-IIB cervical cancer. Unlike the United States and some other countries, most of operable women with IB-IIB cervical cancer received radical surgery other than radiotherapy in China. Patients with recurrence risk factors (lymph node metastasis, deep stromal invasion, positive lymphatic vascular space, et al. ) also received adjuvant therapy after surgery, such as radiotherapy or chemoradiotherapy that are recommended in the NCCN guidelines. However, in China a substantial part of patients especially those admitted to tertiary hospitals received several courses of chemotherapy instead of radiotherapy if they had recurrence risk factors . In our previous study, we found that patients with intermediate risk factors (deep stromal invasion, positive lymphatic vascular space, bulky tumor\>4cm) had better disease-free survival and recurrence-free survival when they received chemotherapy compared with radiotherapy. The objective in this study is to investigate whether the advantage of postoperative chemotherapy is a result of circulating tumor cells (CTC) in some of the patients with intermediate risk factors.

Interventions

None listed

Sponsors

Huazhong University of Science and Technology
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patients with histologically confirmed Ib\ IIa (FIGO)cervical carcinoma without previous treatments * Age between 18-70 * With the presence of these three pathological risk factors after radical surgery:(1) positive lymphatic vascular space,(2)outer one-third invasion of the cervical stroma, (3) bulky tumor≥4cm * At least 3 months of disease-free survival

Exclusion criteria

* The presence of other uncontrolled life-threatening disease (Suffering from myocardial infarction or stroke, or unstable angina, decompensated heart failure, or a history of deep vein thrombosis) * Receiving other anti-cancer therapy, such as traditional Chinese drug * Don't be able to finish the whole treatment(chemotherapy or radiotherapy) * liver dysfunction (ALT、AST\>2.5×ULN) * renal dysfunction (Creatinine\>1.5×ULN) * WBC\<4,000/mm3 or PLT\<100,000/mm3 * Received preoperative radiotherapy

Design outcomes

Primary

MeasureTime frame
The occurrence rate of CTCs, distant metastasis-free survival, disease-free survival, metastatic sites3 years

Secondary

MeasureTime frame
Overall survival3 years

Countries

China

Contacts

Primary ContactMa Ding, M.D.
dma@tjh.tjmu.edu.cn86-27-8362681

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026