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Multi-institutional retrospective study on chemotherapy and pelvic radiotherapy for stage IVB cervical cancer.

Multi-institutional retrospective study on chemotherapy and pelvic radiotherapy for stage IVB cervical cancer. - JGOG1088S/JROSG22-1

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000052234
Enrollment
300
Registered
2023-11-01
Start date
2023-11-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Stage IVB cervical cancer

Interventions

None listed

Sponsors

Japanese Gynecologic Oncology Group (JGOG) Japanese Radiation Oncology Study Group (JROSG)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1) Eighteen years of age or older at the time of initial examination. 2) Patients who has a histopathological diagnosis of cervical cancer and the histological type is either squamous cell carcinoma, adenocarcinoma, or adenosquamous carcinoma. 3) Patients diagnosed with stage IVB (FIGO2018, Nissanpu 2020) at first presentation. Cases in which distant metastasis is limited to inguinal lymph node metastasis are excluded. 4) Patients who received chemotherapy with a treatment start date between January 1, 2016 and December 31, 2020. Chemotherapy in this section must have been administered as either (1) or (2) below. Radiotherapy is not required. (1) Patients must have received at least 4 courses of platinum doublet. (Bevacizumab is not required.) (2) Concurrent chemoradiotherapy with platinum drugs was administered.

Exclusion criteria

Exclusion criteria: 1) Patients who refused data registration. 2) Synchronous or metachronous (within 5 years) malignancies except for carcinoma in situ or mucosal tumors curatively treated with local therapy. 3) Patients who received surgery on the primary tumor during the course of treatment.

Design outcomes

Primary

MeasureTime frame
Overall survival

Secondary

MeasureTime frame
Progression-free survival, rate of urinary tract and gastrointestinal tract adverse events (CTCAE Ver 5.0 Grade 3 or higher), rate of genital bleeding requiring blood transfusion

Countries

Japan

Contacts

Public ContactKeisuke Tsuchida

Kanagawa Cancer Center Department of Radiation Oncology

keisuke.ray.tsuchida@gmail.com045-520-2222

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026