From IB2 to IIIB locally advanced cervical cancers: report of a ten-year experience
Creators
- 1. Radiotherapy Department, Lucien Neuwirth Cancer Institute, 108 bis avenue Albert Raimond, BP60008, 42271 Saint-Priest-en-Jarez cedex (France)
- 2. Public Health Department, Lucien Neuwirth Cancer Institute, 108 bis avenue Albert Raimond, BP60008, 42271 Saint-Priest-en-Jarez cedex (France)
- 3. Chelsea and Westminster Hospital, 369 Fulham Road, London, SW10 9NH (United Kingdom)
- 4. Obstetrics and Gynecology Department, Saint Etienne University Hospital Medical Center, avenue Albert Raimond, BP60008, 42271 Saint-Priest-en-Jarez cedex (France)
- 5. Research Group in Cancer Biology, National Cancer Institute, Bogotá (Colombia)
- 6. Research Group in Radiobiology Clinical, Molecular and Cellular, National Cancer Institute, Bogotá (Colombia)
Description
Despite screening campaigns, cervical cancers remain among the most prevalent malignancies and carry significant mortality, especially in developing countries. Most studies report outcomes of patients receiving the usual standard of care. It is possible that these selected patients may not correctly represent patients in a real-world setting, which may be a limitation in interpreting outcomes. This study was undertaken to identify prognostic factors, management strategies and outcomes of locally advanced cervical cancers (LACC) treated in daily clinical practice. Medical files of all consecutive patients treated with curative intent for LACC in a French Cancer Care Center between 2004 and 2014 were reviewed retrospectively. Ninety-four patients were identified. Performance status was ≥ 2 in 10.6%. Median age at diagnosis was 63.0. Based on the International Federation of Gynecology and Obstetrics classification, tumours were classified as follows: 10.6% IB2, 22.3% IIA, 51.0% IIB, 4.3% IIIA and 11.7% IIIB. Pelvic lymph nodes were involved in 34.0% of cases. Radiotherapy was delivered for all patients. Radiotherapy technique was intensity modulated radiation therapy or volumetric modulated arc therapy in 39.4% of cases. A concurrent cisplatin chemotherapy was delivered in 68.1% of patients. Brachytherapy was performed in 77.7% of cases. The recommended standard care (concurrent chemoradiotherapy with at least five chemotherapy cycles during radiotherapy, followed by brachytherapy) was delivered in 43.6%. The median overall treatment time was 56 days. Complete tumour sterilisation was achieved in 55.2% of cases. Mean follow-up was 54.3 months. Local recurrence rate was 18.1%. Five-year overall survival was 61.9% (95% Confident Interval (CI) = 52.3–73.2) and five-year disease-specific survival was 68.5% (95% CI = 59.2–79.2). Poor performance status, lymph nodes metastasis and absence of concurrent chemotherapy were identified as poor prognostic factors in multivariate analysis. Less than 50% of patients received the standard care. Because LACC patients and disease are heterogeneous, treatment tailoring appears to be common in current clinical practice. However, guidelines for tailoring management are not currently available. More data about real-world settings are required in order to to optimise clinical trials' aims and designs, and make them translatable in daily clinical practice. retrospectively registered.
Availability note (English)
Available from http://dx.doi.org/10.1186/s13014-018-0963-8; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796580Additional details
Identifiers
Publishing Information
- Journal Title
- Radiation Oncology (Online)
- Journal Volume
- 13
- Journal Page Range
- vp.
- ISSN
- 1748-717X
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 49082524
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- BRACHYTHERAPY; CHEMOTHERAPY; CLINICAL TRIALS; COMBINED THERAPY; LYMPH NODES; MULTIVARIATE ANALYSIS; NEOPLASMS; PATIENTS
- Descriptors DEC
- DISEASES; LYMPHATIC SYSTEM; MATHEMATICS; MEDICINE; NUCLEAR MEDICINE; RADIOLOGY; RADIOTHERAPY; STATISTICS; TESTING; THERAPY
Optional Information
- Copyright
- Copyright (c) The Author(s). 2018
- Notes
- PMCID: PMC5796580; PMID: 29394940; PUBLISHER-ID: 963; OAI: oai:pubmedcentral.nih.gov:5796580