Clinical efficacy and toxicity of radio-chemotherapy and magnetic resonance imaging-guided brachytherapy for locally advanced cervical cancer patients: A mono-institutional experience

Authors

  • Ferenc Lakosi Department of Radiation Oncology, University Hospital of Liège, Liège, Belgium
  • Marjoelin de Cuypere Department of Gynecology, University Hospital of Liège, Liège, Belgium
  • Paul Viet Nguyen Department of Radiation Oncology, University Hospital of Liège, Liège, Belgium
  • Nicolas Jansen Department of Radiation Oncology, University Hospital of Liège, Liège, Belgium
  • Bernard Warlimont Department of Radiation Oncology, University Hospital of Liège, Liège, Belgium
  • Akos Gulyban Department of Radiation Oncology, University Hospital of Liège, Liège, Belgium
  • Christine Gennigens Department of Clinical Oncology, University Hospital of Liège, Liège, Belgium
  • Laurence Seidel Department of Biostatistics, University Hospital of Liège, Liège, Belgium
  • Katty Delbecque Department of Pathology, University Hospital of Liège, Liège, Belgium
  • Philippe Coucke Department of Radiation Oncology, University Hospital of Liège, Liège, Belgium
  • Johanne Hermesse Department of Radiation Oncology, University Hospital of Liège, Liège, Belgium
  • Frederic Kridelka Department of Gynecology, University Hospital of Liège, Liège, Belgium

DOI:

https://doi.org/10.3109/0284186X.2015.1062542

Abstract

Background. To evaluate efficacy and toxicity of radio-chemotherapy (RCT) and MR-guided pulsed-dose-rate (PDR) adaptive brachytherapy (IGABT) for locally advanced cervical cancer (LACC).

Material and methods. Between 2007 and 2014 85 patients with FIGO stage 1B1 N+ or ≥ 1B2 cervical cancer were treated with RCT+ IGABT. The treatment consisted of a pelvic± paraaortic external beam radiotherapy (EBRT) (45–50.4 Gy ± 10 Gy boost to primary tumor and/or to pathologic lymph nodes) with concurrent cisplatin followed by 25–35 Gy of PDR IGABT in 30–50 pulses. The ratio of 3D-CFRT/IMRT was 61/24 patients. Dose-volume parameters of high-risk clinical target volume (HR-CTV), intermediate-risk clinical target volume (IR-CTV) and D2cm3 organs at risk (OARs) were reported. Local control (LC), cancer-specific survival (CCS) and overall survival (OS) were analyzed actuarially and morbidity crude rates were scored using CTCAEv4.0.

Results. Mean follow-up was 36 months (range 6–94). The mean D90 and D98 for HR-CTV was 84.4 ± 9 Gy and 77 ± 8.1 Gy, while for IR-CTV was 69.1 ± 4.3 Gy and 64.8 ± 4.3 Gy, respectively. The mean D2cm3 for OARs was the following: bladder: 77.3 ± 10.5 Gy, rectum: 65 ± 6.8 Gy, sigmoid: 63 ± 7.9 Gy and intestine: 64.0 ± 9.1 Gy. Three year LC, CSS and OS were: 94%, 85% and 81%. The three-year regional- and distant control rates were 95% and 74%. Node negative patients had significantly higher three-year CSS (100 vs. 72%, p = 0.016) and OS (92 vs. 72%, p = 0.001) compared to node positive ones. Three-year actuarial late Grade ≥ 3 morbidity was the following: GI: 8%, GU: 5%, Vaginal: 8%. The frequency of Grade ≥ 3 hematological toxicities including anemia/leukopenia/neutropenia/thrombocytopenia were 8.6%/34.7%/24.3%/24.3%, respectively.

Conclusion. This large mono-institutional experience builds up further evidences that IGABT in conjunction with RCT should be the standard of care for patients suffering LACC.

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Published

2015-10-21

How to Cite

Lakosi, F., de Cuypere, M., Viet Nguyen, P., Jansen, N., Warlimont, B., Gulyban, A., … Kridelka, F. (2015). Clinical efficacy and toxicity of radio-chemotherapy and magnetic resonance imaging-guided brachytherapy for locally advanced cervical cancer patients: A mono-institutional experience. Acta Oncologica, 54(9), 1558–1566. https://doi.org/10.3109/0284186X.2015.1062542