Cervical cancer remains a major health problem worldwide, despite advances
in screening. For patients with locally advanced stage disease, failure to
obtain local-regional control usually results in death. In an effort to imp
rove local regional tumour control, neoadjuvant and concurrent chemoradiati
on have been tested. Recently, 5 randomised trials performed by the Gynecol
ogic Oncology Group, Radiation Therapy Oncology Group and the Southwest Onc
ology Group studying cisplatin-based chemoradiation have demonstrated a sig
nificant survival advantage. Three of the trials compared cisplatin-based c
oncurrent chemotherapy and radiation to radiation alone and 2 trials compar
ed cisplatin-based concurrent chemotherapy and radiation to radiation with
hydroxyurea. In all trials, cisplatin-based chemotherapy administered concu
rrently with radiation therapy was the mon effective therapy, reducing the
risk of death by 30 to 50%. Acute toxicities, principally neutropenia and g
astrointestinal, were more common with chemoradiation but were transient an
d rates of late complications were similar between treatment groups. Based
on the results of these 5 randomised trials, the National Cancer Institute
released a Clinical Announcement stating that cisplatin-based chemotherapy
as used in these trials concurrently with radiation therapy should be the n
ew standard of therapy for high risk early stage and locally advanced stage
cervical cancer.