Neoadjuvant chemotherapy in bulky stage ib-iia cervical cancer: results of a quick course with vincristine, bleomycin, and cisplatin

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Abstract

We retrospectively analyzed 51 consecutive patients with bulky International Federation of Gynecology and Obstetrics stage IB-IIA cervical cancer who were treated with vincristine (1 mg/m2), bleomycin (25 mg/m2; days 1Y3), and cisplatin (50 mg/m2) every 10 days between 1995 and 2005 to assess the efficacy and the safety of a quick course of neoadjuvant chemotherapy. A clinical response occurred in 37 patients (72.5%), including 7 patients (13.7%) with a complete response and 30 patients (58.8%) with a partial response; 13 patients (25.5%) had a stable disease, and 1 patient (2.0%) had a progressive disease. Among the 50 patients who were surgically explored, 42 patients had a radical hysterectomy with pelvic and para-aortic lymphadenectomy; radical surgery was aborted in 8 patients because of paracervical and para-aortic lymph node involvement. Hematologic toxicity was the most common adverse event with anemia occurring most frequently, followed by leukopenia. Importantly, pulmonary toxicity occurred in 7 patients, 2 of whom died of complications from pulmonary fibrosis 1 and 3 months after radical surgery.With a median follow-up of 53 months (range, 2Y129 months), the estimated 2- and 5- year survival rates were 74.9% and 61.3%, respectively. In conclusion, the survival benefit of a quick course of neoadjuvant chemotherapy consisting of vincristine, bleomycin, and cisplatin may be uncertain despite the significant clinical response in bulky International Federation of Gynecology and Obstetrics stage IB2-IIA cervical cancer. Special care is required to monitor bleomycin-induced pulmonary toxicity. ©2009 by IGCS and ESGO.

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Ki, K. D., Song, D. H., Tong, S. Y., Lim, M. C., Lee, J. M., & Lee, S. K. (2009). Neoadjuvant chemotherapy in bulky stage ib-iia cervical cancer: results of a quick course with vincristine, bleomycin, and cisplatin. International Journal of Gynecological Cancer, 19(1), 50–53. https://doi.org/10.1111/IGJ.0b013e318197f8be

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