alexa Weekly cisplatin 20 mg m2 in patients with carcinoma of cervix receiving pelvic radiotherapy at Srinagarind Hospital: a randomized controlled trial.
Oncology

Oncology

Journal of Cancer Science & Therapy

Author(s): Punushapai U, Yuenyao P, Chumworathayi B, Luanratanakorn S, Udomthavornsuk B

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Abstract OBJECTIVES: To evaluate treatment response and acute treatment-related toxicity of concurrent chemoradiotherapy with cisplatin 20 mg/m2 , compared to 40 mg/m2 as the standard, in locally advanced cervical cancer. STUDY DESIGN: A prospective randomized controlled trial in Srinagarind Hospital, Faculty of Medicine, Khon Kaen University, Khon Kaen. SUBJECTS: 140 patients, >60 years old with biopsy-proven previously untreated invasive carcinoma of cervix, FIGO stage IB2-IVA, undergoing concurrent chemoradiotherapy with adequate bone marrow, renal and liver functions, between April and December 2009. METHODS: All patients were randomly assigned (half in each group)to receive weekly cisplatin at a dose of 40 mg/m2 compared to 20 mg/m2, concurrent with radiotherapy for 6 cycles. Main outcome measures included clinical response, cytological response, and acute treatment-related toxicity. RESULTS: All 140 patients completed 6 cycles of weekly cisplatin. 80\% had squamous cell carcinomas; about half were FIGO stage IIIB. The 40 mg/m2 group showed unplanned interruptions in 13/70 (18.6\%), which was significantly different from the 5/70 (7.1\%) in the 20 mg/m2 group (p=0.02), resulting in prolonged treatment time (p=0.026). Complete responses were found in 69/70 (98.6\%) and 68/70 (97.1\%), respectively, with no significant difference. Hematological and gastrointestinal toxicities were most frequently observed. Acute toxicities in the first group was significantly higher when compared to the second group (p<0.05) as follows; grade 1-2 leukopenia (14.8\% vs. 6.4\%), grade 1-2 neutropenia (9.3\% vs. 2.6\%), grade 2 N/V (3.8\% vs. 1\%), grade 2 diarrhea (2.4\% vs. 0.7\%), and grade 1 sensory neuropathy (4.5\% vs. 1.2\%). No treatment related deaths were encountered. CONCLUSION: This prospective trial has sufficient data to support the conclusion that concurrent chemoradiotherapy with weekly cisplatin 40 mg/m2 in locally advanced cervical cancer gives good treatment outcomes. When reducing the cisplatin dose to 20 mg/m2, treatment responses were still comparable to the standard, but acute toxicity could be reduced. However, there are insufficient data to assess long term treatment outcomes and late treatment related toxicity, because of the short follow-up time.
This article was published in Asian Pac J Cancer Prev and referenced in Journal of Cancer Science & Therapy

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