首页> 外文期刊>Gynecologic Oncology: An International Journal >Outcome of stage IVA cervical cancer patients with disease limited to the pelvis in the era of chemoradiation: a Gynecologic Oncology Group study.
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Outcome of stage IVA cervical cancer patients with disease limited to the pelvis in the era of chemoradiation: a Gynecologic Oncology Group study.

机译:妇科肿瘤学小组的一项研究,在放化疗时代,仅限于骨盆的IVA期宫颈癌患者的结果。

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OBJECTIVES: To evaluate the outcome of stage IVA cervical cancer treated with radiation and concurrent cisplatin-based chemotherapy. METHODS: We conducted a retrospective study of stage IVA cervical cancer patients from four trials (Gynecologic Oncology Group protocols 56, 85, 120, and 165) treated with radiotherapy with or without concurrent cisplatin-based chemotherapy. Patient records were reviewed for demographic and tumor features, treatment, and progression-free survival (PFS) and overall survival (OS). Stage IVA patients were compared to stage IIIB patients from these same studies. RESULTS: Among the 51 stage IVA patients studied, 92% were stage IVA on the basis of bladder involvement. The median PFS was 10.1 months (95% CI=6.3-14.5 months) and median OS was 21.2 months (95% CI=13.3-30.5 months). The 3 year survival was 32%. On univariate analysis, only advanced age was associated with OS (p=0.0115) but age had only marginal effect on PFS (p=0.083). Pathologic proven pelvic nodal metastasis was of marginal significance for both PFS and OS, p=0.059 and 0.064, respectively. Despite similar patient characteristics, the use of cisplatin-based chemotherapy had no impact on PFS or OS but was underpowered to address this question. When compared to stage IIIB patients, stage IVA patients had a poorer performance status (p=0.0231), larger tumor size (p=0.0302), and more frequent bilateral parametrial involvement (0.0063). CONCLUSION: Patients with stage IVA disease had poor median survival of only 21 months with only 32% 3 year survival. Stage IVA patients have larger tumor size, more bilateral parametrial involvement, and poorer survival when compared to stage IIIB patients.
机译:目的:评估接受放疗和顺铂同步化疗的IVA期宫颈癌的疗效。方法:我们进行了一项回顾性研究,研究了四项接受放疗并同时不进行顺铂为基础的化疗的试验(妇科肿瘤学组规程56、85、120和165)。回顾了患者记录的人口统计学和肿瘤特征,治疗,无进展生存期(PFS)和总体生存期(OS)。将来自这些相同研究的IVA期患者与IIIB期患者进行了比较。结果:在研究的51个IVA期患者中,有92%是基于膀胱受累的IVA期。中位PFS为10.1个月(95%CI = 6.3-14.5个月),中位OS​​为21.2个月(95%CI = 13.3-30.5个月)。 3年生存率为32%。在单因素分析中,只有高龄与OS相关(p = 0.0115),但年龄对PFS仅具有边际影响(p = 0.083)。经病理证实的盆腔淋巴结转移对PFS和OS均无统计学意义,分别为p = 0.059和0.064。尽管患者具有相似的特征,但基于顺铂的化疗对PFS或OS没有影响,但不足以解决该问题。与IIIB期患者相比,IVA期患者的表现状态较差(p = 0.0231),肿瘤尺寸较大(p = 0.0302)和双侧子宫旁组织受累更为频繁(0.0063)。结论:IVA期患者的中位生存期仅为21个月,3年生存率仅为32%。与IIIB期患者相比,IVA期患者的肿瘤更大,双侧子宫旁组织受累更大,并且生存期较差。

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