宫颈小细胞癌患者的临床预后因素和治疗结果:一项基于单一机构的回顾性研究

Niketa Thakur, Sonal Patel
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摘要

宫颈小细胞癌(SCCC)在宫颈恶性肿瘤中相对不常见,与常见的鳞状病变相比,SCCC更容易发展为淋巴结和远处转移。目前对SCCC的潜在预后因素、最佳治疗方式和生存结果缺乏了解。目的:本研究的目的是将临床病理参数和不同的治疗方案与SCCC的生存结果(无进展生存期(PFS)和总生存期(OS))联系起来。材料与方法:回顾性研究2005年1月至2014年12月接受治疗的确诊SCCC患者。结果:共分析21例患者。中位发病年龄为47岁。所有患者均表现为晚期(IIB-IVB),组织学分化程度高。中位PFS和OS分别为5个月和6个月。与其他治疗方式相比,接受多药铂和依托泊苷根治性同步放化疗(CCRT)加近距离放疗的患者有更好的PFS (P = 0.028)和更好的OS趋势。有额外神经内分泌成分、CCRT后未接受近距离治疗和根治性放疗后未接受预防性颅脑照射的SCCC患者的中位OS明显较差(P < 0.05)。顺铂加依托泊苷CCRT方案的PFS和OS优于单纯顺铂加依托泊苷CCRT方案(P > 0.05)。此外,年龄>40岁、肿瘤大小≤4cm、淋巴结阴性的患者有更好的OS趋势。在7个月的中位随访中,42.9%的病例复发。结论:多药铂+依托泊苷化疗加近距离放疗仍然是局部晚期SCCC的主要治疗方法。治疗时应考虑预后因素。
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Clinical prognostic factors and treatment outcomes in patients with small cell carcinoma of the cervix: A single institution-based retrospective study
Introduction: Small cell carcinoma of the cervix (SCCC) is relatively uncommon among cervical malignancies and is more likely to develop lymph node and distant metastasis compared to the common squamous histological variant. There is a lack of knowledge about potential prognostic factors, optimal treatment modalities, and survival outcome of SCCC. Aim: The aim of this study is to correlate clinicopathologic parameters and different treatment schedules with survival outcomes of SCCC as progression-free survival (PFS) and overall survival (OS). Materials and Methods: A retrospective study was conducted on diagnosed SCCC patients taking treatment from January 2005 to December 2014. Results: A total of 21 patients were analyzed. The median age of presentation was 47 years. All the patients presented at an advanced stage (IIB-IVB) with high-grade histological differentiation. The median PFS and OS were 5 and 6 months, respectively. The patient receiving multi-agent platinum- and etoposide-based radical concurrent chemoradiotherapy (CCRT) plus brachytherapy had significantly better PFS (P = 0.028) and a trend toward better OS versus other treatment modalities. The median OS was found to be significantly poor in SCCC patients having an additional neuroendocrine component, not receiving brachytherapy after CCRT, and not receiving prophylactic cranial irradiation after radical radiotherapy (P < 0.05). Cisplatinum- plus etoposide-based CCRT schedule had a trend toward better PFS and OS than that of only cisplatinum-based CCRT (P > 0.05). Furthermore, a trend toward better OS was seen for age >40 years, tumor size ≤4 cm, and lymph node-negative status. Relapse was seen in 42.9% of the cases over a 7-month median follow-up. Conclusions: CCRT using multi-agent platinum- plus etoposide-based chemotherapy followed by brachytherapy remains the mainstay of treatment in locally advanced SCCC. The prognostic factors should be considered for customizing treatment.
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