Department of Radiation Oncology, Baskent University Faculty of Medicine, Adana, Turkey,
Eur J Nucl Med Mol Imaging. 2014 Jul;41(7):1336-42. doi: 10.1007/s00259-014-2719-5. Epub 2014 Feb 22.
We sought to evaluate failure patterns and prognostic factors predictive of recurrences and survival in cervical cancer patients who are treated with definitive chemoradiotherapy (ChRT), who have a subsequent complete metabolic response (CMR) with (18) F-fluorodeoxyglucose positron-emission tomography (FDG-PET) after treatment.
The records of 152 cervical cancer patients who were treated with definitive chemoradiotherapy were evaluated. All patients underwent pre-treatment positron emission tomography (PET-CT), and post-treatment PET-CT was performed within a median of 3.9 months (range, 3.0-9.8 months) after the completion of ChRT. The prognoses of partial response/progressive disease (PR/PD) cases (30 patients, 18 %) and CMR cases (122 patients, %82) were evaluated. Univariate and multivariate analysis effecting the treatment outcome was performed in CMR cases.
The median follow-ups for all patients and surviving patients were 28.7 (range, 3.3-78.7 months) and 33.2 months (range, 6.23-78.7 months), respectively. Four-year overall survival (OS) rate was significantly better in patients with CMR compared to patients with PR/PD (66.9 % vs. 12.4 %, p < 0.001, respectively). Patients with PR/PD had higher maximum standardized uptake value (SUVmax) of primary cervical tumor (26.4 ± 10.1 vs. 15.9 ± 6.3; p < 0.001) and larger tumor (6.4 cm ± 2.3 cm vs. 5.0 cm ± 1.4 cm; p < 0.001) compared to patients with CMR. Of the 122 patients with post-treatment CMRs, 25 (21 %) developed local, locoregional, or distant failure. In univariate analysis, tumor size ≥ 5 cm, 'International Federation of Obstetricians and Gynecologists' (FIGO) stage ≥ IIB, and pelvic and/or para-aortic lymph node metastasis were predictive of both overall survival (OS) and disease-free survival (DFS), while histology was predictive of only OS. In multivariate analysis, tumor size, stage and lymph node metastasis were predictive of OS and DFS.
Although CMR is associated with better outcomes, relapses remain problematic, especially in patients with bulky tumors (≥ 5 cm), extensive stage (≥ IIB) or pelvic and/or para-aortic lymph node metastasis. These findings could support the need for more aggressive treatment or adjuvant chemotherapy regimens.
我们旨在评估接受根治性放化疗(ChRT)治疗后出现完全代谢缓解(CMR)的宫颈癌患者的失败模式和预测复发及生存的预后因素,这些患者在治疗后接受了(18)F-氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)。
评估了 152 名接受根治性放化疗的宫颈癌患者的记录。所有患者均接受了治疗前正电子发射断层扫描(PET-CT),在 ChRT 完成后中位数为 3.9 个月(范围,3.0-9.8 个月)进行了治疗后 PET-CT。评估了部分缓解/进展性疾病(PR/PD)病例(30 例,18%)和 CMR 病例(122 例,82%)的预后。在 CMR 病例中进行了单变量和多变量分析,以评估治疗结果的影响因素。
所有患者和存活患者的中位随访时间分别为 28.7(范围,3.3-78.7 个月)和 33.2 个月(范围,6.23-78.7 个月)。与 PR/PD 患者相比,CMR 患者的四年总生存率(OS)明显更好(66.9%比 12.4%,p<0.001)。PR/PD 患者的原发宫颈肿瘤最大标准化摄取值(SUVmax)(26.4±10.1 比 15.9±6.3;p<0.001)和肿瘤大小(6.4 cm±2.3 cm 比 5.0 cm±1.4 cm;p<0.001)均高于 CMR 患者。在 122 例治疗后 CMR 的患者中,25 例(21%)发生了局部、局部区域或远处复发。在单变量分析中,肿瘤大小≥5 cm、国际妇产科联合会(FIGO)分期≥IIB 以及盆腔和/或腹主动脉旁淋巴结转移与总生存(OS)和无病生存(DFS)均相关,而组织学仅与 OS 相关。在多变量分析中,肿瘤大小、分期和淋巴结转移与 OS 和 DFS 相关。
尽管 CMR 与更好的结果相关,但复发仍然是个问题,特别是在肿瘤较大(≥5 cm)、广泛期(≥IIB)或盆腔和/或腹主动脉旁淋巴结转移的患者中。这些发现可能支持需要更积极的治疗或辅助化疗方案。