Wiley Rachel L, Bondre Ioana L, Jalloul Randa, Klopp Ann H, Taylor Jolyn S, Ramondetta Lois M
Department of Obstetrics, Gynecology and Reproductive Sciences, The University of Texas Health Science Center, Houston, TX, USA.
Anderson Cancer Center, Department of Radiation Oncology, Houston, TX, USA.
Gynecol Oncol Rep. 2022 Mar 23;40:100963. doi: 10.1016/j.gore.2022.100963. eCollection 2022 Apr.
Platinum-based chemotherapy and bevacizumab is the standard treatment for stage IVB cervical cancer. When metastases resolve, the benefit of radiating the primary tumor is unclear. We investigate the effect of pelvic radiation on PFS following chemotherapy and bevacizumab in stage IVB cervical cancer.
This is a retrospective series of 29 patients with stage IVB cervical cancer treated with platinum-based chemotherapy and bevacizumab. 3 subgroups were evaluated: definitive pelvic radiation, palliative radiation, and no radiation. The primary outcome was the mean PFS. Progression was determined radiographically. Kaplan-Meier method and the log-rank test for equality analyzed OS and PFS.
The median OS was 38.4 months. 11 patients (38%) received definitive radiation, 9 (31%) received palliative and 9 (31%) received no radiation. 7/8 in the palliative group, 7/10 who received no radiation and all in the definitive group experienced progression. The median PFS was 7.5 months and not statistically different (p = 0.62). The median OS was not attained in the definitive group, was 23 months [19.6, -] for the palliative group and 19 months [24.9-45.4] for the no radiation group (p = 0.13). OS was higher in patients receiving definitive radiation vs all others (median OS survival not reached vs 6.6 months, p = 0.04). No difference in PFS between those receiving definitive radiation vs others (12 months vs 5.1 months p = 0.32).
Definitive radiation is associated with improved survival among in stage IVB cervical cancer treated with chemotherapy and bevacizumab. This association could be due to treatment, patient, or disease factors associated with improved oncologic outcomes. In absence of higher-level data, shared decision-making with consideration for comorbidities and performance status should be employed.
铂类化疗联合贝伐单抗是IVB期宫颈癌的标准治疗方案。当转移灶消退时,对原发肿瘤进行放疗的益处尚不清楚。我们研究了盆腔放疗对IVB期宫颈癌化疗联合贝伐单抗后无进展生存期(PFS)的影响。
这是一项对29例接受铂类化疗联合贝伐单抗治疗的IVB期宫颈癌患者的回顾性研究。评估了3个亚组:根治性盆腔放疗、姑息性放疗和未放疗。主要结局是平均PFS。通过影像学确定疾病进展。采用Kaplan-Meier法和对数秩检验分析总生存期(OS)和PFS。
中位OS为38.4个月。11例患者(38%)接受了根治性放疗,9例(31%)接受了姑息性放疗,9例(31%)未接受放疗。姑息性放疗组8例中有7例、未放疗组10例中有7例以及根治性放疗组所有患者均出现疾病进展。中位PFS为7.5个月,无统计学差异(p = 0.62)。根治性放疗组未达到中位OS,姑息性放疗组为23个月[19.6,-],未放疗组为19个月[24.9 - 45.4](p = 0.13)。接受根治性放疗的患者OS高于其他所有患者(中位OS未达到 vs 6.6个月,p = 0.04)。接受根治性放疗与其他患者的PFS无差异(12个月 vs 5.1个月,p = 0.32)。
在接受化疗和贝伐单抗治疗的IVB期宫颈癌患者中,根治性放疗与生存期改善相关。这种关联可能归因于与肿瘤学结局改善相关的治疗、患者或疾病因素。在缺乏更高水平数据的情况下,应考虑合并症和体能状态进行共同决策。