Eng Kevin H, Morrell Kayla, Starbuck Kristen, Spring-Robinson Chandra, Khan Aalia, Cleason Dana, Akman Levent, Zsiros Emese, Odunsi Kunle, Szender J Brian
Department of Biostatistics and Bioinformatics, Roswell Park Cancer Institute, Buffalo, NY, United States.
Department of Biostatistics and Bioinformatics, Roswell Park Cancer Institute, Buffalo, NY, United States.
Gynecol Oncol. 2017 Jul;146(1):52-57. doi: 10.1016/j.ygyno.2017.05.005. Epub 2017 May 8.
The presence of miliary disease during initial ovarian cancer debulking may reflect a distinct mode of peritoneal spread independent from size-based tumor staging and may explain variation in response to treatment and survival outcomes. To infer the prevalence, presentation and clinical implications of miliary disease we reviewed existing surgical records.
Reports were available for 1008 primary debulking surgeries for ovarian, primary peritoneal or fallopian tube cancer between 2001 and 2015 (685 reports from 2005 to 2015). Clinical outcome data was available for 938 patients. We analyzed a high-stage sub-cohort for survival (N=436).
Most records were evaluable for miliary disease (761/938); for these, the miliary phenotype was highly prevalent (249/761, 32.7%) and often accompanied by ascites (185/249, 74%). While optimal debulking rates were unaffected by miliary disease, total resection (R0) rates were poorer. Liver, stomach, spleen or bladder appeared to be sporadically involved while the omentum, mesentery, bowel, peritoneum and diaphragm were affected simultaneously (Spearman rho>0.5). Overall, miliary disease was associated with worse progression free survival, overall survival, and time from relapse to death independent of stage. Survival effects were particularly strong for Stage IV disease where median overall survival varied by over 30months (log-rank p=0.002).
Miliary disease is an identifiable surgical phenotype reflecting a distinct clinical trajectory that adds prognostic information to standard disease burden-based staging. These findings should permit further retrospective investigation in a wider cohort and prompt the consideration of prospective structured operative reporting standards and treatment strategies.
初次卵巢癌肿瘤细胞减灭术中粟粒样病灶的存在可能反映了一种独立于基于肿瘤大小的分期的独特腹膜播散方式,并且可以解释治疗反应和生存结果的差异。为了推断粟粒样病灶的患病率、表现及临床意义,我们回顾了现有的手术记录。
有2001年至2015年间1008例卵巢癌、原发性腹膜癌或输卵管癌初次肿瘤细胞减灭术的报告(2005年至2015年的报告有685份)。938例患者有临床结局数据。我们分析了一个用于生存分析的高分期亚队列(N = 436)。
大多数记录可用于评估粟粒样病灶(761/938);在这些记录中,粟粒样表型非常普遍(249/761,32.7%),且常伴有腹水(185/249,74%)。虽然最佳肿瘤细胞减灭率不受粟粒样病灶的影响,但完全切除(R0)率较低。肝脏、胃、脾脏或膀胱似乎偶尔受累,而大网膜、肠系膜、肠、腹膜和膈肌同时受累(Spearman秩相关系数>0.5)。总体而言,粟粒样病灶与无进展生存期、总生存期较差以及复发至死亡时间相关,且与分期无关。对于IV期疾病,生存效应尤为显著,其中位总生存期相差超过30个月(对数秩检验p = 0.002)。
粟粒样病灶是一种可识别的手术表型,反映了一种独特的临床病程,为基于标准疾病负担的分期增加了预后信息。这些发现应允许在更广泛的队列中进行进一步的回顾性研究,并促使考虑前瞻性结构化手术报告标准和治疗策略。