Kumar Anup Kasi Loknath, Satyan Megha Teeka, Holzbeierlein Jeffrey, Mirza Moben, Van Veldhuizen Peter
Division of Hematology and Oncology, University of Kansas Medical Center, Kansas City, Kansas, USA.
J Med Case Rep. 2014 May 13;8:147. doi: 10.1186/1752-1947-8-147.
Granulocyte colony-stimulating factor produced by nonhematopoietic malignant cells is able to induce a leukemoid reaction by excessive stimulation of leukocyte production. Expression of granulocyte colony-stimulating factor and its functional receptors have been confirmed in bladder cancer cells. In vitro studies have demonstrated that granulocyte colony-stimulating factor/receptor exhibits a high affinity binding and this biological axis increases proliferation of the carcinoma. Urothelial carcinoma of the bladder is rarely associated with a leukemoid reaction and autocrine growth induced by paraneoplastic production of granulocyte colony-stimulating factor. In the world literature, there have been less than 35 cases reported in the last 35 years. The clinicopathological aspects, biology, prognosis and management of granulocyte colony-stimulating factor-secreting bladder cancers are poorly understood.
A 39-year-old Caucasian woman with an invasive high-grade urothelial carcinoma presented with hematuria and low-grade fevers. Laboratory tests revealed an elevated white blood cell count and absolute neutrophil count and an elevated 24-hour urine protein. Upon further evaluation she was found to have locally advanced high-grade urothelial carcinoma without nodal or distant metastasis. Her serum granulocyte colony-stimulating factor level was 10 times the normal limit. This led to the diagnosis of a paraneoplastic leukemoid reaction. Her white blood cell count immediately normalized after cystectomy but increased in concordance with recurrence of her disease. Unfortunately, she rapidly progressed and expired within 10 months from the time of first diagnosis.
This is one of the few cases reported that illustrates the existence of a distinct and highly aggressive subtype of bladder cancer which secretes granulocyte colony-stimulating factor. Patients presenting with a leukemoid reaction should be tested for granulocyte colony-stimulating factor/receptor biological axis. Moreover, granulocyte colony-stimulating factor could be a potential neoplastic marker as it can follow the clinical course of the underlying tumor and thus be useful for monitoring its evolution. Neoadjuvant chemotherapy should be considered in these patients due to the aggressive nature of these tumors. With a better understanding of the biology, this autocrine growth signal could be a potential target for therapy in future.
非造血恶性细胞产生的粒细胞集落刺激因子能够通过过度刺激白细胞生成诱导类白血病反应。粒细胞集落刺激因子及其功能性受体在膀胱癌细胞中的表达已得到证实。体外研究表明,粒细胞集落刺激因子/受体表现出高亲和力结合,并且这一生物学轴会增加癌细胞的增殖。膀胱尿路上皮癌很少与类白血病反应以及副肿瘤性产生粒细胞集落刺激因子所诱导的自分泌生长相关。在世界文献中,过去35年报道的病例不足35例。分泌粒细胞集落刺激因子的膀胱癌的临床病理特征、生物学特性、预后及治疗了解甚少。
一名39岁患有浸润性高级别尿路上皮癌的白人女性,出现血尿和低热。实验室检查显示白细胞计数和绝对中性粒细胞计数升高,24小时尿蛋白升高。进一步评估发现她患有局部晚期高级别尿路上皮癌,无淋巴结或远处转移。她的血清粒细胞集落刺激因子水平是正常上限的10倍。这导致诊断为副肿瘤性类白血病反应。膀胱切除术后她的白细胞计数立即恢复正常,但随着疾病复发而升高。不幸的是,她病情迅速进展,自首次诊断起10个月内死亡。
这是少数报告的病例之一,说明了存在一种独特且高度侵袭性的分泌粒细胞集落刺激因子的膀胱癌亚型。出现类白血病反应的患者应检测粒细胞集落刺激因子/受体生物学轴。此外,粒细胞集落刺激因子可能是一种潜在的肿瘤标志物,因为它可以跟踪潜在肿瘤的临床进程,从而有助于监测其演变。由于这些肿瘤具有侵袭性,应考虑对这些患者进行新辅助化疗。随着对其生物学特性的更好理解,这种自分泌生长信号未来可能成为治疗靶点。