O'Sullivan G C, Collins J K, Kelly J, Morgan J, Madden M, Shanahan F
Department of Surgery and Medicine, National University of Ireland, Cork, Ireland.
Gut. 1997 Apr;40(4):512-5. doi: 10.1136/gut.40.4.512.
Micrometastases within bone marrow have been shown to indicate a poor prognosis in patients with epithelial tumours. However, the degree to which micrometastases represent true residual disease or cell shedding and metastatic potential, is unclear.
To explore whether micrometastases represent residual disease, bone marrow taken from carefully staged patients before and after (> 6 months) "curative" resection of a primary gastrointestinal cancer was studied prospectively.
PATIENTS/METHODS: Seventy two consecutive patients were studied; the only exclusions were patients with known overt metastatic disease at the time of surgery. Micrometastatic cells were quantified per 10(5) marrow cells by flow cytometry after staining for contaminant cytokeratin-18 positive cells.
Micrometastases were detected preoperatively in 22% (16/72) of all patients, comprising 11 (23%) of 48 with colorectal cancer, five (33%) of 15 with gastric adenocarcinoma and none (0%) of nine with oesophageal squamous cancer. Although fewer metastatic cells were detected in postoperative bone marrow, and clearance of marrow deposits was evident in most patients, the persistence of micrometastases in five of 16 patients after resection, without evidence of tumour recurrence, indicates a subset with true residual disease. Detection of micrometastases postoperatively (persistent or newly developed) was significantly associated with development of overt metastases during the subsequent 12-18 months of follow up (nine of 19 patients) when compared with patients testing negative for micrometastases (eight of 53; p < 0.01).
Preoperative detection of micrometastases may reflect either transient shedding of cells, metastatic potential or residual disease, but postoperative micrometastases indicate minimal residual disease. Identification of these patients is important because they may benefit from adjuvant therapy.
骨髓中的微转移已被证明提示上皮性肿瘤患者预后不良。然而,微转移在多大程度上代表真正的残留疾病、细胞脱落及转移潜能尚不清楚。
为探讨微转移是否代表残留疾病,对精心分期的原发性胃肠道癌患者在“根治性”切除术前及术后(>6个月)采集的骨髓进行前瞻性研究。
患者/方法:对72例连续患者进行研究;唯一排除标准为手术时已知有明显转移疾病的患者。对污染的细胞角蛋白-18阳性细胞染色后,通过流式细胞术对每10⁵个骨髓细胞中的微转移细胞进行定量。
所有患者中22%(16/72)术前检测到微转移,其中48例结直肠癌患者中有11例(23%),15例胃腺癌患者中有5例(33%),9例食管鳞癌患者中无一例(0%)。虽然术后骨髓中检测到的转移细胞较少,且大多数患者骨髓沉积物清除明显,但16例患者中有5例术后微转移持续存在,且无肿瘤复发证据,提示存在真正残留疾病的亚组。与微转移检测阴性的患者(53例中有8例)相比,术后(持续或新出现)检测到微转移与随后12 - 18个月随访期间发生明显转移显著相关(19例患者中有9例)(p<0.01)。
术前检测到的微转移可能反映细胞的短暂脱落、转移潜能或残留疾病,但术后微转移提示最小残留疾病。识别这些患者很重要,因为他们可能从辅助治疗中获益。