Kaufman C S, Jacobson-Kaufman L, Thorndike-Christ T, Kaufman L, Tabár L
Bellingham Breast Center, 2940 Squalicum Parkway, Bellingham, WA 98225, USA.
Am J Surg. 2001 Oct;182(4):377-83. doi: 10.1016/s0002-9610(01)00741-3.
We have investigated a method, the Kaufman axillary treatment scale (KATS), to help assign patients with a clinically negative axilla to one of three current options of axillary management: standard axillary dissection, sentinel node sampling followed by axillary dissection if the sentinel node is positive, or no axillary surgery at all. The KATS score uses preoperative data to guide the choice of axillary treatment.
The KATS score is calculated by adding the preoperative values of tumor size, patient age, and pathologic grade. Values range from 1 to 4 for size (1 to 9 mm, 10 to 14 mm, 15 to 19 mm, and 20 to 30 mm), 1 to 3 for age (70 years and over, 50 to 69 years, less than 50 years), and 1 to 2 for grade (low or not low) to calculate the score. The KATS score ranges from 3 to 9. We have applied this score against the SEER (Surveillance, Epidemiology, and End Results) tumor registry of 529 patients with invasive breast cancer with known pathologic data. We then validated it by applying it to our own set of 190 patients using preoperative data. The chi-square test and logistic regression analysis were used for P values (all two sided), univariate and multivariate analysis, odds ratio and confidence intervals utilizing SPSS statistics software.
In the SEER database using American Joint Committee on Cancer pathologic size alone, no sizable group was identified with a positive node rate neither below 8% (T1a) nor above 48% (T2). KATS scores of 3 and 4 (68 patients, group 1) identify patients with an average node positive rate of 4.4% (P <0.02, group 1 versus 2). Those patients with KATS scores of 5, 6, and 7 (341 patients, group 2) carry an average node positive rate of 22% (P <0.001, group 2 versus 3). KATS scores of 8 and 9 (120 patients, group 3) identify patients with an average node positive rate of 50% (P <0.001, group 3 versus 1). Similar results were found on our own group of 190 patients using preoperative available data. KATS scores of 3 or 4 (11 patients, group 1) had no positive nodes. Group 2 (100 patients, KATS score 5, 6, and 7) had an average 30% node positive rate. Group 3 (79 patients, KATS score 8 and 9) had 61% node positive rate. The KATS score allows the clinician to separate patients into three axillary management groups. Group 1 are those patients who may need no axillary surgery at all. Group 2 are patients who would benefit from sentinel node mapping. Group 3 has a node positive rate (61%) similar to that of clinically palpable nodes (since not all clinically palpable nodes are positive). Group 3 patients may be considered for standard axillary dissection, similar to the palpable node patient. If group 3 patients have sentinel node mapping, more than half of these patients require axillary dissection and the impact of false negative sentinel node procedures may become clinically significant.
An axillary treatment score has been developed to aid in the triage of patients toward reasonable axillary treatment choices for the benefit of the patient. The KATS score is a guideline and not a mandate. The KATS score attempts to use breakpoints that are both clinically practical and validated by scientific data. Like many other attempts to categorize patients, there is a continuum of data points along any variable. The treating physician utilizing the full array of available data on each patient makes the final clinical decision of axillary management.
我们研究了一种方法,即考夫曼腋窝治疗量表(KATS),以帮助将腋窝临床阴性的患者分配至当前三种腋窝管理方案之一:标准腋窝清扫术;前哨淋巴结取样,若前哨淋巴结阳性则随后进行腋窝清扫术;或完全不进行腋窝手术。KATS评分利用术前数据来指导腋窝治疗方案的选择。
KATS评分通过将肿瘤大小、患者年龄和病理分级的术前值相加来计算。肿瘤大小的取值范围为1至4(1至9毫米、10至14毫米、15至19毫米以及20至30毫米),年龄的取值范围为1至3(70岁及以上、50至69岁、小于50岁),分级的取值范围为1至2(低级别或非低级别),据此计算得分。KATS评分范围为3至9。我们将该评分应用于529例有已知病理数据的浸润性乳腺癌患者的SEER(监测、流行病学和最终结果)肿瘤登记数据库。然后,我们通过将其应用于我们自己的190例患者的数据集并利用术前数据进行验证。使用SPSS统计软件进行卡方检验和逻辑回归分析以得出P值(均为双侧)、单因素和多因素分析、比值比和置信区间。
在SEER数据库中,仅使用美国癌症联合委员会的病理大小,未识别出阳性淋巴结率既低于8%(T1a)也高于48%(T2)的相当规模的组。KATS评分为3和4的患者(68例,第1组)的平均阳性淋巴结率为4.4%(P<0.02,第1组与第2组相比)。KATS评分为5、6和7的患者(341例,第2组)的平均阳性淋巴结率为22%(P<0.001,第2组与第3组相比)。KATS评分为8和9的患者(120例,第3组)的平均阳性淋巴结率为50%(P<0.001,第3组与第1组相比)。在我们自己的190例患者组中,使用术前可用数据也发现了类似结果。KATS评分为3或4的患者(11例,第1组)无阳性淋巴结。第2组(100例,KATS评分为5、6和7)的平均阳性淋巴结率为30%。第3组(79例,KATS评分为8和9)的阳性淋巴结率为61%。KATS评分使临床医生能够将患者分为三个腋窝管理组。第1组是那些可能根本不需要进行腋窝手术的患者。第2组是那些将从前哨淋巴结定位中获益的患者。第3组的阳性淋巴结率(61%)与临床可触及淋巴结的阳性率相似(因为并非所有临床可触及淋巴结都是阳性的)。第3组患者可考虑进行标准腋窝清扫术,类似于可触及淋巴结患者。如果第3组患者进行前哨淋巴结定位,这些患者中超过一半需要进行腋窝清扫术,并且前哨淋巴结假阴性程序的影响可能在临床上变得显著。
已开发出一种腋窝治疗评分,以帮助对患者进行分类,从而为患者选择合理的腋窝治疗方案。KATS评分是一个指导原则而非指令。KATS评分试图使用既具有临床实用性又经过科学数据验证的断点。与许多其他对患者进行分类的尝试一样,沿着任何变量都存在一系列数据点。治疗医生利用每个患者的全部可用数据做出腋窝管理的最终临床决策。