食管胃结合部腺癌新辅助化疗后CT检查征象

CT features of adenocarcinoma of esophagogastric junction after neoadjuvant chemotherapy

  • 摘要: 目的:探讨食管胃结合部腺癌(AEG)新辅助化疗后CT检查征象。
    方法:采用回顾性描述性研究方法。收集2010年2月至2014年11月北京大学肿瘤医院收治的59例行新辅助化疗AEG患者的临床病理资料;男51例,女8例;中位年龄为63岁,年龄范围为46~82岁。患者新辅助化疗前后均行增强CT检查。观察指标:(1)AEG病理学检查及新辅助化疗情况。(2)AEG CT检查结果:①CT检查定性指标分析。②CT检查定量指标分析。偏态分布的计量资料以M(P25,P75)或M(范围)表示,组间比较采用Mann- Whitney U检验。计数资料以绝对数表示,组间比较采用x2检验。
    结果:(1)AEG病理学检查及新辅助化疗情况:59例AEG患者中,肿瘤分化程度为高分化腺癌1例,中分化腺癌40例,低分化腺癌18例;新辅助化疗疗效为13例治疗有效[病理学肿瘤退缩分级(TRG)0级6例、病理学TRG 1级7例],46例反应不良(病理学TRG 2级12例、病理学TRG 3级34例)。(2)AEG CT检查结果。①CT检查定性指标分析:13例新辅助化疗治疗有效患者,新辅助化疗前肿瘤表面溃疡、肿瘤分层强化、外膜侵犯、壁外静脉血管侵犯(EMVI)阳性分别为13、5、10、2例;新辅助化疗后肿瘤表面溃疡变浅或消失、肿瘤分层强化模式改变、外膜侵犯、EMVI阳性分别为13、7、3、1例;46例新辅助化疗反应不良患者,新辅助化疗前上述指标分别为28、18、37、22例,新辅助化疗后上述指标分别为23、7、33、21例。两者新辅助化疗前肿瘤分层强化、外膜侵犯比较,差异均无统计学意义 (x2=0.002,0.000,P>0.05);肿瘤表面溃疡、EMVI阳性比较,差异均有统计学意义(x2=5.591,4.421,P<0.05)。两者新辅助化疗后肿瘤分层强化模式改变、外膜侵犯、EMVI阳性比较,差异均有统计学意义(x2=6.359,10.090,4.728,P<0.05);肿瘤表面溃疡变浅或消失比较,差异无统计学意义(x2=1.239,P>0.05)。②CT检查定量指标分析:13例新辅助治疗有效患者,新辅助化疗前肿瘤最大厚度、肿瘤最大面积、肿瘤CT强化值分别为1.37 cm(0.94 cm,1.88 cm)、8.9 cm2(4.7 cm2,9.9 cm2)、53 HU(47 HU,63 HU),新辅助化疗后上述指标分别为1.17 cm(0.79 cm,1.29 cm)、4.4 cm2(2.5 cm2,6.1 cm2)cm2、30 HU(25 HU,53 HU),新辅助化疗后肿瘤最大厚度变化率、肿瘤最大面积变化率、肿瘤CT强化值变化率分别为-23%(-42%,9%)、-51% (-60%,-21%)、-44%(-51%,19%)。46例新辅助治疗反应不良患者新辅助化疗前肿瘤最大厚度、肿瘤最大面积、肿瘤CT强化值分别为1.57 cm(1.21 cm,1.96 cm)、9.4 cm2(6.6 cm2,13.1 cm2)、60 HU(53 HU, 66 HU),新辅助化疗后上述指标分别为1.16 cm(0.94 cm,1.37 cm)、6.2 cm2(4.8 cm2,8.1 cm2)、55 HU (47 HU,65 HU),新辅助化疗后肿瘤最大厚度变化率、肿瘤最大面积变化率、肿瘤CT强化值变化率分别为 -27%(-38%,-9%)、-33%(-47%,-12%)、-9%(-22%,9%)。两者新辅助化疗前肿瘤最大厚度、肿瘤最大面积、肿瘤CT强化值比较,差异均无统计学意义(Z=-1.372,-1.372,-1.331,P>0.05);两者新辅助化疗后肿瘤最大厚度比较,差异无统计学意义(Z=-0.503,P>0.05),两者新辅助化疗后肿瘤最大面积、肿瘤CT强化值比较,差异均有统计学意义(Z=-2.743,-3.049,P<0.05);两者新辅助化疗后肿瘤最大厚度变化率、肿瘤最大面积变化率比较,差异均无统计学意义(Z=0.000,-1.481,P>0.05);两者新辅助化疗后肿瘤CT强化值变化率比较,差异有统计学意义(Z=-3.231,P<0.05)。
    结论:AEG新辅助化疗治疗有效的CT检查表现为肿瘤分层强化模式的改变、肿瘤最大面积缩小、肿瘤CT强化值减低,外膜侵犯和EMVI阴性。

     

    Abstract: Objective:To investigate the computed tomography (CT) features of adenocarcinoma of esophagogastric junction (AEG) after neoadjuvant chemotherapy.
    Methods:The retrospective and descriptive study was conducted. The clinicopathological data of 59 patients with AEG who underwent neoadjuvant chemotherapy in Peking University Cancer Hospital from February 2010 to November 2014 were collected. There were 51 males and 8 females, aged from 46 to 82 years, with a median age of 63 years. All the 59 patients underwent enhanced CT examination before and after neoadjuvant chemotherapy. Observation indicators: (1) pathological examination and neoadjuvant chemotherapy of patients with AEG; (2) results of CT examination in patients with AEG, including ① qualitative indicators of CT and ② quantitative indicators of CT. Measurement data with skewed distribution were represented as M(P25,P75) or M (range), and comparison between groups was analyzed using the Mann-Whitney U test. Count data were described as absolute numbers, and comparison between groups was analyzed by the chi-square test.
    Results:(1) Pathological examination and neoadjuvant chemotherapy of patients with AEG: of the 59 patients with AEG, high-differentiated adenocarcinoma was observed in 1 patient, moderate-differentiated adenocarcinoma in 40 patients, and low-differentiated adenocarcinoma in 18 patients. Effective response to neoadjuvant chemotherapy was observed in 13 patients, including 6 patients of pathological tumor regression grading (pTRG) 0 and 7 of pTRG 1; poor response was observed in 46 patients, including 12 patients of pTRG 2 and 34 patients of pTRG 3. (2) Results of CT examination in patients with AEG. ① Qualitative indicators of CT: for the 13 patients with effective response to neoadjuvant chemotherapy, 13 had the presence of ulcers, 5 had layered enhancement, 10 had infiltration of adventitia surface, and 2 had positive extramural venous invasion (EMVI) before neoadjuvant chemotherapy; after neoadjuvant chemotherapy, 13 had shallowed or disappeared ulcers, 7 patients had changed enhancement pattern, 3 had infiltration of adventitia surface, and 1 had positive EMVI. For the 46 patients with poor response to neoadjuvant chemotherapy, 28 had the presence of ulcers, 18 had layered enhancement, 37 had infiltration of adventitia surface, and 22 had positive EMVI before neoadjuvant chemotherapy; after neoadjuvant chemotherapy, 23 had shallowed or disappeared ulcers, 7 patients had changed layered enhancement pattern, 33 had infiltration of adventitia surface and 21 had positive EMVI, respectively. There was no significant difference in the layered enhancement or infiltration of adventitia surface before neoadjuvant chemotherapy between patients with different treatment response (x2=0.002, 0.000, P>0.05). There were significant differences in the presence of ulcers and positive EMVI before neoadjuvant chemotherapy between patients with different treatment response (x2=5.591, 4.421, P<0.05). After neoadjuvant chemotherapy, there were significant differences in the changes of layered enhancement pattern, infiltration of adventitia surface and positive EMVI between patients with different treatment response (x2=6.359, 10.090, 4.728, P<0.05); while there was no significant difference in the shallowed or disappeared ulcers between patients with different treatment response (x2=1.239, P>0.05). ② Quantitative indicators of CT: for the 13 patients with good response to neoadjuvant chemotherapy, the maximum tumor height, the maximum tumor area, enhanced CT value of the lesion before neoadjuvant chemotherapy were 1.37 cm(0.94 cm,1.88 cm), 8.9 cm2 (4.7 cm2, 9.9 cm2), 53 HU(47 HU,63 HU), respectively. After neoadjuvant chemotherapy, the above indicators were 1.17 cm (0.79 cm,1.29 cm), 4.4 cm2(2.5 cm2,6.1 cm2), 30 HU(25 HU,53 HU), respectively. The change rates of the maximum tumor height, the maximum tumor area, and enhanced CT value of the lesion were -23% (-42%,9%), -51%(-60 %,-21%), -44%(-51%,19%), respectively. For the 46 patients with poor response to neoadjuvant chemotherapy, the maximum tumor height, the maximum tumor area, enhanced CT value of the lesion were 1.57 cm(1.21 cm,1.96 cm), 9.4 cm2(6.6 cm2,13.1 cm2), 60 HU(53 HU,66 HU) before neoadjuvant chemotherapy, respectively. After neoadjuvant chemotherapy, the above indicators were 1.16 cm(0.94 cm,1.37 cm), 6.2 cm2(4.8 cm2,8.1 cm2), 55 HU(47 HU,65 HU), respectively. The change rates of the maximum tumor height, the maximum tumor area, and enhanced CT value of the lesion were -27%(-38%, -9%), -33%(-47%,-12%), -9%(-22%,9%), respectively. There was no significant difference in the maximum tumor height, the maximum tumor area, enhanced CT value of the lesion before neoadjuvant chemotherapy between patients with different treatment response (Z=-1.372, -1.372, -1.331, P>0.05). There was no significant difference in the maximum tumor height after neoadjuvant chemotherapy between patients with different treatment response (Z= -0.503, P>0.05), while there were significant differences in the maximum tumor area and CT value of the lesion (Z=-2.743,-3.049, P<0.05). There was no significant difference in the change rate of the maximum tumor height or the maximum tumor area between patients with different treatment response (Z=0.000, -1.481, P>0.05), while there was a significant difference in the change rate of CT value of the lesion (Z= -3.231, P<0.05).
    Conclusion:Effective response of AEG to neoadjuvant chemotherapy was characterized by the changes in tumor layered enhancement pattern, reduction in the maximum tumor area, reduced CT value of the lesion, negative infiltration of adventitia surface, and negative EMVI.

     

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