Department of Surgery, City of Hope, 1500 E. Duarte Road, Duarte, CA 91010, USA.
Genes Chromosomes Cancer. 2011 Sep;50(9):689-99. doi: 10.1002/gcc.20891. Epub 2011 May 16.
Rectal cancer response to chemoradiation (CRT) varies from no response to a pathologic complete response (pCR). Identifying predictive biomarkers of response would therefore be useful. We assessed whether chromosomal copy number alterations (CNAs) can assist in predicting pCR. Pretreatment tumor biopsies and paired normal surgical tissues from the proximal resection margin were collected from 95 rectal cancer patients treated with preoperative CRT and total mesorectal excision in a prospective Phase II study. Tumor and control DNA were extracted, and oligonucleotide array-based comparative genomic hybridization (aCGH) was used to identify CNAs, which were correlated with pCR. Ingenuity pathway analysis (IPA) was then used to identify functionally relevant genes in aberrant regions. Finally, a predictive model for pCR was built using support vector machine (SVM), and leave-one-out cross validation assessed the accuracy of aCGH. Chromosomal regions most commonly affected by gains were 20q11.21-q13.33, 13q11.32-23, 7p22.3-p22.2, and 8q23.3-q24.3, and losses were present at 18q11.32-q23, 17p13.3-q11.1, 10q23.1, and 4q32.1-q32.3. The 25 (26%) patients who achieved a pCR had significantly fewer high copy gains overall than non-pCR patients (P = 0.01). Loss of chromosomal region 15q11.1-q26.3 was significantly associated with non-pCR (P < 0.00002; Q-bound < 0.0391), while loss of 12p13.31 was significantly associated with pCR (P < 0.0003; Q-bound < 0.097). IPA identified eight genes in the imbalanced chromosomal regions that associated with tumor response. SVM identified 58 probes that predict pCR with 76% sensitivity, 97% specificity, and positive and negative predictive values of 91% and 92%. Our data indicate that chromosomal CNAs can help identify rectal cancer patients more likely to develop a pCR to CRT.
直肠癌对放化疗(CRT)的反应从无反应到病理完全缓解(pCR)不等。因此,确定预测反应的生物标志物将是有用的。我们评估了染色体拷贝数改变(CNAs)是否有助于预测 pCR。在一项前瞻性 II 期研究中,对 95 例接受术前 CRT 和全直肠系膜切除术的直肠癌患者,采集了治疗前肿瘤活检和近端切除边缘配对的正常手术组织。提取肿瘤和对照 DNA,并用寡核苷酸微阵列比较基因组杂交(aCGH)来识别 CNA,并将其与 pCR 相关。然后使用 IPA 对异常区域中的功能相关基因进行鉴定。最后,使用支持向量机(SVM)构建 pCR 预测模型,并使用留一法交叉验证评估 aCGH 的准确性。最常受增益影响的染色体区域是 20q11.21-q13.33、13q11.32-23、7p22.3-p22.2 和 8q23.3-q24.3,而丢失则发生在 18q11.32-q23、17p13.3-q11.1、10q23.1 和 4q32.1-q32.3。25 名(26%)实现 pCR 的患者总体上具有显著较少的高拷贝增益,而非 pCR 患者则没有(P=0.01)。染色体 15q11.1-q26.3 的缺失与非 pCR 显著相关(P<0.00002;Q 边界<0.0391),而 12p13.31 的缺失与 pCR 显著相关(P<0.0003;Q 边界<0.097)。IPA 在不平衡的染色体区域中鉴定出与肿瘤反应相关的 8 个基因。SVM 鉴定出 58 个探针,以 76%的灵敏度、97%的特异性以及 91%和 92%的阳性和阴性预测值来预测 pCR。我们的数据表明,染色体 CNA 可帮助识别更有可能对 CRT 产生 pCR 的直肠癌患者。