Purpose of investigation. To evaluate whether lymphvascular space involvement (LVSI) is a risk factor for relapse of disease and lymph node metastasis in endometrial cancer. Methods. From 1978 till 2003, 609 patients ...Purpose of investigation. To evaluate whether lymphvascular space involvement (LVSI) is a risk factor for relapse of disease and lymph node metastasis in endometrial cancer. Methods. From 1978 till 2003, 609 patients with epithelial endometrial cancer were treated at the Groningen University Medical Center. The association of LVSI and relapse of disease was evaluated in the total group of 609 patients and in a ‘ low’ and ‘ high’ risk stage I endometrial cancer group. In 239 surgically staged patients, the relation of LVSI and lymph node metastasis was investigated. Results. The median age at diagnosis was 63 years (range 27- 92 years) with a median follow- up of 58 months (range 0- 236 months). More than half of the patients (56% ) received adjuvant radiotherapy. LVSI was present in 123 patients (25,6% ), and a prognostic factor for relapse of disease (multivariate analysis, P < 0.0001). In the ‘ low’ and ‘ high’ risk stage I endometrial cancer patients an increase of 2.6 times in relapse of disease was observed in the presence of LVSI. LVSI positive tumors were more likely to have metastasized to the pelvic lymph nodes (multivariate analysis, P = 0.001). In patients with proven negative nodes, LVSI was a prognostic factor for relapse of disease (univariate analysis, P = 0.02). Conclusion. LVSI is a predictor of nodal disease and an independent prognostic factor for relapse of disease in all stages of endometrial cancer. Patients with stage I endometrial cancer with positive LVSI are at risk for relapse of disease and might therefore benefit from adjuvant therapy. Content. The presence of lymphvascular space involvement (LVSI) in endometrial cancer is significantly and independently associated with an increased risk of pelvic lymph node metastases and/or relapse of disease.展开更多
Background: Tumor ulceration (TU) is considered the second most important prognostic factor after Breslow thickness for localized cutaneous malignant melanoma (CMM). However, many studies have not included mitotic rat...Background: Tumor ulceration (TU) is considered the second most important prognostic factor after Breslow thickness for localized cutaneous malignant melanoma (CMM). However, many studies have not included mitotic rate (MR) with TU in these analyses. When both TU and MR are included in the same analysis, MR appears to be the more important than TU and TU loses its significance as an independent prognostic factor. Methods: The relative importance of TU and MR as prognostic factors in localized CMM were compared in a population- based series of 650 consecutive invasive CMM cases ascertained from the Connecticut tumor registry and reviewed by a single dermatopathologist (RLB), during the period between January 15, 1987 and May 15, 1989. Seventeen clinical and histopathological variables including tumor thickness measured in mm, TU recorded as present or absent, and MR recorded as number per mm2 were included in an unconditional logistic regression model and selected for inclusion using a backward stepwise algorithm with death as an endpoint or at least five- years follow- up. Results: Inthemultivariateregression,theindependent prognostic factors included: 1. tumor thickness in millimeters (OR=1.5, 95% CI=1.3- 1.9) 2. moderate mitotic index (between 1 and 6): (OR=8.3, 95% CI 2.4- 28.7), 3. mitotic index (>6): (OR=11.6, 95% CI=3.0- 44.6), 4. solar elastosis: (inversely associated with mortality) (OR=0.4, 95% CI=0.28). After adjustment for MR, TU lost its significance. When MR was left out of the analysis, ulceration then became an independent prognostic factor. The model with ulceration only (excluding MR) showed a relative risk (RR) of 2.4 (95% CI: 1.1- 5.1). In the model with MR only, MR had a RR of 14.5 (95% CIS.9- 53.7). Finally, regression analysis including both TU and MR yielded an RR of 11.6 for MR and 1.7 for TU. Conclusions: Our results suggest that MR as a proxy for tumor proliferation is a more important prognostic factor than TU.展开更多
Background: Hepatocellular carcinoma (HCC) has an indisputable male predominance. “Gender" as an independent prognostic factor for survival is, however, controversial. Goals: Determine the influence of gender on...Background: Hepatocellular carcinoma (HCC) has an indisputable male predominance. “Gender" as an independent prognostic factor for survival is, however, controversial. Goals: Determine the influence of gender on survival in HCC patients, and identify factors that may account for the difference. Methods: A retrospective analysis on a prospectively collected database in a 15-year period, from 1989 to 2003. Results: A total of 3,171 HCC patients were managed in our institution (946 with curative treatment, 1,388 with palliative treatment, and 837 with supportive treatment) and studied. Female patients (n = 520) were 4.3 years older (P = 0.000), had a lower proportion of smokers and drinkers (P = 0.000), and were less likely to be hepatitisB carriers (P = 0.000). Therewas no difference in Child-Pugh status, tumor size, and the use of different treatments between genders. The overall median survival was 25.7 months longer in females after curative treatment (73.6 vs. 47.9 months; P = 0.012). The survival benefit in female patients was observed in early-stage diseases and persisted when only hepatitis B surface antigen-positive patientswere analyzed (96.4 vs. 47.9 months; P = 0.044). With multivariate analysis, gender, indocyanine green test value at 15 minutes, number of tumor nodules, size of tumor, major vascular invasion, invasion of adjacent organs, and tumor rupture were the independent variables for survival. More importantly, in female patients, history of using oral contraceptive was an independent factor with survival benefit (P = 0.004). Conclusion: Gender is an independent variable for survival after curative treatment of HCC. A survival benefit was observed in females. History of using oral contraceptive is associated with a better long-term survival in female patients.展开更多
PURPOSE:The purpose of this national study was to evaluate the results of treatment for young rectal cancer patients.METHODS:This prospective study from the Norwegian Rectal Cancer Project includes all 2,283 patients ...PURPOSE:The purpose of this national study was to evaluate the results of treatment for young rectal cancer patients.METHODS:This prospective study from the Norwegian Rectal Cancer Project includes all 2,283 patients younger than aged 70 years with adenocarcinoma of the rectum from November 1993 to December 1999.Patients younger than aged 40 years(n = 45) ,40 to 44 years(n = 87) ,45 to 49 years(n = 153) ,and 50 to 69 years(n = 1998) were compared for patient and tumor characteristics and five-year overall survival.Patients treated for cure(n = 1,354) were evaluated for local recurrence,distant metastasis,and disease-free survival.RESULTS:Patients younger than aged 40 years had significantly higher frequencies of poorly differentiated tumors(27 vs.12-16 percent;P = 0.014) ,N2-stage(37 vs.13-18 percent;P = 0.001) ,and distant metastases(38 vs.19-24 percent;P = 0.019) compared with older patients.Among those treated for cure,56 percent of the patients younger than aged 40 years developed distant metastases compared with 20 to 26 percent of the older patients(P = 0.003) .Overall five-year survival was 54 percent for patients younger than aged 40 years compared with 71 to 88 percent for the older patients(P = 0.029) .Age younger than 40 years was a significant independent prognostic factor and increased the risk for metastasis and death.CONCLUSIONS:Patients younger than aged 40 years had a more advanced stage at the time of diagnosis and poor prognosis compared with older patients.Young patients treated for cure more often developed distant metastases and had inferior survival.展开更多
Background. Intrinsic radiosensitivity using the clonogenic assay and the cell surviving fraction at 2 Gy (SF2) has been shown to be an independent prognostic factor for patient response to radiotherapy in carcinoma o...Background. Intrinsic radiosensitivity using the clonogenic assay and the cell surviving fraction at 2 Gy (SF2) has been shown to be an independent prognostic factor for patient response to radiotherapy in carcinoma of the cervix. The clonogenic assay has significant shortcomings, making it unsuitable for routine clinical use. The ATP cell viability assay (ATP- CVA) has been shown to have a high tumor evaluability rate, technical simplicity, and reproducibility in chemosensitivity testing. Aims. This study compares the ATP- CVA with the clonogenic assay in the in vitro radiosensitivity testing of cervical cancer cell lines. Correlation of in vitro radiosensitivity and in vivo patient response was also determined. Methods. Five cervical carcinoma cell lines (SiHa, HeLa, Caski, C- 33A, and C4- 1) were tested using the ATP- CVA and the clonogenic assay. Survival curves were plotted and the mean SF2 values obtained by the two different assay methods were compared using ANOVA to see if there were significant differences. Mean SF2 values obtained from 27 cervical cancers were compared with clinical outcomes. Results. The SF2 values for the cell lines ranged from 0.28 to 0.67 when tested using the ATP- CVA. Using the clonogenic assay, the SF2 values ranged from 0.27 to 0.70. ANOVA with Bonferroni pairwise multiple comparison showed no significant difference between the mean SF2 values for the individual cell lines between the two assay methods. Twenty- three cervical cancer samples (85% ) were evaluable for SF2 using ATP- CVA. The mean SF2 values of patients who had locoregional failure were significantly higher than those who achieved local control (P < 0.01). Conclusions. Testing intrinsic radiosensitivity using the surviving fraction at 2 Gy (SF2) is comparable using the two assay methods of ATP- CVA and clonogenic assay. The ATP- CVA should be further investigated in the testing of intrinsic radiosensitivity in patients with cervical cancer.展开更多
Objective. Recurrent ovarian carcinoma is considered an incurable dis ease and second-line chemotherapy is administered for extension of survival and palliati on. The impact of continued antineoplastic treatment in pa...Objective. Recurrent ovarian carcinoma is considered an incurable dis ease and second-line chemotherapy is administered for extension of survival and palliati on. The impact of continued antineoplastic treatment in patients with stable dis ease without a demonstrable response is uncertain. The aim of this analysis was to assess the value of a stabilization of the tumor size in second-line chemoth erapy as an indicator of survival. Methods. Retrospective, single-institution s tudy of 487 consecutive patients with primary epithelial ovarian carcinoma. Incl usion criteria: (1) FIGO stage IC-IV epithelial ovarian carcinoma; (2) first-l ine chemotherapy with Paclitaxel and a Platinum-compound; (3) refractory, persi stent, or recurrent disease diagnosed by imaging methods; and (4) intravenous se cond-line chemotherapy with single Topotecan or Paclitaxel-Carboplatin. Univar iate and multivariate analyses of survival with theWorld Health Organization (WH O) tumor response parameter included as a time-dependent variable were performe d. Results. The response rates were (N = 100): complete response (CR) 27%, part ial response (PR) 14%, stable disease (SD) 41%and progressive disease (PD) 18 %. In a multivariate Cox regression analysis of survival, SD was found to be an independent prognostic factor for survival and the death hazard ratio was 0.37 (SD versus PD; 95%CI: 0.16-0.86; P = 0.02). There was no statistically signifi cant difference in survival between patients with PR and SD (P = 0.09). Conclusi on. In secondline chemotherapy of ovarian cancer,patients demonstrating SD have a survival benefit compared to patients with PD measured by theWHO tumor respons e criteria.展开更多
AIM: Colorectal cancers result from the accumulation of several distinct genetic alterations. This study was to investigate the frequency and prognostic value of loss of heterozygosity (LOH) and microsatellite instabi...AIM: Colorectal cancers result from the accumulation of several distinct genetic alterations. This study was to investigate the frequency and prognostic value of loss of heterozygosity (LOH) and microsatellite instability (MSI) at 14 genetic loci located near or within regions containing important genes implicated in colorectal tumorigenesis. METHODS: We studied colorectal cancers with corresponding normal mucosae in 207 patients (139 males and 68 females, mean age at the time of tumor resection 66.2±12.4 years, range 22-88 years). There were 37 right-sided colonic tumors, 85 left-sided colonic tumors and 85 rectal tumors. The distribution of tumor staging was stage Ⅰ in 25, stage Ⅱ in 73, stage Ⅲ in 68, and stage Ⅳ in 41. We analyzed the LOH and MSI of HPC1, hMSH2, hMLH1, APC, MET, P53, NH23-H1, DCC, BAT25, BAT26, D17S250, MYCL1 and D8S254 with fluorescent polymerase chain reaction and denatured gel electrophoresis. High-frequency LOH was determined to be greater than three, or more than 50% of the informative marker with LOH. High-frequency MSI (MSI-H) was determined as more than four markers with instability (>30%). Correlations of LOH and MSI with clinical outcomes and pathological features were analyzed and compared. RESULTS: The occurrence of MSI-H was 7.25%, located predominantly in the right colons (7/15) and had a higher frequency of poor differentiation (6/15) and mucin production (7/15). LOH in at least one genetic locus occurred in 78.7% of the tumors and was significantly associated with disease progression. Of the 166 potentially cured patients, 45 developed tumor recurrence within 36 mo of follow-up. Clinicopathological factors affecting 3-year disease-free survival (DFS) were TNM staging, grade of differentiation, preoperative CEA level, and high LOH status. Patients with high LOH tumors had a significantly lower DFS (50%) compared with patients with low LOH tumors (84%). Of the patients developing subsequent tumor recurrence, the number and percentage of LOH were 2.97 and 46.8% respectively, similar to the stage IV disease patients. TNM staging had the most significant impact on DFS, followed by high LOH status. CONCLUSION: Clinical manifestations of LOH and MSI are different in colorectal cancer patients. High-frequency LOH is associated with high metastatic potential of colorectal cancers.展开更多
文摘Purpose of investigation. To evaluate whether lymphvascular space involvement (LVSI) is a risk factor for relapse of disease and lymph node metastasis in endometrial cancer. Methods. From 1978 till 2003, 609 patients with epithelial endometrial cancer were treated at the Groningen University Medical Center. The association of LVSI and relapse of disease was evaluated in the total group of 609 patients and in a ‘ low’ and ‘ high’ risk stage I endometrial cancer group. In 239 surgically staged patients, the relation of LVSI and lymph node metastasis was investigated. Results. The median age at diagnosis was 63 years (range 27- 92 years) with a median follow- up of 58 months (range 0- 236 months). More than half of the patients (56% ) received adjuvant radiotherapy. LVSI was present in 123 patients (25,6% ), and a prognostic factor for relapse of disease (multivariate analysis, P < 0.0001). In the ‘ low’ and ‘ high’ risk stage I endometrial cancer patients an increase of 2.6 times in relapse of disease was observed in the presence of LVSI. LVSI positive tumors were more likely to have metastasized to the pelvic lymph nodes (multivariate analysis, P = 0.001). In patients with proven negative nodes, LVSI was a prognostic factor for relapse of disease (univariate analysis, P = 0.02). Conclusion. LVSI is a predictor of nodal disease and an independent prognostic factor for relapse of disease in all stages of endometrial cancer. Patients with stage I endometrial cancer with positive LVSI are at risk for relapse of disease and might therefore benefit from adjuvant therapy. Content. The presence of lymphvascular space involvement (LVSI) in endometrial cancer is significantly and independently associated with an increased risk of pelvic lymph node metastases and/or relapse of disease.
文摘Background: Tumor ulceration (TU) is considered the second most important prognostic factor after Breslow thickness for localized cutaneous malignant melanoma (CMM). However, many studies have not included mitotic rate (MR) with TU in these analyses. When both TU and MR are included in the same analysis, MR appears to be the more important than TU and TU loses its significance as an independent prognostic factor. Methods: The relative importance of TU and MR as prognostic factors in localized CMM were compared in a population- based series of 650 consecutive invasive CMM cases ascertained from the Connecticut tumor registry and reviewed by a single dermatopathologist (RLB), during the period between January 15, 1987 and May 15, 1989. Seventeen clinical and histopathological variables including tumor thickness measured in mm, TU recorded as present or absent, and MR recorded as number per mm2 were included in an unconditional logistic regression model and selected for inclusion using a backward stepwise algorithm with death as an endpoint or at least five- years follow- up. Results: Inthemultivariateregression,theindependent prognostic factors included: 1. tumor thickness in millimeters (OR=1.5, 95% CI=1.3- 1.9) 2. moderate mitotic index (between 1 and 6): (OR=8.3, 95% CI 2.4- 28.7), 3. mitotic index (>6): (OR=11.6, 95% CI=3.0- 44.6), 4. solar elastosis: (inversely associated with mortality) (OR=0.4, 95% CI=0.28). After adjustment for MR, TU lost its significance. When MR was left out of the analysis, ulceration then became an independent prognostic factor. The model with ulceration only (excluding MR) showed a relative risk (RR) of 2.4 (95% CI: 1.1- 5.1). In the model with MR only, MR had a RR of 14.5 (95% CIS.9- 53.7). Finally, regression analysis including both TU and MR yielded an RR of 11.6 for MR and 1.7 for TU. Conclusions: Our results suggest that MR as a proxy for tumor proliferation is a more important prognostic factor than TU.
文摘目的探究脑特异性新生血管抑制因子1(BAI1)在结直肠癌中的表达与结直肠癌患者临床病理学特征的关系。方法 2016年5月~2017年7月,购买包含有208个结直肠癌和8个正常结肠组织及其临床信息的组织芯片。查询癌症基因组图谱数据库,内含192例结直肠癌患者的m RNA表达信息。通过免疫组化检测组织芯片正常结肠组织与结直肠癌组织中BAI1表达的情况,检测BAI1表达与结直肠癌患者临床病理特征的关系,采用Kaplan-Meier法和Log-rank秩检验方法进行生存曲线。最后使用Cox回归模型进行单变量分析和多变量分析,判断BAI1对预后的判断价值。结果 BAI1在结直肠癌组织中的含量较正常组织显著上升(P<0.001)。高BAI1表达与临床分期(P=0.004)和肿瘤浸润(P=0.006)相关。癌症基因组图谱(TCGA)中结直肠癌患者的BAI1m RNA表达进一步提示了较晚的临床分期(P=0.027)、较严重的肿瘤浸润(P=0.021)的结直肠癌中BAI1表达水平更高。Kaplan-Meier生存曲线提示BAI1 m RNA高表达的患者比低表达水平的患者总生存期明显减少(P=0.02)。BAI1 m RNA的高表达是结直肠癌预后的独立影响因素(HR=2.895,95%CI:1.012~8.281,P=0.047)。结论 BAI1与结直肠癌的恶性相关。BAI1的高表达可能提示结直肠癌患者的不良预后。
文摘Background: Hepatocellular carcinoma (HCC) has an indisputable male predominance. “Gender" as an independent prognostic factor for survival is, however, controversial. Goals: Determine the influence of gender on survival in HCC patients, and identify factors that may account for the difference. Methods: A retrospective analysis on a prospectively collected database in a 15-year period, from 1989 to 2003. Results: A total of 3,171 HCC patients were managed in our institution (946 with curative treatment, 1,388 with palliative treatment, and 837 with supportive treatment) and studied. Female patients (n = 520) were 4.3 years older (P = 0.000), had a lower proportion of smokers and drinkers (P = 0.000), and were less likely to be hepatitisB carriers (P = 0.000). Therewas no difference in Child-Pugh status, tumor size, and the use of different treatments between genders. The overall median survival was 25.7 months longer in females after curative treatment (73.6 vs. 47.9 months; P = 0.012). The survival benefit in female patients was observed in early-stage diseases and persisted when only hepatitis B surface antigen-positive patientswere analyzed (96.4 vs. 47.9 months; P = 0.044). With multivariate analysis, gender, indocyanine green test value at 15 minutes, number of tumor nodules, size of tumor, major vascular invasion, invasion of adjacent organs, and tumor rupture were the independent variables for survival. More importantly, in female patients, history of using oral contraceptive was an independent factor with survival benefit (P = 0.004). Conclusion: Gender is an independent variable for survival after curative treatment of HCC. A survival benefit was observed in females. History of using oral contraceptive is associated with a better long-term survival in female patients.
文摘PURPOSE:The purpose of this national study was to evaluate the results of treatment for young rectal cancer patients.METHODS:This prospective study from the Norwegian Rectal Cancer Project includes all 2,283 patients younger than aged 70 years with adenocarcinoma of the rectum from November 1993 to December 1999.Patients younger than aged 40 years(n = 45) ,40 to 44 years(n = 87) ,45 to 49 years(n = 153) ,and 50 to 69 years(n = 1998) were compared for patient and tumor characteristics and five-year overall survival.Patients treated for cure(n = 1,354) were evaluated for local recurrence,distant metastasis,and disease-free survival.RESULTS:Patients younger than aged 40 years had significantly higher frequencies of poorly differentiated tumors(27 vs.12-16 percent;P = 0.014) ,N2-stage(37 vs.13-18 percent;P = 0.001) ,and distant metastases(38 vs.19-24 percent;P = 0.019) compared with older patients.Among those treated for cure,56 percent of the patients younger than aged 40 years developed distant metastases compared with 20 to 26 percent of the older patients(P = 0.003) .Overall five-year survival was 54 percent for patients younger than aged 40 years compared with 71 to 88 percent for the older patients(P = 0.029) .Age younger than 40 years was a significant independent prognostic factor and increased the risk for metastasis and death.CONCLUSIONS:Patients younger than aged 40 years had a more advanced stage at the time of diagnosis and poor prognosis compared with older patients.Young patients treated for cure more often developed distant metastases and had inferior survival.
文摘Background. Intrinsic radiosensitivity using the clonogenic assay and the cell surviving fraction at 2 Gy (SF2) has been shown to be an independent prognostic factor for patient response to radiotherapy in carcinoma of the cervix. The clonogenic assay has significant shortcomings, making it unsuitable for routine clinical use. The ATP cell viability assay (ATP- CVA) has been shown to have a high tumor evaluability rate, technical simplicity, and reproducibility in chemosensitivity testing. Aims. This study compares the ATP- CVA with the clonogenic assay in the in vitro radiosensitivity testing of cervical cancer cell lines. Correlation of in vitro radiosensitivity and in vivo patient response was also determined. Methods. Five cervical carcinoma cell lines (SiHa, HeLa, Caski, C- 33A, and C4- 1) were tested using the ATP- CVA and the clonogenic assay. Survival curves were plotted and the mean SF2 values obtained by the two different assay methods were compared using ANOVA to see if there were significant differences. Mean SF2 values obtained from 27 cervical cancers were compared with clinical outcomes. Results. The SF2 values for the cell lines ranged from 0.28 to 0.67 when tested using the ATP- CVA. Using the clonogenic assay, the SF2 values ranged from 0.27 to 0.70. ANOVA with Bonferroni pairwise multiple comparison showed no significant difference between the mean SF2 values for the individual cell lines between the two assay methods. Twenty- three cervical cancer samples (85% ) were evaluable for SF2 using ATP- CVA. The mean SF2 values of patients who had locoregional failure were significantly higher than those who achieved local control (P < 0.01). Conclusions. Testing intrinsic radiosensitivity using the surviving fraction at 2 Gy (SF2) is comparable using the two assay methods of ATP- CVA and clonogenic assay. The ATP- CVA should be further investigated in the testing of intrinsic radiosensitivity in patients with cervical cancer.
文摘Objective. Recurrent ovarian carcinoma is considered an incurable dis ease and second-line chemotherapy is administered for extension of survival and palliati on. The impact of continued antineoplastic treatment in patients with stable dis ease without a demonstrable response is uncertain. The aim of this analysis was to assess the value of a stabilization of the tumor size in second-line chemoth erapy as an indicator of survival. Methods. Retrospective, single-institution s tudy of 487 consecutive patients with primary epithelial ovarian carcinoma. Incl usion criteria: (1) FIGO stage IC-IV epithelial ovarian carcinoma; (2) first-l ine chemotherapy with Paclitaxel and a Platinum-compound; (3) refractory, persi stent, or recurrent disease diagnosed by imaging methods; and (4) intravenous se cond-line chemotherapy with single Topotecan or Paclitaxel-Carboplatin. Univar iate and multivariate analyses of survival with theWorld Health Organization (WH O) tumor response parameter included as a time-dependent variable were performe d. Results. The response rates were (N = 100): complete response (CR) 27%, part ial response (PR) 14%, stable disease (SD) 41%and progressive disease (PD) 18 %. In a multivariate Cox regression analysis of survival, SD was found to be an independent prognostic factor for survival and the death hazard ratio was 0.37 (SD versus PD; 95%CI: 0.16-0.86; P = 0.02). There was no statistically signifi cant difference in survival between patients with PR and SD (P = 0.09). Conclusi on. In secondline chemotherapy of ovarian cancer,patients demonstrating SD have a survival benefit compared to patients with PD measured by theWHO tumor respons e criteria.
基金Supported by grants from the Veterans General Hospital-Taipei,VGH90348 and VGH910305
文摘AIM: Colorectal cancers result from the accumulation of several distinct genetic alterations. This study was to investigate the frequency and prognostic value of loss of heterozygosity (LOH) and microsatellite instability (MSI) at 14 genetic loci located near or within regions containing important genes implicated in colorectal tumorigenesis. METHODS: We studied colorectal cancers with corresponding normal mucosae in 207 patients (139 males and 68 females, mean age at the time of tumor resection 66.2±12.4 years, range 22-88 years). There were 37 right-sided colonic tumors, 85 left-sided colonic tumors and 85 rectal tumors. The distribution of tumor staging was stage Ⅰ in 25, stage Ⅱ in 73, stage Ⅲ in 68, and stage Ⅳ in 41. We analyzed the LOH and MSI of HPC1, hMSH2, hMLH1, APC, MET, P53, NH23-H1, DCC, BAT25, BAT26, D17S250, MYCL1 and D8S254 with fluorescent polymerase chain reaction and denatured gel electrophoresis. High-frequency LOH was determined to be greater than three, or more than 50% of the informative marker with LOH. High-frequency MSI (MSI-H) was determined as more than four markers with instability (>30%). Correlations of LOH and MSI with clinical outcomes and pathological features were analyzed and compared. RESULTS: The occurrence of MSI-H was 7.25%, located predominantly in the right colons (7/15) and had a higher frequency of poor differentiation (6/15) and mucin production (7/15). LOH in at least one genetic locus occurred in 78.7% of the tumors and was significantly associated with disease progression. Of the 166 potentially cured patients, 45 developed tumor recurrence within 36 mo of follow-up. Clinicopathological factors affecting 3-year disease-free survival (DFS) were TNM staging, grade of differentiation, preoperative CEA level, and high LOH status. Patients with high LOH tumors had a significantly lower DFS (50%) compared with patients with low LOH tumors (84%). Of the patients developing subsequent tumor recurrence, the number and percentage of LOH were 2.97 and 46.8% respectively, similar to the stage IV disease patients. TNM staging had the most significant impact on DFS, followed by high LOH status. CONCLUSION: Clinical manifestations of LOH and MSI are different in colorectal cancer patients. High-frequency LOH is associated with high metastatic potential of colorectal cancers.