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. 2014 Nov;2(11):108. doi: 10.3978/j.issn.2305-5839.2014.09.06

Table 2. The main clinical evidence for CTC detection in various types of cancer.

Type of cancer Tumor stage Clinical results References
Breast cancer (BC) Metastatic CTCs ≥5/7.5 mL associated with reduced PFS and OS (9,92)
CTCs C 5/7.5 mL at any time point during chemotherapy associated with adverse clinical outcome (90)
CTCs C 5/7.5 mL after the initiation of a new systemic therapy were associated with shorter median PFS and higher incidence of radiographic disease progression (95,96)
Lack of prediction in HER2-positive disease treated with targeted therapy (99)
Change in CTC level during the course of chemotherapy was a surrogate marker monitoring therapeutic efficacy and was correlated with OS (147)
Stages I-III A low cutoff of 1 CTC was feasible. CTC detection was not associated with primary tumor response but was an independent prognostic factor for early relapse and OS after neoadjuvant therapy (17,70,148,149)
CTC detection incidence in early-stage disease paralleled with cancer stage. Each of CTC biomarker significantly correlated with ALN metastasis (150)
CTC detection before adjuvant chemotherapy was independent predictor of DFS and OS. The persistence of CTCs after adjuvant treatment significantly correlates with a decreased DFS (66,68,103)
Prostate cancer Metastatic CTCs ≥5/7.5 mL was associated with poor OS (108,151)
Patients with unfavorable pre- or post-treatment CTC count had shorter OS and its predictive ability was superior to PSA level at all-time points (152)
CTC count predicted OS and was a sensitive marker in monitoring disease status during treatment, especially in early-stage disease (114)
CTC number as a continuous variable was prognostic for survival of patients with CRPC starting first-line chemotherapy (115)
CTCs ≥4/7.5 mL was associated with poor OS, and their presence correlates with radiographic findings and classic markers (110)
CTCs ≥2/7.5 mL was associated with disease status and clinical indicators of PSA and PSM (111)
CTCs ≥1.8/mL was associated with shorter OS (112)
Localized disease No correlation between the number of CTC and known prognostic factor in localized prostate cancer patients (121)
Colorectal cancer Metastatic The CTCs level at baseline and follow-up was an independent predictor of PFS and OS, which correlate well with radiographic findings (123)
The presence of at least 1 CTC at baseline count was found to be predictive for poor prognosis (124)
Unfavorable baseline CTC was associated with worse PFS in patients receiving first- or second-line therapy, irinotecan, having liver involvement, ≥65 years, and ECOG PS of zero (126)
CTC count was a reliable surrogate biomarker of predicting clinical outcome and assessing Japanese patients responsive to oxaliplatin-based chemotherapy (127)
CTC count during treatment could become a new predictor of therapy response (128,130,153,154)
Stage I-III Patients with persistent presence of CTC even postoperatively exhibited higher incidence of postoperative relapse and poor relapse-free survival rate (131)
Molecular assessment for micrometastasis in sentinel lymph node along with CTC count may help to identify patients at high risk for recurrence and thus who could benefit from adjuvant therapy (129,130)
Lung cancer Localized and metastatic The number of CTC was a robust surrogate prognostic indicator to predict the presence of distant metastasis. CTC status correlated with clinical and pathological stage (134)
CTC enumeration well correlated with radiographic response at the end of two cycles of chemotherapy (135)
CTCs decreased in all patients after on cycle of chemotherapy supporting CTC as a pharmacodynamic biomarker for small cell lung cancer (SCLC) (137)
Stages III-IV CTC detection at baseline and change in CTC number after one cycle of chemotherapy was a prognostic factor for tumor response, PFS and OS (136,138,140-144)
Stages I-IV CTC level ≥5 was associated with worse survival of patients with resectable NSCLC (145)

CTCs, circulating tumor cells; PFS, progression-free; OS, overall survival; DFS, disease-free survival; CRPC, castration-resistant prostate cancer; NSCLC, non-small cell lung cancer.