2020
DOI: 10.3389/fonc.2020.595107
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Re-Evaluation of the Survival Paradox Between Stage IIB/IIC and Stage IIIA Colon Cancer

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Cited by 17 publications
(16 citation statements)
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“…The Western medicine predictors were determined according to the predictor in the reported prognostic model (25) and the actual record of the case data in this study. The details are as follows: (1) Age at diagnosis; (2) primary tumor (T stage); (3) number of positive lymph nodes; (4) whether the number of detected lymph nodes was less than 12; (5) whether there was lymphatic, vascular and nerve invasion; (6) tumor site;…”
Section: Model Predictorsmentioning
confidence: 99%
“…The Western medicine predictors were determined according to the predictor in the reported prognostic model (25) and the actual record of the case data in this study. The details are as follows: (1) Age at diagnosis; (2) primary tumor (T stage); (3) number of positive lymph nodes; (4) whether the number of detected lymph nodes was less than 12; (5) whether there was lymphatic, vascular and nerve invasion; (6) tumor site;…”
Section: Model Predictorsmentioning
confidence: 99%
“…These linear approaches may cause a phenomenon known as the "survival paradox": T4N0 CRC had a significantly worse outcome than T1-2N1 cancer regardless of adjuvant chemotherapy, 12 which may mislead clinicians into over-or underestimating the disease prognosis. 13 To deal with these challenges, methods based on machine learning (ML), a subfield of artificial intelligence with the goal of developing algorithms capable of learning from data automatically, 14 were used in the present study. ML is able to use complex algorithms for large datasets with multidimensional variables to capture high-dimensional, nonlinear relationships among clinical features to make data-driven outcome predictions.…”
Section: Introductionmentioning
confidence: 99%
“…These linear approaches may cause a phenomenon known as the “survival paradox”: T4N0 CRC had a significantly worse outcome than T1-2N1 cancer regardless of adjuvant chemotherapy, 12 which may mislead clinicians into over- or underestimating the disease prognosis. 13 …”
Section: Introductionmentioning
confidence: 99%
“…While for stage III CRC adjuvant systemic therapy is mandatory, stage II CRC must be firstly assessed for potential risk/benefits of therapy and prognosis. Currently, adjuvant chemotherapy for stage II CRC is recommended to patents with less than 12 lymph nodes analyzed after surgery and poor prognostic features (such as poorly differentiated histology, lymphatic/vascular invasion, positive margins, obstruction/perforation, comorbidities) [11]. Currently, the options of adjuvant therapy for high-risk stage II CRC are FOLFOX (5-fluorouracil, leucovorin, and oxaliplatin), CAPEOX (capecitabine and oxaliplatin), capecitabine, or 5-fluorouracil/leucovorin for 3-6 months.…”
Section: Introduction 1standard Of Care Of Colorectal Cancermentioning
confidence: 99%
“…Inevitably, distinct drug responses and inconsistent survival outcomes are not uncommon within a single stage, which is even more pronounced regarding stages II and III [17]. The existence of a survival paradox between stages IIB/IIC and IIIA (T1-2, N1, M0 or T1, N2, M0) is a widely known phenomenon in CRC patients, and numerous causes had been described to contribute to an inferior survival in IIB/IIC compared with that of stage IIIA [11]. One explanation might be the insufficient use of systemic adjuvant chemotherapy in stage II CRC, since it is part of the standard care of treatment used in stage III CRC [18].…”
Section: Introduction 1standard Of Care Of Colorectal Cancermentioning
confidence: 99%