2005
DOI: 10.1097/01.sla.0000161983.82345.85
|View full text |Cite
|
Sign up to set email alerts
|

Proposed Revision of the Esophageal Cancer Staging System to Accommodate Pathologic Response (pP) Following Preoperative Chemoradiation (CRT)

Abstract: Our analyses demonstrate that following CRT, pTNM continues to predict survival. The extent of pathologic response following CRT is an independent risk factor for survival (pP) and should be incorporated in the pTNM esophageal cancer staging system to better predict patient outcome in esophageal cancer.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

11
112
2
3

Year Published

2006
2006
2020
2020

Publication Types

Select...
8
1

Relationship

0
9

Authors

Journals

citations
Cited by 144 publications
(128 citation statements)
references
References 19 publications
11
112
2
3
Order By: Relevance
“…However, several authors have criticised the TNM oesophageal staging system, claiming that it poorly stratifies what is a heterogeneous group of patients who have variable prognostic outcomes and undergo different treatment regimens [12][13][14][15][16][17][18][19][20][21][22][23]. The UICC has responded to these recommendations in its seventh edition of TNM staging, released in 2010, by modifying all three aspects of the scoring system.…”
Section: Introductionmentioning
confidence: 99%
“…However, several authors have criticised the TNM oesophageal staging system, claiming that it poorly stratifies what is a heterogeneous group of patients who have variable prognostic outcomes and undergo different treatment regimens [12][13][14][15][16][17][18][19][20][21][22][23]. The UICC has responded to these recommendations in its seventh edition of TNM staging, released in 2010, by modifying all three aspects of the scoring system.…”
Section: Introductionmentioning
confidence: 99%
“…A pCR occurs in approximately 15 -30% of cases, and 3-year survival rates of approximately 60% irrespective of the applied protocol, type of histology and tumour stage are achieved (Geh et al, 2001). A further subdivision of pathological response to neoadjuvant regimens, the tumour regression grade (TRG) (Mandard et al, 1994), may also identify patterns of incomplete response that may impact on treatment outcome, and the addition of the pathologic response to pTNM staging has been recently advocated (Swisher et al, 2005). Where a cohort of patients may benefit from neoadjuvant CRT, with pCR and TRG the surrogate markers, many patients will not be helped, and their prognosis may be worsened by delay in surgery and by the added risks of surgery in patients on multimodal protocols (Ancona et al, 2001;Fiorica et al, 2004).…”
mentioning
confidence: 99%
“…Applying this scoring system, patients with less than 10% residual tumor cells after neoadjuvant treatment are classifi ed as histopathological responders (score 1a, complete response and score 1b, less than 10% residual tumor cells). In other publications, only patients with complete tumor regression are classifi ed as histopathological responders [26,27]. In contrast, Shah et al [28] defi ned patients with less than 50% residual tumor cells as histopathological responders.…”
Section: Response Evaluationmentioning
confidence: 99%
“…It is generally accepted that responders have a signifi cantly improved survival compared to that in nonresponding patients [12]. Unfortunately, no standardized scores for clinical or histopathological response evaluation have been established so far, which makes studies hard to compare [5,22,27,28]. There is a need for the homogenization of clinical and histopathological response scores after induction chemotherapy.…”
Section: The New Credomentioning
confidence: 99%