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We are analyzing https://link.springer.com/article/10.1245/s10434-011-2086-4.

Title:
Significance of Pathologic Response to Preoperative Therapy in Pancreatic Cancer | Annals of Surgical Oncology
Description:
Pathologic response to preoperative therapy is increasingly recognized as an important prognostic factor in solid tumors. The impact of pathologic response on survival in pancreatic adenocarcinoma is not well established. Data on 135 consecutive patients treated with chemoradiation followed by pancreatectomy for adenocarcinoma of the pancreatic head and/or body between July 1987 and May 2009 were reviewed. Histopathologic examination was performed in 107 patients to determine pathologic response, defined as minor (<50% fibrosis relative to residual neoplastic cells), partial (50–94% fibrosis), or major (95–100% fibrosis). Minor, partial, and major pathologic response rates were 17% (n = 18), 64% (n = 68), and 19% (n = 21), including a 7% (n = 8) complete pathologic response rate. Pathologic response correlated with R0 resection (P = 0.019), negative lymph nodes (P = 0.006), and smaller tumor size (P = 0.001). Median survival rates by pathologic response were as follows: 17 months [95% confidence interval (CI), 0–36 months] for minor response, 20 months (95% CI, 17–23 months) for partial response, and 66 months (95% CI, 8–124 months) for major response (minor versus partial response, P = not significant; partial versus major response, P < 0.001). On multivariate analysis, major pathologic response was the only factor significantly associated with improved survival (P = 0.025; hazard ratio, 2.26). Major pathologic response to preoperative therapy occurs in a minority of patients with pancreatic adenocarcinoma and is independently associated with prolonged survival.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Non-Profit & Charity
  • Telecommunications
  • Health & Fitness

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 7,626,182 visitors per month in the current month.

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How Does Link.springer.com Make Money? {💸}

We find it hard to spot revenue streams.

Not all websites focus on profit; some are designed to educate, connect people, or share useful tools. People create websites for numerous reasons. And this could be one such example. Link.springer.com has a secret sauce for making money, but we can't detect it yet.

Keywords {🔍}

article, pancreatic, response, cancer, pubmed, google, scholar, pathologic, adenocarcinoma, oncol, cas, preoperative, surg, resectable, patients, ann, chemoradiotherapy, survival, chemoradiation, pancreas, hoffman, major, months, chemotherapy, clin, privacy, cookies, content, oncology, therapy, chun, partial, borderline, outcome, neoadjuvant, usa, analysis, data, publish, search, surgical, significance, cooper, head, minor, complete, resection, access, clinical, gemcitabine,

Topics {✒️}

month download article/chapter negative lymph nodes de campos-lobato lf contemporary single-institution experience preoperative gemcitabine-based chemoradiation advanced pancreatic cancer doxorubicin-based neoadjuvant chemotherapy full article pdf article chun resected pancreatic cancer gemcitabine-based chemoradiation privacy choices/manage cookies related subjects smaller tumor size wayne state university andre konski md pathologic complete response resectable pancreatic adenocarcinoma combined modality treatment expert consensus statement breast cancer patients determine pathologic response pathologic response correlated major pathologic response randomised controlled trial barbara burtness md igor astsaturov md serum ca19-9 response article annals pancreatic cancer european economic area residual neoplastic cells defining venous involvement varadhachary gr localized gastric carcinoma surgical margin status randomized controlled trial evans db conditions privacy policy hepatobiliary pancreat surg surgical oncology aims important prognostic factor preoperative endorectal ultrasonography paclitaxel-based chemoradiotherapy preoperative therapy occurs median survival rates ann surg oncol accepting optional cookies check access instant access

Questions {❓}

  • Does neoadjuvant chemoradiation downstage locally advanced pancreatic cancer?

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Significance of Pathologic Response to Preoperative Therapy in Pancreatic Cancer
         description:Pathologic response to preoperative therapy is increasingly recognized as an important prognostic factor in solid tumors. The impact of pathologic response on survival in pancreatic adenocarcinoma is not well established. Data on 135 consecutive patients treated with chemoradiation followed by pancreatectomy for adenocarcinoma of the pancreatic head and/or body between July 1987 and May 2009 were reviewed. Histopathologic examination was performed in 107 patients to determine pathologic response, defined as minor (<50% fibrosis relative to residual neoplastic cells), partial (50–94% fibrosis), or major (95–100% fibrosis). Minor, partial, and major pathologic response rates were 17% (n = 18), 64% (n = 68), and 19% (n = 21), including a 7% (n = 8) complete pathologic response rate. Pathologic response correlated with R0 resection (P = 0.019), negative lymph nodes (P = 0.006), and smaller tumor size (P = 0.001). Median survival rates by pathologic response were as follows: 17 months [95% confidence interval (CI), 0–36 months] for minor response, 20 months (95% CI, 17–23 months) for partial response, and 66 months (95% CI, 8–124 months) for major response (minor versus partial response, P = not significant; partial versus major response, P < 0.001). On multivariate analysis, major pathologic response was the only factor significantly associated with improved survival (P = 0.025; hazard ratio, 2.26). Major pathologic response to preoperative therapy occurs in a minority of patients with pancreatic adenocarcinoma and is independently associated with prolonged survival.
         datePublished:2011-09-27T00:00:00Z
         dateModified:2011-09-27T00:00:00Z
         pageStart:3601
         pageEnd:3607
         sameAs:https://doi.org/10.1245/s10434-011-2086-4
         keywords:
            Pancreatic Cancer
            Gemcitabine
            Pancreatic Adenocarcinoma
            Pathologic Response
            Negative Lymph Node
            Surgical Oncology
            Oncology
            Surgery
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               name:Yun Shin Chun
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                     name:Fox Chase Cancer Center
                     address:
                        name:Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, USA
                        type:PostalAddress
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               name:Harry S. Cooper
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                     name:Fox Chase Cancer Center
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                        name:Department of Pathology, Fox Chase Cancer Center, Philadelphia, USA
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               name:Steven J. Cohen
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                        type:PostalAddress
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               name:Andre Konski
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                        name:Department of Radiation Oncology, Wayne State University, Detroit, USA
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               name:Michael J. Hall
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                        name:Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, USA
                        type:PostalAddress
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               name:John P. Hoffman
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                     name:Fox Chase Cancer Center
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      headline:Significance of Pathologic Response to Preoperative Therapy in Pancreatic Cancer
      description:Pathologic response to preoperative therapy is increasingly recognized as an important prognostic factor in solid tumors. The impact of pathologic response on survival in pancreatic adenocarcinoma is not well established. Data on 135 consecutive patients treated with chemoradiation followed by pancreatectomy for adenocarcinoma of the pancreatic head and/or body between July 1987 and May 2009 were reviewed. Histopathologic examination was performed in 107 patients to determine pathologic response, defined as minor (<50% fibrosis relative to residual neoplastic cells), partial (50–94% fibrosis), or major (95–100% fibrosis). Minor, partial, and major pathologic response rates were 17% (n = 18), 64% (n = 68), and 19% (n = 21), including a 7% (n = 8) complete pathologic response rate. Pathologic response correlated with R0 resection (P = 0.019), negative lymph nodes (P = 0.006), and smaller tumor size (P = 0.001). Median survival rates by pathologic response were as follows: 17 months [95% confidence interval (CI), 0–36 months] for minor response, 20 months (95% CI, 17–23 months) for partial response, and 66 months (95% CI, 8–124 months) for major response (minor versus partial response, P = not significant; partial versus major response, P < 0.001). On multivariate analysis, major pathologic response was the only factor significantly associated with improved survival (P = 0.025; hazard ratio, 2.26). Major pathologic response to preoperative therapy occurs in a minority of patients with pancreatic adenocarcinoma and is independently associated with prolonged survival.
      datePublished:2011-09-27T00:00:00Z
      dateModified:2011-09-27T00:00:00Z
      pageStart:3601
      pageEnd:3607
      sameAs:https://doi.org/10.1245/s10434-011-2086-4
      keywords:
         Pancreatic Cancer
         Gemcitabine
         Pancreatic Adenocarcinoma
         Pathologic Response
         Negative Lymph Node
         Surgical Oncology
         Oncology
         Surgery
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            name:Yun Shin Chun
            affiliation:
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                  address:
                     name:Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, USA
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
            name:Harry S. Cooper
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                  name:Fox Chase Cancer Center
                  address:
                     name:Department of Pathology, Fox Chase Cancer Center, Philadelphia, USA
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                     type:PostalAddress
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            name:Andre Konski
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                  address:
                     name:Department of Radiation Oncology, Wayne State University, Detroit, USA
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                     name:Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, USA
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                  address:
                     name:Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, USA
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            name:Michael J. Hall
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                  name:Fox Chase Cancer Center
                  address:
                     name:Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, USA
                     type:PostalAddress
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            name:John P. Hoffman
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                     name:Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, USA
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            address:
               name:Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, USA
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      affiliation:
            name:Fox Chase Cancer Center
            address:
               name:Department of Pathology, Fox Chase Cancer Center, Philadelphia, USA
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      name:Steven J. Cohen
      affiliation:
            name:Fox Chase Cancer Center
            address:
               name:Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, USA
               type:PostalAddress
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      name:Andre Konski
      affiliation:
            name:Wayne State University
            address:
               name:Department of Radiation Oncology, Wayne State University, Detroit, USA
               type:PostalAddress
            type:Organization
      name:Barbara Burtness
      affiliation:
            name:Fox Chase Cancer Center
            address:
               name:Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, USA
               type:PostalAddress
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      name:Crystal S. Denlinger
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            name:Fox Chase Cancer Center
            address:
               name:Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, USA
               type:PostalAddress
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      name:Igor Astsaturov
      affiliation:
            name:Fox Chase Cancer Center
            address:
               name:Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, USA
               type:PostalAddress
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      name:Michael J. Hall
      affiliation:
            name:Fox Chase Cancer Center
            address:
               name:Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, USA
               type:PostalAddress
            type:Organization
      name:John P. Hoffman
      affiliation:
            name:Fox Chase Cancer Center
            address:
               name:Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, USA
               type:PostalAddress
            type:Organization
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      name:Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, USA
      name:Department of Pathology, Fox Chase Cancer Center, Philadelphia, USA
      name:Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, USA
      name:Department of Radiation Oncology, Wayne State University, Detroit, USA
      name:Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, USA
      name:Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, USA
      name:Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, USA
      name:Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, USA
      name:Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, USA
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