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Tumor Regression Grade in Gastric Cancer After Preoperative Therapy

Background The Cancer Staging Manual , 8th edition, now includes post-neoadjuvant therapy (ypTNM) staging for gastric cancer patients. Our purpose was to determine whether the tumor regression grade (TRG) of the primary tumor is useful for predicting the survival of these patients. Methods We perfor...

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Published in:Journal of gastrointestinal surgery 2021-06, Vol.25 (6), p.1380-1387
Main Authors: Ikoma, Naruhiko, Estrella, Jeannelyn S., Blum Murphy, Mariela, Das, Prajnan, Minsky, Bruce D., Mansfield, Paul, Ajani, Jaffer A., Badgwell, Brian D.
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creator Ikoma, Naruhiko
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description Background The Cancer Staging Manual , 8th edition, now includes post-neoadjuvant therapy (ypTNM) staging for gastric cancer patients. Our purpose was to determine whether the tumor regression grade (TRG) of the primary tumor is useful for predicting the survival of these patients. Methods We performed a retrospective review of an institutional database and identified patients with clinically non-metastatic gastric adenocarcinoma who underwent preoperative chemotherapy or chemoradiation therapy before gastrectomy. Pathology reports were reviewed, and TRG was classified as follows: 0 (complete response), 1 (viable tumor cells ≤ 1–2%), 2 (viable cells ≤ 50%), or 3 (viable cells > 50%). Results Of the 356 patients identified, including 80 (23%) with a gastroesophageal junction tumor, 268 (75%) had undergone preoperative chemoradiation therapy. Fifty-six (16%) had TRG 0, 57 (16%) TRG 1, 128 (36%) TRG 2, and 115 (32%) TRG 3. No association between TRG and pretreatment factors was identified, except for signet-ring cell histologic type and tumor location. A higher TRG was associated with more advanced ypT and ypN categories (both p  
doi_str_mv 10.1007/s11605-020-04688-2
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Our purpose was to determine whether the tumor regression grade (TRG) of the primary tumor is useful for predicting the survival of these patients. Methods We performed a retrospective review of an institutional database and identified patients with clinically non-metastatic gastric adenocarcinoma who underwent preoperative chemotherapy or chemoradiation therapy before gastrectomy. Pathology reports were reviewed, and TRG was classified as follows: 0 (complete response), 1 (viable tumor cells ≤ 1–2%), 2 (viable cells ≤ 50%), or 3 (viable cells &gt; 50%). Results Of the 356 patients identified, including 80 (23%) with a gastroesophageal junction tumor, 268 (75%) had undergone preoperative chemoradiation therapy. Fifty-six (16%) had TRG 0, 57 (16%) TRG 1, 128 (36%) TRG 2, and 115 (32%) TRG 3. No association between TRG and pretreatment factors was identified, except for signet-ring cell histologic type and tumor location. A higher TRG was associated with more advanced ypT and ypN categories (both p  &lt; 0.001), ypM1 ( p  = 0.004), and R1 resection ( p  = 0.052). The median overall survival (OS) duration was 6.6 years, and the 5-year OS rate was 54.1%. TRG 3 was associated with a shorter OS duration than were other TRG scores ( p  = 0.015), while the OS did not differ significantly among the TRG 0–2 groups ( p  = 0.803). On multivariable analysis, TRG was not associated with OS after adjustment for ypN status. Conclusion In gastric cancer patients who underwent preoperative therapy, TRG 3 was associated with advanced ypStage and R1 resection. Patients with TRG 3 had a shorter OS duration because of associated advanced ypStage, particularly ypN+ status.</description><identifier>ISSN: 1091-255X</identifier><identifier>EISSN: 1873-4626</identifier><identifier>DOI: 10.1007/s11605-020-04688-2</identifier><identifier>PMID: 32542556</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adenocarcinoma - pathology ; Adenocarcinoma - therapy ; Cancer therapies ; Chemotherapy ; Ethnicity ; Gastric cancer ; Gastroenterology ; Gastrointestinal surgery ; Humans ; Lymphatic system ; Medicine ; Medicine &amp; Public Health ; Metastasis ; Neoadjuvant Therapy ; Neoplasm Staging ; Oncology ; Original Article ; Pathology ; Prognosis ; Radiation ; Retrospective Studies ; Stomach Neoplasms - pathology ; Stomach Neoplasms - therapy ; Surgery ; Tumors</subject><ispartof>Journal of gastrointestinal surgery, 2021-06, Vol.25 (6), p.1380-1387</ispartof><rights>The Society for Surgery of the Alimentary Tract 2020</rights><rights>The Society for Surgery of the Alimentary Tract 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-8ab42fa745d91c70506a9a597aeb2d755a810e1aa061b838f90fdc983b5ddea93</citedby><cites>FETCH-LOGICAL-c375t-8ab42fa745d91c70506a9a597aeb2d755a810e1aa061b838f90fdc983b5ddea93</cites><orcidid>0000-0002-9825-9234</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32542556$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ikoma, Naruhiko</creatorcontrib><creatorcontrib>Estrella, Jeannelyn S.</creatorcontrib><creatorcontrib>Blum Murphy, Mariela</creatorcontrib><creatorcontrib>Das, Prajnan</creatorcontrib><creatorcontrib>Minsky, Bruce D.</creatorcontrib><creatorcontrib>Mansfield, Paul</creatorcontrib><creatorcontrib>Ajani, Jaffer A.</creatorcontrib><creatorcontrib>Badgwell, Brian D.</creatorcontrib><title>Tumor Regression Grade in Gastric Cancer After Preoperative Therapy</title><title>Journal of gastrointestinal surgery</title><addtitle>J Gastrointest Surg</addtitle><addtitle>J Gastrointest Surg</addtitle><description>Background The Cancer Staging Manual , 8th edition, now includes post-neoadjuvant therapy (ypTNM) staging for gastric cancer patients. Our purpose was to determine whether the tumor regression grade (TRG) of the primary tumor is useful for predicting the survival of these patients. Methods We performed a retrospective review of an institutional database and identified patients with clinically non-metastatic gastric adenocarcinoma who underwent preoperative chemotherapy or chemoradiation therapy before gastrectomy. Pathology reports were reviewed, and TRG was classified as follows: 0 (complete response), 1 (viable tumor cells ≤ 1–2%), 2 (viable cells ≤ 50%), or 3 (viable cells &gt; 50%). Results Of the 356 patients identified, including 80 (23%) with a gastroesophageal junction tumor, 268 (75%) had undergone preoperative chemoradiation therapy. Fifty-six (16%) had TRG 0, 57 (16%) TRG 1, 128 (36%) TRG 2, and 115 (32%) TRG 3. No association between TRG and pretreatment factors was identified, except for signet-ring cell histologic type and tumor location. A higher TRG was associated with more advanced ypT and ypN categories (both p  &lt; 0.001), ypM1 ( p  = 0.004), and R1 resection ( p  = 0.052). The median overall survival (OS) duration was 6.6 years, and the 5-year OS rate was 54.1%. TRG 3 was associated with a shorter OS duration than were other TRG scores ( p  = 0.015), while the OS did not differ significantly among the TRG 0–2 groups ( p  = 0.803). On multivariable analysis, TRG was not associated with OS after adjustment for ypN status. Conclusion In gastric cancer patients who underwent preoperative therapy, TRG 3 was associated with advanced ypStage and R1 resection. 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Our purpose was to determine whether the tumor regression grade (TRG) of the primary tumor is useful for predicting the survival of these patients. Methods We performed a retrospective review of an institutional database and identified patients with clinically non-metastatic gastric adenocarcinoma who underwent preoperative chemotherapy or chemoradiation therapy before gastrectomy. Pathology reports were reviewed, and TRG was classified as follows: 0 (complete response), 1 (viable tumor cells ≤ 1–2%), 2 (viable cells ≤ 50%), or 3 (viable cells &gt; 50%). Results Of the 356 patients identified, including 80 (23%) with a gastroesophageal junction tumor, 268 (75%) had undergone preoperative chemoradiation therapy. Fifty-six (16%) had TRG 0, 57 (16%) TRG 1, 128 (36%) TRG 2, and 115 (32%) TRG 3. No association between TRG and pretreatment factors was identified, except for signet-ring cell histologic type and tumor location. A higher TRG was associated with more advanced ypT and ypN categories (both p  &lt; 0.001), ypM1 ( p  = 0.004), and R1 resection ( p  = 0.052). The median overall survival (OS) duration was 6.6 years, and the 5-year OS rate was 54.1%. TRG 3 was associated with a shorter OS duration than were other TRG scores ( p  = 0.015), while the OS did not differ significantly among the TRG 0–2 groups ( p  = 0.803). On multivariable analysis, TRG was not associated with OS after adjustment for ypN status. Conclusion In gastric cancer patients who underwent preoperative therapy, TRG 3 was associated with advanced ypStage and R1 resection. Patients with TRG 3 had a shorter OS duration because of associated advanced ypStage, particularly ypN+ status.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>32542556</pmid><doi>10.1007/s11605-020-04688-2</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-9825-9234</orcidid></addata></record>
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subjects Adenocarcinoma - pathology
Adenocarcinoma - therapy
Cancer therapies
Chemotherapy
Ethnicity
Gastric cancer
Gastroenterology
Gastrointestinal surgery
Humans
Lymphatic system
Medicine
Medicine & Public Health
Metastasis
Neoadjuvant Therapy
Neoplasm Staging
Oncology
Original Article
Pathology
Prognosis
Radiation
Retrospective Studies
Stomach Neoplasms - pathology
Stomach Neoplasms - therapy
Surgery
Tumors
title Tumor Regression Grade in Gastric Cancer After Preoperative Therapy
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