Preoperative chemoradiation in potentially resectable pancreatic adenocarcinoma: feasibility, treatment effect evaluation and prognostic factors, analysis of the SFRO-FFCD 9704 trial and literature review
We explored the feasibility and the histologic assessment of treatment effect of preoperative chemoradiation in patients presenting with resectable pancreatic adenocarcinoma. Treatment consisted of concurrent radiotherapy (50 Gy within 5 weeks) and chemotherapy with 5-fluorouracil (300 mg/m2/day, 5...
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Veröffentlicht in: | Annals of oncology 2009-08, Vol.20 (8), p.1387-1396 |
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creator | Le Scodan, R. Mornex, F. Girard, N. Mercier, C. Valette, P.-J. Ychou, M. Bibeau, F. Roy, P. Scoazec, J.-Y. Partensky, C. |
description | We explored the feasibility and the histologic assessment of treatment effect of preoperative chemoradiation in patients presenting with resectable pancreatic adenocarcinoma.
Treatment consisted of concurrent radiotherapy (50 Gy within 5 weeks) and chemotherapy with 5-fluorouracil (300 mg/m2/day, 5 days/week, weeks 1–5) and cisplatin (20 mg/m2/day, days 1–5 and 29–33), followed by surgical resection of the pancreatic tumor in patients without progression.
In all, 41 patients were enrolled; 38 (93%) received ≥47 Gy; 30 patients (73%) received ≥75% of the prescribed doses of chemotherapy. Among 40 assessable patients, 27 (67.5%; 95% confidence interval 50.9% to 81.4%) were successfully treated (entire dose of radiation, ≥75% of the chemotherapy dose, no grade 4 non-hematologic toxicity). In all, 26 patients (63%) underwent surgical resection with curative intent and 21 (80.7%) had R0 resection. A total of 13 of 26 specimens (50%) presented a major pathologic response (≥80% of severely degenerative cancer cells), with one complete pathologic response. Operative mortality was 2.8%. The local recurrence and 2-year survival rates were 4% and 32%, respectively, for the 26 operated patients.
This proposed preoperative scheme is feasible, does not prevent successful surgery, and provides antitumoral effect associated with major histopathological response in 50% of patients and a high R0 resection rate. |
doi_str_mv | 10.1093/annonc/mdp015 |
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Treatment consisted of concurrent radiotherapy (50 Gy within 5 weeks) and chemotherapy with 5-fluorouracil (300 mg/m2/day, 5 days/week, weeks 1–5) and cisplatin (20 mg/m2/day, days 1–5 and 29–33), followed by surgical resection of the pancreatic tumor in patients without progression.
In all, 41 patients were enrolled; 38 (93%) received ≥47 Gy; 30 patients (73%) received ≥75% of the prescribed doses of chemotherapy. Among 40 assessable patients, 27 (67.5%; 95% confidence interval 50.9% to 81.4%) were successfully treated (entire dose of radiation, ≥75% of the chemotherapy dose, no grade 4 non-hematologic toxicity). In all, 26 patients (63%) underwent surgical resection with curative intent and 21 (80.7%) had R0 resection. A total of 13 of 26 specimens (50%) presented a major pathologic response (≥80% of severely degenerative cancer cells), with one complete pathologic response. Operative mortality was 2.8%. The local recurrence and 2-year survival rates were 4% and 32%, respectively, for the 26 operated patients.
This proposed preoperative scheme is feasible, does not prevent successful surgery, and provides antitumoral effect associated with major histopathological response in 50% of patients and a high R0 resection rate.</description><identifier>ISSN: 0923-7534</identifier><identifier>EISSN: 1569-8041</identifier><identifier>DOI: 10.1093/annonc/mdp015</identifier><identifier>PMID: 19502533</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Adenocarcinoma - therapy ; Adult ; Aged ; Antineoplastic agents ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; chemoradiation ; Cisplatin - administration & dosage ; Feasibility Studies ; Female ; Fluorouracil - administration & dosage ; Gastroenterology. Liver. Pancreas. Abdomen ; histopathological response ; Humans ; Life Sciences ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Middle Aged ; Neoadjuvant Therapy ; neoadjuvant treatment ; Neoplasm Recurrence, Local - pathology ; pancreatic adenocarcinoma ; Pancreatic Neoplasms - drug therapy ; Pancreatic Neoplasms - radiotherapy ; Pancreatic Neoplasms - surgery ; Pancreatic Neoplasms - therapy ; Pharmacology. Drug treatments ; Survival Rate ; Tumors</subject><ispartof>Annals of oncology, 2009-08, Vol.20 (8), p.1387-1396</ispartof><rights>2009 European Society for Medical Oncology</rights><rights>The Author 2009. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org 2009</rights><rights>2009 INIST-CNRS</rights><rights>The Author 2009. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c606t-ff6f9054d9c3c061b7a1c8c0ce6e0c5ac5be292bc9a3d72abea3d18c429dcee13</citedby><cites>FETCH-LOGICAL-c606t-ff6f9054d9c3c061b7a1c8c0ce6e0c5ac5be292bc9a3d72abea3d18c429dcee13</cites><orcidid>0000-0003-3837-3198</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21798204$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19502533$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-04153141$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Le Scodan, R.</creatorcontrib><creatorcontrib>Mornex, F.</creatorcontrib><creatorcontrib>Girard, N.</creatorcontrib><creatorcontrib>Mercier, C.</creatorcontrib><creatorcontrib>Valette, P.-J.</creatorcontrib><creatorcontrib>Ychou, M.</creatorcontrib><creatorcontrib>Bibeau, F.</creatorcontrib><creatorcontrib>Roy, P.</creatorcontrib><creatorcontrib>Scoazec, J.-Y.</creatorcontrib><creatorcontrib>Partensky, C.</creatorcontrib><title>Preoperative chemoradiation in potentially resectable pancreatic adenocarcinoma: feasibility, treatment effect evaluation and prognostic factors, analysis of the SFRO-FFCD 9704 trial and literature review</title><title>Annals of oncology</title><addtitle>Ann Oncol</addtitle><description>We explored the feasibility and the histologic assessment of treatment effect of preoperative chemoradiation in patients presenting with resectable pancreatic adenocarcinoma.
Treatment consisted of concurrent radiotherapy (50 Gy within 5 weeks) and chemotherapy with 5-fluorouracil (300 mg/m2/day, 5 days/week, weeks 1–5) and cisplatin (20 mg/m2/day, days 1–5 and 29–33), followed by surgical resection of the pancreatic tumor in patients without progression.
In all, 41 patients were enrolled; 38 (93%) received ≥47 Gy; 30 patients (73%) received ≥75% of the prescribed doses of chemotherapy. Among 40 assessable patients, 27 (67.5%; 95% confidence interval 50.9% to 81.4%) were successfully treated (entire dose of radiation, ≥75% of the chemotherapy dose, no grade 4 non-hematologic toxicity). In all, 26 patients (63%) underwent surgical resection with curative intent and 21 (80.7%) had R0 resection. A total of 13 of 26 specimens (50%) presented a major pathologic response (≥80% of severely degenerative cancer cells), with one complete pathologic response. Operative mortality was 2.8%. The local recurrence and 2-year survival rates were 4% and 32%, respectively, for the 26 operated patients.
This proposed preoperative scheme is feasible, does not prevent successful surgery, and provides antitumoral effect associated with major histopathological response in 50% of patients and a high R0 resection rate.</description><subject>Adenocarcinoma - therapy</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>chemoradiation</subject><subject>Cisplatin - administration & dosage</subject><subject>Feasibility Studies</subject><subject>Female</subject><subject>Fluorouracil - administration & dosage</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>histopathological response</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoadjuvant Therapy</subject><subject>neoadjuvant treatment</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>pancreatic adenocarcinoma</subject><subject>Pancreatic Neoplasms - drug therapy</subject><subject>Pancreatic Neoplasms - radiotherapy</subject><subject>Pancreatic Neoplasms - surgery</subject><subject>Pancreatic Neoplasms - therapy</subject><subject>Pharmacology. Drug treatments</subject><subject>Survival Rate</subject><subject>Tumors</subject><issn>0923-7534</issn><issn>1569-8041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk2LFDEQhhtR3HX16FWCIChsu0l_Tva2jI4jDKz4ActeQnV1tZO1O2mT7tH5j_4o0_YwnsRTSPHUW2_lTRQ9Ffy14DK9AGOswYuu7rnI70WnIi9kvOCZuB-dcpmkcZmn2Un0yPs7znkhE_kwOhEy50mepqfRrw-ObE8OBr0jhlvqrINah6s1TBvW24HMoKFt98yRJxygaon1YNBRoJBBTcYiONTGdnDJGgKvK93qYX_OhgnqggKjpgnNjHbQjrM6mJr1zn411k86DeBgnT8PdWj3XntmGzZsiX1afbyOV6vlGyZLngXJ4OZPcxgxGR8dBWs7TT8eRw8aaD09OZxn0ZfV28_Ldby5fvd-ebWJseDFEDdN0UieZ7XEFHkhqhIELpAjFcQxB8wrSmRSoYS0LhOoKJxigVkiayQS6Vn0atbdQqt6pztwe2VBq_XVRk218Px5KjKxm9jnMxtW_T6SH9SdHV1Y0Sshi6LkpUgDFM8QOuu9o-aoKriaYlZzzGqOOfDPDqJj1VH9lz7kGoAXBwA8Qtu4kJf2Ry4RpVwkPAvcy5mzY__fmQeP2g_08wiD-6aKMi1ztb65VXyz5MXt5kZNFsqZp5BESMcpj5oMUq1d-Amqtvofk34D4lrn-Q</recordid><startdate>20090801</startdate><enddate>20090801</enddate><creator>Le Scodan, R.</creator><creator>Mornex, F.</creator><creator>Girard, N.</creator><creator>Mercier, C.</creator><creator>Valette, P.-J.</creator><creator>Ychou, M.</creator><creator>Bibeau, F.</creator><creator>Roy, P.</creator><creator>Scoazec, J.-Y.</creator><creator>Partensky, C.</creator><general>Elsevier Ltd</general><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>H94</scope><scope>K9.</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-3837-3198</orcidid></search><sort><creationdate>20090801</creationdate><title>Preoperative chemoradiation in potentially resectable pancreatic adenocarcinoma: feasibility, treatment effect evaluation and prognostic factors, analysis of the SFRO-FFCD 9704 trial and literature review</title><author>Le Scodan, R. ; Mornex, F. ; Girard, N. ; Mercier, C. ; Valette, P.-J. ; Ychou, M. ; Bibeau, F. ; Roy, P. ; Scoazec, J.-Y. ; Partensky, C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c606t-ff6f9054d9c3c061b7a1c8c0ce6e0c5ac5be292bc9a3d72abea3d18c429dcee13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adenocarcinoma - therapy</topic><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic agents</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>chemoradiation</topic><topic>Cisplatin - administration & dosage</topic><topic>Feasibility Studies</topic><topic>Female</topic><topic>Fluorouracil - administration & dosage</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>histopathological response</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoadjuvant Therapy</topic><topic>neoadjuvant treatment</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>pancreatic adenocarcinoma</topic><topic>Pancreatic Neoplasms - drug therapy</topic><topic>Pancreatic Neoplasms - radiotherapy</topic><topic>Pancreatic Neoplasms - surgery</topic><topic>Pancreatic Neoplasms - therapy</topic><topic>Pharmacology. 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Treatment consisted of concurrent radiotherapy (50 Gy within 5 weeks) and chemotherapy with 5-fluorouracil (300 mg/m2/day, 5 days/week, weeks 1–5) and cisplatin (20 mg/m2/day, days 1–5 and 29–33), followed by surgical resection of the pancreatic tumor in patients without progression.
In all, 41 patients were enrolled; 38 (93%) received ≥47 Gy; 30 patients (73%) received ≥75% of the prescribed doses of chemotherapy. Among 40 assessable patients, 27 (67.5%; 95% confidence interval 50.9% to 81.4%) were successfully treated (entire dose of radiation, ≥75% of the chemotherapy dose, no grade 4 non-hematologic toxicity). In all, 26 patients (63%) underwent surgical resection with curative intent and 21 (80.7%) had R0 resection. A total of 13 of 26 specimens (50%) presented a major pathologic response (≥80% of severely degenerative cancer cells), with one complete pathologic response. Operative mortality was 2.8%. The local recurrence and 2-year survival rates were 4% and 32%, respectively, for the 26 operated patients.
This proposed preoperative scheme is feasible, does not prevent successful surgery, and provides antitumoral effect associated with major histopathological response in 50% of patients and a high R0 resection rate.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>19502533</pmid><doi>10.1093/annonc/mdp015</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-3837-3198</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma - therapy Adult Aged Antineoplastic agents Antineoplastic Combined Chemotherapy Protocols - adverse effects Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biological and medical sciences chemoradiation Cisplatin - administration & dosage Feasibility Studies Female Fluorouracil - administration & dosage Gastroenterology. Liver. Pancreas. Abdomen histopathological response Humans Life Sciences Liver. Biliary tract. Portal circulation. Exocrine pancreas Male Medical sciences Middle Aged Neoadjuvant Therapy neoadjuvant treatment Neoplasm Recurrence, Local - pathology pancreatic adenocarcinoma Pancreatic Neoplasms - drug therapy Pancreatic Neoplasms - radiotherapy Pancreatic Neoplasms - surgery Pancreatic Neoplasms - therapy Pharmacology. Drug treatments Survival Rate Tumors |
title | Preoperative chemoradiation in potentially resectable pancreatic adenocarcinoma: feasibility, treatment effect evaluation and prognostic factors, analysis of the SFRO-FFCD 9704 trial and literature review |
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