Chemotherapy in advanced pancreatic adenosquamous carcinoma: A retrospective multicenter AGEO study

Pancreatic adenosquamous carcinoma (PASC) account for

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Veröffentlicht in:International journal of cancer 2023-05, Vol.152 (9), p.1894-1902
Hauptverfasser: Auvray Kuentz, Marie, Hautefeuille, Vincent, Mestier, Louis, Coutzac, Clélia, Lecomte, Thierry, Nardon, Victor, Artru, Pascal, Turpin, Anthony, Drouillard, Antoine, Malka, David, Tran‐Minh, My‐Linh, Trouilloud, Isabelle, Lièvre, Astrid, Williet, Nicolas, Pernot, Simon, Touchefeu, Yann, Taieb, Julien, Hammel, Pascal, Zaanan, Aziz
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container_end_page 1902
container_issue 9
container_start_page 1894
container_title International journal of cancer
container_volume 152
creator Auvray Kuentz, Marie
Hautefeuille, Vincent
Mestier, Louis
Coutzac, Clélia
Lecomte, Thierry
Nardon, Victor
Artru, Pascal
Turpin, Anthony
Drouillard, Antoine
Malka, David
Tran‐Minh, My‐Linh
Trouilloud, Isabelle
Lièvre, Astrid
Williet, Nicolas
Pernot, Simon
Touchefeu, Yann
Taieb, Julien
Hammel, Pascal
Zaanan, Aziz
description Pancreatic adenosquamous carcinoma (PASC) account for
doi_str_mv 10.1002/ijc.34414
format Article
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The efficacy of modern chemotherapy regimens in patients with advanced PASC is unknown. Patients with advanced PASC from 2008 to 2021 were consecutively included in this retrospective multicenter study. Overall survival (OS) and progression‐free survival (PFS) were evaluated by Kaplan‐Meier method. Ninety‐four PASC from 16 French centers were included (median age, 67.3 years; males, 56.4%; metastatic disease, 85.1%). The first‐line treatment was chemotherapy for 79 patients (84.0%) (37 FOLFIRINOX (FX), 7 Gemcitabine‐nab paclitaxel (GN) and 35 for all other regimen) or best supportive care (BSC) alone for 15 patients (16.0%). No significant difference was observed between FX and GN in terms of PFS (P = .67) or OS (P = .5). Modern regimens pooled together (FX and GN) as compared to all others chemotherapy regimens showed an improvement of overall response rate (39.5% and 9.7%, P = .002), PFS (median, 7.8 vs 4.7 months, P = .02) and OS (median, 12.7 vs 9.2 months, P = .35). This large study evaluating first‐line treatment regimens in advanced PASC suggests that modern regimens as FX or GN may be preferable to all other chemotherapy regimens. These results deserve confirmation in prospective studies. What's new? Pancreatic adenosquamous carcinoma (PASC) is a rare pancreatic cancer subtype of uncertain histological origin. Owing to its scarcity, little is known about the efficacy of chemotherapy for PASC, particularly for advanced disease. Here, investigation of modern chemotherapy regimens in a large multicenter cohort consisting of patients with advanced PASC suggests that more recent regimens based on 5‐fluorouracil, particularly FOLFIRINOX (FX), as well as regimens based on gemcitabine, namely gemcitabine‐nab paclitaxel (GN), are more effective for advanced PASC compared to more conventional regimens. Notably, overall response rates and survival rates were improved in advanced PASC patients on FX and GN regimens.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.34414</identifier><identifier>PMID: 36562310</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>Adenocarcinoma ; Adenosquamous ; adenosquamous carcinoma ; advanced disease ; Aged ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Cancer ; Carcinoma, Adenosquamous - chemically induced ; Carcinoma, Adenosquamous - drug therapy ; Chemotherapy ; Deoxycytidine ; Fluorouracil - therapeutic use ; Gemcitabine ; Humans ; Leucovorin - therapeutic use ; Life Sciences ; Male ; Malignancy ; Medical research ; Metastases ; Paclitaxel ; Paclitaxel - therapeutic use ; Pancreas ; Pancreatic cancer ; Pancreatic carcinoma ; Pancreatic Neoplasms ; Pancreatic Neoplasms - pathology ; Prospective Studies ; Retrospective Studies ; Squamous cell carcinoma ; Survival</subject><ispartof>International journal of cancer, 2023-05, Vol.152 (9), p.1894-1902</ispartof><rights>2022 UICC.</rights><rights>2023 UICC</rights><rights>Attribution - NonCommercial</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3824-b223cc7524d5a1a1863c0ff1359c4f997bea5c316096423aea45d8ed3d6c10da3</cites><orcidid>0000-0002-1258-861X ; 0000-0002-7296-5464 ; 0000-0001-8372-5653 ; 0000-0001-5093-0212 ; 0000-0002-7948-1331</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fijc.34414$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.34414$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,778,782,883,1414,27907,27908,45557,45558</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36562310$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03969427$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Auvray Kuentz, Marie</creatorcontrib><creatorcontrib>Hautefeuille, Vincent</creatorcontrib><creatorcontrib>Mestier, Louis</creatorcontrib><creatorcontrib>Coutzac, Clélia</creatorcontrib><creatorcontrib>Lecomte, Thierry</creatorcontrib><creatorcontrib>Nardon, Victor</creatorcontrib><creatorcontrib>Artru, Pascal</creatorcontrib><creatorcontrib>Turpin, Anthony</creatorcontrib><creatorcontrib>Drouillard, Antoine</creatorcontrib><creatorcontrib>Malka, David</creatorcontrib><creatorcontrib>Tran‐Minh, My‐Linh</creatorcontrib><creatorcontrib>Trouilloud, Isabelle</creatorcontrib><creatorcontrib>Lièvre, Astrid</creatorcontrib><creatorcontrib>Williet, Nicolas</creatorcontrib><creatorcontrib>Pernot, Simon</creatorcontrib><creatorcontrib>Touchefeu, Yann</creatorcontrib><creatorcontrib>Taieb, Julien</creatorcontrib><creatorcontrib>Hammel, Pascal</creatorcontrib><creatorcontrib>Zaanan, Aziz</creatorcontrib><title>Chemotherapy in advanced pancreatic adenosquamous carcinoma: A retrospective multicenter AGEO study</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>Pancreatic adenosquamous carcinoma (PASC) account for &lt;5% of pancreatic malignancies. The efficacy of modern chemotherapy regimens in patients with advanced PASC is unknown. Patients with advanced PASC from 2008 to 2021 were consecutively included in this retrospective multicenter study. Overall survival (OS) and progression‐free survival (PFS) were evaluated by Kaplan‐Meier method. Ninety‐four PASC from 16 French centers were included (median age, 67.3 years; males, 56.4%; metastatic disease, 85.1%). The first‐line treatment was chemotherapy for 79 patients (84.0%) (37 FOLFIRINOX (FX), 7 Gemcitabine‐nab paclitaxel (GN) and 35 for all other regimen) or best supportive care (BSC) alone for 15 patients (16.0%). No significant difference was observed between FX and GN in terms of PFS (P = .67) or OS (P = .5). Modern regimens pooled together (FX and GN) as compared to all others chemotherapy regimens showed an improvement of overall response rate (39.5% and 9.7%, P = .002), PFS (median, 7.8 vs 4.7 months, P = .02) and OS (median, 12.7 vs 9.2 months, P = .35). This large study evaluating first‐line treatment regimens in advanced PASC suggests that modern regimens as FX or GN may be preferable to all other chemotherapy regimens. These results deserve confirmation in prospective studies. What's new? Pancreatic adenosquamous carcinoma (PASC) is a rare pancreatic cancer subtype of uncertain histological origin. Owing to its scarcity, little is known about the efficacy of chemotherapy for PASC, particularly for advanced disease. Here, investigation of modern chemotherapy regimens in a large multicenter cohort consisting of patients with advanced PASC suggests that more recent regimens based on 5‐fluorouracil, particularly FOLFIRINOX (FX), as well as regimens based on gemcitabine, namely gemcitabine‐nab paclitaxel (GN), are more effective for advanced PASC compared to more conventional regimens. Notably, overall response rates and survival rates were improved in advanced PASC patients on FX and GN regimens.</description><subject>Adenocarcinoma</subject><subject>Adenosquamous</subject><subject>adenosquamous carcinoma</subject><subject>advanced disease</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Cancer</subject><subject>Carcinoma, Adenosquamous - chemically induced</subject><subject>Carcinoma, Adenosquamous - drug therapy</subject><subject>Chemotherapy</subject><subject>Deoxycytidine</subject><subject>Fluorouracil - therapeutic use</subject><subject>Gemcitabine</subject><subject>Humans</subject><subject>Leucovorin - therapeutic use</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Malignancy</subject><subject>Medical research</subject><subject>Metastases</subject><subject>Paclitaxel</subject><subject>Paclitaxel - therapeutic use</subject><subject>Pancreas</subject><subject>Pancreatic cancer</subject><subject>Pancreatic carcinoma</subject><subject>Pancreatic Neoplasms</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Prospective Studies</subject><subject>Retrospective Studies</subject><subject>Squamous cell carcinoma</subject><subject>Survival</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUlrHDEQhUVIiCdODvkDQZCLc2hbpaW7ldsweGXAl-QsNFI1o6E3S90T5t9HzniBgE8FVR-v6tUj5Cuwc2CMX4SdOxdSgnxHFsB0VTAO6j1Z5BkrKhDlCfmU0o4xAMXkR3IiSlVyAWxB3GqL3TBtMdrxQENPrd_b3qGnYy4R7RRc7mE_pIfZdsOcqLPRhX7o7E-6pBGnOKQR3RT2SLu5zTz2E0a6vL68p2ma_eEz-dDYNuGXp3pKfl9d_lrdFOv769vVcl04UXNZbDgXzlWKS68sWKhL4VjTgFDayUbraoNWOQEl06XkwqKVytfohS8dMG_FKflx1N3a1owxdDYezGCDuVmuzWOPCV1qyas9ZPbsyI5xeJgxTaYLyWHb2h6zScMrVQOw_K6Mfv8P3Q1z7LOTTNVc11qAfF3u8j9SxOblAmDmMSWTUzL_UsrstyfFedOhfyGfY8nAxRH4E1o8vK1kbu9WR8m_vZCanA</recordid><startdate>20230501</startdate><enddate>20230501</enddate><creator>Auvray Kuentz, Marie</creator><creator>Hautefeuille, Vincent</creator><creator>Mestier, Louis</creator><creator>Coutzac, Clélia</creator><creator>Lecomte, Thierry</creator><creator>Nardon, Victor</creator><creator>Artru, Pascal</creator><creator>Turpin, Anthony</creator><creator>Drouillard, Antoine</creator><creator>Malka, David</creator><creator>Tran‐Minh, My‐Linh</creator><creator>Trouilloud, Isabelle</creator><creator>Lièvre, Astrid</creator><creator>Williet, Nicolas</creator><creator>Pernot, Simon</creator><creator>Touchefeu, Yann</creator><creator>Taieb, Julien</creator><creator>Hammel, Pascal</creator><creator>Zaanan, Aziz</creator><general>John Wiley &amp; 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Malka, David ; Tran‐Minh, My‐Linh ; Trouilloud, Isabelle ; Lièvre, Astrid ; Williet, Nicolas ; Pernot, Simon ; Touchefeu, Yann ; Taieb, Julien ; Hammel, Pascal ; Zaanan, Aziz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3824-b223cc7524d5a1a1863c0ff1359c4f997bea5c316096423aea45d8ed3d6c10da3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adenocarcinoma</topic><topic>Adenosquamous</topic><topic>adenosquamous carcinoma</topic><topic>advanced disease</topic><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Cancer</topic><topic>Carcinoma, Adenosquamous - chemically induced</topic><topic>Carcinoma, Adenosquamous - drug therapy</topic><topic>Chemotherapy</topic><topic>Deoxycytidine</topic><topic>Fluorouracil - therapeutic use</topic><topic>Gemcitabine</topic><topic>Humans</topic><topic>Leucovorin - therapeutic use</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Malignancy</topic><topic>Medical research</topic><topic>Metastases</topic><topic>Paclitaxel</topic><topic>Paclitaxel - therapeutic use</topic><topic>Pancreas</topic><topic>Pancreatic cancer</topic><topic>Pancreatic carcinoma</topic><topic>Pancreatic Neoplasms</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>Prospective Studies</topic><topic>Retrospective Studies</topic><topic>Squamous cell carcinoma</topic><topic>Survival</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Auvray Kuentz, Marie</creatorcontrib><creatorcontrib>Hautefeuille, Vincent</creatorcontrib><creatorcontrib>Mestier, Louis</creatorcontrib><creatorcontrib>Coutzac, Clélia</creatorcontrib><creatorcontrib>Lecomte, Thierry</creatorcontrib><creatorcontrib>Nardon, Victor</creatorcontrib><creatorcontrib>Artru, Pascal</creatorcontrib><creatorcontrib>Turpin, Anthony</creatorcontrib><creatorcontrib>Drouillard, Antoine</creatorcontrib><creatorcontrib>Malka, David</creatorcontrib><creatorcontrib>Tran‐Minh, My‐Linh</creatorcontrib><creatorcontrib>Trouilloud, Isabelle</creatorcontrib><creatorcontrib>Lièvre, Astrid</creatorcontrib><creatorcontrib>Williet, Nicolas</creatorcontrib><creatorcontrib>Pernot, Simon</creatorcontrib><creatorcontrib>Touchefeu, Yann</creatorcontrib><creatorcontrib>Taieb, Julien</creatorcontrib><creatorcontrib>Hammel, Pascal</creatorcontrib><creatorcontrib>Zaanan, Aziz</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; 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The efficacy of modern chemotherapy regimens in patients with advanced PASC is unknown. Patients with advanced PASC from 2008 to 2021 were consecutively included in this retrospective multicenter study. Overall survival (OS) and progression‐free survival (PFS) were evaluated by Kaplan‐Meier method. Ninety‐four PASC from 16 French centers were included (median age, 67.3 years; males, 56.4%; metastatic disease, 85.1%). The first‐line treatment was chemotherapy for 79 patients (84.0%) (37 FOLFIRINOX (FX), 7 Gemcitabine‐nab paclitaxel (GN) and 35 for all other regimen) or best supportive care (BSC) alone for 15 patients (16.0%). No significant difference was observed between FX and GN in terms of PFS (P = .67) or OS (P = .5). Modern regimens pooled together (FX and GN) as compared to all others chemotherapy regimens showed an improvement of overall response rate (39.5% and 9.7%, P = .002), PFS (median, 7.8 vs 4.7 months, P = .02) and OS (median, 12.7 vs 9.2 months, P = .35). This large study evaluating first‐line treatment regimens in advanced PASC suggests that modern regimens as FX or GN may be preferable to all other chemotherapy regimens. These results deserve confirmation in prospective studies. What's new? Pancreatic adenosquamous carcinoma (PASC) is a rare pancreatic cancer subtype of uncertain histological origin. Owing to its scarcity, little is known about the efficacy of chemotherapy for PASC, particularly for advanced disease. Here, investigation of modern chemotherapy regimens in a large multicenter cohort consisting of patients with advanced PASC suggests that more recent regimens based on 5‐fluorouracil, particularly FOLFIRINOX (FX), as well as regimens based on gemcitabine, namely gemcitabine‐nab paclitaxel (GN), are more effective for advanced PASC compared to more conventional regimens. 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subjects Adenocarcinoma
Adenosquamous
adenosquamous carcinoma
advanced disease
Aged
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Cancer
Carcinoma, Adenosquamous - chemically induced
Carcinoma, Adenosquamous - drug therapy
Chemotherapy
Deoxycytidine
Fluorouracil - therapeutic use
Gemcitabine
Humans
Leucovorin - therapeutic use
Life Sciences
Male
Malignancy
Medical research
Metastases
Paclitaxel
Paclitaxel - therapeutic use
Pancreas
Pancreatic cancer
Pancreatic carcinoma
Pancreatic Neoplasms
Pancreatic Neoplasms - pathology
Prospective Studies
Retrospective Studies
Squamous cell carcinoma
Survival
title Chemotherapy in advanced pancreatic adenosquamous carcinoma: A retrospective multicenter AGEO study
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