Adaptive Neoadjuvant Chemotherapy Guided by (18)F-FDG PET in Resectable Non-Small Cell Lung Cancers: The NEOSCAN Trial
Although perioperative chemotherapy improves survival in patients with resectable lung cancers, systemic recurrence remains common. Neoadjuvant chemotherapy permits response assessment and an opportunity to switch treatment regimens. Response measured by fludeoxyglucose ((18)F-FDG) positron emission...
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Veröffentlicht in: | Journal of thoracic oncology 2016-04, Vol.11 (4), p.537 |
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creator | Chaft, Jamie E Dunphy, Mark Naidoo, Jarushka Travis, William D Hellmann, Matthew Woo, Kaitlin Downey, Robert Rusch, Valerie Ginsberg, Michelle S Azzoli, Christopher G Kris, Mark G |
description | Although perioperative chemotherapy improves survival in patients with resectable lung cancers, systemic recurrence remains common. Neoadjuvant chemotherapy permits response assessment and an opportunity to switch treatment regimens. Response measured by fludeoxyglucose ((18)F-FDG) positron emission tomography (PET) correlates with clinical outcomes better than computed tomography (CT) does. This trial assessed PET-measured response rate to alternative chemotherapy in patients with a suboptimal PET response after two cycles of neoadjuvant chemotherapy.
This phase II study enrolled patients with resectable stage IB-IIIA lung cancers (primary tumor ≥ 2 cm and peak standard uptake value [SUVpeak] ≥ 4.5). Patients had a pretreatment (18)F-FDG PET/CT scan before two cycles of cisplatin (or carboplatin) plus gemcitabine (squamous cell carcinoma) or pemetrexed (adenocarcinoma) and then a repeat PET/CT scan. If SUVpeak in the primary tumor decreased by at least 35%, patients continued the initial chemotherapy. Individuals with less than a 35% PET response were switched to vinorelbine plus docetaxel. Postoperative radiotherapy was recommended to all patients with positive N2 nodes. A Simon's optimal two-stage design was used to evaluate the primary end point of a PET Response in Solid Tumors-defined response rate to vinorelbine plus docetaxel in previously nonresponding patients.
Forty patients were enrolled. Fifteen patients (38% [95% confidence interval: 38-53]) had less than a 35% decrease in SUVpeak, and 13 received vinorelbine plus docetaxel. The study met its primary end point with 10 of 15 PET metabolic responses to alternate therapy (67%). Chemotherapy toxicities never precluded surgical exploration.
Utilizing (18)F-FDG PET/CT to assess response and change preoperative chemotherapy in nonresponding patients can improve radiographic measures of response. This adaptive approach can also be used to test new drugs, attempting to optimize perioperative chemotherapy to achieve better long-term outcomes. |
doi_str_mv | 10.1016/j.jtho.2015.12.104 |
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This phase II study enrolled patients with resectable stage IB-IIIA lung cancers (primary tumor ≥ 2 cm and peak standard uptake value [SUVpeak] ≥ 4.5). Patients had a pretreatment (18)F-FDG PET/CT scan before two cycles of cisplatin (or carboplatin) plus gemcitabine (squamous cell carcinoma) or pemetrexed (adenocarcinoma) and then a repeat PET/CT scan. If SUVpeak in the primary tumor decreased by at least 35%, patients continued the initial chemotherapy. Individuals with less than a 35% PET response were switched to vinorelbine plus docetaxel. Postoperative radiotherapy was recommended to all patients with positive N2 nodes. A Simon's optimal two-stage design was used to evaluate the primary end point of a PET Response in Solid Tumors-defined response rate to vinorelbine plus docetaxel in previously nonresponding patients.
Forty patients were enrolled. Fifteen patients (38% [95% confidence interval: 38-53]) had less than a 35% decrease in SUVpeak, and 13 received vinorelbine plus docetaxel. The study met its primary end point with 10 of 15 PET metabolic responses to alternate therapy (67%). Chemotherapy toxicities never precluded surgical exploration.
Utilizing (18)F-FDG PET/CT to assess response and change preoperative chemotherapy in nonresponding patients can improve radiographic measures of response. This adaptive approach can also be used to test new drugs, attempting to optimize perioperative chemotherapy to achieve better long-term outcomes.</description><identifier>EISSN: 1556-1380</identifier><identifier>DOI: 10.1016/j.jtho.2015.12.104</identifier><identifier>PMID: 26724474</identifier><language>eng</language><publisher>United States</publisher><subject>Adult ; Aged ; Carcinoma, Non-Small-Cell Lung - diagnostic imaging ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - pathology ; Female ; Fluorodeoxyglucose F18 - analysis ; Humans ; Lung Neoplasms - diagnostic imaging ; Lung Neoplasms - drug therapy ; Lung Neoplasms - pathology ; Male ; Middle Aged ; Neoadjuvant Therapy ; Neoplasm Staging ; Positron-Emission Tomography - methods</subject><ispartof>Journal of thoracic oncology, 2016-04, Vol.11 (4), p.537</ispartof><rights>Copyright © 2015 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26724474$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chaft, Jamie E</creatorcontrib><creatorcontrib>Dunphy, Mark</creatorcontrib><creatorcontrib>Naidoo, Jarushka</creatorcontrib><creatorcontrib>Travis, William D</creatorcontrib><creatorcontrib>Hellmann, Matthew</creatorcontrib><creatorcontrib>Woo, Kaitlin</creatorcontrib><creatorcontrib>Downey, Robert</creatorcontrib><creatorcontrib>Rusch, Valerie</creatorcontrib><creatorcontrib>Ginsberg, Michelle S</creatorcontrib><creatorcontrib>Azzoli, Christopher G</creatorcontrib><creatorcontrib>Kris, Mark G</creatorcontrib><title>Adaptive Neoadjuvant Chemotherapy Guided by (18)F-FDG PET in Resectable Non-Small Cell Lung Cancers: The NEOSCAN Trial</title><title>Journal of thoracic oncology</title><addtitle>J Thorac Oncol</addtitle><description>Although perioperative chemotherapy improves survival in patients with resectable lung cancers, systemic recurrence remains common. Neoadjuvant chemotherapy permits response assessment and an opportunity to switch treatment regimens. Response measured by fludeoxyglucose ((18)F-FDG) positron emission tomography (PET) correlates with clinical outcomes better than computed tomography (CT) does. This trial assessed PET-measured response rate to alternative chemotherapy in patients with a suboptimal PET response after two cycles of neoadjuvant chemotherapy.
This phase II study enrolled patients with resectable stage IB-IIIA lung cancers (primary tumor ≥ 2 cm and peak standard uptake value [SUVpeak] ≥ 4.5). Patients had a pretreatment (18)F-FDG PET/CT scan before two cycles of cisplatin (or carboplatin) plus gemcitabine (squamous cell carcinoma) or pemetrexed (adenocarcinoma) and then a repeat PET/CT scan. If SUVpeak in the primary tumor decreased by at least 35%, patients continued the initial chemotherapy. Individuals with less than a 35% PET response were switched to vinorelbine plus docetaxel. Postoperative radiotherapy was recommended to all patients with positive N2 nodes. A Simon's optimal two-stage design was used to evaluate the primary end point of a PET Response in Solid Tumors-defined response rate to vinorelbine plus docetaxel in previously nonresponding patients.
Forty patients were enrolled. Fifteen patients (38% [95% confidence interval: 38-53]) had less than a 35% decrease in SUVpeak, and 13 received vinorelbine plus docetaxel. The study met its primary end point with 10 of 15 PET metabolic responses to alternate therapy (67%). Chemotherapy toxicities never precluded surgical exploration.
Utilizing (18)F-FDG PET/CT to assess response and change preoperative chemotherapy in nonresponding patients can improve radiographic measures of response. This adaptive approach can also be used to test new drugs, attempting to optimize perioperative chemotherapy to achieve better long-term outcomes.</description><subject>Adult</subject><subject>Aged</subject><subject>Carcinoma, Non-Small-Cell Lung - diagnostic imaging</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Female</subject><subject>Fluorodeoxyglucose F18 - analysis</subject><subject>Humans</subject><subject>Lung Neoplasms - diagnostic imaging</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoadjuvant Therapy</subject><subject>Neoplasm Staging</subject><subject>Positron-Emission Tomography - methods</subject><issn>1556-1380</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kE1Lw0AYhBdBrFb_gAfZox4S993sV72V2FahtGLjuWyyb0xCvshHof_egHqZgeGZOQwh98B8YKCeC78YssbnDKQPfMrEBbkGKZUHgWEzctP3BWNCMmGuyIwrzYXQ4pqcls62Q35CusPGumI82XqgYYZVM2TY2fZMN2Pu0NH4TB_BPK299euGfqwimtf0E3tMBhuXU72pvUNly5KGOMl2rL9paOsEu_6FRtkErPaHcLmjUZfb8pZcprbs8e7P5-RrvYrCN2-737yHy63XAleDJ5VLBcZOBlqkKtCA2iykgEQ4TGMTc2RSoUktM5BImeoFAwsLEyjJnVY8mJOH3912jCt0x7bLK9udj_8HBD9i4loA</recordid><startdate>201604</startdate><enddate>201604</enddate><creator>Chaft, Jamie E</creator><creator>Dunphy, Mark</creator><creator>Naidoo, Jarushka</creator><creator>Travis, William D</creator><creator>Hellmann, Matthew</creator><creator>Woo, Kaitlin</creator><creator>Downey, Robert</creator><creator>Rusch, Valerie</creator><creator>Ginsberg, Michelle S</creator><creator>Azzoli, Christopher G</creator><creator>Kris, Mark G</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>201604</creationdate><title>Adaptive Neoadjuvant Chemotherapy Guided by (18)F-FDG PET in Resectable Non-Small Cell Lung Cancers: The NEOSCAN Trial</title><author>Chaft, Jamie E ; Dunphy, Mark ; Naidoo, Jarushka ; Travis, William D ; Hellmann, Matthew ; Woo, Kaitlin ; Downey, Robert ; Rusch, Valerie ; Ginsberg, Michelle S ; Azzoli, Christopher G ; Kris, Mark G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p126t-56df4ebd5374f6371e789541c4defb8b2e056e8fa081c55f7901a1983652d7623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Carcinoma, Non-Small-Cell Lung - diagnostic imaging</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Female</topic><topic>Fluorodeoxyglucose F18 - analysis</topic><topic>Humans</topic><topic>Lung Neoplasms - diagnostic imaging</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoadjuvant Therapy</topic><topic>Neoplasm Staging</topic><topic>Positron-Emission Tomography - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chaft, Jamie E</creatorcontrib><creatorcontrib>Dunphy, Mark</creatorcontrib><creatorcontrib>Naidoo, Jarushka</creatorcontrib><creatorcontrib>Travis, William D</creatorcontrib><creatorcontrib>Hellmann, Matthew</creatorcontrib><creatorcontrib>Woo, Kaitlin</creatorcontrib><creatorcontrib>Downey, Robert</creatorcontrib><creatorcontrib>Rusch, Valerie</creatorcontrib><creatorcontrib>Ginsberg, Michelle S</creatorcontrib><creatorcontrib>Azzoli, Christopher G</creatorcontrib><creatorcontrib>Kris, Mark G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Journal of thoracic oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chaft, Jamie E</au><au>Dunphy, Mark</au><au>Naidoo, Jarushka</au><au>Travis, William D</au><au>Hellmann, Matthew</au><au>Woo, Kaitlin</au><au>Downey, Robert</au><au>Rusch, Valerie</au><au>Ginsberg, Michelle S</au><au>Azzoli, Christopher G</au><au>Kris, Mark G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adaptive Neoadjuvant Chemotherapy Guided by (18)F-FDG PET in Resectable Non-Small Cell Lung Cancers: The NEOSCAN Trial</atitle><jtitle>Journal of thoracic oncology</jtitle><addtitle>J Thorac Oncol</addtitle><date>2016-04</date><risdate>2016</risdate><volume>11</volume><issue>4</issue><spage>537</spage><pages>537-</pages><eissn>1556-1380</eissn><abstract>Although perioperative chemotherapy improves survival in patients with resectable lung cancers, systemic recurrence remains common. Neoadjuvant chemotherapy permits response assessment and an opportunity to switch treatment regimens. Response measured by fludeoxyglucose ((18)F-FDG) positron emission tomography (PET) correlates with clinical outcomes better than computed tomography (CT) does. This trial assessed PET-measured response rate to alternative chemotherapy in patients with a suboptimal PET response after two cycles of neoadjuvant chemotherapy.
This phase II study enrolled patients with resectable stage IB-IIIA lung cancers (primary tumor ≥ 2 cm and peak standard uptake value [SUVpeak] ≥ 4.5). Patients had a pretreatment (18)F-FDG PET/CT scan before two cycles of cisplatin (or carboplatin) plus gemcitabine (squamous cell carcinoma) or pemetrexed (adenocarcinoma) and then a repeat PET/CT scan. If SUVpeak in the primary tumor decreased by at least 35%, patients continued the initial chemotherapy. Individuals with less than a 35% PET response were switched to vinorelbine plus docetaxel. Postoperative radiotherapy was recommended to all patients with positive N2 nodes. A Simon's optimal two-stage design was used to evaluate the primary end point of a PET Response in Solid Tumors-defined response rate to vinorelbine plus docetaxel in previously nonresponding patients.
Forty patients were enrolled. Fifteen patients (38% [95% confidence interval: 38-53]) had less than a 35% decrease in SUVpeak, and 13 received vinorelbine plus docetaxel. The study met its primary end point with 10 of 15 PET metabolic responses to alternate therapy (67%). Chemotherapy toxicities never precluded surgical exploration.
Utilizing (18)F-FDG PET/CT to assess response and change preoperative chemotherapy in nonresponding patients can improve radiographic measures of response. This adaptive approach can also be used to test new drugs, attempting to optimize perioperative chemotherapy to achieve better long-term outcomes.</abstract><cop>United States</cop><pmid>26724474</pmid><doi>10.1016/j.jtho.2015.12.104</doi></addata></record> |
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subjects | Adult Aged Carcinoma, Non-Small-Cell Lung - diagnostic imaging Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - pathology Female Fluorodeoxyglucose F18 - analysis Humans Lung Neoplasms - diagnostic imaging Lung Neoplasms - drug therapy Lung Neoplasms - pathology Male Middle Aged Neoadjuvant Therapy Neoplasm Staging Positron-Emission Tomography - methods |
title | Adaptive Neoadjuvant Chemotherapy Guided by (18)F-FDG PET in Resectable Non-Small Cell Lung Cancers: The NEOSCAN Trial |
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