Fatal pneumonitis associated with intensity-modulated radiation therapy for mesothelioma

Purpose: To describe the initial experience at Dana-Farber Cancer Institute/Brigham and Women’s Hospital with intensity-modulated radiation therapy (IMRT) as adjuvant therapy after extrapleural pneumonectomy (EPP) and adjuvant chemotherapy. Methods and Materials: The medical records of patients trea...

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Veröffentlicht in:International journal of radiation oncology, biology, physics biology, physics, 2006-07, Vol.65 (3), p.640-645
Hauptverfasser: Allen, Aaron M., Czerminska, Maria, Jänne, Pasi A., Sugarbaker, David J., Bueno, Raphael, Harris, Jay R., Court, Laurence, Baldini, Elizabeth H.
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container_end_page 645
container_issue 3
container_start_page 640
container_title International journal of radiation oncology, biology, physics
container_volume 65
creator Allen, Aaron M.
Czerminska, Maria
Jänne, Pasi A.
Sugarbaker, David J.
Bueno, Raphael
Harris, Jay R.
Court, Laurence
Baldini, Elizabeth H.
description Purpose: To describe the initial experience at Dana-Farber Cancer Institute/Brigham and Women’s Hospital with intensity-modulated radiation therapy (IMRT) as adjuvant therapy after extrapleural pneumonectomy (EPP) and adjuvant chemotherapy. Methods and Materials: The medical records of patients treated with IMRT after EPP and adjuvant chemotherapy were retrospectively reviewed. IMRT was given to a dose of 54 Gy to the clinical target volume in 1.8 Gy daily fractions. Treatment was delivered with a dynamic multileaf collimator using a sliding window technique. Eleven of 13 patients received heated intraoperative cisplatin chemotherapy (225 mg/m 2). Two patients received neoadjuvant intravenous cisplatin/pemetrexed, and 10 patients received adjuvant cisplatin/pemetrexed chemotherapy after EPP but before radiation therapy. All patients received at least 2 cycles of intravenous chemotherapy. The contralateral lung was limited to a V20 (volume of lung receiving 20 Gy or more) of 20% and a mean lung dose (MLD) of 15 Gy. All patients underwent fluorodeoxyglucose positron emission tomography (FDG-PET) for staging, and any FDG-avid areas in the hemithorax were given a simultaneous boost of radiotherapy to 60 Gy. Statistical comparisons were done using two-sided t test. Results: Thirteen patients were treated with IMRT from December 2004 to September 2005. Six patients developed fatal pneumonitis after treatment. The median time from completion of IMRT to the onset of radiation pneumonitis was 30 days (range 5–57 days). Thirty percent of patients (4 of 13) developed acute Grade 3 nausea and vomiting. One patient developed acute Grade 3 thrombocytopenia. The median V20, MLD, and V5 (volume of lung receiving 5 Gy or more) for the patients who developed pneumonitis was 17.6% (range, 15.3–22.3%), 15.2 Gy (range, 13.3–17 Gy), and 98.6% (range, 81–100%), respectively, as compared with 10.9% (range, 5.5–24.7%) ( p = 0.08), 12.9 Gy (range, 8.7–16.9 Gy) ( p = 0.07), and 90% (range, 66–98.3%) ( p = 0.20), respectively, for the patients who did not develop pneumonitis. Conclusions: Intensity-modulated RT treatment for mesothelioma after EPP and adjuvant chemotherapy resulted in a high rate of fatal pneumonitis when standard dose parameters were used. We therefore recommend caution in the utilization of this technique. Our data suggest that with IMRT, metrics such as V5 and MLD should be considered in addition to V20 to determine tolerance levels in future patients.
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Methods and Materials: The medical records of patients treated with IMRT after EPP and adjuvant chemotherapy were retrospectively reviewed. IMRT was given to a dose of 54 Gy to the clinical target volume in 1.8 Gy daily fractions. Treatment was delivered with a dynamic multileaf collimator using a sliding window technique. Eleven of 13 patients received heated intraoperative cisplatin chemotherapy (225 mg/m 2). Two patients received neoadjuvant intravenous cisplatin/pemetrexed, and 10 patients received adjuvant cisplatin/pemetrexed chemotherapy after EPP but before radiation therapy. All patients received at least 2 cycles of intravenous chemotherapy. The contralateral lung was limited to a V20 (volume of lung receiving 20 Gy or more) of 20% and a mean lung dose (MLD) of 15 Gy. All patients underwent fluorodeoxyglucose positron emission tomography (FDG-PET) for staging, and any FDG-avid areas in the hemithorax were given a simultaneous boost of radiotherapy to 60 Gy. Statistical comparisons were done using two-sided t test. Results: Thirteen patients were treated with IMRT from December 2004 to September 2005. Six patients developed fatal pneumonitis after treatment. The median time from completion of IMRT to the onset of radiation pneumonitis was 30 days (range 5–57 days). Thirty percent of patients (4 of 13) developed acute Grade 3 nausea and vomiting. One patient developed acute Grade 3 thrombocytopenia. The median V20, MLD, and V5 (volume of lung receiving 5 Gy or more) for the patients who developed pneumonitis was 17.6% (range, 15.3–22.3%), 15.2 Gy (range, 13.3–17 Gy), and 98.6% (range, 81–100%), respectively, as compared with 10.9% (range, 5.5–24.7%) ( p = 0.08), 12.9 Gy (range, 8.7–16.9 Gy) ( p = 0.07), and 90% (range, 66–98.3%) ( p = 0.20), respectively, for the patients who did not develop pneumonitis. Conclusions: Intensity-modulated RT treatment for mesothelioma after EPP and adjuvant chemotherapy resulted in a high rate of fatal pneumonitis when standard dose parameters were used. We therefore recommend caution in the utilization of this technique. Our data suggest that with IMRT, metrics such as V5 and MLD should be considered in addition to V20 to determine tolerance levels in future patients.</description><identifier>ISSN: 0360-3016</identifier><identifier>EISSN: 1879-355X</identifier><identifier>DOI: 10.1016/j.ijrobp.2006.03.012</identifier><identifier>PMID: 16751058</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; CARCINOMAS ; CHEMOTHERAPY ; Chemotherapy, Adjuvant ; Cisplatin - administration &amp; dosage ; COLLIMATORS ; Female ; FLUORODEOXYGLUCOSE ; Glutamates - administration &amp; dosage ; Guanine - administration &amp; dosage ; Guanine - analogs &amp; derivatives ; HOSPITALS ; Humans ; Intensity-modulated radiation therapy ; LUNGS ; Male ; Mean lung dose ; MEDICAL RECORDS ; Mesothelioma ; Mesothelioma - drug therapy ; Mesothelioma - radiotherapy ; Mesothelioma - surgery ; Middle Aged ; NAUSEA ; PATIENTS ; Pemetrexed ; Pneumonectomy ; PNEUMONITIS ; POSITRON COMPUTED TOMOGRAPHY ; RADIATION DOSES ; Radiation Pneumonitis - etiology ; Radiation Pneumonitis - mortality ; RADIOLOGY AND NUCLEAR MEDICINE ; RADIOTHERAPY ; Radiotherapy, Adjuvant ; Radiotherapy, Intensity-Modulated - adverse effects ; Radiotherapy, Intensity-Modulated - mortality ; Respiratory Insufficiency - mortality ; Retrospective Studies ; VOMITING</subject><ispartof>International journal of radiation oncology, biology, physics, 2006-07, Vol.65 (3), p.640-645</ispartof><rights>2006 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c434t-7e1bc8131d8b79053a05a821e7a2b4dc37a547a5b9467628196e87e5fa8f550b3</citedby><cites>FETCH-LOGICAL-c434t-7e1bc8131d8b79053a05a821e7a2b4dc37a547a5b9467628196e87e5fa8f550b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijrobp.2006.03.012$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16751058$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/20842890$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Allen, Aaron M.</creatorcontrib><creatorcontrib>Czerminska, Maria</creatorcontrib><creatorcontrib>Jänne, Pasi A.</creatorcontrib><creatorcontrib>Sugarbaker, David J.</creatorcontrib><creatorcontrib>Bueno, Raphael</creatorcontrib><creatorcontrib>Harris, Jay R.</creatorcontrib><creatorcontrib>Court, Laurence</creatorcontrib><creatorcontrib>Baldini, Elizabeth H.</creatorcontrib><title>Fatal pneumonitis associated with intensity-modulated radiation therapy for mesothelioma</title><title>International journal of radiation oncology, biology, physics</title><addtitle>Int J Radiat Oncol Biol Phys</addtitle><description>Purpose: To describe the initial experience at Dana-Farber Cancer Institute/Brigham and Women’s Hospital with intensity-modulated radiation therapy (IMRT) as adjuvant therapy after extrapleural pneumonectomy (EPP) and adjuvant chemotherapy. Methods and Materials: The medical records of patients treated with IMRT after EPP and adjuvant chemotherapy were retrospectively reviewed. IMRT was given to a dose of 54 Gy to the clinical target volume in 1.8 Gy daily fractions. Treatment was delivered with a dynamic multileaf collimator using a sliding window technique. Eleven of 13 patients received heated intraoperative cisplatin chemotherapy (225 mg/m 2). Two patients received neoadjuvant intravenous cisplatin/pemetrexed, and 10 patients received adjuvant cisplatin/pemetrexed chemotherapy after EPP but before radiation therapy. All patients received at least 2 cycles of intravenous chemotherapy. The contralateral lung was limited to a V20 (volume of lung receiving 20 Gy or more) of 20% and a mean lung dose (MLD) of 15 Gy. All patients underwent fluorodeoxyglucose positron emission tomography (FDG-PET) for staging, and any FDG-avid areas in the hemithorax were given a simultaneous boost of radiotherapy to 60 Gy. Statistical comparisons were done using two-sided t test. Results: Thirteen patients were treated with IMRT from December 2004 to September 2005. Six patients developed fatal pneumonitis after treatment. The median time from completion of IMRT to the onset of radiation pneumonitis was 30 days (range 5–57 days). Thirty percent of patients (4 of 13) developed acute Grade 3 nausea and vomiting. One patient developed acute Grade 3 thrombocytopenia. The median V20, MLD, and V5 (volume of lung receiving 5 Gy or more) for the patients who developed pneumonitis was 17.6% (range, 15.3–22.3%), 15.2 Gy (range, 13.3–17 Gy), and 98.6% (range, 81–100%), respectively, as compared with 10.9% (range, 5.5–24.7%) ( p = 0.08), 12.9 Gy (range, 8.7–16.9 Gy) ( p = 0.07), and 90% (range, 66–98.3%) ( p = 0.20), respectively, for the patients who did not develop pneumonitis. Conclusions: Intensity-modulated RT treatment for mesothelioma after EPP and adjuvant chemotherapy resulted in a high rate of fatal pneumonitis when standard dose parameters were used. We therefore recommend caution in the utilization of this technique. Our data suggest that with IMRT, metrics such as V5 and MLD should be considered in addition to V20 to determine tolerance levels in future patients.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>CARCINOMAS</subject><subject>CHEMOTHERAPY</subject><subject>Chemotherapy, Adjuvant</subject><subject>Cisplatin - administration &amp; dosage</subject><subject>COLLIMATORS</subject><subject>Female</subject><subject>FLUORODEOXYGLUCOSE</subject><subject>Glutamates - administration &amp; dosage</subject><subject>Guanine - administration &amp; dosage</subject><subject>Guanine - analogs &amp; derivatives</subject><subject>HOSPITALS</subject><subject>Humans</subject><subject>Intensity-modulated radiation therapy</subject><subject>LUNGS</subject><subject>Male</subject><subject>Mean lung dose</subject><subject>MEDICAL RECORDS</subject><subject>Mesothelioma</subject><subject>Mesothelioma - drug therapy</subject><subject>Mesothelioma - radiotherapy</subject><subject>Mesothelioma - surgery</subject><subject>Middle Aged</subject><subject>NAUSEA</subject><subject>PATIENTS</subject><subject>Pemetrexed</subject><subject>Pneumonectomy</subject><subject>PNEUMONITIS</subject><subject>POSITRON COMPUTED TOMOGRAPHY</subject><subject>RADIATION DOSES</subject><subject>Radiation Pneumonitis - etiology</subject><subject>Radiation Pneumonitis - mortality</subject><subject>RADIOLOGY AND NUCLEAR MEDICINE</subject><subject>RADIOTHERAPY</subject><subject>Radiotherapy, Adjuvant</subject><subject>Radiotherapy, Intensity-Modulated - adverse effects</subject><subject>Radiotherapy, Intensity-Modulated - mortality</subject><subject>Respiratory Insufficiency - mortality</subject><subject>Retrospective Studies</subject><subject>VOMITING</subject><issn>0360-3016</issn><issn>1879-355X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LxDAQhoMoun78A5GC59ZJ0zTpRRBxVRC8KHgLaTpls2ybkmSV_fdmreDNQwhhnjcz8xBySaGgQOubdWHX3rVTUQLUBbACaHlAFlSKJmecfxySBbAacpbgE3IawhoAKBXVMTmhteAUuFyQj6WOepNNI24HN9poQ6ZDcMbqiF32ZeMqs2PEMdi4ywfXbTc_Ba-7RFg3ZnGFXk-7rHc-GzC49N5YN-hzctTrTcCL3_uMvC8f3u6f8pfXx-f7u5fcVKyKuUDaGkkZ7WQrGuBMA9eypCh02VadYULzKp22qWpRl5I2NUqBvNey5xxadkau539diFYFYyOalXHjiCaqEmRVygYSVc2U8S4Ej72avB203ykKaq9TrdWsU-11KmAq6Uyxqzk2bdsBu7_Qr78E3M4AphU_Lfr9BDga7KzfD9A5-3-Hb-V5iVc</recordid><startdate>20060701</startdate><enddate>20060701</enddate><creator>Allen, Aaron M.</creator><creator>Czerminska, Maria</creator><creator>Jänne, Pasi A.</creator><creator>Sugarbaker, David J.</creator><creator>Bueno, Raphael</creator><creator>Harris, Jay R.</creator><creator>Court, Laurence</creator><creator>Baldini, Elizabeth H.</creator><general>Elsevier Inc</general><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>OTOTI</scope></search><sort><creationdate>20060701</creationdate><title>Fatal pneumonitis associated with intensity-modulated radiation therapy for mesothelioma</title><author>Allen, Aaron M. ; 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Methods and Materials: The medical records of patients treated with IMRT after EPP and adjuvant chemotherapy were retrospectively reviewed. IMRT was given to a dose of 54 Gy to the clinical target volume in 1.8 Gy daily fractions. Treatment was delivered with a dynamic multileaf collimator using a sliding window technique. Eleven of 13 patients received heated intraoperative cisplatin chemotherapy (225 mg/m 2). Two patients received neoadjuvant intravenous cisplatin/pemetrexed, and 10 patients received adjuvant cisplatin/pemetrexed chemotherapy after EPP but before radiation therapy. All patients received at least 2 cycles of intravenous chemotherapy. The contralateral lung was limited to a V20 (volume of lung receiving 20 Gy or more) of 20% and a mean lung dose (MLD) of 15 Gy. All patients underwent fluorodeoxyglucose positron emission tomography (FDG-PET) for staging, and any FDG-avid areas in the hemithorax were given a simultaneous boost of radiotherapy to 60 Gy. Statistical comparisons were done using two-sided t test. Results: Thirteen patients were treated with IMRT from December 2004 to September 2005. Six patients developed fatal pneumonitis after treatment. The median time from completion of IMRT to the onset of radiation pneumonitis was 30 days (range 5–57 days). Thirty percent of patients (4 of 13) developed acute Grade 3 nausea and vomiting. One patient developed acute Grade 3 thrombocytopenia. The median V20, MLD, and V5 (volume of lung receiving 5 Gy or more) for the patients who developed pneumonitis was 17.6% (range, 15.3–22.3%), 15.2 Gy (range, 13.3–17 Gy), and 98.6% (range, 81–100%), respectively, as compared with 10.9% (range, 5.5–24.7%) ( p = 0.08), 12.9 Gy (range, 8.7–16.9 Gy) ( p = 0.07), and 90% (range, 66–98.3%) ( p = 0.20), respectively, for the patients who did not develop pneumonitis. Conclusions: Intensity-modulated RT treatment for mesothelioma after EPP and adjuvant chemotherapy resulted in a high rate of fatal pneumonitis when standard dose parameters were used. We therefore recommend caution in the utilization of this technique. Our data suggest that with IMRT, metrics such as V5 and MLD should be considered in addition to V20 to determine tolerance levels in future patients.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>16751058</pmid><doi>10.1016/j.ijrobp.2006.03.012</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0360-3016
ispartof International journal of radiation oncology, biology, physics, 2006-07, Vol.65 (3), p.640-645
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1879-355X
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Adult
Aged
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
CARCINOMAS
CHEMOTHERAPY
Chemotherapy, Adjuvant
Cisplatin - administration & dosage
COLLIMATORS
Female
FLUORODEOXYGLUCOSE
Glutamates - administration & dosage
Guanine - administration & dosage
Guanine - analogs & derivatives
HOSPITALS
Humans
Intensity-modulated radiation therapy
LUNGS
Male
Mean lung dose
MEDICAL RECORDS
Mesothelioma
Mesothelioma - drug therapy
Mesothelioma - radiotherapy
Mesothelioma - surgery
Middle Aged
NAUSEA
PATIENTS
Pemetrexed
Pneumonectomy
PNEUMONITIS
POSITRON COMPUTED TOMOGRAPHY
RADIATION DOSES
Radiation Pneumonitis - etiology
Radiation Pneumonitis - mortality
RADIOLOGY AND NUCLEAR MEDICINE
RADIOTHERAPY
Radiotherapy, Adjuvant
Radiotherapy, Intensity-Modulated - adverse effects
Radiotherapy, Intensity-Modulated - mortality
Respiratory Insufficiency - mortality
Retrospective Studies
VOMITING
title Fatal pneumonitis associated with intensity-modulated radiation therapy for mesothelioma
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