Chemotherapy, irradiation, and surgery for function-preserving therapy of primary extremity soft tissue sarcomas initial treatment with ifosfamide, mitomycin, doxorubicin, and cisplatin plus granulocyte macrophage-colony-stimulating factor

Most institutional teams utilize multimodality therapy in their efforts to cure patients with primary high-grade extremity soft tissue sarcomas, although the value of adjuvant systemic chemotherapy is still disputed by some oncologists. This single-institution Phase II study describes an effort to c...

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Veröffentlicht in:Cancer 2002-02, Vol.94 (3), p.786-792
Hauptverfasser: EDMONSON, John H, PETERSEN, Ivy A, FOO, May L, PRITCHARD, Douglas J, BUCKNER, Jan C, STAFFORD, Scott L, SHIVES, Thomas C, MAHONEY, Michelle R, ROCK, Michael G, HADDOCK, Michael G, SIM, Franklin H, MAPLES, William J, O'CONNOR, Mary I, GUNDERSON, Leonard L
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container_issue 3
container_start_page 786
container_title Cancer
container_volume 94
creator EDMONSON, John H
PETERSEN, Ivy A
FOO, May L
PRITCHARD, Douglas J
BUCKNER, Jan C
STAFFORD, Scott L
SHIVES, Thomas C
MAHONEY, Michelle R
ROCK, Michael G
HADDOCK, Michael G
SIM, Franklin H
MAPLES, William J
O'CONNOR, Mary I
GUNDERSON, Leonard L
description Most institutional teams utilize multimodality therapy in their efforts to cure patients with primary high-grade extremity soft tissue sarcomas, although the value of adjuvant systemic chemotherapy is still disputed by some oncologists. This single-institution Phase II study describes an effort to control metastasis by the use of two cycles of chemotherapy as the initial preoperative treatment. Between March 1994 and October 1997, 20 women and 19 men with primary extremity or limb girdle high-grade soft tissue sarcomas were registered to a study of preoperative ifosfamide, mitomycin, doxorubicin, cisplatin (IMAP) plus granulocyte macrophage-colony-stimulating factor (GM-CSF) followed by preoperative irradiation and subsequent limb-sparing surgery. The two sequential monthly cycles of IMAP involved intravenous ifosfamide, 2500 mg/m(2), and mesna, 2500 mg/m(2), on Day 0, followed by identical doses of these agents plus intravenous mitomycin, 4 mg/m(2), doxorubicin, 40 mg/m(2), and cisplatin, 60 mg/m(2), on Day 1. Sargramostim (GM-CSF) 250 microg/m(2) was given subcutaneously every 12 hours for 4 days beginning 6 days before the chemotherapy, and then for 14 more days beginning the day after chemotherapy was completed. At the beginning of the third month, external beam irradiation was administered daily, 5 days each week for 5 consecutive weeks to total preoperative doses of 4500 centigrays (cGy). This was accompanied by reduced doses of MAP chemotherapy (mitomycin, 6 mg/m(2), doxorubicin, 30 mg/m(2), and cisplatin, 45 mg/m(2)) intravenously on Days 0, 21, and 42 of the radiation therapy segment. Approximately 1 month after preoperative irradiation ended, each patient had complete surgical excision with curative intent, using limb-sparing techniques when possible. Radiation to total doses of 5500-6500 cGy was accomplished by delivery of an additional 1000-2000 cGy to the tumor bed via intraoperative electron beam, brachytherapy, or external beam irradiation at the completion of surgery. All except 5 patients had tumors at least 5 cm in diameter. Chemotherapy toxicity grade three or higher consisted primarily of vomiting (23%), leukopenia (54%), and thrombocytopenia (77%). Six patients have died of metastatic sarcoma, and one other died in a motorcycle accident. Kaplan-Meier curves indicate estimated 5-year survival of approximately 80% and freedom from metastasis at 2 years of approximately 85%. IMAP plus GM-CSF is satisfactory as initial treatment for primar
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This single-institution Phase II study describes an effort to control metastasis by the use of two cycles of chemotherapy as the initial preoperative treatment. Between March 1994 and October 1997, 20 women and 19 men with primary extremity or limb girdle high-grade soft tissue sarcomas were registered to a study of preoperative ifosfamide, mitomycin, doxorubicin, cisplatin (IMAP) plus granulocyte macrophage-colony-stimulating factor (GM-CSF) followed by preoperative irradiation and subsequent limb-sparing surgery. The two sequential monthly cycles of IMAP involved intravenous ifosfamide, 2500 mg/m(2), and mesna, 2500 mg/m(2), on Day 0, followed by identical doses of these agents plus intravenous mitomycin, 4 mg/m(2), doxorubicin, 40 mg/m(2), and cisplatin, 60 mg/m(2), on Day 1. Sargramostim (GM-CSF) 250 microg/m(2) was given subcutaneously every 12 hours for 4 days beginning 6 days before the chemotherapy, and then for 14 more days beginning the day after chemotherapy was completed. At the beginning of the third month, external beam irradiation was administered daily, 5 days each week for 5 consecutive weeks to total preoperative doses of 4500 centigrays (cGy). This was accompanied by reduced doses of MAP chemotherapy (mitomycin, 6 mg/m(2), doxorubicin, 30 mg/m(2), and cisplatin, 45 mg/m(2)) intravenously on Days 0, 21, and 42 of the radiation therapy segment. Approximately 1 month after preoperative irradiation ended, each patient had complete surgical excision with curative intent, using limb-sparing techniques when possible. Radiation to total doses of 5500-6500 cGy was accomplished by delivery of an additional 1000-2000 cGy to the tumor bed via intraoperative electron beam, brachytherapy, or external beam irradiation at the completion of surgery. All except 5 patients had tumors at least 5 cm in diameter. Chemotherapy toxicity grade three or higher consisted primarily of vomiting (23%), leukopenia (54%), and thrombocytopenia (77%). Six patients have died of metastatic sarcoma, and one other died in a motorcycle accident. Kaplan-Meier curves indicate estimated 5-year survival of approximately 80% and freedom from metastasis at 2 years of approximately 85%. IMAP plus GM-CSF is satisfactory as initial treatment for primary extremity soft tissue sarcomas in two monthly cycles preceding irradiation. The prescribed irradiation was generally tolerable and effective in permitting limb-sparing surgery. Although the outcome of patients treated on this regimen has been favorable, the metastasis problem has not been eliminated.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/cncr.10259</identifier><identifier>PMID: 11857314</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>New York, NY: Wiley-Liss</publisher><subject><![CDATA[Adult ; Aged ; Aged, 80 and over ; Antineoplastic agents ; Antineoplastic Combined Chemotherapy Protocols - administration & dosage ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Cisplatin - administration & dosage ; Combined Modality Therapy ; Combined treatments (chemotherapy of immunotherapy associated with an other treatment) ; Doxorubicin - administration & dosage ; Female ; Granulocyte-Macrophage Colony-Stimulating Factor - administration & dosage ; Humans ; Ifosfamide - administration & dosage ; Infusions, Intravenous ; Injections, Subcutaneous ; Leukopenia - chemically induced ; Male ; Medical sciences ; Mesna - administration & dosage ; Middle Aged ; Mitomycin - administration & dosage ; Neoadjuvant Therapy ; Pharmacology. Drug treatments ; Sarcoma - drug therapy ; Sarcoma - radiotherapy ; Sarcoma - surgery ; Soft Tissue Neoplasms - drug therapy ; Soft Tissue Neoplasms - radiotherapy ; Soft Tissue Neoplasms - surgery ; Thrombocytopenia - chemically induced ; Treatment Outcome ; Vomiting - chemically induced]]></subject><ispartof>Cancer, 2002-02, Vol.94 (3), p.786-792</ispartof><rights>2002 INIST-CNRS</rights><rights>Copyright 2002 American Cancer Society. 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This single-institution Phase II study describes an effort to control metastasis by the use of two cycles of chemotherapy as the initial preoperative treatment. Between March 1994 and October 1997, 20 women and 19 men with primary extremity or limb girdle high-grade soft tissue sarcomas were registered to a study of preoperative ifosfamide, mitomycin, doxorubicin, cisplatin (IMAP) plus granulocyte macrophage-colony-stimulating factor (GM-CSF) followed by preoperative irradiation and subsequent limb-sparing surgery. The two sequential monthly cycles of IMAP involved intravenous ifosfamide, 2500 mg/m(2), and mesna, 2500 mg/m(2), on Day 0, followed by identical doses of these agents plus intravenous mitomycin, 4 mg/m(2), doxorubicin, 40 mg/m(2), and cisplatin, 60 mg/m(2), on Day 1. Sargramostim (GM-CSF) 250 microg/m(2) was given subcutaneously every 12 hours for 4 days beginning 6 days before the chemotherapy, and then for 14 more days beginning the day after chemotherapy was completed. At the beginning of the third month, external beam irradiation was administered daily, 5 days each week for 5 consecutive weeks to total preoperative doses of 4500 centigrays (cGy). This was accompanied by reduced doses of MAP chemotherapy (mitomycin, 6 mg/m(2), doxorubicin, 30 mg/m(2), and cisplatin, 45 mg/m(2)) intravenously on Days 0, 21, and 42 of the radiation therapy segment. Approximately 1 month after preoperative irradiation ended, each patient had complete surgical excision with curative intent, using limb-sparing techniques when possible. Radiation to total doses of 5500-6500 cGy was accomplished by delivery of an additional 1000-2000 cGy to the tumor bed via intraoperative electron beam, brachytherapy, or external beam irradiation at the completion of surgery. All except 5 patients had tumors at least 5 cm in diameter. Chemotherapy toxicity grade three or higher consisted primarily of vomiting (23%), leukopenia (54%), and thrombocytopenia (77%). Six patients have died of metastatic sarcoma, and one other died in a motorcycle accident. Kaplan-Meier curves indicate estimated 5-year survival of approximately 80% and freedom from metastasis at 2 years of approximately 85%. IMAP plus GM-CSF is satisfactory as initial treatment for primary extremity soft tissue sarcomas in two monthly cycles preceding irradiation. The prescribed irradiation was generally tolerable and effective in permitting limb-sparing surgery. Although the outcome of patients treated on this regimen has been favorable, the metastasis problem has not been eliminated.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration &amp; dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Cisplatin - administration &amp; dosage</subject><subject>Combined Modality Therapy</subject><subject>Combined treatments (chemotherapy of immunotherapy associated with an other treatment)</subject><subject>Doxorubicin - administration &amp; dosage</subject><subject>Female</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor - administration &amp; dosage</subject><subject>Humans</subject><subject>Ifosfamide - administration &amp; dosage</subject><subject>Infusions, Intravenous</subject><subject>Injections, Subcutaneous</subject><subject>Leukopenia - chemically induced</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mesna - administration &amp; dosage</subject><subject>Middle Aged</subject><subject>Mitomycin - administration &amp; dosage</subject><subject>Neoadjuvant Therapy</subject><subject>Pharmacology. Drug treatments</subject><subject>Sarcoma - drug therapy</subject><subject>Sarcoma - radiotherapy</subject><subject>Sarcoma - surgery</subject><subject>Soft Tissue Neoplasms - drug therapy</subject><subject>Soft Tissue Neoplasms - radiotherapy</subject><subject>Soft Tissue Neoplasms - surgery</subject><subject>Thrombocytopenia - chemically induced</subject><subject>Treatment Outcome</subject><subject>Vomiting - chemically induced</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkcuO1DAQRS0EYpqBDR-AvGGDOuBH3EkvUYuXNBIbkNhF5VfaKLYj24HJV_MLuHsizaqqVKdKt-oi9JqS95QQ9kEFlWrGxPEJ2lFy7BpCW_YU7QghfSNa_usGvcj5dy07JvhzdENpLzpO2x36dzobH8vZJJjXPXYpgXZQXAx7DEHjvKTRpBXbmLBdgrp0mjmZbNIfF0a8TeJo8Zych4qa-5KMd2XFOdqCi8t5MThDUtFDxi644mDCFYLiTSj4rytn7GzMFrzTZo_rcPSrclWDjvcxLdJdi4sg5fI8VYEBz9OS8ZggLFNUazHYg0pxPsNoGhWnGNYmF-eXKz1iC6rE9BI9szBl82qLt-jn508_Tl-bu-9fvp0-3jWKdaw0naHQGyGJBi47wgURkrXsaHjPZXuk2hB2kLq3uuetYUB7KVrJmZX6IDoB_Ba9e9hbJeWcjB229wyUDBfXhotrw9W1Cr95gOdFeqMf0c2mCrzdAMgKJluPrn945Hh7aFlF_wOzKamt</recordid><startdate>20020201</startdate><enddate>20020201</enddate><creator>EDMONSON, John H</creator><creator>PETERSEN, Ivy A</creator><creator>FOO, May L</creator><creator>PRITCHARD, Douglas J</creator><creator>BUCKNER, Jan C</creator><creator>STAFFORD, Scott L</creator><creator>SHIVES, Thomas C</creator><creator>MAHONEY, Michelle R</creator><creator>ROCK, Michael G</creator><creator>HADDOCK, Michael G</creator><creator>SIM, Franklin H</creator><creator>MAPLES, William J</creator><creator>O'CONNOR, Mary I</creator><creator>GUNDERSON, Leonard L</creator><general>Wiley-Liss</general><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></search><sort><creationdate>20020201</creationdate><title>Chemotherapy, irradiation, and surgery for function-preserving therapy of primary extremity soft tissue sarcomas initial treatment with ifosfamide, mitomycin, doxorubicin, and cisplatin plus granulocyte macrophage-colony-stimulating factor</title><author>EDMONSON, John H ; PETERSEN, Ivy A ; FOO, May L ; PRITCHARD, Douglas J ; BUCKNER, Jan C ; STAFFORD, Scott L ; SHIVES, Thomas C ; MAHONEY, Michelle R ; ROCK, Michael G ; HADDOCK, Michael G ; SIM, Franklin H ; MAPLES, William J ; O'CONNOR, Mary I ; GUNDERSON, Leonard L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c272t-7e1a8e5b0da3b703505b2429e383b491de026bd8fd834e2a18b54b32fbd6575a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic agents</topic><topic>Antineoplastic Combined Chemotherapy Protocols - administration &amp; dosage</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Cisplatin - administration &amp; dosage</topic><topic>Combined Modality Therapy</topic><topic>Combined treatments (chemotherapy of immunotherapy associated with an other treatment)</topic><topic>Doxorubicin - administration &amp; dosage</topic><topic>Female</topic><topic>Granulocyte-Macrophage Colony-Stimulating Factor - administration &amp; dosage</topic><topic>Humans</topic><topic>Ifosfamide - administration &amp; dosage</topic><topic>Infusions, Intravenous</topic><topic>Injections, Subcutaneous</topic><topic>Leukopenia - chemically induced</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mesna - administration &amp; dosage</topic><topic>Middle Aged</topic><topic>Mitomycin - administration &amp; dosage</topic><topic>Neoadjuvant Therapy</topic><topic>Pharmacology. Drug treatments</topic><topic>Sarcoma - drug therapy</topic><topic>Sarcoma - radiotherapy</topic><topic>Sarcoma - surgery</topic><topic>Soft Tissue Neoplasms - drug therapy</topic><topic>Soft Tissue Neoplasms - radiotherapy</topic><topic>Soft Tissue Neoplasms - surgery</topic><topic>Thrombocytopenia - chemically induced</topic><topic>Treatment Outcome</topic><topic>Vomiting - chemically induced</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>EDMONSON, John H</creatorcontrib><creatorcontrib>PETERSEN, Ivy A</creatorcontrib><creatorcontrib>FOO, May L</creatorcontrib><creatorcontrib>PRITCHARD, Douglas J</creatorcontrib><creatorcontrib>BUCKNER, Jan C</creatorcontrib><creatorcontrib>STAFFORD, Scott L</creatorcontrib><creatorcontrib>SHIVES, Thomas C</creatorcontrib><creatorcontrib>MAHONEY, Michelle R</creatorcontrib><creatorcontrib>ROCK, Michael G</creatorcontrib><creatorcontrib>HADDOCK, Michael G</creatorcontrib><creatorcontrib>SIM, Franklin H</creatorcontrib><creatorcontrib>MAPLES, William J</creatorcontrib><creatorcontrib>O'CONNOR, Mary I</creatorcontrib><creatorcontrib>GUNDERSON, Leonard L</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>EDMONSON, John H</au><au>PETERSEN, Ivy A</au><au>FOO, May L</au><au>PRITCHARD, Douglas J</au><au>BUCKNER, Jan C</au><au>STAFFORD, Scott L</au><au>SHIVES, Thomas C</au><au>MAHONEY, Michelle R</au><au>ROCK, Michael G</au><au>HADDOCK, Michael G</au><au>SIM, Franklin H</au><au>MAPLES, William J</au><au>O'CONNOR, Mary I</au><au>GUNDERSON, Leonard L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chemotherapy, irradiation, and surgery for function-preserving therapy of primary extremity soft tissue sarcomas initial treatment with ifosfamide, mitomycin, doxorubicin, and cisplatin plus granulocyte macrophage-colony-stimulating factor</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>2002-02-01</date><risdate>2002</risdate><volume>94</volume><issue>3</issue><spage>786</spage><epage>792</epage><pages>786-792</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>Most institutional teams utilize multimodality therapy in their efforts to cure patients with primary high-grade extremity soft tissue sarcomas, although the value of adjuvant systemic chemotherapy is still disputed by some oncologists. This single-institution Phase II study describes an effort to control metastasis by the use of two cycles of chemotherapy as the initial preoperative treatment. Between March 1994 and October 1997, 20 women and 19 men with primary extremity or limb girdle high-grade soft tissue sarcomas were registered to a study of preoperative ifosfamide, mitomycin, doxorubicin, cisplatin (IMAP) plus granulocyte macrophage-colony-stimulating factor (GM-CSF) followed by preoperative irradiation and subsequent limb-sparing surgery. The two sequential monthly cycles of IMAP involved intravenous ifosfamide, 2500 mg/m(2), and mesna, 2500 mg/m(2), on Day 0, followed by identical doses of these agents plus intravenous mitomycin, 4 mg/m(2), doxorubicin, 40 mg/m(2), and cisplatin, 60 mg/m(2), on Day 1. Sargramostim (GM-CSF) 250 microg/m(2) was given subcutaneously every 12 hours for 4 days beginning 6 days before the chemotherapy, and then for 14 more days beginning the day after chemotherapy was completed. At the beginning of the third month, external beam irradiation was administered daily, 5 days each week for 5 consecutive weeks to total preoperative doses of 4500 centigrays (cGy). This was accompanied by reduced doses of MAP chemotherapy (mitomycin, 6 mg/m(2), doxorubicin, 30 mg/m(2), and cisplatin, 45 mg/m(2)) intravenously on Days 0, 21, and 42 of the radiation therapy segment. Approximately 1 month after preoperative irradiation ended, each patient had complete surgical excision with curative intent, using limb-sparing techniques when possible. Radiation to total doses of 5500-6500 cGy was accomplished by delivery of an additional 1000-2000 cGy to the tumor bed via intraoperative electron beam, brachytherapy, or external beam irradiation at the completion of surgery. All except 5 patients had tumors at least 5 cm in diameter. Chemotherapy toxicity grade three or higher consisted primarily of vomiting (23%), leukopenia (54%), and thrombocytopenia (77%). Six patients have died of metastatic sarcoma, and one other died in a motorcycle accident. Kaplan-Meier curves indicate estimated 5-year survival of approximately 80% and freedom from metastasis at 2 years of approximately 85%. IMAP plus GM-CSF is satisfactory as initial treatment for primary extremity soft tissue sarcomas in two monthly cycles preceding irradiation. The prescribed irradiation was generally tolerable and effective in permitting limb-sparing surgery. Although the outcome of patients treated on this regimen has been favorable, the metastasis problem has not been eliminated.</abstract><cop>New York, NY</cop><pub>Wiley-Liss</pub><pmid>11857314</pmid><doi>10.1002/cncr.10259</doi><tpages>7</tpages></addata></record>
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identifier ISSN: 0008-543X
ispartof Cancer, 2002-02, Vol.94 (3), p.786-792
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recordid cdi_crossref_primary_10_1002_cncr_10259
source MEDLINE; Wiley Online Library Journals Frontfile Complete; Wiley Online Library Free Content; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Adult
Aged
Aged, 80 and over
Antineoplastic agents
Antineoplastic Combined Chemotherapy Protocols - administration & dosage
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Cisplatin - administration & dosage
Combined Modality Therapy
Combined treatments (chemotherapy of immunotherapy associated with an other treatment)
Doxorubicin - administration & dosage
Female
Granulocyte-Macrophage Colony-Stimulating Factor - administration & dosage
Humans
Ifosfamide - administration & dosage
Infusions, Intravenous
Injections, Subcutaneous
Leukopenia - chemically induced
Male
Medical sciences
Mesna - administration & dosage
Middle Aged
Mitomycin - administration & dosage
Neoadjuvant Therapy
Pharmacology. Drug treatments
Sarcoma - drug therapy
Sarcoma - radiotherapy
Sarcoma - surgery
Soft Tissue Neoplasms - drug therapy
Soft Tissue Neoplasms - radiotherapy
Soft Tissue Neoplasms - surgery
Thrombocytopenia - chemically induced
Treatment Outcome
Vomiting - chemically induced
title Chemotherapy, irradiation, and surgery for function-preserving therapy of primary extremity soft tissue sarcomas initial treatment with ifosfamide, mitomycin, doxorubicin, and cisplatin plus granulocyte macrophage-colony-stimulating factor
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