Therapeutic efficacy of alpha-RIT using a 213Bi-anti-hCD138 antibody in a mouse model of ovarian peritoneal carcinomatosis
Purpose: Ovarian peritoneal carcinomatosis is a pathology for which effective cures are currently lacking. New research protocols seek to eradicate residual micrometastases following cytoreductive surgery by using Hyperthermic Intraperitoneal Chemotherapy (HIPEC), or Radioimmunotherapy (RIT). This s...
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doaj-d6696dd5770e41f29067b2122ac295712020-11-25T00:50:49ZengFrontiers Media S.A.Frontiers in Medicine2296-858X2015-12-01210.3389/fmed.2015.00088168884Therapeutic efficacy of alpha-RIT using a 213Bi-anti-hCD138 antibody in a mouse model of ovarian peritoneal carcinomatosisAurélie eDerrien0Aurélie eDerrien1Aurélie eDerrien2Aurélie eDerrien3Sébastien eGouard4Sébastien eGouard5Sébastien eGouard6Catherine eMaurel7Catherine eMaurel8Catherine eMaurel9Marie-Helene eGaugler10Marie-Helene eGaugler11Marie-Helene eGaugler12Frank eBruchertseifer13Alfred eMorgenstern14Alain eFaivre-Chauvet15Alain eFaivre-Chauvet16Alain eFaivre-Chauvet17Alain eFaivre-Chauvet18Jean-Marc eClasse19Jean-Marc eClasse20Jean-Marc eClasse21Jean-Marc eClasse22Michel eChérel23Michel eChérel24Michel eChérel25Michel eChérel26Nantes-Angers Cancer Research Center (CRCNA) UMR 892 Inserm6299 CNRSNantes UniversityPoitiers University HospitalNantes-Angers Cancer Research Center (CRCNA) UMR 892 Inserm6299 CNRSNantes UniversityNantes-Angers Cancer Research Center (CRCNA) UMR 892 Inserm6299 CNRSNantes UniversityNantes-Angers Cancer Research Center (CRCNA) UMR 892 Inserm6299 CNRSNantes UniversityEuropean Commission, Joint Research Centre, Institute for Transuranium ElementsEuropean Commission, Joint Research Centre, Institute for Transuranium ElementsNantes-Angers Cancer Research Center (CRCNA) UMR 892 Inserm6299 CNRSNantes UniversityNantes University HospitalNantes-Angers Cancer Research Center (CRCNA) UMR 892 Inserm6299 CNRSNantes UniversityICO institut de Cancerologie de l'Ouest - Centre René GauducheauNantes-Angers Cancer Research Center (CRCNA) UMR 892 Inserm6299 CNRSNantes UniversityICO institut de Cancerologie de l'Ouest - Centre René GauducheauPurpose: Ovarian peritoneal carcinomatosis is a pathology for which effective cures are currently lacking. New research protocols seek to eradicate residual micrometastases following cytoreductive surgery by using Hyperthermic Intraperitoneal Chemotherapy (HIPEC), or Radioimmunotherapy (RIT). This study aims to firstly develop alpha-RIT using an anti-CD138 mAb radiolabeled with an alpha-emitter, bismuth 213 (213Bi-B-B4) and HIPEC in a nude mouse model, and secondly to compare and combine these techniques.Material and Methods: A murine model of postoperative ovarian peritoneal carcinomatosis was established. A pilot group of six mice received an intraperitoneal injection of luciferase-tagged SHIN-3 cells and bioluminescence was measured every day. Cytoreductive surgery was performed at day 14 (n=4) and 29 (n=2). Because the residual bioluminescence signal measured after surgery was equivalent to that obtained 3 days after the graft, HIPEC or alpha-RIT treatments were applied 3 days after the graft. Ten mice were treated by HIPEC with cisplatine (37.5 mg/mL), 11 with 7.4 MBq of 213Bi-B-B4, 7 with 11.1 MBq of 213Bi-B-B4 and 10 mice were treated with the combined therapy (HIPEC + 7.4 MBq of 213Bi-B-B4). Eleven mice received no treatment. Bioluminescence imaging and survival were assessed.Results: Alpha-RIT 7.4 MBq and 11.1 MBq significantly improved survival (p=0.0303 and p=0.0070 respectively) whereas HIPEC and HIPEC + alpha-RIT treatments did not significantly ameliorate survival as compared to the control group.Conclusions: Survival was significantly increased by alpha-RIT treatment in mice with peritoneal carcinomatosis of ovarian origin, however HIPEC alone or in combination with alpha-RIT had no significant effect.http://journal.frontiersin.org/Journal/10.3389/fmed.2015.00088/fullRadioimmunotherapyHIPECCD138alpha-particlesovarian peritoneal carcinomatosis |
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language |
English |
format |
Article |
sources |
DOAJ |
author |
Aurélie eDerrien Aurélie eDerrien Aurélie eDerrien Aurélie eDerrien Sébastien eGouard Sébastien eGouard Sébastien eGouard Catherine eMaurel Catherine eMaurel Catherine eMaurel Marie-Helene eGaugler Marie-Helene eGaugler Marie-Helene eGaugler Frank eBruchertseifer Alfred eMorgenstern Alain eFaivre-Chauvet Alain eFaivre-Chauvet Alain eFaivre-Chauvet Alain eFaivre-Chauvet Jean-Marc eClasse Jean-Marc eClasse Jean-Marc eClasse Jean-Marc eClasse Michel eChérel Michel eChérel Michel eChérel Michel eChérel |
spellingShingle |
Aurélie eDerrien Aurélie eDerrien Aurélie eDerrien Aurélie eDerrien Sébastien eGouard Sébastien eGouard Sébastien eGouard Catherine eMaurel Catherine eMaurel Catherine eMaurel Marie-Helene eGaugler Marie-Helene eGaugler Marie-Helene eGaugler Frank eBruchertseifer Alfred eMorgenstern Alain eFaivre-Chauvet Alain eFaivre-Chauvet Alain eFaivre-Chauvet Alain eFaivre-Chauvet Jean-Marc eClasse Jean-Marc eClasse Jean-Marc eClasse Jean-Marc eClasse Michel eChérel Michel eChérel Michel eChérel Michel eChérel Therapeutic efficacy of alpha-RIT using a 213Bi-anti-hCD138 antibody in a mouse model of ovarian peritoneal carcinomatosis Frontiers in Medicine Radioimmunotherapy HIPEC CD138 alpha-particles ovarian peritoneal carcinomatosis |
author_facet |
Aurélie eDerrien Aurélie eDerrien Aurélie eDerrien Aurélie eDerrien Sébastien eGouard Sébastien eGouard Sébastien eGouard Catherine eMaurel Catherine eMaurel Catherine eMaurel Marie-Helene eGaugler Marie-Helene eGaugler Marie-Helene eGaugler Frank eBruchertseifer Alfred eMorgenstern Alain eFaivre-Chauvet Alain eFaivre-Chauvet Alain eFaivre-Chauvet Alain eFaivre-Chauvet Jean-Marc eClasse Jean-Marc eClasse Jean-Marc eClasse Jean-Marc eClasse Michel eChérel Michel eChérel Michel eChérel Michel eChérel |
author_sort |
Aurélie eDerrien |
title |
Therapeutic efficacy of alpha-RIT using a 213Bi-anti-hCD138 antibody in a mouse model of ovarian peritoneal carcinomatosis |
title_short |
Therapeutic efficacy of alpha-RIT using a 213Bi-anti-hCD138 antibody in a mouse model of ovarian peritoneal carcinomatosis |
title_full |
Therapeutic efficacy of alpha-RIT using a 213Bi-anti-hCD138 antibody in a mouse model of ovarian peritoneal carcinomatosis |
title_fullStr |
Therapeutic efficacy of alpha-RIT using a 213Bi-anti-hCD138 antibody in a mouse model of ovarian peritoneal carcinomatosis |
title_full_unstemmed |
Therapeutic efficacy of alpha-RIT using a 213Bi-anti-hCD138 antibody in a mouse model of ovarian peritoneal carcinomatosis |
title_sort |
therapeutic efficacy of alpha-rit using a 213bi-anti-hcd138 antibody in a mouse model of ovarian peritoneal carcinomatosis |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Medicine |
issn |
2296-858X |
publishDate |
2015-12-01 |
description |
Purpose: Ovarian peritoneal carcinomatosis is a pathology for which effective cures are currently lacking. New research protocols seek to eradicate residual micrometastases following cytoreductive surgery by using Hyperthermic Intraperitoneal Chemotherapy (HIPEC), or Radioimmunotherapy (RIT). This study aims to firstly develop alpha-RIT using an anti-CD138 mAb radiolabeled with an alpha-emitter, bismuth 213 (213Bi-B-B4) and HIPEC in a nude mouse model, and secondly to compare and combine these techniques.Material and Methods: A murine model of postoperative ovarian peritoneal carcinomatosis was established. A pilot group of six mice received an intraperitoneal injection of luciferase-tagged SHIN-3 cells and bioluminescence was measured every day. Cytoreductive surgery was performed at day 14 (n=4) and 29 (n=2). Because the residual bioluminescence signal measured after surgery was equivalent to that obtained 3 days after the graft, HIPEC or alpha-RIT treatments were applied 3 days after the graft. Ten mice were treated by HIPEC with cisplatine (37.5 mg/mL), 11 with 7.4 MBq of 213Bi-B-B4, 7 with 11.1 MBq of 213Bi-B-B4 and 10 mice were treated with the combined therapy (HIPEC + 7.4 MBq of 213Bi-B-B4). Eleven mice received no treatment. Bioluminescence imaging and survival were assessed.Results: Alpha-RIT 7.4 MBq and 11.1 MBq significantly improved survival (p=0.0303 and p=0.0070 respectively) whereas HIPEC and HIPEC + alpha-RIT treatments did not significantly ameliorate survival as compared to the control group.Conclusions: Survival was significantly increased by alpha-RIT treatment in mice with peritoneal carcinomatosis of ovarian origin, however HIPEC alone or in combination with alpha-RIT had no significant effect. |
topic |
Radioimmunotherapy HIPEC CD138 alpha-particles ovarian peritoneal carcinomatosis |
url |
http://journal.frontiersin.org/Journal/10.3389/fmed.2015.00088/full |
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