Local transdermal therapy to the breast for breast cancer prevention and DCIS therapy: preclinical and clinical evaluation

Purpose Women at high risk of breast cancer and those with carcinoma in situ need non-toxic, well-tolerated preventive interventions. One promising approach is drug delivery through the breast skin (local transdermal therapy, LTT). Our goal was to test novel drugs for LTT, to establish that LTT is a...

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Published inCancer chemotherapy and pharmacology Vol. 76; no. 6; pp. 1235 - 1246
Main Authors Lee, Oukseub, Ivancic, David, Allu, Subhashini, Shidfar, Ali, Kenney, Kara, Helenowski, Irene, Sullivan, Megan E., Muzzio, Miguel, Scholtens, Denise, Chatterton, Robert T., Bethke, Kevin P., Hansen, Nora M., Khan, Seema A.
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer Berlin Heidelberg 01.12.2015
Springer Nature B.V
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Abstract Purpose Women at high risk of breast cancer and those with carcinoma in situ need non-toxic, well-tolerated preventive interventions. One promising approach is drug delivery through the breast skin (local transdermal therapy, LTT). Our goal was to test novel drugs for LTT, to establish that LTT is applicable to non-steroidal drugs. Methods Athymic nude rats were treated with oral tamoxifen, transdermal 4-hydroxytamoxifen (4-OHT) or endoxifen gel applied daily to the axillary mammary gland for 6 weeks (Study 1). Study 2 was identical to Study 1, testing transdermal telapristone acetate (telapristone) gel versus subcutaneous implant. At euthanasia, mammary glands and blood were collected. In Study 3, consenting women requiring mastectomy were randomized to diclofenac patch applied to the abdomen or the breast for 3 days preoperatively. At surgery, eight tissue samples per breast were collected from predetermined locations, along with venous blood. Drug concentrations were measured using liquid chromatography–tandem mass spectroscopy. Results Mammary tissue concentrations of 4-OHT, endoxifen, and telapristone were significantly higher in the axillary glands of the gel-treated animals, compared to inguinal glands or to systemically treated animals. Plasma concentrations were similar in gel and systemically treated animals. The clinical trial showed significantly higher mammary concentrations when diclofenac was applied to the breast skin versus the abdominal skin, but concentrations were variable. Conclusions These results demonstrate that lipophilic drugs can be developed for LTT; although the nude rat is suitable for testing drug permeability, delivery is systemic. In human, however, transdermal application to the breast skin provides local delivery.
AbstractList Women at high risk of breast cancer and those with carcinoma in situ need non-toxic, well-tolerated preventive interventions. One promising approach is drug delivery through the breast skin (local transdermal therapy, LTT). Our goal was to test novel drugs for LTT, to establish that LTT is applicable to non-steroidal drugs. Athymic nude rats were treated with oral tamoxifen, transdermal 4-hydroxytamoxifen (4-OHT) or endoxifen gel applied daily to the axillary mammary gland for 6 weeks (Study 1). Study 2 was identical to Study 1, testing transdermal telapristone acetate (telapristone) gel versus subcutaneous implant. At euthanasia, mammary glands and blood were collected. In Study 3, consenting women requiring mastectomy were randomized to diclofenac patch applied to the abdomen or the breast for 3 days preoperatively. At surgery, eight tissue samples per breast were collected from predetermined locations, along with venous blood. Drug concentrations were measured using liquid chromatography-tandem mass spectroscopy. Mammary tissue concentrations of 4-OHT, endoxifen, and telapristone were significantly higher in the axillary glands of the gel-treated animals, compared to inguinal glands or to systemically treated animals. Plasma concentrations were similar in gel and systemically treated animals. The clinical trial showed significantly higher mammary concentrations when diclofenac was applied to the breast skin versus the abdominal skin, but concentrations were variable. These results demonstrate that lipophilic drugs can be developed for LTT; although the nude rat is suitable for testing drug permeability, delivery is systemic. In human, however, transdermal application to the breast skin provides local delivery.
Purpose Women at high risk of breast cancer and those with carcinoma in situ need non-toxic, well-tolerated preventive interventions. One promising approach is drug delivery through the breast skin (local transdermal therapy, LTT). Our goal was to test novel drugs for LTT, to establish that LTT is applicable to non-steroidal drugs. Methods Athymic nude rats were treated with oral tamoxifen, transdermal 4-hydroxytamoxifen (4-OHT) or endoxifen gel applied daily to the axillary mammary gland for 6 weeks (Study 1). Study 2 was identical to Study 1, testing transdermal telapristone acetate (telapristone) gel versus subcutaneous implant. At euthanasia, mammary glands and blood were collected. In Study 3, consenting women requiring mastectomy were randomized to diclofenac patch applied to the abdomen or the breast for 3 days preoperatively. At surgery, eight tissue samples per breast were collected from predetermined locations, along with venous blood. Drug concentrations were measured using liquid chromatography-tandem mass spectroscopy. Results Mammary tissue concentrations of 4-OHT, endoxifen, and telapristone were significantly higher in the axillary glands of the gel-treated animals, compared to inguinal glands or to systemically treated animals. Plasma concentrations were similar in gel and systemically treated animals. The clinical trial showed significantly higher mammary concentrations when diclofenac was applied to the breast skin versus the abdominal skin, but concentrations were variable. Conclusions These results demonstrate that lipophilic drugs can be developed for LTT; although the nude rat is suitable for testing drug permeability, delivery is systemic. In human, however, transdermal application to the breast skin provides local delivery.
Purpose Women at high risk of breast cancer and those with carcinoma in situ need non-toxic, well-tolerated preventive interventions. One promising approach is drug delivery through the breast skin (local transdermal therapy, LTT). Our goal was to test novel drugs for LTT, to establish that LTT is applicable to non-steroidal drugs. Methods Athymic nude rats were treated with oral tamoxifen, transdermal 4-hydroxytamoxifen (4-OHT) or endoxifen gel applied daily to the axillary mammary gland for 6 weeks (Study 1). Study 2 was identical to Study 1, testing transdermal telapristone acetate (telapristone) gel versus subcutaneous implant. At euthanasia, mammary glands and blood were collected. In Study 3, consenting women requiring mastectomy were randomized to diclofenac patch applied to the abdomen or the breast for 3 days preoperatively. At surgery, eight tissue samples per breast were collected from predetermined locations, along with venous blood. Drug concentrations were measured using liquid chromatography–tandem mass spectroscopy. Results Mammary tissue concentrations of 4-OHT, endoxifen, and telapristone were significantly higher in the axillary glands of the gel-treated animals, compared to inguinal glands or to systemically treated animals. Plasma concentrations were similar in gel and systemically treated animals. The clinical trial showed significantly higher mammary concentrations when diclofenac was applied to the breast skin versus the abdominal skin, but concentrations were variable. Conclusions These results demonstrate that lipophilic drugs can be developed for LTT; although the nude rat is suitable for testing drug permeability, delivery is systemic. In human, however, transdermal application to the breast skin provides local delivery.
Author Ivancic, David
Lee, Oukseub
Kenney, Kara
Chatterton, Robert T.
Helenowski, Irene
Scholtens, Denise
Muzzio, Miguel
Bethke, Kevin P.
Allu, Subhashini
Shidfar, Ali
Khan, Seema A.
Hansen, Nora M.
Sullivan, Megan E.
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  organization: Department of Surgery, The Robert H. Lurie Cancer Center of Northwestern University
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  organization: Department of Surgery, The Robert H. Lurie Cancer Center of Northwestern University
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  fullname: Allu, Subhashini
  organization: Department of Surgery, The Robert H. Lurie Cancer Center of Northwestern University, Department of Medicine, The Robert H. Lurie Cancer Center of Northwestern University
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  givenname: Ali
  surname: Shidfar
  fullname: Shidfar, Ali
  organization: Department of Surgery, The Robert H. Lurie Cancer Center of Northwestern University
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  surname: Kenney
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  organization: Illinois Institute of Technology Research Institute
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  organization: Department of Preventive Medicine, The Robert H. Lurie Cancer Center of Northwestern University
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  fullname: Chatterton, Robert T.
  organization: Department of Obstetrics and Gynecology, The Robert H. Lurie Cancer Center of Northwestern University
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  givenname: Kevin P.
  surname: Bethke
  fullname: Bethke, Kevin P.
  organization: Department of Surgery, The Robert H. Lurie Cancer Center of Northwestern University, Department of Medicine, The Robert H. Lurie Cancer Center of Northwestern University
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  givenname: Nora M.
  surname: Hansen
  fullname: Hansen, Nora M.
  organization: Department of Surgery, The Robert H. Lurie Cancer Center of Northwestern University, Department of Medicine, The Robert H. Lurie Cancer Center of Northwestern University
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  givenname: Seema A.
  surname: Khan
  fullname: Khan, Seema A.
  email: skhan@nmh.org
  organization: Department of Surgery, The Robert H. Lurie Cancer Center of Northwestern University, Department of Medicine, The Robert H. Lurie Cancer Center of Northwestern University, Northwestern University Feinberg School of Medicine
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Keywords 4-Hydroxytamoxifen
Breast
Transdermal therapy
Endoxifen
Telapristone
Diclofenac
Language English
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SSID ssj0004133
Score 2.3298135
Snippet Purpose Women at high risk of breast cancer and those with carcinoma in situ need non-toxic, well-tolerated preventive interventions. One promising approach is...
Women at high risk of breast cancer and those with carcinoma in situ need non-toxic, well-tolerated preventive interventions. One promising approach is drug...
Purpose Women at high risk of breast cancer and those with carcinoma in situ need non-toxic, well-tolerated preventive interventions. One promising approach is...
SourceID proquest
crossref
pubmed
springer
SourceType Aggregation Database
Index Database
Publisher
StartPage 1235
SubjectTerms Administration, Cutaneous
Administration, Oral
Adult
Animals
Antineoplastic Agents - administration & dosage
Antineoplastic Agents - therapeutic use
Breast - drug effects
Breast - pathology
Breast Neoplasms - prevention & control
Cancer Research
Carcinoma, Intraductal, Noninfiltrating - drug therapy
Diclofenac - administration & dosage
Diclofenac - therapeutic use
Drug Evaluation, Preclinical - methods
Female
Gels
Humans
Mammary Glands, Animal - drug effects
Medicine
Medicine & Public Health
Middle Aged
Norpregnadienes - administration & dosage
Norpregnadienes - pharmacology
Oncology
Original Article
Outcome Assessment (Health Care)
Pharmacology/Toxicology
Pilot Projects
Preoperative Period
Random Allocation
Rats, Nude
Tamoxifen - administration & dosage
Tamoxifen - analogs & derivatives
Tamoxifen - pharmacology
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Title Local transdermal therapy to the breast for breast cancer prevention and DCIS therapy: preclinical and clinical evaluation
URI https://link.springer.com/article/10.1007/s00280-015-2848-y
https://www.ncbi.nlm.nih.gov/pubmed/26560487
https://www.proquest.com/docview/1733841395
Volume 76
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