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 in | Cancer chemotherapy and pharmacology Vol. 76; no. 6; pp. 1235 - 1246 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.12.2015
Springer Nature B.V |
Subjects | |
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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. |
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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. |
Author_xml | – sequence: 1 givenname: Oukseub surname: Lee fullname: Lee, Oukseub organization: Department of Surgery, The Robert H. Lurie Cancer Center of Northwestern University – sequence: 2 givenname: David surname: Ivancic fullname: Ivancic, David organization: Department of Surgery, The Robert H. Lurie Cancer Center of Northwestern University – sequence: 3 givenname: Subhashini surname: Allu 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 – sequence: 4 givenname: Ali surname: Shidfar fullname: Shidfar, Ali organization: Department of Surgery, The Robert H. Lurie Cancer Center of Northwestern University – sequence: 5 givenname: Kara surname: Kenney fullname: Kenney, Kara organization: Department of Medicine, The Robert H. Lurie Cancer Center of Northwestern University – sequence: 6 givenname: Irene surname: Helenowski fullname: Helenowski, Irene organization: Department of Preventive Medicine, The Robert H. Lurie Cancer Center of Northwestern University – sequence: 7 givenname: Megan E. surname: Sullivan fullname: Sullivan, Megan E. organization: Department of Pathology, The Robert H. Lurie Cancer Center of Northwestern University – sequence: 8 givenname: Miguel surname: Muzzio fullname: Muzzio, Miguel organization: Illinois Institute of Technology Research Institute – sequence: 9 givenname: Denise surname: Scholtens fullname: Scholtens, Denise organization: Department of Preventive Medicine, The Robert H. Lurie Cancer Center of Northwestern University – sequence: 10 givenname: Robert T. surname: Chatterton fullname: Chatterton, Robert T. organization: Department of Obstetrics and Gynecology, The Robert H. Lurie Cancer Center of Northwestern University – sequence: 11 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 – sequence: 12 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 – sequence: 13 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 |
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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... |
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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 |
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