Page last updated: 2024-10-24

chloroquine and Atypical Ductal Hyperplasia

chloroquine has been researched along with Atypical Ductal Hyperplasia in 2 studies

Chloroquine: The prototypical antimalarial agent with a mechanism that is not well understood. It has also been used to treat rheumatoid arthritis, systemic lupus erythematosus, and in the systemic therapy of amebic liver abscesses.
chloroquine : An aminoquinoline that is quinoline which is substituted at position 4 by a [5-(diethylamino)pentan-2-yl]amino group at at position 7 by chlorine. It is used for the treatment of malaria, hepatic amoebiasis, lupus erythematosus, light-sensitive skin eruptions, and rheumatoid arthritis.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Martinez-Outschoorn, UE1
Pavlides, S1
Whitaker-Menezes, D1
Daumer, KM1
Milliman, JN1
Chiavarina, B1
Migneco, G1
Witkiewicz, AK1
Martinez-Cantarin, MP1
Flomenberg, N1
Howell, A1
Pestell, RG1
Lisanti, MP1
Sotgia, F1
Zeilhofer, HU1
Mollenhauer, J1
Brune, K1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Preventing Invasive Breast Neoplasia With Chloroquine (PINC) Trial[NCT01023477]Phase 1/Phase 212 participants (Actual)Interventional2009-12-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Average Change in the Longest Diameter of the Breast MRI Target Lesion

One of the primary outcomes of this study was to measure the impact of weekly chloroquine on the amount of DCIS seen on MRI.The tumor response was evaluated by RECIST criteria. Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR The longest diameter of the target lesion or primary area of non-mass enhancement was measured by digital calipers. For one patient, the longest diameter was difficult to measure due to the presence of a significant post biopsy resolving hematoma at the biopsy site. Further correlation was made based on the extent of the pre-treatment microcalcifications and post treatment areas of non-mass enhancement. (NCT01023477)
Timeframe: Immediately preceding study drug treatment and again after treatment prior to surgery. The total time interval was up to 8 weeks

Interventionpercentage length change (Mean)
Chloroquine Standard Dose (500mg/Week)6
Chloroquine Low Dose (250mg/Week)43

Effect of Chloroquine on Proliferating Cell Nuclear Antigen (PCNA) Proliferation Index

We evaluated the effect of therapy on cellular proliferation as measured by the change in proliferating cell nuclear antigen (PCNA) proliferation index. PCNA , which is elevated during the G1/S phase of the cell cycle, may be used as a marker of cellular proliferation. The PCNA proliferation index was measured as the number of PCNA positive stained cells in the DCIS lesion/ total number of cells in the lesion. The change in the PCNA index is equal to the mean PCNA proliferation index pre-treatment minus the mean PCNA proliferation index post-treatment. (NCT01023477)
Timeframe: At the time of breast biopsy and again at time of surgery.

InterventionChange in PCNA proliferation index (Mean)
Chloroquine Standard Dose (500mg/Week)50.4
Chloroquine Low Dose (250mg/Week)56.71

Total Number of Treatment-Related Adverse Events

One of the outcomes was to ensure the safety of weekly chloroquine. Patients were followed clinically during the treatment with chloroquine and during their surgery and postoperative period ( including radiation therapy). Patients were verbally assessed for additional symptoms or concerns. Patients were also examined by the provider during treatment and follow up visits to the surgeon. (NCT01023477)
Timeframe: The patients were monitored from the time of diagnosis through 6 months of surgical follow up.

InterventionAdverse Events (mortality, SAE, AE) (Number)
Chloroquine Standard Dose (500mg/Week)0
Chloroquine Low Dose (250mg/Week)0

Impact of Chloroquine Treatment on the Cell Signaling Kinase Levels in DCIS Lesions.

"The study evaluated the effect of chloroquine treatment on the proteomic signaling profiles of the DCIS lesions. Post treatment surgical specimens were evaluated by immunohistochemical staining to measure cell signaling kinase levels for CD68 and HMGB1. CD68 (Cluster Determinant 68) is a marker of macrophages/monocytes in the breast ducts. and HMGB1 (High Mobility Group Box 1) is involved in oxidative stress-mediated autophagy. HMGB1 is a non-histone DNA binding protein. The number of positive cells were quantified and recorded.~." (NCT01023477)
Timeframe: At the time of surgery

,
InterventionPositive cells (Mean)
HMGB1CD68
Chloroquine Low Dose (250mg/Week)47.89163.2
Chloroquine Standard Dose (500mg/Week)33.9318.3

Other Studies

2 other studies available for chloroquine and Atypical Ductal Hyperplasia

ArticleYear
Tumor cells induce the cancer associated fibroblast phenotype via caveolin-1 degradation: implications for breast cancer and DCIS therapy with autophagy inhibitors.
    Cell cycle (Georgetown, Tex.), 2010, Jun-15, Volume: 9, Issue:12

    Topics: Actins; Autophagy; Biomarkers, Tumor; Breast Neoplasms; Calcium-Binding Proteins; Calponins; Carcino

2010
Selective growth inhibition of ductal pancreatic adenocarcinoma cells by the lysosomotropic agent chloroquine.
    Cancer letters, 1989, Volume: 44, Issue:1

    Topics: Auranofin; Carcinoma, Intraductal, Noninfiltrating; Cell Division; Chloroquine; Humans; Pancreatic N

1989