Blood test may guide chemo decisions for advanced breast cancer
NCT ID NCT01349842
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether measuring circulating tumor cells (CTCs) in the blood can help doctors decide when to switch chemotherapy for women with metastatic breast cancer that has worsened after two prior treatments. The trial involved 265 women and compared standard care with CTC-guided treatment decisions. The goal was to see if this approach improves overall survival and quality of life.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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265 people
The number who actually took part.
- Started
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Mar 2010
- Finished
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Nov 2018
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Women over the age of 18 years. * WHO performance status: 0 to 4. * Metastatic breast cancer. * Progression after 2 lines of chemotherapy with decision to initiate third-line chemotherapy. * Disease evaluable by CTC (CTC-positive before starting chemotherapy). * Histology: lobular or ductal adenocarcinoma. * Information of the patient and signature of the informed consent form by the patient or her legal representative. Exclusion Criteria: * Disease not evaluable by CTC (CTC-negative before starting chemotherapy). * History of other potentially metastatic cancer (stage III or IV cancer) different from breast cancer. * Histology other than lobular or ductal adenocarcinoma. * Pregnant woman, women likely to become pregnant or nursing mothers. * Persons deprived of their freedom or under guardianship. * Women unable to comply with the medical follow-up of the study for geographical, social or mental reasons.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Centre Georges Francois Leclerc
Dijon, 21079, France
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Chu Limoges
Limoges, 87042, France
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Clinique Victor Hugo
Le Mans, 72000, France
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Hopital Saint Louis
Paris, 75475, France
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Institut Curie
Paris, 75005, France
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Institut Rene Huguenin Curie
Saint-Cloud, 92210, France
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Institut de Canacerologie de L'Ouest
Saint-Herblain, 44805, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a blood test reveal when breast cancer treatment stops working?
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- Zapping a few growing tumors may keep breast cancer drugs working longer
- Can a Two-Drug combo outsmart resistant breast and ovarian cancers?