Breast Cancer and PregnancyEMBARCAMNCT04603820
Registry Study of Pregnancy and Breast Cancer
An observational study of Breast Cancer and Pregnancy, run by Spanish Breast Cancer Research Group at 28 sites in Spain.
Trial summary
An ambispective observational registry study of pregnancy and breast cancer Read more about this study
- Who is it for?
- Ages 18 years and older, women only
- Conditions the study is for
- Breast Cancer and Pregnancy
- How many people
- 866 participants
- Where
- 28 sitesSpain
- Study dates
- 18 Nov 2019to Jan 2030
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- Women only
- No healthy volunteers
- Adult, Older adult
Study population: Patients with breast cancer in any of these three situations: 1. Patients with gestational breast cancer, defined as breast cancer diagnosed during pregnancy, breastfeeding or up to a year after delivery. 2. Patients who become pregnant after a breast cancer diagnosis. 3. Patients with breast cancer who have followed any fertility preservation technique prior to the start of breast cancer treatment.
Who may be able to join
- The patient should have signed and dated the informed consent form (ICF). The enrollment of patients who have died is allowed.
- Women aged ≥ 18 years.
- Patients in one of the following situations:
- Patients with breast cancer diagnosis during pregnancy, breastfeeding or within the year after delivery.
- Patients with breast cancer who become pregnant after treatment.
- Patients with breast cancer who were subjected to any fertility preservation method prior to the start of breast cancer treatment.
Show all 9Show fewer
- The patients referred to in the previous section and the patients who meet these characteristics prospectively could be enrolled retrospectively upon registry opening.
- All cases diagnosed at the same site may be included. In order to prevent duplications, in case the patient followed her treatment and follow-up at another site, she will be enrolled as per the site where the diagnosis was made, requesting information of the treatment and progression, when possible.
- Availability of clinical, epidemiological and progress data.
Who cannot join
- Patients who do not wish to participate in the study for any reason could not be included in the study.
Trial locations and contacts
28 sites in 1 country.
28 sites in 1 country
Spain28 sites
Complejo Hospitalario de Galicia (CHUAC)
A Coruña, La Coruña, 15009
Hospital General Universitario de Albacete
Albacete, 02006
Hospital General Universitario de Alicante
Alicante, 03010
Hospital Universitari Germans Trias i Pujol
Badalona, Barcelona, 08916
Hospital del Mar
Barcelona, 08003
Hospital Clinic i Provincial
Barcelona, 08036
Hospital Universitario de Basurto
Bilbao, Bizkaia, 48013
Hospital San Pedro de Alcántara
Cáceres, 10003
Complejo Hospitalario Reina Sofía
Córdoba, 14004
Hospital Clínico Universitario Virgen de la Arrixaca
El Palmar, Murcia, 30120
Hospital Universitario San Cecilio
Granada, 18016
Hospital Universitario Doctor Negrín
Las Palmas de Gran Canaria, Las Palmas, 35010
Hospital Universitario Severo Ochoa
Leganés, Madrid, 28911
Hospital General Universitario Gregorio Marañón
Madrid, 28007
Hospital Clínico San Carlos
Madrid, 28040
Hospital Universitario Puerta de Hierro
Majadahonda, Madrid, 28222
Hospital Central de Asturias
Oviedo, Principality of Asturias, 33011
Hospital Unviersitari Son Espases
Palma de Mallorca, Balearic Islands, 07120
Complejo Hospitalario de Navarra
Pamplona, Navarre, 31008
Hospital Universitario de Salamanca
Salamanca, 37007
Hospital Nuestra Señora de la Candelaria
Santa Cruz de Tenerife, Canary Islands, 38010
Hospital Universitario Virgen del Rocío
Seville, 41013
Hospital Universitario Mutua de Terrassa
Terrassa, Barcelona, 08221
Hospital Virgen de la Salud de Toledo
Toledo, 45004
Instituto Valenciano de Oncología
Valencia, 46009
Hospital Clínico Universitario de Valencia
Valencia, 46010
Hospital Universitari i Politecnic La Fè
Valencia, 46026
Hospital Universitario Miguel Servet
Zaragoza, 50009
About this study
Official title: An Ambispective Observational Registry Study of Pregnancy and Breast Cancer
An ambispective observational registry study of pregnancy and breast cancer
Read the detailed description
A multicenter, observational, non-post-marketing (non-PMS), ambispective (retrospective and prospective from the registry opening) study which will enroll patients with breast cancer in any of these three situations:
- Patients with gestational breast cancer, defined as breast cancer diagnosed during pregnancy, breastfeeding or up to a year after delivery.
- Patients who become pregnant after a breast cancer diagnosis.
- Patients with breast cancer who have followed any fertility preservation technique prior to the start of breast cancer treatment.
It is estimated a minimum recruitment period of approximately 3 years from the study activation. The study will remain open as long as possible in order to collect as much information as possible. GEICAM will actively search for funding for this.
Patients may also be concurrently enrolled in an interventional clinical trial. This observational registry study of pregnancy and breast cancer that collects significant data obtained from standard clinical practice, regarding the clinical characteristics of patients with breast cancer in any of the three situations described above. These data will allow the performance of both descriptive and exploratory analyses in order to evaluate the associations between different breast cancer subtypes and risk factors observed.
Finally, this study will collect high quality molecular data derived from the analysis of biological samples (paraffin-embedded tumor and peripheral blood samples) to reach a better understanding of the biological mechanisms involved in breast cancer in relation to pregnancy.
No treatment regimen will be protocol specified. This is an observational study in which clinical decisions concerning the optimum management strategy for a particular patient are taken independently of and/or prior to, any decision by the physician to invite a patient to participate in the study. The treating physician will make all treatment decisions according to his/her regular clinical practice independent of this study.
- Conditions
- Breast Cancer and Pregnancy
- Keywords
- Pregnancy, Gestational breast cancer, Fertility preservation technique, Breast Cancer
- Medical subject headings
- Breast Neoplasms
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of participants with breast cancer diagnosis during the gestation, breastfeeding, first year after the delivery (not during breastfeeding period), after a pregnancy and followed by any fertility preservation method before the anticancer treatment
Data for this study will be recorded into the electronic case report form (eCRF) via web using Remote Data Capture (RDC) from Oracle Clinical®. Once patient has signed the ICF or verified that the data of deceased patients can be included, designated site personnel will complete the register of each patient in the eCRF, where an identification number will automatically be assigned.
Data will be recorded in the eCRF at the time of patient enrollment and approximately every year.
Measured: Baseline visit
Race of participants with breast cancer diagnosis during the gestation, breastfeeding, first year after the delivery (not during breastfeeding period), after a pregnancy and followed by any fertility preservation method before the anticancer treatment
Data for this study will be recorded into the eCRF via web using RDC (Remote Data Capture) from Oracle Clinical®. Once patient has signed the ICF or verified that the data of deceased patients can be included, designated site personnel will complete the register of each patient in the eCRF, where an identification number will automatically be assigned.
Data will be recorded in the eCRF at the time of patient enrollment and approximately every year.
Measured: Baseline visit
Age of participants with breast cancer diagnosis during the gestation, breastfeeding, first year after the delivery (not during breastfeeding period), after a pregnancy and followed by any fertility preservation method before the anticancer treatment
Data for this study will be recorded into the eCRF via web using RDC (Remote Data Capture) from Oracle Clinical®. Once patient has signed the ICF or verified that the data of deceased patients can be included, designated site personnel will complete the register of each patient in the eCRF, where an identification number will automatically be assigned.
Data will be recorded in the eCRF at the time of patient enrollment and approximately every year.
Measured: Baseline visit
Secondary outcomes (19)
Clinicopathological characteristics of cancer: Tumor size
Assess the clinicopathological characteristics of cancer in the patients enrolled in the study. For this, it is used the Tumor, Node, Metastasis (TNM) staging system is the most common way that doctors stage breast cancer. Patient scans and tests give some information about the stage of the cancer.
Tumor (T) size describes the size of the tumour. Larger T is associated with inferior survival.
Tumor cannot be assessed (TX): can't be assessed. Tis: ductal carcinoma in situ. T1: tumour is 2 centimetres (cm) across or less. T1mi: tumour is 0.1cm across or less T1a: tumour >0.1 cm but <0.5 cm T1b: tumour >0.5 cm but <1 cm T1c: tumour >1 cm but <2 cm T2: tumour >2 cm but <5 cm across. T3: tumour >5 cm across. T4a: tumour has spread into the chest wall T4b: tumour has spread into the skin and the breast might be swollen T4c: tumour has spread to both the skin and the chest wall T4d: inflammatory carcinoma
Measured: 3 years
Clinicopathological characteristics of cancer: lymph node condition
Assess the clinicopathological characteristics of cancer in the patients enrolled in the study. For this, it is used the Tumor, Node, Metastasis (TNM) staging system is the most common way that doctors stage breast cancer. Patient scans and tests give some information about the stage of the cancer.
Lymph Node (N) conditions describes whether the cancer has spread to the Lymph Nodes (LN). Prognosis is better when cancer has not spread to the LN. The more LN that contain cancer, the poorer prognosis tends to be.
Node cannot be assessed (NX): LN can't be assessed N0: no Cancer Cells (CC) N1: CC in the LN in the armpit but the nodes are not stuck to surrounding tissues.
N2a: CC in the LN in the armpit, which are stuck to each other and to other structures.
N2b: CC in the LN behind the breast bone. N3a: CC in LN below the collarbone. N3b: CC in LN in the armpit and behind the breastbone. N3c: CC in LN above the collarbone.
Measured: 3 years
Clinicopathological characteristics of cancer: metastasis presence
Assess the clinicopathological characteristics of cancer in the patients enrolled in the study. For this, it is used the Tumor, Node, Metastasis (TNM) staging system is the most common way that doctors stage breast cancer. Patient scans and tests give some information about the stage of the cancer.
Metastasis (M) describes whether the cancer has spread to a different part of the body.
M0 means that there is no sign that the cancer has spread. cMo(i+) means there is no sign of the cancer on physical examination, scans or x-rays. But cancer cells are present in blood, bone marrow, or lymph nodes far away from the breast cancer - the cells are found by laboratory tests M1 means the cancer has spread to another part of the body.
Measured: 3 years
Clinicopathological characteristics of cancer: histopathological differentiation degree
Cancer cells are given a Grade (G) when they are removed from the breast and checked under a microscope. The G is based on how much the cancer cells look like normal cells.
G1 or well differentiated (score 3, 4, or 5): cells are slower-growing, and look more like normal breast tissue.
G2 or moderately differentiated (score 6, 7): cells are growing at a speed of and look like cells somewhere between G1 and 3.
G3 or poorly differentiated (score 8, 9): cells look very different from normal and will probably grow and spread faster.
The histopathological differentiation is analyzed on tumor samples. The collection of a sample of the primary archival tumor and/or a sample of metastatic lesions will be requested, when available.
Measured: 3 years
Clinicopathological characteristics of cancer: hormonal receptor status
Receptors (R) are proteins in or on cells that can attach to certain substances in the blood. Normal breast cells and some breast cancer cells have R that attach to the hormones estrogen and progesterone, and depend on these hormones to grow.
Breast cancer cells may have one, both, or none of these R:
- Estrogen Receptors (ER) -positive: are called ER-positive (or ER+) cancers.
- Progesterone Receptors (PR) -positive: are called PR-positive (or PR+) cancers.
- Hormone receptor (HR) -positive: If the cancer cell has one or both of the R above, the term hormone-receptive positive (also called hormone-positive or HR+) breast cancer may be used.
- HR-negative: If the cancer cell has neither the ER nor the PR, it's called hormone-receptor negative (also called hormone-negative or HR-).
The hormonal R status is analyzed on tumor samples. The collection of a sample of the primary archival tumor and/or a sample of metastatic lesions will be requested, when available.
Measured: 3 years
Clinicopathological characteristics of cancer: human epidermal growth factor receptor 2 (HER2) condition
HER2 is a growth-promoting protein on the outside of all breast cells. Cells with higher than normal levels of HER2 are called HER2+. These cancers tend to grow and spread faster than other breast cancers, but are much more likely to respond to treatment with drugs that target the HER2 protein.
A biopsy or surgery sample of the cancer is tested with either immunohistochemical stains (IHC) or Fluorescent in situ hybridization (FISH).
- IHC result 0 or 1+: cancer is considered HER2-negative. These cancers do not respond to treatment with drugs that target HER2.
- IHC result is 3+: the cancer is HER2-positive. These cancers are usually treated with drugs that target HER2.
- IHC result is 2+: HER2 status of the tumor is not clear and is called "equivocal." HER2 status needs to be tested with FISH to clarify the result.
HER2 is analyzed on tumor samples. The collection of a sample of the primary archival tumor and/or a sample of metastatic lesions will be requested, when available.
Measured: 3 years
Clinicopathological characteristics of cancer: Ki67 proliferation index
Ki-67 is a protein in cells that increases as they prepare to divide into new cells. A staining process can measure the percentage of tumor cells that are positive for Ki-67. The more positive cells there are, the more quickly they are dividing and forming new cells. In breast cancer, a result of less than 10% is considered low, 10-20% borderline, and high if more than 20%.
Ki-67 is analyzed on tumor samples. The collection of a sample of the primary archival tumor and/or a sample of metastatic lesions will be requested, when available.
Measured: 3 years
Clinicopathological characteristics of cancer: BRCA1 and 2 mutations
BRCA1 and BRCA2 are human genes that produce tumor suppressor proteins. These proteins help repair damaged DNA and, therefore, play a role in ensuring the stability of each cell's genetic material. When either of these genes is mutated, or altered, such that its protein product is not made or does not function correctly, DNA damage may not be repaired properly. As a result, cells are more likely to develop additional genetic alterations that can lead to cancer.
People who have inherited mutations in BRCA1 and BRCA2 tend to develop breast and ovarian cancers at younger ages than people who do not have these mutations.
BRCA1 and 2 mutations are analyzed on whole blood samples, that are preferably collected at the enrolment visit (after signing the informed consent).
Measured: 3 years
Disease-free survival (DFS) of pregnant women with breast cancer, pregnant patients after breast cancer and patients who have undergone techniques for the preservation of fertility.
Disease-free survival (DFS): It is defined as the time from date of initial breast cancer surgery to the date of the first documented relapse event (local, regional and/or distant) of the disease, second breast or non-breast primary tumor, or death due to any cause, whichever occurs first. In the event that none of the previous events were observed, censoring the last contact date will be considered.
Measured: 3 years
Event-free survival (EFS) of pregnant women with breast cancer, pregnant patients after breast cancer and patients who have undergone techniques for the preservation of fertility.
Event-free survival (EFS): It is defined as the time from date of breast cancer diagnosis to the date of the first documented event of disease progression which excludes the potentially curative surgery, relapse (local, regional and/or distant) of the disease after the curative surgery, second breast or non-breast primary tumor, or death due to any cause, whichever occurs first. In the event that none of the previous events were observed, censoring the last contact date will be considered.
Measured: 3 years
Progression-free survival (PFS) of pregnant women with breast cancer, pregnant patients after breast cancer and patients who have undergone techniques for the preservation of fertility.
Progression-free survival (PFS): It is defined as the time from the start date of a specific treatment to the documentation of disease progression on such treatment, or death due to any cause, whichever occurs first. In the event that none of the previous events were observed, censoring the last contact date will be considered.
Measured: 3 years
Overall survival (OS) of pregnant women with breast cancer, pregnant patients after breast cancer and patients who have undergone techniques for the preservation of fertility.
Overall survival (OS): It is defined as the time from date of initial breast cancer diagnosis to the date of death due to any cause.
Measured: 3 years
Correlation of the molecular profiles identified with the patients' clinicopathological and epidemiological characteristics and their disease evolution.
Measured: 3 years
Association between gestational breast cancer and a specific genotype or gene expression profile.
Measured: 3 years
Number of patients with breast cancer managed to get pregnant, spontaneously or through in vitro fertilization (IVF) methods
Number of patients with breast cancer managed to get pregnant, spontaneously or through in vitro fertilization (IVF) methods, considering both the patients with early disease and the patients with advanced disease.
Measured: 3 years
Number of patients with breast cancer that have followed fertility preservation techniques and what type of techniques were used.
Measured: 3 years
Enumerate the potential risks of fertility preservation techniques in women with breast cancer.
Measured: 3 years
Pregnancy outcome from women diagnosed with gestational breast cancer or women with breast cancer diagnosis who became pregnant.
Measured: 3 years
Progress of the babies born from women diagnosed with gestational breast cancer or women with breast cancer diagnosis who became pregnant.
Regarding the live-born children, serious diseases and age until the progression is known.
Measured: 3 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Oct 2020
- Study start18 Nov 2019
- Primary completionJan 2030 (estimated)
- Study completionJan 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Breast Cancer and PregnancyStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case only
- Time perspective
- Other
- Enrolment
- 866 participants (actual)
Sponsor and investigators
- Lead sponsor
- Spanish Breast Cancer Research Group
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Study Director, Study director, Instituto Valenciano de Oncología, Valencia, EspañaStudy Director, Study director, Hospital Universitario Reina Sofía de Córdoba, Córdoba, EspañaStudy Director, Study director, Hospital Clínico Universitario de Valencia, Valencia, EspañaStudy Director, Study director, Centro Nacional de Epidemiología. Instituto de Salud Carlos III, Madrid, España
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04603820
- Sponsor's protocol ID
- GEICAM/2017-07
- Acronym
- EMBARCAM
- Status last verified
- Dec 2025
- First submitted
- 10 Jun 2020
- Last updated
- 18 Dec 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 18 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- An Ambispective Observational Registry Study of Pregnancy and Breast Cancer
- ClinicalTrials.gov ID
- NCT04603820
- Acronym / sponsor ID
- EMBARCAM / GEICAM/2017-07
- Conditions
- Breast Cancer and Pregnancy
- Keywords
- Pregnancy, Gestational breast cancer, Fertility preservation technique, Breast Cancer
- Study type
- Observational
- Recruitment status
- Active, not recruiting
- Enrolment
- 866 participants (actual)
- Lead sponsor
- Spanish Breast Cancer Research GroupUniversity, hospital or other
- Study start
- 18 Nov 2019 (actual)
- Primary completion
- Jan 2030 (estimated)
- Study completion
- Jan 2030 (estimated)
- First posted
- 27 Oct 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
An ambispective observational registry study of pregnancy and breast cancer
Detailed description
A multicenter, observational, non-post-marketing (non-PMS), ambispective (retrospective and prospective from the registry opening) study which will enroll patients with breast cancer in any of these three situations:
- Patients with gestational breast cancer, defined as breast cancer diagnosed during pregnancy, breastfeeding or up to a year after delivery.
- Patients who become pregnant after a breast cancer diagnosis.
- Patients with breast cancer who have followed any fertility preservation technique prior to the start of breast cancer treatment.
It is estimated a minimum recruitment period of approximately 3 years from the study activation. The study will remain open as long as possible in order to collect as much information as possible. GEICAM will actively search for funding for this.
Patients may also be concurrently enrolled in an interventional clinical trial. This observational registry study of pregnancy and breast cancer that collects significant data obtained from standard clinical practice, regarding the clinical characteristics of patients with breast cancer in any of the three situations described above. These data will allow the performance of both descriptive and exploratory analyses in order to evaluate the associations between different breast cancer subtypes and risk factors observed.
Finally, this study will collect high quality molecular data derived from the analysis of biological samples (paraffin-embedded tumor and peripheral blood samples) to reach a better understanding of the biological mechanisms involved in breast cancer in relation to pregnancy.
No treatment regimen will be protocol specified. This is an observational study in which clinical decisions concerning the optimum management strategy for a particular patient are taken independently of and/or prior to, any decision by the physician to invite a patient to participate in the study. The treating physician will make all treatment decisions according to his/her regular clinical practice independent of this study.
Study design
- Observational model
- Case only
- Time perspective
- Other
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients with breast cancer in any of these three situations: 1. Patients with gestational breast cancer, defined as breast cancer diagnosed during pregnancy, breastfeeding or up to a year after delivery. 2. Patients who become pregnant after a breast cancer diagnosis. 3. Patients with breast cancer who have followed any fertility preservation technique prior to the start of breast cancer treatment.
Key inclusion criteria (9 listed)
- The patient should have signed and dated the informed consent form (ICF). The enrollment of patients who have died is allowed.
- Women aged ≥ 18 years.
- Patients in one of the following situations:
- The patients referred to in the previous section and the patients who meet these characteristics prospectively could be enrolled retrospectively upon registry opening.
- All cases diagnosed at the same site may be included. In order to prevent duplications, in case the patient followed her treatment and follow-up at another site, she will be enrolled as per the site where the diagnosis was made, requesting information of the treatment and progression, when possible.
Key exclusion criteria (1 listed)
- Patients who do not wish to participate in the study for any reason could not be included in the study.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Number of participants with breast cancer diagnosis during the gestation, breastfeeding, first year after the delivery (not during breastfeeding period), after a pregnancy and followed by any fertility preservation method before the anticancer treatment
Time frame: Baseline visit
Data for this study will be recorded into the electronic case report form (eCRF) via web using Remote Data Capture (RDC) from Oracle Clinical®. Once patient has signed the ICF or verified that the data of deceased patients can be included, designated site personnel will complete the register of each patient in the eCRF, where an identification number will automatically be assigned. Data will be recorded in the eCRF at the time of patient enrollment and approximately every year.
Race of participants with breast cancer diagnosis during the gestation, breastfeeding, first year after the delivery (not during breastfeeding period), after a pregnancy and followed by any fertility preservation method before the anticancer treatment
Time frame: Baseline visit
Data for this study will be recorded into the eCRF via web using RDC (Remote Data Capture) from Oracle Clinical®. Once patient has signed the ICF or verified that the data of deceased patients can be included, designated site personnel will complete the register of each patient in the eCRF, where an identification number will automatically be assigned. Data will be recorded in the eCRF at the time of patient enrollment and approximately every year.
Age of participants with breast cancer diagnosis during the gestation, breastfeeding, first year after the delivery (not during breastfeeding period), after a pregnancy and followed by any fertility preservation method before the anticancer treatment
Time frame: Baseline visit
Data for this study will be recorded into the eCRF via web using RDC (Remote Data Capture) from Oracle Clinical®. Once patient has signed the ICF or verified that the data of deceased patients can be included, designated site personnel will complete the register of each patient in the eCRF, where an identification number will automatically be assigned. Data will be recorded in the eCRF at the time of patient enrollment and approximately every year.
19 secondary outcomes
Clinicopathological characteristics of cancer: Tumor size
Time frame: 3 years
Clinicopathological characteristics of cancer: lymph node condition
Time frame: 3 years
Clinicopathological characteristics of cancer: metastasis presence
Time frame: 3 years
Clinicopathological characteristics of cancer: histopathological differentiation degree
Time frame: 3 years
Clinicopathological characteristics of cancer: hormonal receptor status
Time frame: 3 years
Clinicopathological characteristics of cancer: human epidermal growth factor receptor 2 (HER2) condition
Time frame: 3 years
Clinicopathological characteristics of cancer: Ki67 proliferation index
Time frame: 3 years
Clinicopathological characteristics of cancer: BRCA1 and 2 mutations
Time frame: 3 years
Disease-free survival (DFS) of pregnant women with breast cancer, pregnant patients after breast cancer and patients who have undergone techniques for the preservation of fertility.
Time frame: 3 years
Event-free survival (EFS) of pregnant women with breast cancer, pregnant patients after breast cancer and patients who have undergone techniques for the preservation of fertility.
Time frame: 3 years
Progression-free survival (PFS) of pregnant women with breast cancer, pregnant patients after breast cancer and patients who have undergone techniques for the preservation of fertility.
Time frame: 3 years
Overall survival (OS) of pregnant women with breast cancer, pregnant patients after breast cancer and patients who have undergone techniques for the preservation of fertility.
Time frame: 3 years
Correlation of the molecular profiles identified with the patients' clinicopathological and epidemiological characteristics and their disease evolution.
Time frame: 3 years
Association between gestational breast cancer and a specific genotype or gene expression profile.
Time frame: 3 years
Number of patients with breast cancer managed to get pregnant, spontaneously or through in vitro fertilization (IVF) methods
Time frame: 3 years
Number of patients with breast cancer that have followed fertility preservation techniques and what type of techniques were used.
Time frame: 3 years
Enumerate the potential risks of fertility preservation techniques in women with breast cancer.
Time frame: 3 years
Pregnancy outcome from women diagnosed with gestational breast cancer or women with breast cancer diagnosis who became pregnant.
Time frame: 3 years
Progress of the babies born from women diagnosed with gestational breast cancer or women with breast cancer diagnosis who became pregnant.
Time frame: 3 years
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Dec 2025.
- Spanish Breast Cancer Research Group (GEICAM) is a Spanish Breast Cancer Research GroupLink provided by the sponsor.
Related trials for Breast Cancer and Pregnancy
Recruiting
The Vanguard Study: Testing a New Way to Screen for Cancer
Bladder Carcinoma, Breast Carcinoma
Active, not recruitingPhase 1
A Phase 1 Study of XL309 (ISM3091) Alone and in Combination in Participants With Advanced Solid Tumors
Advanced Solid Tumor
RecruitingPhase 1
A Phase I Study of CG-7321 Monotherapy or Combination Therapy in Advanced Solid Tumors
Advanced Solid Tumors, Breast Cancer
RecruitingPhase 2
Immunotherapy Using Tumor Infiltrating Lymphocytes for Patients With Metastatic Cancer
Metastatic Colorectal Cancer, Metastatic Pancreatic Cancer
RecruitingPhase 1
A Study With NKT3964 for Adults With Advanced/Metastatic Solid Tumors
Solid Tumor, Advanced Solid Tumor
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Study Director study director
Instituto Valenciano de Oncología, Valencia, España
Study Director study director
Hospital Universitario Reina Sofía de Córdoba, Córdoba, España
Study Director study director
Hospital Clínico Universitario de Valencia, Valencia, España
28 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Breast Cancer and Pregnancy, run by Spanish Breast Cancer Research Group at 28 sites in Spain.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 9 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 18 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 28 sites in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of participants with breast cancer diagnosis during the gestation, breastfeeding, first year after the delivery (not during breastfeeding period), after a pregnancy and followed by any fertility preservation method before the anticancer treatment (time frame: Baseline visit). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Dec 2025.