Lymphoma, HodgkinLinf-inositolNCT05410314
Nutritional Supplement Based on Myo-inositol-D-chiro-inositoln in Long-term Survivors of Lymphoma
An observational study of Lymphoma, Hodgkin and Menstrual Irregularity, run by University of Bari Aldo Moro at 1 site in Italy.
Trial summary
The progressive improvement of lymphoma treatment has led to an important prolongation of patient survival and life expectancy. Therefore, the principal International scientific societies of oncology, recommend Long-term Survivors of Lymphoma to join fertility programs. Read more about this study
- Who is it for?
- Ages 25 to 44 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Lymphoma, Hodgkin, Menstrual Irregularity, Fertility Disorders
- What is being tested?
- Myo-Inositol and D-Chiro-Inositol (MIC)
- Type of treatment
- Pill or oral medicine
- How many people
- 90 participants
- Where
- 1 siteItaly
- Study dates
- 7 Feb 2020to 7 Dec 2021
- Phase
- Observational
- Are there results?
- None posted in the registry
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 25 to 44 years
- Women only
- Healthy volunteers accepted
- Adult
Study population: From January 2020 to January 2021, 90 Long-term Survivors of Lymphoma female patients, average age 34 years (range 25-44) were considered eligible for the study. Each patient was informed about the procedures and signed informed consent before the surgery to allow data collection for research purposes.
Who may be able to join
- Patients with Classical Hodgkin lymphoma (cHL) and Diffuse Large B-cell lymphoma (DLBCL) long survival
Who cannot join
None listed.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Nutritional Supplement Based on Myo-inositol-D-chiro-inositol: Effectiveness on the Reproductive System Functionality in Long-term Survivors of Lymphoma
The progressive improvement of lymphoma treatment has led to an important prolongation of patient survival and life expectancy. Therefore, the principal International scientific societies of oncology, recommend Long-term Survivors of Lymphoma to join fertility programs. Specifically, fertile age patients should be assisted by a multi-disciplinary team including specialists dedicated to fertility preservation in oncology, in order to support the completion of the reproductive project. In general population, the use of Inositol was spready considered an effectives choice to contrast ovarian dysfunction with consequently improvement of reproductive outcomes, so it may represent an adjuvant strategy for this purpose. Therefore, the investigators conducted a pilot study to evaluate the potentialities of this nutritional supplement with the aim to optimize the reproductive function in Long-term Survivors of Lymphoma. Despite the limited number of cases and short observational time, this pilot investigation could represent a potential cornerstone for further insights, discussions, and applications
Read the detailed description
Anticancer regimens are usually used to treat patients with lymphoproliferative neoplasms with a consequently transitory or permanent damage to their reproductive functionalities. Rates of gonadotoxicity of each chemotherapy could be modulated according to dose intensity, number of courses, and type of agent or combination. Classical Hodgkin lymphoma (cHL) and Diffuse Large B-cell lymphoma (DLBCL), including primary mediastinal Large B-cell Lymphoma (PMBL) have usually higher incidence in the 2nd or 3rd decade of life and presents cure rates of more than 75% 3,4 These histotypes need a poli-chemotherapy with ABVD (adriamycin, bleomycin, vinblastine, dacarbazine), which involves the association of alkylating and non-alkylating agents.
The autologous hemato-poietic stem cell transplant (ASCT) is needed in about the 10% of cHL and the 40% of DLBCL and has higher impact on fertility compared to ABVD 6. Therefore, both the chemotherapy (damaging the primordial follicle pool and then the ovarian reserve, OR) and the radiotherapy (exclusively secondary to under diaphragmatic and pelvic irradiation) could represent a risk of gonadotoxicity . In this scenario, data concerning fertility in cHL have been mainly evaluated by the German Hodgkin Study Group (GHSG) and the European Organization for Research and Treatment of Cancer (EORTC) through amenorrhea and anti-Mullerian hormone (AMH) evaluation. Indeed, amenorrhea has been used in numerous research to assess the gonadotoxicity of oncological treatment and reflect ovarian function . Furthermore, AMH could represent a gonadotoxicity marker, since it decreases during chemotherapy and could improve after the end of treatment, depending upon specific treatment schemes . Literature showed that after early-stage disease treatment (2 -4 cycle), more than 90% of patients reported a low gonadotoxic effect with a regular menstrual cycle after therapy (median recovery of 1 year). For advanced stage diseases (treated with 6 courses of ABVD) the gonadotoxic effect vary on base of patient's aged. Indeed, the complete AMH restoring during the 3-years follow-up period, was detected in all women under 35 years, and only 37% of older ones . Moreover, in a Cochrane meta-analysis, gonadotropin-releasing hormone agonist (GnRHa)seems to be effective in shielding the ovaries during chemotherapy, in terms of treatment-related premature ovarian failure, ovulation and menstruation recovery.
Beyond the ovarian suppression with GnRHa, there are several well-established procedures (oocyte cryopreservation, ovarian cortex cryopreservation for woman and sperm cryopreservation for men) that could prevent impact of these therapies in young patients. Therefore, considering the increased life expectation nowadays of Long-term Survivors of Lymphoma (patients in complete remission of the disease for more than 5 years) a fertility program with multi-disciplinary counselling is indicated. Particularly, in order to assess the damages upcoming after anticancer therapies on reproductive organs, international scientific societies such as the American Society for Reproductive Medicine (ASRM) (Ethics Committee of American Society for Reproductive Medicine, 2013), the American Society of Clinical Oncology (ASCO), the European Society for Medical Oncology (ESMO) as well as the International Society for Fertility Preservation (ISFP), strongly recommend a personalized and multidisciplinary counseling for each patient. In particular, the surveillance programs for the management of long-term lymphoma survivors should involve a team with onco-hematologists, radiotherapists, cardiologists, an endocrinologist, a psychologist, gynecologist, urologist and a nutritional biologist. The goal is to provide individualized therapeutic possibilities to restore endocrine function. Following these recommendations, an ambulatorial service dedicated to fertile patients with oncological disease was instituted in our Clinic of Gynecology Oncology, aiming to perform a careful assessment of the fertility state and support the reproductive project of those patients.
In these women,the investigators primarily estimated AMH, Follicle stimulating hormone (FSH), Luteinizing hormones (LH), 17β-estradiol ,in association to antral follicles count (AFC) assessed by ultrasonography during the cycle follicular phase. During this clinical evaluation, several patients often reported menstrual irregularities due to anovulatory cycles (50%), dysmenorrhea (20%) and abnormal uterine bleeding (30%).
Considering these elements, one of the potential therapeutic options could be considered the oral supplementation with Myo-Inositol and D-Chiro-Inositol (MIC). Indeed, MIC over the years has tiptoed to come alongside the classic pharmacological therapies, with robust compliance, safety, and effectiveness. MIC showed great potentiality to contrast ovarian dysfunction and optimize the reproductive function.
Therefore, the investigators conducted a prospective observational controlled study, with the aim to assess the effects of oral supplementation with MIC on ovarian function parameters in Long-term Survivors of Lymphoma.
- Being tested
- Myo-Inositol and D-Chiro-Inositol (MIC)
- Medical subject headings
- Hodgkin Disease, Menstruation Disturbances
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Myo-Inositol and D-Chiro-Inositol (MIC)Drug
Both groups were followed up for 12 months, in T0 (during first evaluation), and T12 (after twelve months) with blood test for AMH (ng/ml).
| Study group | Role | What they receive |
|---|---|---|
| cHL (85%) and DLBCL (15%) | Patients enrolled in this study are cHL (85%) and DLBCL (15%) long-term survivors, treated mainly with ABVD+ radiotherapy (not under diaphragmatic and pelvic irradiation), without relapse (during quinquennial follow-up) who are followed at the clinic dedicated to fertility in oncology of our Department, which is a regional referral center for this purpose. Therefore, the investigators conducted a prospective observational controlled study on two groups: the first one (A group) underwent oral supplementation with MIC for 12 months; the second group (B group) underwent follow-up without any nutritional supplement for 12 months Receives: Drug: Myo-Inositol and D-Chiro-Inositol (MIC) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of Lymphoma long-term survivors treated with myo-inositol-D-chiro-inositol: evaluation of the results on the reproduction apparatus
The investigatirs conducted a prospective observational controlled study on two groups: the first one (A group) underwent oral supplementation with myo-inositol-D-chiro-inositol for 12 months; the second group (B group) underwent follow-up without any nutritional supplement for 12 months.Moreover, the investigators reported for each patient the menstrual frequency ( oligomenorrhea <25 days , normal flow 25-36 days , polymenorrhea >36 days), the duration of the cycle (short < 3 days, normal: 3-7 days , long >7 days), the amount of the menstrual cycle (poor <30 ml, normal 30-80 ml, >80 ml abundant) and dysmenorrhea and dyspareunia (visual analogue scale VAS pain scale = 1 -10).In addition, results of blood tests and clinical data about menstrual regularity and dysmenorrhea, were reported on the same database.In addition, results of blood tests and clinical data about menstrual regularity and dysmenorrhea, were reported on the same database.
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Jun 2022
- Study start7 Feb 2020
- Primary completion7 Feb 2021
- Study completion7 Dec 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Lymphoma, HodgkinStudies 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-control
- Time perspective
- Other
- Enrolment
- 90 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Bari Aldo Moro
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, MIRIAM DELLINO, University of Bari Aldo Moro
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05410314
- Sponsor's protocol ID
- UNIBA
- Acronym
- Linf-inositol
- Status last verified
- May 2022
- First submitted
- 29 May 2022
- Last updated
- 8 Jun 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: From January 2020 to January 2021, 90 Long-term Survivors of Lymphoma female patients, average age 34 years (range 25-44) were considered eligible for the study.
Study at a glance
From the registry record, last updated by the sponsor on 8 Jun 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Nutritional Supplement Based on Myo-inositol-D-chiro-inositol: Effectiveness on the Reproductive System Functionality in Long-term Survivors of Lymphoma
- ClinicalTrials.gov ID
- NCT05410314
- Acronym / sponsor ID
- Linf-inositol / UNIBA
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 90 participants (actual)
- Lead sponsor
- University of Bari Aldo MoroUniversity, hospital or other
- Study start
- 7 Feb 2020 (actual)
- Primary completion
- 7 Feb 2021 (actual)
- Study completion
- 7 Dec 2021 (actual)
- First posted
- 8 Jun 2022 (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.
The progressive improvement of lymphoma treatment has led to an important prolongation of patient survival and life expectancy. Therefore, the principal International scientific societies of oncology, recommend Long-term Survivors of Lymphoma to join fertility programs. Specifically, fertile age patients should be assisted by a multi-disciplinary team including specialists dedicated to fertility preservation in oncology, in order to support the completion of the reproductive project. In general population, the use of Inositol was spready considered an effectives choice to contrast ovarian dysfunction with consequently improvement of reproductive outcomes, so it may represent an adjuvant strategy for this purpose. Therefore, the investigators conducted a pilot study to evaluate the potentialities of this nutritional supplement with the aim to optimize the reproductive function in Long-term Survivors of Lymphoma. Despite the limited number of cases and short observational time, this pilot investigation could represent a potential cornerstone for further insights, discussions, and applications
Detailed description
Anticancer regimens are usually used to treat patients with lymphoproliferative neoplasms with a consequently transitory or permanent damage to their reproductive functionalities. Rates of gonadotoxicity of each chemotherapy could be modulated according to dose intensity, number of courses, and type of agent or combination. Classical Hodgkin lymphoma (cHL) and Diffuse Large B-cell lymphoma (DLBCL), including primary mediastinal Large B-cell Lymphoma (PMBL) have usually higher incidence in the 2nd or 3rd decade of life and presents cure rates of more than 75% 3,4 These histotypes need a poli-chemotherapy with ABVD (adriamycin, bleomycin, vinblastine, dacarbazine), which involves the association of alkylating and non-alkylating agents.
The autologous hemato-poietic stem cell transplant (ASCT) is needed in about the 10% of cHL and the 40% of DLBCL and has higher impact on fertility compared to ABVD 6. Therefore, both the chemotherapy (damaging the primordial follicle pool and then the ovarian reserve, OR) and the radiotherapy (exclusively secondary to under diaphragmatic and pelvic irradiation) could represent a risk of gonadotoxicity . In this scenario, data concerning fertility in cHL have been mainly evaluated by the German Hodgkin Study Group (GHSG) and the European Organization for Research and Treatment of Cancer (EORTC) through amenorrhea and anti-Mullerian hormone (AMH) evaluation. Indeed, amenorrhea has been used in numerous research to assess the gonadotoxicity of oncological treatment and reflect ovarian function . Furthermore, AMH could represent a gonadotoxicity marker, since it decreases during chemotherapy and could improve after the end of treatment, depending upon specific treatment schemes . Literature showed that after early-stage disease treatment (2 -4 cycle), more than 90% of patients reported a low gonadotoxic effect with a regular menstrual cycle after therapy (median recovery of 1 year). For advanced stage diseases (treated with 6 courses of ABVD) the gonadotoxic effect vary on base of patient's aged. Indeed, the complete AMH restoring during the 3-years follow-up period, was detected in all women under 35 years, and only 37% of older ones . Moreover, in a Cochrane meta-analysis, gonadotropin-releasing hormone agonist (GnRHa)seems to be effective in shielding the ovaries during chemotherapy, in terms of treatment-related premature ovarian failure, ovulation and menstruation recovery.
Beyond the ovarian suppression with GnRHa, there are several well-established procedures (oocyte cryopreservation, ovarian cortex cryopreservation for woman and sperm cryopreservation for men) that could prevent impact of these therapies in young patients. Therefore, considering the increased life expectation nowadays of Long-term Survivors of Lymphoma (patients in complete remission of the disease for more than 5 years) a fertility program with multi-disciplinary counselling is indicated. Particularly, in order to assess the damages upcoming after anticancer therapies on reproductive organs, international scientific societies such as the American Society for Reproductive Medicine (ASRM) (Ethics Committee of American Society for Reproductive Medicine, 2013), the American Society of Clinical Oncology (ASCO), the European Society for Medical Oncology (ESMO) as well as the International Society for Fertility Preservation (ISFP), strongly recommend a personalized and multidisciplinary counseling for each patient. In particular, the surveillance programs for the management of long-term lymphoma survivors should involve a team with onco-hematologists, radiotherapists, cardiologists, an endocrinologist, a psychologist, gynecologist, urologist and a nutritional biologist. The goal is to provide individualized therapeutic possibilities to restore endocrine function. Following these recommendations, an ambulatorial service dedicated to fertile patients with oncological disease was instituted in our Clinic of Gynecology Oncology, aiming to perform a careful assessment of the fertility state and support the reproductive project of those patients.
In these women,the investigators primarily estimated AMH, Follicle stimulating hormone (FSH), Luteinizing hormones (LH), 17β-estradiol ,in association to antral follicles count (AFC) assessed by ultrasonography during the cycle follicular phase. During this clinical evaluation, several patients often reported menstrual irregularities due to anovulatory cycles (50%), dysmenorrhea (20%) and abnormal uterine bleeding (30%).
Considering these elements, one of the potential therapeutic options could be considered the oral supplementation with Myo-Inositol and D-Chiro-Inositol (MIC). Indeed, MIC over the years has tiptoed to come alongside the classic pharmacological therapies, with robust compliance, safety, and effectiveness. MIC showed great potentiality to contrast ovarian dysfunction and optimize the reproductive function.
Therefore, the investigators conducted a prospective observational controlled study, with the aim to assess the effects of oral supplementation with MIC on ovarian function parameters in Long-term Survivors of Lymphoma.
Study design
- Observational model
- Case-control
- Time perspective
- Other
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| cHL (85%) and DLBCL (15%) | – | Drug: Myo-Inositol and D-Chiro-Inositol (MIC)Patients enrolled in this study are cHL (85%) and DLBCL (15%) long-term survivors, treated mainly with ABVD+ radiotherapy (not under diaphragmatic and pelvic irradiation), without relapse (during quinquennial follow-up) who are followed at the clinic dedicated to fertility in oncology of our Department, which is a regional referral center for this purpose. Therefore, the investigators conducted a prospective observational controlled study on two groups: the first one (A group) underwent oral supplementation with MIC for 12 months; the second group (B group) underwent follow-up without any nutritional supplement for 12 months |
Who may qualify
- Ages
- 25 to 44 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
- Study population
- From January 2020 to January 2021, 90 Long-term Survivors of Lymphoma female patients, average age 34 years (range 25-44) were considered eligible for the study. Each patient was informed about the procedures and signed informed consent before the surgery to allow data collection for research purposes.
Key inclusion criteria (1 listed)
- Patients with Classical Hodgkin lymphoma (cHL) and Diffuse Large B-cell lymphoma (DLBCL) long survival
Key exclusion criteria (0 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Myo-Inositol and D-Chiro-Inositol (MIC)Both groups were followed up for 12 months, in T0 (during first evaluation), and T12 (after twelve months) with blood test for AMH (ng/ml). | Drug | cHL (85%) and DLBCL (15%) |
Primary outcome
Number of Lymphoma long-term survivors treated with myo-inositol-D-chiro-inositol: evaluation of the results on the reproduction apparatus
Time frame: 12 months
The investigatirs conducted a prospective observational controlled study on two groups: the first one (A group) underwent oral supplementation with myo-inositol-D-chiro-inositol for 12 months; the second group (B group) underwent follow-up without any nutritional supplement for 12 months.Moreover, the investigators reported for each patient the menstrual frequency ( oligomenorrhea <25 days , normal flow 25-36 days , polymenorrhea >36 days), the duration of the cycle (short < 3 days, normal: 3-7 days , long >7 days), the amount of the menstrual cycle (poor <30 ml, normal 30-80 ml, >80 ml abundant) and dysmenorrhea and dyspareunia (visual analogue scale VAS pain scale = 1 -10).In addition, results of blood tests and clinical data about menstrual regularity and dysmenorrhea, were reported on the same database.In addition, results of blood tests and clinical data about menstrual regularity and dysmenorrhea, were reported on the same database.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 Jun 2022.
- Individual participant dataSharing planned: No. From January 2020 to January 2021, 90 Long-term Survivors of Lymphoma female patients, average age 34 years (range 25-44) were considered eligible for the study.
Related trials for Lymphoma, Hodgkin
RecruitingPhase 2
Ibrutinib Combination Therapy in Transplant Ineligible Individuals With Newly Diagnosed Primary CNS Lymphoma
Non-hodgkin Lymphoma
RecruitingObservational study
Blood, Urine, and Tissue Collection for Cutaneous Lymphoma, Eczema, and Atopic Dermatitis Research
Cutaneous T-cell Lymphoma, Sezary Syndrome
Active, not recruitingPhase 2
Brentuximab Vedotin and Combination Chemotherapy in Treating Patients With CD30-Positive Peripheral T-cell Lymphoma
Adult T-Cell Leukemia/Lymphoma, Anaplastic Large Cell Lymphoma, ALK-Negative
Active, not recruitingPhase 1/2
Study of Oral MRT-2359 in Selected Cancer Patients
NSCLC, SCLC
Active, not recruitingObservational study
Multi-omics Profiling of Relapsed Extranodal Natural Killer (NK)/T-cell Lymphoma
Extranodal NK/T-cell Lymphoma, Nasal Type
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.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Lymphoma, Hodgkin and Menstrual Irregularity, run by University of Bari Aldo Moro at 1 site in Italy.
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 1 inclusion and 0 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: finished, as of the sponsor's last update on 8 Jun 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Italy. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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 Lymphoma long-term survivors treated with myo-inositol-D-chiro-inositol: evaluation of the results on the reproduction apparatus (time frame: 12 months). 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 8 Jun 2022.