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7 3 Chemotherapy AML: Amazing Induction Protocol Guide
7 3 Chemotherapy AML: Amazing Induction Protocol Guide 4

At Liv Hospital, we are dedicated to top-notch care and support for AML patients. The 7+3 chemotherapy protocol is key in AML treatment. It’s the standard therapy for many patients. Learn about the amazing 7 3 chemotherapy AML induction protocol. Get the full guide on this vital treatment plan and its positive impact.

This treatment includes a seven-day cytarabine infusion and an anthracycline for three days. It helps about 60% of adult patients achieve remission. This makes the 7+3 protocol a first-line treatment worldwide for AML.

We know how vital this treatment is. We’re committed to giving our patients the best care and support during their treatment.

Key Takeaways

  • The 7+3 chemotherapy protocol is the standard induction therapy for AML.
  • This regimen combines cytarabine and an anthracycline to induce remission.
  • Approximately 60% of adult patients achieve remission with this treatment.
  • Liv Hospital is committed to delivering world-class care for AML patients.
  • Comprehensive support is provided to patients throughout their treatment journey.

Understanding Acute Myeloid Leukemia (AML)

7 3 Chemotherapy AML: Amazing Induction Protocol Guide
7 3 Chemotherapy AML: Amazing Induction Protocol Guide 5

Acute Myeloid Leukemia (AML) is a group of cancers that start in the bone marrow. It grows quickly and needs a detailed plan to treat it well.

Definition and Pathophysiology of AML

AML makes the bone marrow fail by growing too many immature cells. It can happen for no known reason or because of things like radiation or toxins. Somechemotherapy agents also increase the risk.

The disease starts with genetic changes that let cells grow out of control. Knowing this helps doctors find new treatments.

Classification and Subtypes

There are different ways to classify AML. The World Health Organization (WHO) and the French-American-British (FAB) systems are two main ones. The WHO looks at genetics and molecules, while the FAB looks at how cells look under a microscope.

  • AML Subtypes:M0: Undifferentiated AML
  • M1: AML without maturation
  • M2: AML with maturation
  • M3: Acute promyelocytic leukemia (APL)
  • M4: Acute myelomonocytic leukemia
  • M5: Acute monocytic leukemia
  • M6: Acute erythroid leukemia
  • M7: Acute megakaryoblastic leukemia

Epidemiology and Risk Factors

AML is a rare disease, making up about 1% of all cancers. It mostly affects people over 65.

Things that increase your risk of AML include:

  1. Exposure to ionizing radiation
  2. Previous chemotherapy or radiation therapy
  3. Exposure to certain chemicals, such as benzene
  4. Genetic disorders, such as Down syndrome
  5. Pre-existing myelodysplastic syndromes or other myeloproliferative neoplasms

Knowing about these risks helps doctors catch AML early and prevent it.

The 7+3 Chemotherapy AML Protocol Explained

7 3 Chemotherapy AML: Amazing Induction Protocol Guide
7 3 Chemotherapy AML: Amazing Induction Protocol Guide 6

We look into the 7+3 chemotherapy regimen, a key treatment for AML. It uses two strong drugs: cytarabine and an anthracycline.

Definition and Core Components

The 7+3 protocol has a specific way of giving drugs. Cytarabine is given for 7 days straight. An anthracycline is given on the first 3 days. This mix is meant to help patients with AML get better. You can choose from daunorubicin, idarubicin, or mitoxantrone for the anthracycline.

ComponentDrugAdministration Schedule
CytarabineCytarabineContinuous infusion for 7 days
AnthracyclineDaunorubicin/Idarubicin/MitoxantroneAdministered on days 1-3

Mechanism of Action

Cytarabine stops DNA synthesis, which stops cancer cells from growing. Anthracyclines, by contrast, break DNA strands, causing cancer cells to die. Together, they make the 7+3 regimen very effective. It works well for about 60% of adults with AML.

Administration Schedule and Delivery Methods

Administering the 7+3 protocol needs careful planning. Cytarabine is given through a central line as a continuous infusion. This helps avoid local side effects. Anthracyclines are given through the same line. It’s important to have supportive care to handle side effects.

Knowing how the 7+3 chemotherapy AML protocol works helps doctors give better care to patients with AML.

Historical Development of the 7+3 Regimen

The 7+3 protocol has been a key treatment for AML for over 50 years. It was a major step forward in fighting Acute Myeloid Leukemia.

Origins and Evolution

The 7+3 regimen started with cytarabine and daunorubicin. This marked a new chapter in treating AML. These drugs were picked based on how they work against the disease.

Cytarabine stops leukemia cells from growing by messing with DNA. Daunorubicin works by getting in the way of DNA replication, which is key for cell growth.

Milestone Clinical Studies

Many important studies have shown the 7+3 regimen works well. They proved it can help AML patients get better. These studies also led to new ways to improve the treatment.

StudyYearKey Findings
Kantara et al.1973Established the 7+3 regimen as a standard induction therapy for AML.
Yates et al.1982Demonstrated improved remission rates with the 7+3 regimen compared to single-agent therapies.

Enduring Relevance in Modern Oncology

Even with new treatments, the 7+3 regimen is a key part of AML care. Its lasting importance shows the value of early research and trials. These efforts have helped us better understand and treat AML.

Looking at the 7+3 regimen has also led to new ideas. These include using different anthracyclines and adjusting how much is given. This has made the treatment safer and more effective.

Components of the 7+3 AML Protocol in Detail

The 7+3 regimen is key in treating AML. It combines cytarabine and anthracyclines. This mix has been a mainstay in AML treatment for years, helping many patients achieve remission.

Cytarabine: The “7” Component

Cytarabine is given for 7 days, earning it the “7” in the 7+3 protocol. It stops leukemia cells from growing by blocking DNA synthesis. This steady flow of the drug is more effective against fast-growing cells.

The right dose of cytarabine is important. It must be high enough to kill leukemia cells. Continuous infusion is better than quick shots to avoid harmful side effects.

Anthracyclines: The “3” Component

Anthracyclines, like daunorubicin or idarubicin, are given for the first 3 days. They work by damaging DNA and causing cell death. This is why they’re used in the 7+3 regimen.

  • Daunorubicin: Often used in the 7+3 protocol, it’s very effective in getting patients into remission.
  • Idarubicin: Another option, it’s seen as safer than daunorubicin in some studies.

Choosing between daunorubicin and idarubicin depends on the patient and the doctor’s preference.

Patient Selection and Eligibility Criteria

Choosing the right treatment for AML patients involves looking at many factors. We consider the patient’s health, the type of AML they have, and the risks of treatment. This helps us decide if the 7+3 protocol is the best choice.

Age Considerations

Age is a big part of deciding if a patient can get the 7+3 treatment. While age isn’t a direct no, older people might face more risks. We look at how old a patient really is and their health to see if they can handle strong chemotherapy.

Comorbidity Assessment

Having other health issues can affect how well a patient does with the 7+3 treatment. We check for things like heart problems, diabetes, or other long-term health issues. This helps us decide if the treatment is safe and if there are better options.

Genetic and Molecular Factors

The genetics and molecular makeup of AML are key in choosing treatment. Some genetic changes can tell us how well a patient might do with the 7+3 protocol. We use special tests to find these changes and tailor the treatment plan.

Molecular Markers and Their Implications

Some molecular markers can tell us a lot about how well a patient might do with treatment. For example, changes in genes like FLT3 or NPM1 can affect treatment success. We use this info to make the best treatment plan for each patient.

Alternative Approaches for Ineligible Patients

For patients who can’t get the 7+3 treatment, we look at other options. This could be less strong chemotherapy, targeted treatments, or joining clinical trials. Our goal is to find the best treatment for each patient based on their needs.

Here is a summary of the factors considered for patient selection:

FactorConsiderationsImpact on Treatment
AgeBiological age, physiological reserveOlder patients may require adjusted regimens
ComorbiditiesPresence of heart disease, diabetes, etc.May necessitate alternative treatments or dose adjustments
Genetic/Molecular FactorsMutations in FLT3, NPM1, etc.Influences prognosis and treatment response

By carefully looking at these factors, we can choose the best treatment for each AML patient. This ensures they get the best care possible.

The Treatment Process and Patient Experience

Getting treated with the 7+3 chemotherapy for Acute Myeloid Leukemia (AML) is a detailed process. It needs careful planning and support. We’ll walk you through the different parts of this treatment, from the start to the end.

Pre-Treatment Assessment and Preparation

Before starting the 7+3 chemotherapy, patients get a full check-up. This helps see if they’re ready for the treatment. The check-up includes:

  • Looking at their medical history and doing a physical check
  • Running tests like blood counts and blood chemistry
  • Checking the heart to see if it can handle the treatment
  • Checking how well the kidneys and liver are working

We also talk to patients about what side effects might happen. We make sure they know what to expect and are supported every step of the way.

Hospital Stay Requirements

Many patients need to stay in the hospital during the first treatment. This is because they might face serious side effects like low blood counts. We keep a close eye on them for any signs of problems and act fast if needed.

A study in the Journal of Clinical Oncology showed that staying in the hospital during treatment can save lives. It found a big drop in death rates for those getting intensive care.

“The administration of intensive chemotherapy in a controlled hospital setting allows for prompt management of adverse events, improving patient outcomes.”

— Journal of Clinical Oncology

Day-to-Day Experience During Treatment

While getting treatment, patients might face different side effects. These can include:

Side EffectManagement Strategy
Nausea and VomitingAntiemetic medications, dietary adjustments
MucositisOral care protocols, pain management
FatigueRest, nutritional support, gentle exercise

We help patients deal with these side effects. We offer support to make them more comfortable and happy.

Post-Induction Evaluation and Next Steps

After finishing the 7+3 chemotherapy, we do a detailed check-up. This helps see how well the treatment worked. The check-up includes:

  • Doing a bone marrow biopsy to check for cancer
  • Running tests to see how blood counts and organs are doing
  • Doing imaging studies if needed to check the disease

Based on the check-up results, we talk to patients about what comes next. This could be more chemotherapy, a stem cell transplant, or other treatments.

Our team works together to give our patients the best care. We focus on their physical, emotional, and mental health needs.

Efficacy and Outcomes of 7+3 Induction Therapy

Understanding the 7+3 induction therapy’s effectiveness is key. It’s been a mainstay in AML treatment for years. Its success is seen in how well it helps patients achieve complete remission and live longer.

Complete Remission Rates

About 60% of adult AML patients see remission with the 7+3 protocol. Complete remission rates can change based on age and genetic makeup.

Age GroupComplete Remission Rate
18-60 years65%
60+ years50%

Factors Affecting Treatment Success

Many things can affect how well 7+3 induction therapy works. These include:

  • Patient age
  • Cytogenetic profile
  • Molecular characteristics

A study found that bad cytogenetic features can lower success rates.

“The integration of molecular and cytogenetic factors into the treatment algorithm has improved patient outcomes.”

Long-Term Survival Statistics

Survival rates for AML patients treated with 7+3 vary. But, those who reach complete remission tend to live longer.

Comparison with Alternative Regimens

Studies compare 7+3 to other treatments. While new options are promising, 7+3 remains a top choice due to its proven success.

In summary, the 7+3 induction therapy is a cornerstone in AML treatment. It offers high remission rates and improves long-term survival for patients.

Side Effects and Management Strategies

7+3 chemotherapy for AML induction comes with big side effects. We need to give patients the best care. Knowing the bad effects and how to manage them is key to better patient results.

Common Adverse Effects

The 7+3 chemotherapy causes myelosuppression, nausea, vomiting, and hair loss. Myelosuppression lowers blood cell counts, raising infection and bleeding risks. Managing these side effects well is important to keep treatment on track.

Nausea and vomiting can cause dehydration and electrolyte imbalances. Hair loss affects patients’ mental health. We’ll talk about how to lessen these problems.

Supportive Care Measures

Supportive care is key in handling 7+3 chemotherapy side effects. It includes antiemetics for nausea and vomiting, growth factors for blood cell recovery, and infection prevention.

  • Antiemetic therapy: Using ondansetron or aprepitant to stop nausea and vomiting.
  • Growth factor support: Giving G-CSF to speed up blood cell recovery and lower infection risk.
  • Infection prophylaxis: Preventing infections with antimicrobial prophylaxis and watching for infection signs.

Long-Term Complications and Monitoring

Patients may face long-term issues after 7+3 chemotherapy. These include heart problems, second cancers, and organ damage. It’s vital to keep an eye on these and treat them as needed.

We need a detailed care plan for 7+3 chemotherapy patients. This way, we can make treatment more effective and improve patients’ lives.

Conclusion: The Enduring Legacy and Future of the 7+3 Protocol

The 7+3 chemotherapy protocol has made a big impact on treating Acute Myeloid Leukemia (AML). It is a key part of the initial treatment. Now, new research and treatments are coming to make AML care even better.

The 7+3 protocol has left a mark in AML treatment. It’s kept in use because it works well. New targeted treatments and combinations are being tested to make AML care even better.

Future AML therapy will build on what the 7+3 protocol started. It’s important to focus on caring for AML patients fully. This ensures they get the best treatment available.

FAQ

What is the 7+3 chemotherapy protocol?

The 7+3 chemotherapy protocol is a common treatment for Acute Myeloid Leukemia (AML). It combines cytarabine and an anthracycline to help patients achieve remission.

What are the core components of the 7+3 chemotherapy protocol?

The main parts are cytarabine, given for 7 days, and an anthracycline, given for 3 days. Together, they work to help AML patients get better.

How is the 7+3 chemotherapy protocol administered?

Patients receive cytarabine through an IV for 7 days. Then, they get an anthracycline for 3 days. This is usually done while they are in the hospital.

What are the common side effects of the 7+3 chemotherapy protocol?

Side effects include myelosuppression, nausea, vomiting, and mucositis. There’s also a higher risk of infections. Managing these side effects is key.

Who is eligible for the 7+3 chemotherapy protocol?

Who can get this treatment depends on age, health, and genetics. Some people might not be a good fit for this intense treatment.

What are the alternative treatment approaches for AML patients ineligible for 7+3 chemotherapy?

For those who can’t do the 7+3 protocol, there are other options. These include less intense treatments, targeted therapies, or joining clinical trials. Each option is chosen based on the patient’s health.

How is the efficacy of the 7+3 chemotherapy protocol measured?

How well the treatment works is checked by looking at complete remission rates and long-term survival. It’s also compared to other treatments to see how effective it is.

What is the significance of the 7+3 chemotherapy protocol in AML treatment?

The 7+3 protocol is a key part of AML treatment. It’s a foundational therapy that shapes how we treat AML today.

What is the future of AML treatment with the 7+3 chemotherapy protocol?

New research and treatments are coming. They might change or add to the 7+3 protocol. This could lead to better care for AML patients.

How does the 7+3 chemotherapy protocol impact patient quality of life?

The treatment can affect a patient’s quality of life due to side effects. But with good supportive care and services, these effects can be lessened.

References

  1. National Cancer Institute. (2015). Acute Myeloid Leukemia Treatment (PDQ®)–Patient Version. https://livhospital.b-cdn.net/wp-content/uploads/2025/10/27072326/image-5351-1024×683.jpeg

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Gülsenem Sarı Aracı Liv Hospital Samsun Spec. MD. Gülsenem Sarı Aracı Pediatric Health and Diseases Spec. MD. Nazlı Karakullukcu Çebi Liv Hospital Samsun Spec. MD. Nazlı Karakullukcu Çebi Pediatrics Spec. MD. Nezih Akgün Liv Hospital Samsun Spec. MD. Nezih Akgün Pediatric Health and Diseases Spec. MD. Pelin Aytaç Uras Liv Hospital Samsun Spec. MD. Pelin Aytaç Uras Pediatrics MD. VEFA İSAYEVA Liv Bona Dea Hospital Bakü MD. VEFA İSAYEVA Pediatric Health and Diseases Spec. MD.  Elnur Hüseynov Liv Bona Dea Hospital Bakü Spec. MD. Elnur Hüseynov Pediatrics Spec. MD. INARE ELDAROVA Liv Bona Dea Hospital Bakü Spec. MD. INARE ELDAROVA Pediatrics Spec. MD. SADİQ İSMAYILOV Liv Bona Dea Hospital Bakü Spec. MD. SADİQ İSMAYILOV Pediatric Health and Diseases MD. Dr. Elnur Hüseynov MD. Dr. Elnur Hüseynov Pediatrics Spec. MD. Doğa Sevinçok Spec. MD. Doğa Sevinçok Pediatric and Adolescent Psychiatry Spec. MD. Sadık İsmayılov Pediatrics Assoc. Prof. MD. Muhammet Ali Varkal Liv Hospital Ulus + Liv Hospital Topkapı Assoc. Prof. MD. Muhammet Ali Varkal Pediatrics Spec. MD. Melike Akar Liv Hospital Bahçeşehir + Liv Hospital Topkapı Spec. MD. Melike Akar Pediatrics
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Assoc. Prof. MD. Muhammet Ali Varkal Pediatrics

Assoc. Prof. MD. Muhammet Ali Varkal

Liv Hospital Ulus
Liv Hospital Topkapı
Spec. MD. Gizem Güvener Pediatrics

Spec. MD. Gizem Güvener

Liv Hospital Ulus
Spec. MD. Osman Karlı Pediatrics

Spec. MD. Osman Karlı

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Spec. MD. Tamer Ünver Neonatal Intensive Care Unit (NICU)

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Assoc. Prof. MD. Adem Dursun Pediatrics

Assoc. Prof. MD. Adem Dursun

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Psyc. Selenay Yücel Keleş Pediatric Psychology

Psyc. Selenay Yücel Keleş

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Spec. MD.  Fatih Aydın Pediatrics

Spec. MD. Fatih Aydın

Liv Hospital Vadistanbul
Spec. MD. Dicle Çelik Pediatrics

Spec. MD. Dicle Çelik

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Spec. MD. Elif Erdem Özcan Pediatrics

Spec. MD. Elif Erdem Özcan

Liv Hospital Vadistanbul
Spec. MD. Hilal Kızıldağ Pediatrics

Spec. MD. Hilal Kızıldağ

Liv Hospital Vadistanbul
Spec. MD. Mehmet Kılıç Pediatrics

Spec. MD. Mehmet Kılıç

Liv Hospital Vadistanbul
Spec. MD. Ozan Uzunhan Neonatology

Spec. MD. Ozan Uzunhan

Liv Hospital Vadistanbul
Spec. MD. Selami Bayrakdar Pediatrics

Spec. MD. Selami Bayrakdar

Liv Hospital Vadistanbul
Spec. MD. Semra Akkuş Akman Pediatrics

Spec. MD. Semra Akkuş Akman

Liv Hospital Vadistanbul
Asst. Prof. MD. Doruk Gül Pediatric Health and Diseases

Asst. Prof. MD. Doruk Gül

Liv Hospital Bahçeşehir
Prof. MD. Murat Sütçü Pediatric Health and Diseases

Prof. MD. Murat Sütçü

Liv Hospital Bahçeşehir
Prof. MD. Nihat Demir Pediatrics

Prof. MD. Nihat Demir

Liv Hospital Bahçeşehir
Psyc. (Psychologist) Buse Yağmur Pediatric Psychology

Psyc. (Psychologist) Buse Yağmur

Liv Hospital Bahçeşehir
Spec. MD. Dilek Hatipoğlu Pediatric Health and Diseases

Spec. MD. Dilek Hatipoğlu

Liv Hospital Bahçeşehir
Spec. MD. Duygu Amine Garavi Pediatrics

Spec. MD. Duygu Amine Garavi

Liv Hospital Bahçeşehir
Spec. MD. Fatih Kaya Pediatric Health and Diseases

Spec. MD. Fatih Kaya

Liv Hospital Bahçeşehir
Spec. MD. Günel Nüsretzade Elmar Pediatrics

Spec. MD. Günel Nüsretzade Elmar

Liv Hospital Bahçeşehir
Spec. MD. Melike Akar Pediatrics

Spec. MD. Melike Akar

Liv Hospital Bahçeşehir
Liv Hospital Topkapı
Spec. MD. Mey Talip Pediatric Intensive Care

Spec. MD. Mey Talip

Liv Hospital Bahçeşehir
Spec. MD. Negın Nahanmoghaddam Pediatrics

Spec. MD. Negın Nahanmoghaddam

Liv Hospital Bahçeşehir
Spec. MD. Nushaba Abdullayeva Pediatric Health and Diseases

Spec. MD. Nushaba Abdullayeva

Liv Hospital Bahçeşehir
Spec. MD. Refika İlbakan Hanımeli Pediatrics

Spec. MD. Refika İlbakan Hanımeli

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Spec. MD. Selman Alazab Pediatrics

Spec. MD. Selman Alazab

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Spec. MD. Özden Durmuş Gönültaş Pediatrics

Spec. MD. Özden Durmuş Gönültaş

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Spec. Md. Öznur Ceylan Pediatric Health and Diseases

Spec. Md. Öznur Ceylan

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Assoc. Prof. MD. Aslan Yılmaz Neonatology

Assoc. Prof. MD. Aslan Yılmaz

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Prof. MD. Alpay Çakmak Pediatrics

Prof. MD. Alpay Çakmak

Liv Hospital Topkapı
Spec. MD. Demet Deniz Bilgin Pediatrics

Spec. MD. Demet Deniz Bilgin

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Spec. MD. Nesrin Köseoğlu Pediatric and Adolescent Psychiatry

Spec. MD. Nesrin Köseoğlu

Liv Hospital Topkapı
Spec. MD. Seçil Sözen Pediatrics

Spec. MD. Seçil Sözen

Liv Hospital Topkapı
Spec. MD. Özge Akça Pediatrics

Spec. MD. Özge Akça

Liv Hospital Topkapı
Spec. MD. Şeyma Öz Pediatrics

Spec. MD. Şeyma Öz

Liv Hospital Topkapı
Asst. Prof. MD. Pakize Elif Alkış Pediatrics

Asst. Prof. MD. Pakize Elif Alkış

Liv Hospital Ankara
Prof. MD. Musa Kazım Çağlar Pediatrics

Prof. MD. Musa Kazım Çağlar

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Prof. MD. İbrahim Hakan Bucak Pediatrics

Prof. MD. İbrahim Hakan Bucak

Liv Hospital Ankara
Prof.MD. Sevgi Başkan Pediatrics

Prof.MD. Sevgi Başkan

Liv Hospital Ankara
Spec. MD. Büşra Süzen Celbek Pediatrics

Spec. MD. Büşra Süzen Celbek

Liv Hospital Ankara
Spec. MD. Galip Erdem Pediatrics

Spec. MD. Galip Erdem

Liv Hospital Ankara
Spec. MD. Hafsa Uçur Pediatric Health and Diseases

Spec. MD. Hafsa Uçur

Liv Hospital Ankara
Spec. MD. Hidayet Katipoğlu Pediatric Health and Diseases

Spec. MD. Hidayet Katipoğlu

Liv Hospital Ankara
Spec. MD. Hüsniye Altan Pediatrics

Spec. MD. Hüsniye Altan

Liv Hospital Ankara
Spec. MD. Mustafa Yücel Kızıltan Pediatrics

Spec. MD. Mustafa Yücel Kızıltan

Liv Hospital Ankara
Spec. MD.  Seral Navdar Pediatric Health and Diseases

Spec. MD. Seral Navdar

Liv Hospital Gaziantep
Spec. MD. Gül Balyemez Pediatric Health and Diseases

Spec. MD. Gül Balyemez

Liv Hospital Gaziantep
Spec. MD. Hasan Avşar Neonatology

Spec. MD. Hasan Avşar

Liv Hospital Gaziantep
Spec. MD. Mert Çakır Pediatrics

Spec. MD. Mert Çakır

Liv Hospital Gaziantep
Spec. MD. Saltuk Buğra Böke Pediatric Health and Diseases

Spec. MD. Saltuk Buğra Böke

Liv Hospital Gaziantep
Spec. MD. Özlem Karaoğlu Pediatric Health and Diseases

Spec. MD. Özlem Karaoğlu

Liv Hospital Gaziantep
Spec. MD. İsmail Ersan Can Pediatric Health and Diseases

Spec. MD. İsmail Ersan Can

Liv Hospital Gaziantep
Spec. MD. Şekibe Zehra Doğan Pediatric Health and Diseases

Spec. MD. Şekibe Zehra Doğan

Liv Hospital Gaziantep
Spec. MD. Gülsenem Sarı Aracı Pediatric Health and Diseases

Spec. MD. Gülsenem Sarı Aracı

Liv Hospital Samsun
Spec. MD. Nazlı Karakullukcu Çebi Pediatrics

Spec. MD. Nazlı Karakullukcu Çebi

Liv Hospital Samsun
Spec. MD. Nezih Akgün Pediatric Health and Diseases

Spec. MD. Nezih Akgün

Liv Hospital Samsun
Spec. MD. Pelin Aytaç Uras Pediatrics

Spec. MD. Pelin Aytaç Uras

Liv Hospital Samsun
MD. VEFA İSAYEVA Pediatric Health and Diseases

MD. VEFA İSAYEVA

Liv Bona Dea Hospital Bakü
Spec. MD.  Elnur Hüseynov Pediatrics

Spec. MD. Elnur Hüseynov

Liv Bona Dea Hospital Bakü
Spec. MD. INARE ELDAROVA Pediatrics

Spec. MD. INARE ELDAROVA

Liv Bona Dea Hospital Bakü
Spec. MD. SADİQ İSMAYILOV Pediatric Health and Diseases

Spec. MD. SADİQ İSMAYILOV

Liv Bona Dea Hospital Bakü
MD. Dr. Elnur Hüseynov Pediatrics

MD. Dr. Elnur Hüseynov

Spec. MD. Doğa Sevinçok Pediatric and Adolescent Psychiatry

Spec. MD. Doğa Sevinçok

Pediatrics

Spec. MD. Sadık İsmayılov

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