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Diffuse intrinsic pontine gliomas (DIPG)DDiffuse intrinsic pontine gliomas (DIPG)Diffuse intrinsic pontine gliomas (DIPG)EnglishNeurology;OncologyChild (0-12 years);Teen (13-18 years)BrainNervous systemConditions and diseasesAdult (19+)NA2021-09-24T04:00:00Z10.700000000000049.50000000000001487.00000000000Health (A-Z) - ConditionsHealth A-Z<p>Diffuse intrinsic pontine gliomas (DIPG) are a type of malignant brain tumour. Learn about the symptoms, diagnosis, treatment and outlook for DIPG. </p><p>Diffuse intrinsic pontine gliomas (DIPG) are a type of brain tumour that arises from the <a href="/article?contentid=1307&language=english">pons, a part of the brainstem</a> which is located at the base of the brain. The brainstem controls vital functions such as breathing, heart rate, the sleep-wake cycle, etc. Additionally, many of the nerves that control the muscles of our face, eyes, and tongue arise from the brainstem. </p><p>Because of their location, these tumours are difficult to treat as it is impossible to remove a tumour in the brainstem without severe damage to vital functions controlled by the brainstem. Instead of surgical removal, the main treatment for DIPG is radiation therapy.</p><p>DIPGs are usually diagnosed in children aged 5 to 10, however they can be seen at any age, including in toddlers and in teenagers. </p><p>You and your child will have a dedicated, supportive care team who will help you make decisions about your child’s care and can offer other resources and supports in areas such as family support, mental health and finances. </p><h2>Key points</h2><ul><li>Diffuse intrinsic pontine gliomas are malignant tumors that arise from the pons in the brainstem, at the lower part of the brain.</li><li>The brainstem controls breathing, heart rate function , the body’s wake-sleep cycle and the cranial nerves.</li><li>Diffuse intrinsic pontine gliomas are difficult to treat, and complete removal of the tumor is not possible because of their location and their invasive nature. </li><li>The most common symptoms are crossed eyes, balance problems, muscle weakness on one side of the body, swallowing problems, speech problems, drowsiness, hearing loss, and personality changes.</li><li>The cause of diffuse pontine gliomas is unknown.</li><li>The main treatment for diffuse intrinsic pontine gliomas is radiation therapy.</li><li>Chemotherapy may be given as part of a clinical trial or at a later stage when the tumour is progressing.</li><li>Your child’s health-care team will support you in your decision making throughout your child’s treatment and offer resources and supports that you and your family can access. </li></ul><h2>What are the symptoms of a diffuse pontine glioma?</h2><p>When the DIPG tumour presses on the brainstem and the nerves that control the muscles of the face, eyes and tongue, symptoms appear. </p><p>Patients diagnosed with DIPG present with the following symptoms:</p><ul><li>crossed eyes</li><li>facial asymmetry (crooked smile)</li><li>balance problems (ataxia)</li><li>muscle weakness on one side of the body (hemiparesis)</li><li>swallowing problems (dysphagia)</li><li>speech problems (dysarthria)</li><li>drowsiness</li><li>hearing loss</li><li>personality changes</li></ul><p>Sleep problems are also frequently described, for example nighttime laughter is usually noted before other symptoms appear.</p><p>Most symptoms develop quickly, over a period of 1 to 2 weeks. Sometimes symptoms can develop over a longer time, but usually less than 3 months.</p><h2>What causes a diffuse intrinsic pontine glioma? </h2><p>The cause of DIPG is unknown. Research has shown that DIPGs rise from brain cells that are unable to properly develop into a mature normal brain cell. There is no way to predict that a child will get brain cancer. </p><p>There is no definite proof that there is a connection between environmental factors such as food, chemicals or radiation and the development of brain cancer in children. </p><h3>Biology of DIPG</h3><p>Doctors and scientists’ understanding of the biological behaviour of DIPGs has significantly improved in recent years. It is now known that most of these tumors are characterized by a mutation in a protein called histone. The main function of histone proteins is to protect the DNA. </p><p>Most recently, scientists have also learned that not all DIPGs behave the same way. Some may be dormant (inactive or not growing quickly) for a long time while others are very aggressive. Certain medication can be used to target different tumor components to slow down its growth. </p><h2>How many children have diffuse intrinsic pontine gliomas?</h2><p>DIPGs account for about 10% of brain tumours in children.</p><h2>How are diffuse intrinsic pontine gliomas diagnosed?</h2><p>Doctors and other health-care professionals use well-established diagnostic tests to see if a brain tumour is causing your child’s symptoms. These tests will include a physical examination, and brain scans such as <a href="/article?contentid=1270&language=english">magnetic resonance imaging (MRI)</a>. The diagnosis is usually made based on the signs and symptoms in your child, and on the results of the MRI study. </p><p>When the DIPG tumour looks typical on an MRI, a biopsy is not required to confirm the diagnosis. </p><h2>How are diffuse pontine intrinsic gliomas treated?</h2><p>While there are different treatments that may be recommended for your child, the main type of treatment for DIPG is radiation therapy.</p><p>The treatment team is led by a doctor called a neuro-oncologist. They take the responsibility for your child’s care and make the decisions about your child’s treatment plan.</p><h3>Radiation for DIPG</h3><p>DIPGs are treated with<a href="/article?contentid=1353&language=english"> radiation therapy</a>, which are high-energy X-rays, gamma rays, or electrons that destroy tumour cells and shrink tumours. This treatment can reduce symptoms significantly, but there may be some permanent damage to the brainstem caused by the tumour which can not be repaired by the radiation treatment.</p><h3>Steroids for DIPG</h3><p><a href="/article?contentid=1354&language=english">Steroids</a>, an anti-inflammatory medication, are often given to improve some of the symptoms of gliomas. Steroids decrease the swelling (edema) within and around the tumour and often cause significant improvement of the symptoms. Usually doctors start steroid treatment immediately after the initial MRI, unless your child has very mild symptoms. They will continue the steroid until there is evidence that your child gets better. </p><h3>Surgery for DIPG</h3><p><a href="/article?contentid=1351&language=english">Surgery</a> is not part of the standard treatment for DIPG because it is too damaging to this part of the brain and it does not improve the outcome. However, surgery may be considered if a tumour component grows outside the brainstem (exophytic component). </p><p><a href="/article?contentid=1335&language=english">Biopsy </a>of these tumors may be considered as part of diagnosis to confirm the diagnosis and sometimes to find changes that can be amenable to treatment with new drugs.</p><h3>Other treatments for DIPG</h3><p>There are several other types of treatment being considered. Treatments targeting molecules expressed by the tumor cells have been developed and may be offered to certain patients. The use of those “targeted agents” is dependent on the finding of an alteration in the tumor cells obtained through a biopsy. However, these treatments target only a small minority of DIPG tumours and for the large proportion there is no targeted treatment that will specifically ‘turn off’ the tumour, or stop it from growing.</p><h3>Chemotherapy for DIPG</h3><p>In DIPG, the effectiveness of chemotherapy is uncertain. In DIPGs, chemotherapy has not shown effective killing of the tumor cells and is not routinely offered. Although many trials have been done using chemotherapy, there is no evidence that it improves survival.</p><p>In DIPG, chemotherapy is given in one of the following circumstances:</p><ul><li>As part of a clinical trial to evaluate the benefits of new chemotherapy drugs or drug combinations in addition to radiation</li><li>At a later stage when the child's tumour shows signs of progression (getting worse). The aim in this case is to try to decrease the symptoms of progression and to help improve quality of life</li></ul><div class="row"><div class="col-md-6"> <a href="https://www.sickkidsfoundation.com/podcast"> <img src="https://assets.aboutkidshealth.ca/AKHAssets/foundation_banners/SKF%20Logo-%28Standard%29_New_Small_FINAL.jpg" alt="SickKids VS Podcast link" style="margin-top:1rem;" /> </a> <p></p></div><div class="col-md-6"><p>SickKids VS takes you to the frontlines in the fight for child health, where big questions drive big breakthroughs: Where do we start when a child’s disease is unknown? Can we heal the brain? How should we talk to kids about dying? Behind each quest, is a remarkable family and story. <a href="https://www.sickkidsfoundation.com/podcast">Listen now</a> and subscribe.</p><p><a href="https://www.sickkidsfoundation.com/podcast/despair">HOW SHOULD WE TALK TO KIDS ABOUT DYING? SickKids VS DESPAIR</a></p></div></div>
Gliomes pontiques intrinsèques diffus (DIPG)GGliomes pontiques intrinsèques diffus (DIPG)Diffuse pontine gliomasFrenchNeurology;OncologyChild (0-12 years);Teen (13-18 years)BrainNervous systemConditions and diseasesAdult (19+)NA2021-09-24T04:00:00Z11.000000000000036.000000000000043.0000000000000Health (A-Z) - ConditionsHealth A-Z<p>Apprendre au sujet des gliomes pontiques intrinsèques diffus (DIPG). Examen approfondi des causes, des symptômes, du traitement et des résultats pour un enfant atteint de DIPG.</p><p>Les gliomes pontiques intrinsèques diffus (DIPG) sont un type de tumeur cérébrale qui provient du <a href="/article?contentid=1307&language=french">pont, une partie du tronc cérébral</a> située à la base du cerveau. Le tronc cérébral contrôle les fonctions vitales telles que la respiration, la fréquence cardiaque, le cycle sommeil-veille, etc. En outre, de nombreux nerfs qui contrôlent les muscles du visage, des yeux et de la langue proviennent du tronc cérébral.</p><p>En raison de leur siège, ces tumeurs sont difficiles à traiter, car il est impossible d’enlever une tumeur dans le tronc cérébral sans endommager gravement les fonctions vitales contrôlées par le tronc cérébral. Au lieu de l’ablation chirurgicale, le principal traitement des DIPG est la radiothérapie.</p><p>Les DIPG sont généralement diagnostiqués chez les enfants âgés de 5 à 10 ans, mais on peut les observer à tout âge, y compris chez les tout-petits et les adolescents.</p><p>Vous et votre enfant disposerez d’une équipe de soins dévouée qui vous aidera à prendre des décisions concernant les soins à donner à votre enfant et qui pourra offrir d’autres ressources et mesures de soutien dans des domaines comme le soutien familial, la santé mentale et les finances.</p><h2>À retenir</h2><ul><li>Les gliomes pontiques intrinsèques diffus sont des tumeurs malignes qui naissent du pont dans le tronc cérébral, à la partie inférieure du cerveau.</li><li>Le tronc cérébral contrôle la respiration, la fréquence cardiaque, le cycle veille-sommeil et les nerfs crâniens.</li><li>Les gliomes pontiques intrinsèques diffus sont difficiles à traiter et l’ablation complète de la tumeur n’est pas possible en raison de leur emplacement et de leur nature invasive.</li><li>Les symptômes les plus courants sont les yeux croisés, les problèmes d’équilibre, la faiblesse musculaire d’un côté du corps, les problèmes de déglutition, les problèmes d’élocution, la somnolence, la perte d’audition et les changements de personnalité.</li><li>La cause des gliomes pontiques diffus n’est pas connue.</li><li>Le principal traitement des gliomes pontiques intrinsèques diffus est la radiothérapie.</li><li>La chimiothérapie peut être administrée dans le cadre d’un essai clinique ou à un stade ultérieur lorsque la tumeur progresse.</li><li>L’équipe de soins de santé de votre enfant vous aidera dans votre prise de décision tout au long du traitement de votre enfant et vous indiquera les ressources et le soutien auxquels vous et votre famille pourrez avoir accès. </li></ul><h2>Quels sont les symptômes du gliome pontique diffus?</h2><p>Lorsque le DIPG exerce une pression sur le tronc cérébral et les nerfs qui contrôlent les muscles du visage, des yeux et de la langue, des symptômes se manifestent. </p><p>Les patients qui ont reçu un diagnostic de DIPG présentent les symptômes suivants :</p><ul><li>yeux croisés</li><li>asymétrie faciale (sourire tordu)</li><li>problèmes d’équilibre (ataxie)</li><li>faiblesse musculaire d’un côté du corps (hémiparésie)</li><li>problèmes de déglutition (dysphagie)</li><li>troubles de l’élocution (dysarthrie)</li><li>somnolence</li><li>perte d’audition</li><li>changements de personnalité</li></ul><p>Les problèmes de sommeil sont également fréquemment décrits; par exemple, on note généralement un rire nocturne avant l’apparition d’autres symptômes.</p><p>La plupart des symptômes se développent rapidement, sur une période d’une à deux semaines. Parfois, les symptômes peuvent se développer sur une période plus longue, mais généralement moins de trois mois.</p><h2>Qu’est-ce qui cause un gliome pontique intrinsèque diffus?</h2><p>La cause du DIPG est inconnue. La recherche a montré que les DIPG proviennent de cellules cérébrales incapables de se développer correctement pour devenir une cellule cérébrale normale mature. Il n’y a aucun moyen de prédire qu’un enfant aura un cancer du cerveau.</p><p>Il n’existe aucune preuve concluante qu’il existe un lien entre les facteurs environnementaux tels que l’alimentation, les produits chimiques ou les rayonnements et le développement du cancer du cerveau chez les enfants.</p><h3>Biologie du DIPG</h3><p>Ces dernières années, les médecins et les scientifiques ont considérablement amélioré leur compréhension du comportement biologique des DIPG. On sait maintenant que la plupart de ces tumeurs sont caractérisées par une mutation dans une protéine appelée histone. La fonction principale des histones est de protéger l’ADN.</p><p>Plus récemment, les scientifiques ont également appris que tous les DIPG ne se comportent pas de la même manière. Certains peuvent rester latents (rester inactifs ou ne pas croître rapidement) pendant longtemps, tandis que d’autres sont très agressifs. Certains médicaments peuvent être utilisés pour cibler différentes composantes de la tumeur afin de ralentir sa croissance.</p><h2>Combien d’enfants ont des gliomes pontiques intrinsèques diffus?</h2><p>Les DIPG représentent environ 10 % des tumeurs cérébrales chez l’enfant.</p><h2>Comment diagnostique-t-on les gliomes pontiques intrinsèques diffus?</h2><p>Les médecins et autres professionnels de la santé utilisent des tests diagnostiques bien établis pour déterminer si une tumeur cérébrale est à l’origine des symptômes de votre enfant. Ces tests comprendront un examen physique et une scintigraphie cérébrale, comme une <a href="/article?contentid=1270&language=french">imagerie par résonance magnétique (IRM)</a>. Le diagnostic est généralement posé en fonction des signes et symptômes de votre enfant et des résultats de l’étude IRM.</p><p>Lorsque le DIPG semble typique à l’IRM, une biopsie n’est pas nécessaire pour confirmer le diagnostic.</p><h2>Comment traite-t-on les gliomes pontiques intrinsèques diffus?</h2><p>Bien qu’il existe différents traitements qui peuvent être recommandés pour votre enfant, le principal type de traitement pour le DIPG est la radiothérapie.</p><p>L’équipe soignante est dirigée par un médecin appelé neuro-oncologue. Il prend la responsabilité des soins de votre enfant et les décisions concernant son plan de traitement.</p><p>Le médecin vous expliquera le type de tumeur qu’a votre enfant, selon ce que les tests diagnostiques et la stadification auront révélé à l’équipe. L’équipe vous informera des effets attendus de cette tumeur sur votre enfant dans les mois et les années à venir, selon ce que l’on sait sur la tumeur. C’est ce qu’on appelle le pronostic.</p><p>Il se peut que l’équipe discute de la possibilité d’inscrire votre enfant à un essai clinique ou de le traiter selon la norme de soins, qui est un plan de traitement pour une tumeur particulière. Vous devrez donner votre consentement au plan pour que le traitement puisse commencer. Les patients adolescents peuvent également être invités à donner leur consentement.</p><p>Votre équipe vous parlera également de la pose d'une ligne intraveineuse appelée ligne centrale. Cela aidera les médecins à administrer les traitements de manière plus sûre et à éviter de multiples piqûres pour les tests sanguins. Vous obtiendrez plus d'informations sur l'insertion de ligne dans les détails lors de la réunion.</p><h3>Traitement des DIPG par rayonnement</h3><p>Les DIPG sont traités par <a href="/article?contentid=1353&language=french">radiothérapie</a>, c’est-à-dire des rayons X, des rayons gamma ou des électrons à haute énergie qui détruisent les cellules tumorales et réduisent la taille des tumeurs. Ce traitement peut réduire considérablement les symptômes, mais il peut y avoir des lésions permanentes du tronc cérébral causées par la tumeur, qui sont impossibles à réparer par la radiothérapie.</p><h3>Traitement des DIPG par stéroïdes</h3><p>Les <a href="/article?contentid=1354&language=french">stéroïdes</a>, des médicaments anti-inflammatoires, sont souvent administrés pour améliorer certains des symptômes des gliomes. Les stéroïdes diminuent le gonflement (œdème) à l’intérieur et autour de la tumeur et entraînent souvent une amélioration considérable des symptômes. En général, les médecins commencent le traitement par stéroïdes immédiatement après l’IRM initiale, sauf si votre enfant présente des symptômes très légers. Ils continueront d’administrer des stéroïdes jusqu’à ce qu’il y ait des preuves que votre enfant va mieux.</p><h3>Traitement des DIPG par chirurgie</h3><p>La <a href="/article?contentid=1351&language=french">chirurgie</a> ne fait pas partie du traitement standard des DIPG, parce qu’elle cause trop de lésions à cette partie du cerveau et qu’elle n’améliore pas le résultat thérapeutique. Cependant, une intervention chirurgicale peut être envisagée si une composante de la tumeur se développe en dehors du tronc cérébral (composante exophytique).</p><p>La <a href="/article?contentid=1335&language=french">biopsie</a> de certaines de ces tumeurs peut être considérée comme faisant partie du diagnostic pour confirmer le diagnostic et parfois pour trouver des changements qui peuvent se prêter au traitement par de nouveaux médicaments.</p><h3>Autres traitements des DIPG</h3><p>Plusieurs autres types de traitement sont envisagés. Des traitements ciblant des molécules exprimées par les cellules tumorales ont été développés et peuvent être proposés à certains patients. L’utilisation de ces « agents ciblés » dépend de la découverte d’une altération des cellules tumorales obtenues par biopsie. </p><p>Cependant, ces traitements ne ciblent qu’une petite minorité de DIPG et, pour la majeure partie d’entre eux, il n’existe pas de traitement ciblé qui va spécifiquement « désactiver » la tumeur ou l’empêcher de continuer à croître.</p><h3>Traitement des DIPG par chimiothérapie</h3><p>L’efficacité de la chimiothérapie pour traiter les DIPG est incertaine. Dans le cas des DIPG, la chimiothérapie n’a pas révélé une destruction efficace des cellules tumorales et n’est pas systématiquement proposée. Bien que de nombreux essais aient été réalisés à l’aide de la chimiothérapie, rien ne prouve qu’elle améliore la survie.</p><p>Dans le cas des DIPG, la chimiothérapie est administrée dans l’une des circonstances suivantes :</p><ul><li>Dans le cadre d’un essai clinique visant à évaluer les avantages de nouveaux médicaments de chimiothérapie ou de nouvelles associations de médicaments en plus de la radiothérapie.</li><li>À un stade ultérieur, lorsque la tumeur de l’enfant montre des signes de progression (aggravation) L’objectif dans ce cas est d’essayer de diminuer les symptômes de progression et d’aider à améliorer la qualité de vie.<br></li></ul>

 

 

 

 

Diffuse intrinsic pontine gliomas (DIPG)1311.00000000000Diffuse intrinsic pontine gliomas (DIPG)Diffuse intrinsic pontine gliomas (DIPG)DEnglishNeurology;OncologyChild (0-12 years);Teen (13-18 years)BrainNervous systemConditions and diseasesAdult (19+)NA2021-09-24T04:00:00Z10.700000000000049.50000000000001487.00000000000Health (A-Z) - ConditionsHealth A-Z<p>Diffuse intrinsic pontine gliomas (DIPG) are a type of malignant brain tumour. Learn about the symptoms, diagnosis, treatment and outlook for DIPG. </p><p>Diffuse intrinsic pontine gliomas (DIPG) are a type of brain tumour that arises from the <a href="/article?contentid=1307&language=english">pons, a part of the brainstem</a> which is located at the base of the brain. The brainstem controls vital functions such as breathing, heart rate, the sleep-wake cycle, etc. Additionally, many of the nerves that control the muscles of our face, eyes, and tongue arise from the brainstem. </p><p>Because of their location, these tumours are difficult to treat as it is impossible to remove a tumour in the brainstem without severe damage to vital functions controlled by the brainstem. Instead of surgical removal, the main treatment for DIPG is radiation therapy.</p><p>DIPGs are usually diagnosed in children aged 5 to 10, however they can be seen at any age, including in toddlers and in teenagers. </p><p>You and your child will have a dedicated, supportive care team who will help you make decisions about your child’s care and can offer other resources and supports in areas such as family support, mental health and finances. </p><h2>Key points</h2><ul><li>Diffuse intrinsic pontine gliomas are malignant tumors that arise from the pons in the brainstem, at the lower part of the brain.</li><li>The brainstem controls breathing, heart rate function , the body’s wake-sleep cycle and the cranial nerves.</li><li>Diffuse intrinsic pontine gliomas are difficult to treat, and complete removal of the tumor is not possible because of their location and their invasive nature. </li><li>The most common symptoms are crossed eyes, balance problems, muscle weakness on one side of the body, swallowing problems, speech problems, drowsiness, hearing loss, and personality changes.</li><li>The cause of diffuse pontine gliomas is unknown.</li><li>The main treatment for diffuse intrinsic pontine gliomas is radiation therapy.</li><li>Chemotherapy may be given as part of a clinical trial or at a later stage when the tumour is progressing.</li><li>Your child’s health-care team will support you in your decision making throughout your child’s treatment and offer resources and supports that you and your family can access. </li></ul><h2>What are the symptoms of a diffuse pontine glioma?</h2><p>When the DIPG tumour presses on the brainstem and the nerves that control the muscles of the face, eyes and tongue, symptoms appear. </p><p>Patients diagnosed with DIPG present with the following symptoms:</p><ul><li>crossed eyes</li><li>facial asymmetry (crooked smile)</li><li>balance problems (ataxia)</li><li>muscle weakness on one side of the body (hemiparesis)</li><li>swallowing problems (dysphagia)</li><li>speech problems (dysarthria)</li><li>drowsiness</li><li>hearing loss</li><li>personality changes</li></ul><p>Sleep problems are also frequently described, for example nighttime laughter is usually noted before other symptoms appear.</p><p>Most symptoms develop quickly, over a period of 1 to 2 weeks. Sometimes symptoms can develop over a longer time, but usually less than 3 months.</p><h2>What causes a diffuse intrinsic pontine glioma? </h2><p>The cause of DIPG is unknown. Research has shown that DIPGs rise from brain cells that are unable to properly develop into a mature normal brain cell. There is no way to predict that a child will get brain cancer. </p><p>There is no definite proof that there is a connection between environmental factors such as food, chemicals or radiation and the development of brain cancer in children. </p><h3>Biology of DIPG</h3><p>Doctors and scientists’ understanding of the biological behaviour of DIPGs has significantly improved in recent years. It is now known that most of these tumors are characterized by a mutation in a protein called histone. The main function of histone proteins is to protect the DNA. </p><p>Most recently, scientists have also learned that not all DIPGs behave the same way. Some may be dormant (inactive or not growing quickly) for a long time while others are very aggressive. Certain medication can be used to target different tumor components to slow down its growth. </p><h2>How many children have diffuse intrinsic pontine gliomas?</h2><p>DIPGs account for about 10% of brain tumours in children.</p><h2>How are diffuse intrinsic pontine gliomas diagnosed?</h2><p>Doctors and other health-care professionals use well-established diagnostic tests to see if a brain tumour is causing your child’s symptoms. These tests will include a physical examination, and brain scans such as <a href="/article?contentid=1270&language=english">magnetic resonance imaging (MRI)</a>. The diagnosis is usually made based on the signs and symptoms in your child, and on the results of the MRI study. </p><p>When the DIPG tumour looks typical on an MRI, a biopsy is not required to confirm the diagnosis. </p><h2>How are diffuse pontine intrinsic gliomas treated?</h2><p>While there are different treatments that may be recommended for your child, the main type of treatment for DIPG is radiation therapy.</p><p>The treatment team is led by a doctor called a neuro-oncologist. They take the responsibility for your child’s care and make the decisions about your child’s treatment plan.</p><h3>Radiation for DIPG</h3><p>DIPGs are treated with<a href="/article?contentid=1353&language=english"> radiation therapy</a>, which are high-energy X-rays, gamma rays, or electrons that destroy tumour cells and shrink tumours. This treatment can reduce symptoms significantly, but there may be some permanent damage to the brainstem caused by the tumour which can not be repaired by the radiation treatment.</p><h3>Steroids for DIPG</h3><p><a href="/article?contentid=1354&language=english">Steroids</a>, an anti-inflammatory medication, are often given to improve some of the symptoms of gliomas. Steroids decrease the swelling (edema) within and around the tumour and often cause significant improvement of the symptoms. Usually doctors start steroid treatment immediately after the initial MRI, unless your child has very mild symptoms. They will continue the steroid until there is evidence that your child gets better. </p><h3>Surgery for DIPG</h3><p><a href="/article?contentid=1351&language=english">Surgery</a> is not part of the standard treatment for DIPG because it is too damaging to this part of the brain and it does not improve the outcome. However, surgery may be considered if a tumour component grows outside the brainstem (exophytic component). </p><p><a href="/article?contentid=1335&language=english">Biopsy </a>of these tumors may be considered as part of diagnosis to confirm the diagnosis and sometimes to find changes that can be amenable to treatment with new drugs.</p><h3>Other treatments for DIPG</h3><p>There are several other types of treatment being considered. Treatments targeting molecules expressed by the tumor cells have been developed and may be offered to certain patients. The use of those “targeted agents” is dependent on the finding of an alteration in the tumor cells obtained through a biopsy. However, these treatments target only a small minority of DIPG tumours and for the large proportion there is no targeted treatment that will specifically ‘turn off’ the tumour, or stop it from growing.</p><h3>Chemotherapy for DIPG</h3><p>In DIPG, the effectiveness of chemotherapy is uncertain. In DIPGs, chemotherapy has not shown effective killing of the tumor cells and is not routinely offered. Although many trials have been done using chemotherapy, there is no evidence that it improves survival.</p><p>In DIPG, chemotherapy is given in one of the following circumstances:</p><ul><li>As part of a clinical trial to evaluate the benefits of new chemotherapy drugs or drug combinations in addition to radiation</li><li>At a later stage when the child's tumour shows signs of progression (getting worse). The aim in this case is to try to decrease the symptoms of progression and to help improve quality of life</li></ul><h2>What is the outcome for a child with a diffuse intrinsic pontine glioma?</h2><p>After diagnosis, the survival time is on average 9 to 12 months. This is because brainstem gliomas are difficult to treat. To improve the outcome, doctors have tried giving higher amounts of radiation, or using chemotherapy medications to kill the tumour cells. Research is underway to achieve better results. When the tumour recurs (grows back after initially responding to treatment), the focus of treatment is on managing symptoms to make sure the child is as comfortable as possible.</p><h2>Recurrence of diffuse intrinsic pontine gliomas</h2><p>Repeated radiation therapy to the tumor area has been the only treatment proven to improve symptoms and prolong the life of patients with DIPG at recurrence. Such treatment is usually offered to children who had a good response to initial treatment and at least 4 to 6 months of remission following radiotherapy. The second radiation treatment will give a lower dose, as the brainstem cannot tolerate a high dose of radiotherapy twice.</p><p>Unfortunately, no chemotherapy or high-dose chemotherapy treatment has yet shown any benefit in curing a recurrence. When a DIPG recurs, the focus of care is to manage symptoms with the fewest side effects possible. Sometimes chemotherapy drugs taken by mouth are offered. </p><p>Because of their <a href="/article?contentid=1354&language=english">side effects</a>, steroids are usually avoided at the time of recurrence, except when a second radiation treatment is planned.</p><p>Surgery to place a shunt is sometimes considered when a recurrence occurs, if the child has <a href="/article?contentid=858&language=english">hydrocephalus</a> due to the blockage of the flow of cerebrospinal fluid in the brain by the growing tumour. However, a shunt is not a treatment for DIPG itself; the objective of the shunt placement is to improve the symptoms associated with hydrocephalus and improve the child's quality of life.</p><div class="row"><div class="col-md-6"> <a href="https://www.sickkidsfoundation.com/podcast"> <img src="https://assets.aboutkidshealth.ca/AKHAssets/foundation_banners/SKF%20Logo-%28Standard%29_New_Small_FINAL.jpg" alt="SickKids VS Podcast link" style="margin-top:1rem;" /> </a> <p></p></div><div class="col-md-6"><p>SickKids VS takes you to the frontlines in the fight for child health, where big questions drive big breakthroughs: Where do we start when a child’s disease is unknown? Can we heal the brain? How should we talk to kids about dying? Behind each quest, is a remarkable family and story. <a href="https://www.sickkidsfoundation.com/podcast">Listen now</a> and subscribe.</p><p><a href="https://www.sickkidsfoundation.com/podcast/despair">HOW SHOULD WE TALK TO KIDS ABOUT DYING? SickKids VS DESPAIR</a></p></div></div>Diffuse intrinsic pontine gliomas (DIPG)False

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