通用中文 | 诺华CAR-T疗法 | 通用外文 | Tisagenlecleucel |
品牌中文 | 品牌外文 | Kymriah | |
其他名称 | CTL019CART CAR-T | ||
公司 | 诺华(Novartis) | 产地 | 美国(USA) |
含量 | 包装 | ||
剂型给药 | 液体 静脉 | 储存 | 2度-8度(冰箱冷藏,禁止冷冻) |
适用范围 | 急性淋巴细胞白血病(ALL) 弥漫性大B细胞淋巴瘤(DLBCL) |
通用中文 | 诺华CAR-T疗法 |
通用外文 | Tisagenlecleucel |
品牌中文 | |
品牌外文 | Kymriah |
其他名称 | CTL019CART CAR-T |
公司 | 诺华(Novartis) |
产地 | 美国(USA) |
含量 | |
包装 | |
剂型给药 | 液体 静脉 |
储存 | 2度-8度(冰箱冷藏,禁止冷冻) |
适用范围 | 急性淋巴细胞白血病(ALL) 弥漫性大B细胞淋巴瘤(DLBCL) |
2017年8月30日,FDA官方网站宣布批准诺华CAR-T细胞疗法正式上市,用于治疗复发性或难治性儿童、青少年B-细胞急性淋巴细胞白血病,其商品名为Kymriah(tisagenlecleucel)。
FDA称其为“一项历史性的行动,使美国第一种基因治疗方法得以实现,从而采取了一种新的治疗癌症、其他严重和危及生命的疾病的方法。”
FDA专员Scott Gottlieb博士说:“我们正在进入一个新的医疗创新前沿,能够重编病人自己的细胞来攻击致命的癌症,基因和细胞疗法等新技术能够在转化医学和治疗许多难治性疾病方面创造拐点。FDA致力于帮助加快开发和审查有潜力挽救生命的突破性治疗。”
今年果然是CAR-T疗法的大年。
在此前两天,吉利德Gilead与Kite制药联合宣布,双方董事会已经达成最终收购协议,吉利德将以每股180美元的现金价格收购Kite,溢价29%。该项交易金额约为119亿美元,预计整个交易将在2017年第四季度完成。
吉利德巨资出手拿下了CAR-T三巨头之一,传统药企与新兴技术的结合充满想象。
2017年7月12日,美国FDA肿瘤药物专家咨询委员会(ODAC)召开针对诺华(Novartis)CAR-T疗法CTL-019(tisagenlecleucel)的评估会议,最终以10:0的投票结果一致推荐批准此疗法上市,是为全球首次。
上述结果将促使FDA在10月3日前做出最终审批决定,其时业内认为获批上市基本没有悬念,绝大多数情况下,FDA都会听从专家咨询委员会的意见。
“咨询委员会小组成员一致赞成,使我们在实现首个批准的CAR-T细胞疗法道路上又迈进了一步。”诺华肿瘤CEO Bruno Striginibiaoshi表示,“诺华开拓了癌症治疗的新领域。”
CAR-T是通过基因工程技术,人工改造肿瘤患者的T细胞,在体外大量培养后生成肿瘤特异性CAR-T细胞,再将其回输入患者体内用以攻击癌细胞。
根据治疗流程,CAR-T细胞免疫治疗包括两大核心环节:一是用于制备CAR-T细胞的基因修饰载体的生产,即生产CAR慢病毒载体;二是CART细胞的制备和应用,包括采集患者的免疫细胞、体外细胞培养、转染、扩增和回输等制备和治疗。
CTL019由宾夕法尼亚大学率先研发,在其嵌合抗原受体中用4-1BB共刺激域来增强细胞反应性以及CTL019注入患者后的持续疗效,可能有助于长时间缓解患者痛苦。
急性淋巴细胞白血病在15岁以下儿童癌症确诊病例中约占25%,是美国最常见的儿童癌。根据美国国家癌症研究所估计,每年约有3100名年龄在20岁以下的患者被诊断为这一疾病。有效的治疗选择十分有限,在多次复发或难治性B-细胞急性淋巴细胞白血病儿童及青少年患者中,五年无病生存率低于10%-30%。
世界上第一例接受CAR-T疗法的小女孩Emily,在接受了16个月化疗后复发。2012年4月她开始接受CAR-T治疗,为她治疗的宾夕法尼亚大学细胞免疫疗法中心主任Carl June博士曾表示:“当时我们非常怀疑培养的T细胞能否对抗她体内的白血病癌细胞。”
这位小女孩在5年后来到上述ODAC审评会现场,成为CTL019直接的疗效证据。
诺华的成功让业内沸腾,并将这一天称为“CAR-T日”,但患者和研发公司都曾面临巨大风险。
CAR-T是一种高度个性化的方法,每个人的细胞和接受过的治疗都不同,如同Emily一样,许多患者在接受CAR-T治疗前已经接受过各种治疗方法,如骨髓移植手术、化疗、靶向治疗等,所获得的T细胞的制备和编程也会各异。
此次获批公告中,FDA方面也表示,Kymriah的剂量是根据使用的患者自身T细胞所产生的定制治疗。“患者的T细胞被收集并送到制造中心,在进行遗传修饰以包括含有特异性蛋白质(嵌合抗原受体或CAR)的新基因,其指导T细胞靶向并杀死具有表面上的特异性抗原(CD19)。一旦细胞被修饰,它们被注入到患者体内以杀死癌细胞。”
而在CAR-T研发第一梯队中,诺华一开始的卡位并不领先。但JUNO的 JACR015在去年的临床研究中先后出现5例脑水肿引起患者死亡;Kite的KTE-C19也在4月底出现1例患者死亡,两家先后折戟让诺华后来居上。
FDA的生物制剂评估中心总监Peter Marks博士说:“Kymriah是一种前所未有的治疗方法,可满足儿童和年轻人对这种严重疾病的重要需求。Kymriah不仅为这些患者提供了一种新的治疗方案,在极其有限的选择中,这也是一种在临床试验中显示出有希望缓解和存活率的治疗方案。”
Kymriah的安全性和有效性在一项多中心临床试验中得到证实。治疗三个月内的总体缓解率为83%。
但FDA提示用Kymriah治疗有潜在的严重副作用。CAR-T治疗过程中会释放出很多杀伤肿瘤细胞的细胞因子,副作用通常表现为发烧、低血压、脑水肿等,此前在评估会议上专家也提出诸多需要关注的问题,包括T细胞的制备、有效性,生产质控和安全性,癌症复发,毒副作用等。
2017年8月30日,FDA官方网站宣布批准诺华CAR-T细胞疗法正式上市,用于治疗复发性或难治性儿童、青少年B-细胞急性淋巴细胞白血病,其商品名为Kymriah(tisagenlecleucel)。
FDA称其为“一项历史性的行动,使美国第一种基因治疗方法得以实现,从而采取了一种新的治疗癌症、其他严重和危及生命的疾病的方法。”
FDA专员Scott Gottlieb博士说:“我们正在进入一个新的医疗创新前沿,能够重编病人自己的细胞来攻击致命的癌症,基因和细胞疗法等新技术能够在转化医学和治疗许多难治性疾病方面创造拐点。FDA致力于帮助加快开发和审查有潜力挽救生命的突破性治疗。”
今年果然是CAR-T疗法的大年。
在此前两天,吉利德Gilead与Kite制药联合宣布,双方董事会已经达成最终收购协议,吉利德将以每股180美元的现金价格收购Kite,溢价29%。该项交易金额约为119亿美元,预计整个交易将在2017年第四季度完成。
吉利德巨资出手拿下了CAR-T三巨头之一,传统药企与新兴技术的结合充满想象。
2017年7月12日,美国FDA肿瘤药物专家咨询委员会(ODAC)召开针对诺华(Novartis)CAR-T疗法CTL-019(tisagenlecleucel)的评估会议,最终以10:0的投票结果一致推荐批准此疗法上市,是为全球首次。
上述结果将促使FDA在10月3日前做出最终审批决定,其时业内认为获批上市基本没有悬念,绝大多数情况下,FDA都会听从专家咨询委员会的意见。
“咨询委员会小组成员一致赞成,使我们在实现首个批准的CAR-T细胞疗法道路上又迈进了一步。”诺华肿瘤CEO Bruno Striginibiaoshi表示,“诺华开拓了癌症治疗的新领域。”
CAR-T是通过基因工程技术,人工改造肿瘤患者的T细胞,在体外大量培养后生成肿瘤特异性CAR-T细胞,再将其回输入患者体内用以攻击癌细胞。
根据治疗流程,CAR-T细胞免疫治疗包括两大核心环节:一是用于制备CAR-T细胞的基因修饰载体的生产,即生产CAR慢病毒载体;二是CART细胞的制备和应用,包括采集患者的免疫细胞、体外细胞培养、转染、扩增和回输等制备和治疗。
CTL019由宾夕法尼亚大学率先研发,在其嵌合抗原受体中用4-1BB共刺激域来增强细胞反应性以及CTL019注入患者后的持续疗效,可能有助于长时间缓解患者痛苦。
急性淋巴细胞白血病在15岁以下儿童癌症确诊病例中约占25%,是美国最常见的儿童癌。根据美国国家癌症研究所估计,每年约有3100名年龄在20岁以下的患者被诊断为这一疾病。有效的治疗选择十分有限,在多次复发或难治性B-细胞急性淋巴细胞白血病儿童及青少年患者中,五年无病生存率低于10%-30%。
世界上第一例接受CAR-T疗法的小女孩Emily,在接受了16个月化疗后复发。2012年4月她开始接受CAR-T治疗,为她治疗的宾夕法尼亚大学细胞免疫疗法中心主任Carl June博士曾表示:“当时我们非常怀疑培养的T细胞能否对抗她体内的白血病癌细胞。”
这位小女孩在5年后来到上述ODAC审评会现场,成为CTL019直接的疗效证据。
诺华的成功让业内沸腾,并将这一天称为“CAR-T日”,但患者和研发公司都曾面临巨大风险。
CAR-T是一种高度个性化的方法,每个人的细胞和接受过的治疗都不同,如同Emily一样,许多患者在接受CAR-T治疗前已经接受过各种治疗方法,如骨髓移植手术、化疗、靶向治疗等,所获得的T细胞的制备和编程也会各异。
此次获批公告中,FDA方面也表示,Kymriah的剂量是根据使用的患者自身T细胞所产生的定制治疗。“患者的T细胞被收集并送到制造中心,在进行遗传修饰以包括含有特异性蛋白质(嵌合抗原受体或CAR)的新基因,其指导T细胞靶向并杀死具有表面上的特异性抗原(CD19)。一旦细胞被修饰,它们被注入到患者体内以杀死癌细胞。”
而在CAR-T研发第一梯队中,诺华一开始的卡位并不领先。但JUNO的 JACR015在去年的临床研究中先后出现5例脑水肿引起患者死亡;Kite的KTE-C19也在4月底出现1例患者死亡,两家先后折戟让诺华后来居上。
FDA的生物制剂评估中心总监Peter Marks博士说:“Kymriah是一种前所未有的治疗方法,可满足儿童和年轻人对这种严重疾病的重要需求。Kymriah不仅为这些患者提供了一种新的治疗方案,在极其有限的选择中,这也是一种在临床试验中显示出有希望缓解和存活率的治疗方案。”
Kymriah的安全性和有效性在一项多中心临床试验中得到证实。治疗三个月内的总体缓解率为83%。
但FDA提示用Kymriah治疗有潜在的严重副作用。CAR-T治疗过程中会释放出很多杀伤肿瘤细胞的细胞因子,副作用通常表现为发烧、低血压、脑水肿等,此前在评估会议上专家也提出诸多需要关注的问题,包括T细胞的制备、有效性,生产质控和安全性,癌症复发,毒副作用等。
Kymriah
Generic Name: tisagenlecleucel (TIS a JEN lek LOO sel)
Brand Names: Kymriah
Medically reviewed on December 3, 2017
What is Kymriah?
Kymriah (tisagenlecleucel) is an immunotherapy medicine used to treat a certain type of acute lymphoblastic leukemia in people who are up to 25 years old.
Kymriah is also used to treat certain adult patients with large B-cell lymphoma.
Kymriah is given after other treatments have failed.
Kymriah is made from your own white blood cells, removed from a small amount of blood drawn from your body.
Kymriah is available under a special program. You must be registered in the program and understand the risks and benefits of this medicine.
Important information
A serious side effect of Kymriah is called cytokine release syndrome, which causes fever, chills, trouble breathing, vomiting, and other symptoms. Your caregivers will have medication available to quickly treat this condition if it occurs.
Kymriah can also cause life-threatening nerve problems. Tell your caregivers or seek emergency medical attention if you have problems with speech, problems with thinking or memory, confusion, or a seizure.
Kymriah side effects
Get emergency medical help if you have signs of an allergic reaction to Kymriah: hives; difficult breathing; swelling of your face, lips, tongue, or throat.
A serious side effect of Kymriah is called cytokine release syndrome (CRS). Tell your caregivers right away if you have signs of this condition: fever, chills, trouble breathing, body aches, vomiting, diarrhea, or feeling light-headed. Your caregivers will have medication available to quickly treat CRS if it occurs.
Also tell your caregivers or seek emergency medical attention if you have signs of life-threatening nerve problems: problems with speech, problems with thinking or memory, confusion, or a seizure.
Also call your doctor at once if you have:
· headaches, unusual tiredness;
· tremors, anxiety, agitation;
· unusual thoughts or behavior;
· trouble speaking or understanding what is said to you; or
· signs of infection - fever, chills, flu symptoms, mouth sores, skin sores, easy bruising or bleeding, cough, trouble breathing.
Common Kymriah side effects may include:
· nausea, vomiting, diarrhea, loss of appetite;
· fever;
· headache, confusion, feeling tired;
· bleeding; or
· fast heartbeats.
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
See also: Side effects (in more detail)
Before taking this medicineTo make sure Kymriah is safe for you, tell your doctor if you have ever had:
· hepatitis B or C;
· HIV (human immunodeficiency virus); or
· if you have received a vaccine in the past 2 weeks.
Women may need pregnancy testing before receiving this medicine. You may also need to use birth control to prevent pregnancy during and shortly after treatment with Kymriah and chemotherapy.
It is not known whether this medicine will harm an unborn baby. Tell your doctor if you are pregnant.
If you receive Kymriah during pregnancy, your baby's blood may need to be tested after it is born. This is to evaluate any effects the medicine may have had on the baby.
It is not known whether tisagenlecleucel passes into breast milk or if it could affect the nursing baby. Tell your doctor if you are breast-feeding.
How is Kymriah given?Your care providers will use an intravenous (IV) needle to draw your blood for collecting the white blood cells. The cells are then frozen and sent to a laboratory where they are made into tisagenlecleucel. This could take 3-4 weeks.
About 2 to 14 days before Kymriah is given, you will be pre-treated with chemotherapy to help prepare your body for tisagenlecleucel.
Just before you receive Kymriah, you will be given other medications to help prevent serious side effects or allergic reaction.
Once your body is ready to receive tisagenlecleucel, your care providers will inject the medicine into a vein through an IV.
For at least 4 weeks, plan to stay near the hospital or clinic where you received Kymriah. Avoid being so far away that it takes you longer than 2 hours to travel back to the hospital.
Serious and sometimes fatal infections may develop after the injection. Call your doctor right away if you have fever, chills, easy bruising, unusual bleeding, or other signs of infection.
This medicine can cause you to have a false positive screening test for HIV (human immunodeficiency virus). Tell any doctor who treats you that you are using Kymriah.
Using Kymriah may increase your risk of developing other types of cancer, or causing your leukemia to come back. Your doctor will need to check your progress for the rest of your life.
If you have ever had hepatitis B, Kymriah can cause this condition to come back or get worse. You will need frequent blood tests to check your liver function during treatment and for several months after you stop using this medicine.
Kymriah dosing informationUsual Adult Dose of Kymriah for Acute Lymphoblastic Leukemia:
Up to Age 25 Years:
-Body Weight 50 kg or less: 0.2 to 5 x 10(6) chimeric antigen receptor (CAR)-positive viable T cells per kg of body weight.
-Body Weight Above 50 kg: 0.1 to 2.5 x 10(8) CAR-positive viable T cells
Duration of Therapy: Infuse this drug 2 to 14 days after completion of lymphodepleting chemotherapy.
Comments:
-Base the dosage on the patient's weight at the time of leukapheresis.
-Administer this drug via IV infusion within 30 minutes of thawing at 10 to 20 mL per minute (adjusted as appropriate for smaller children and smaller volumes); the infusion bag volume ranges from 10 to 50 mL.
-Pre-medicate patients with acetaminophen and diphenhydramine or another H1-antihistamine approximately 30 to 60 minutes prior to infusion of this drug; avoid using corticosteroids at any time except in the case of a life-threatening emergency.
Use: Treatment of patients up to age 25 with B-cell precursor acute lymphoblastic leukemia (ALL) that is refractory or in second or later relapse.
Usual Pediatric Dose for Acute Lymphoblastic Leukemia:
-Body Weight 50 kg or less: 0.2 to 5 x 10(6) chimeric antigen receptor (CAR)-positive viable T cells per kg of body weight.
-Body Weight Above 50 kg: 0.1 to 2.5 x 10(8) CAR-positive viable T cells
Duration of Therapy: Infuse this drug 2 to 14 days after completion of lymphodepleting chemotherapy.
Comments:
-Base the dosage on the patient's weight at the time of leukapheresis.
-Administer this drug via IV infusion within 30 minutes of thawing at 10 to 20 mL per minute, adjusted as appropriate for smaller children and smaller volumes; the infusion bag volume ranges from 10 to 50 mL.
-Pre-medicate patients with acetaminophen and diphenhydramine or another H1-antihistamine approximately 30 to 60 minutes prior to infusion of this drug; avoid using corticosteroids at any time except in the case of a life-threatening emergency.
Use: Treatment of patients up to age 25 with B-cell precursor acute lymphoblastic leukemia (ALL) that is refractory or in second or later relapse.
See also: Dosage Information (in more detail)
What happens if I miss a dose?Call your doctor for instructions if you miss any of your chemotherapy treatment, or if you miss a dose of your medications to prevent side effects of Kymriah.
What happens if I overdose?Since this medicine is given by a healthcare professional in a medical setting, an overdose is unlikely to occur.
What should I avoid after receiving Kymriah?This medicine can cause weakness, drowsiness, confusion, problems with memory or coordination, and seizures. Avoid driving or operating machinery for at least 8 weeks after you are treated with Kymriah.
Do not donate blood, an organ, or any tissues or cells from your own body.
Do not receive a "live" vaccine while using Kymriah, or you could develop a serious infection. Live vaccines include measles, mumps, rubella (MMR), polio, rotavirus, typhoid, yellow fever, varicella (chickenpox), zoster (shingles), and nasal flu (influenza) vaccine.
What other drugs will affect Kymriah?Other drugs may interact with tisagenlecleucel, including prescription and over-the-counter medicines, vitamins, and herbal products. Tell your doctor about all your current medicines and any medicine you start or stop using.
Further informationRemember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use Kymriah only for the indication prescribed.
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
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