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南美洲和中美洲T 细胞治疗市场预测至2030 年- 区域分析- 按模式(研究和商业化)、治疗类型[CAR T 细胞疗法和基于T 细胞受体(TCR) 的] 和适应症(血液恶性肿瘤和实体肿瘤)肿瘤)South & Central America T Cell Therapy Market Forecast to 2030 - Regional Analysis - by Modality (Research and Commercialized), Therapy Type [CAR T-cell Therapy and T-cell Receptor (TCR)-based], and Indication (Hematologic Malignancies and Solid Tumors) |
2022年南美洲和中美洲T细胞治疗市场价值为8,411万美元,预计到2030年将达到2.6559亿美元;预计2022年至2030年CAGR为15.5%。
T 细胞治疗批准数量的增加推动了南美洲和中美洲 T 细胞治疗市场
标靶治疗、更快、更有效的恢復以及减少副作用都是 T 细胞疗法的优点。在全球范围内,细胞疗法由于获得了各种批准而被广泛采用:
2023 年:吉利德旗下 Kite 公司宣布在沙乌地阿拉伯、新加坡和巴西开展业务,作为其商业扩张的一部分。 Kite 已在这三个国家提交了其 CAR T 细胞治疗产品的监管申请。
例如,2022年6月,百时美施贵宝的Breyanzi (lisocabtagene maraleucel) 获得FDA 批准,这是一种CD19 定向嵌合抗原受体(CAR) T 细胞疗法,用于治疗成人大B 细胞淋巴瘤(LBCL ) 患者。
2022年2月,美国食品药物管理局(FDA) 批准Yescarta (axicabtagene ciloleucel) CAR T 细胞疗法用于治疗一线化学免疫疗法难治或一线化学免疫疗法12 个月内復发的大B 细胞淋巴瘤成人患者。 Yescarta 是第一个获得全国综合癌症网络 (NCCN) 1 类推荐的 CAR T 细胞疗法。
2022年2月,FDA核准了ciltacabtagene autoleucel(商品名CARVYKTI)用于治疗经过四线或四线以上治疗(包括蛋白酶体抑制剂、免疫调节剂和抗CD38单株抗体)后復发或难治性多发性骨髓瘤的成年患者。
2022年1月,FDA核准Kimmtrak(tebentafusp-tebn)用于治疗HLA-A*02:01阳性的不可切除或转移性葡萄膜黑色素瘤患者。
2021年3月,Abecma(idecabtagene vicleucel)被FDA核准用于治疗復发或难治性多发性骨髓瘤。该疗法是一种针对 B 细胞成熟抗原 (BCMA) 的转基因自体 T 细胞免疫疗法,适用于治疗患有难治性多发性骨髓瘤的成年患者。
因此,越来越多的 T 细胞疗法获批正在推动市场成长。
南美洲和中美洲 T 细胞治疗市场概述
南美洲和中美洲 T 细胞治疗市场仅限于巴西,因为该产品仅在该国获得批准和商业化。根据《巴西癌症学杂誌》报道,预计 2023 年至 2025 年期间将新增约 704,000 例癌症病例。据估计,巴西每年诊断出超过 12,000 例非何杰金氏淋巴瘤 (NHL) 病例。巴西卫生监管机构(ANVISA) 已在巴西批准了两种CAR T 细胞疗法:tisagenlecleucel(诺华公司),用于治疗患有RR B 细胞急性淋巴细胞白血病(ALL) 的儿科患者和年轻人以及患有復发/难治性(RR) 的成人患者瀰漫性大 B 细胞淋巴瘤和 ciltacabtagene autoleucel (cilta-cel) 用于治疗復发/难治性多发性骨髓瘤 (RRMM) 患者。此外,2022年8月,吉利德旗下公司Kite透过在巴西、新加坡和沙乌地阿拉伯开展业务来扩大业务。 Kite 已提交其 CAR T 细胞治疗产品的监管申请。癌症和淋巴瘤病例的增加以及 T 细胞疗法的应用和临床试验数量的增加预计将在未来几年推动需求。
南美洲和中美洲 T 细胞治疗市场收入及 2030 年预测(百万美元)
南美洲和中美洲 T 细胞治疗市场细分
南美洲和中美洲 T 细胞治疗市场分为模式、治疗类型、适应症和国家。
根据模式,南美洲和中美洲 T 细胞治疗市场分为研究和商业化市场。 2022年,商业化细分市场将占据更大的市场份额。
根据治疗类型,南美洲和中美洲T细胞治疗市场分为CAR T细胞疗法和T细胞受体(TCR)疗法。 2022年,CAR T细胞疗法领域将占据更大的市场份额。
根据适应症,南美洲和中美洲 T 细胞治疗市场分为血液恶性肿瘤和实体肿瘤。 2022 年,血液恶性肿瘤细分市场占据最大市场。
从国家来看,南美洲和中美洲 T 细胞治疗市场仅限于巴西。 2022 年,巴西在南美洲和中美洲 T 细胞治疗市场份额中占据主导地位。
百时美施贵宝公司、吉利德科学公司、杨森全球服务有限责任公司和诺华公司是南美洲和中美洲 T 细胞治疗市场的一些领导公司。
The South & Central America T cell therapy market was valued at US$ 84.11 million in 2022 and is expected to reach US$ 265.59 million by 2030; it is estimated to grow at a CAGR of 15.5% from 2022 to 2030.
Increasing Number of T-Cell Therapy Approvals Fuels the South & Central America T Cell Therapy Market
Targeted treatment, faster and more efficient recovery, and reduced side effects are among the advantages of t cell therapy. Globally, cell therapies are widely adopted owing to the availability of various approval:
In 2023: Kite, a Gilead Company announced launching operations in Saudi Arabia, Singapore, and Brazil as part of its commercial expansion. Kite has filed regulatory applications for its CAR T-cell therapy products in each of the three nations.
For instance, in June 2022, Bristol Myers Squibb received FDA approval for Breyanzi (lisocabtagene maraleucel), a CD19-directed chimeric antigen receptor (CAR) T-cell therapy, for the treatment of adult patients with large B-cell lymphoma (LBCL).
In February 2022, the US Food and Drug Administration (FDA) approved Yescarta (axicabtagene ciloleucel) CAR T-cell therapy for adult patients with large B-cell lymphoma that is refractory to first line chemoimmunotherapy or that relapses within 12 months of first line chemoimmunotherapy. Yescarta is the first CAR T-cell therapy to receive a National Comprehensive Cancer Network (NCCN) Category 1 recommendation.
In February 2022, the FDA approved ciltacabtagene autoleucel (brand name CARVYKTI) for treating adult patients with relapsed or refractory multiple myeloma after four or more prior lines of therapy, including a proteasome inhibitor, an immunomodulatory agent, and an anti-CD38 monoclonal antibody.
In January 2022, the FDA approved Kimmtrak (tebentafusp-tebn) for treating unresectable or metastatic uveal melanoma patients who are HLA-A*02:01 positive.
In March 2021, Abecma (idecabtagene vicleucel) was approved by the FDA for treating relapsed or refractory multiple myeloma. The treatment is a B-cell maturation antigen (BCMA)-directed genetically modified autologous T-cell immunotherapy indicated for treating adult patients with refractory multiple myeloma.
Therefore, the increasing number of approvals for T-cell therapies is fueling the market growth.
South & Central America T Cell Therapy Market Overview
The South & Central America T-cell therapy market is limited to Brazil as the products are only approved and commercially available in the country. According to the Brazilian Journal of Cancerology, it is estimated that ~704,000 new cases of cancer are expected during 2023-2025. More than 12,000 non-Hodgkin lymphoma (NHL) cases in Brazil are estimated to be diagnosed yearly. The Brazilian Health Regulatory Agency (ANVISA) has approved two CAR T-cell therapies in Brazil: tisagenlecleucel (by Novartis) for pediatric patients and young adults with RR B-cell acute lymphoblastic leukemia (ALL) and adults with relapsed/refractory (RR) diffuse large B-cell lymphoma, and ciltacabtagene autoleucel (cilta-cel) for patients with relapsed/refractory multiple myeloma (RRMM). Moreover, in August 2022, Kite, a Gilead Company, expanded its business by launching operations in Brazil, Singapore, and Saudi Arabia. Kite has submitted regulatory applications for its CAR T-cell therapy products. The rising cases of cancer and lymphoma, and the increasing number of applications and clinical trials for T-cell therapies are expected to boost the demand in the coming years.
South & Central America T Cell Therapy Market Revenue and Forecast to 2030 (US$ Mn)
South & Central America T Cell Therapy Market Segmentation
The South & Central America T cell therapy market is segmented into modality , therapy type, indication, and country.
Based on modality, the South & Central America T cell therapy market is bifurcated into research and commercialized. The commercialized segment held a larger market share in 2022.
Based on therapy type, the South & Central America T cell therapy market is divided into CAR T-cell therapy and T-cell Receptor (TCR)-based. The CAR T-cell therapy segment held a larger market share in 2022.
Based on indication, the South & Central America T cell therapy market is bifurcated into hematologic malignancies and solid tumors. The hematologic malignancies segment held the largest market share in 2022.
Based on country, the South & Central America T cell therapy market is limited to Brazil. Brazil dominated the South & Central America T cell therapy market share in 2022.
Bristol-Myers Squibb Co, Gilead Sciences Inc, Janssen Global Services LLC, and Novartis AG are some of the leading companies operating in the South & Central America T cell therapy market.