市場調查報告書
商品編碼
1452637
南美洲和中美洲T 細胞治療市場預測至2030 年- 區域分析- 按模式(研究和商業化)、治療類型[CAR T 細胞療法和基於T 細胞受體(TCR) 的] 和適應症(血液惡性腫瘤和實體腫瘤)腫瘤)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細胞治療市場價值為8,411萬美元,預計到2030年將達到2.6559億美元;預計2022年至2030年CAGR為15.5%。
T 細胞治療批准數量的增加推動了南美洲和中美洲 T 細胞治療市場
標靶治療、更快、更有效的恢復以及減少副作用都是 T 細胞療法的優點。在全球範圍內,細胞療法由於獲得了各種批准而被廣泛採用:
2023 年:吉利德旗下 Kite 公司宣佈在沙烏地阿拉伯、新加坡和巴西開展業務,作為其商業擴張的一部分。 Kite 已在這三個國家提交了其 CAR T 細胞治療產品的監管申請。
例如,2022年6月,百時美施貴寶的Breyanzi (lisocabtagene maraleucel) 獲得FDA 批准,這是一種CD19 定向嵌合抗原受體(CAR) T 細胞療法,用於治療成人大B 細胞淋巴瘤(LBCL ) 患者。
2022年2月,美國食品藥物管理局(FDA) 批准Yescarta (axicabtagene ciloleucel) CAR T 細胞療法用於治療一線化學免疫療法難治或一線化學免疫療法12 個月內復發的大B 細胞淋巴瘤成人患者。 Yescarta 是第一個獲得全國綜合癌症網路 (NCCN) 1 類推薦的 CAR T 細胞療法。
2022年2月,FDA核准了ciltacabtagene autoleucel(商品名CARVYKTI)用於治療經過四線或四線以上治療(包括蛋白酶體抑制劑、免疫調節劑和抗CD38單株抗體)後復發或難治性多發性骨髓瘤的成年患者。
2022年1月,FDA核准Kimmtrak(tebentafusp-tebn)用於治療HLA-A*02:01陽性的不可切除或轉移性葡萄膜黑色素瘤患者。
2021年3月,Abecma(idecabtagene vicleucel)被FDA核准用於治療復發或難治性多發性骨髓瘤。該療法是一種針對 B 細胞成熟抗原 (BCMA) 的基因改造自體 T 細胞免疫療法,適用於治療患有難治性多發性骨髓瘤的成年患者。
因此,越來越多的 T 細胞療法獲批正在推動市場成長。
南美洲和中美洲 T 細胞治療市場概述
南美洲和中美洲 T 細胞治療市場僅限於巴西,因為該產品僅在該國獲得批准和商業化。根據《巴西癌症學雜誌》報道,預計 2023 年至 2025 年期間將新增約 704,000 例癌症病例。據估計,巴西每年診斷出超過 12,000 例非何杰金氏淋巴瘤 (NHL) 病例。巴西衛生監管機構(ANVISA) 已在巴西批准了兩種CAR T 細胞療法:tisagenlecleucel(諾華公司),用於治療患有RR B 細胞急性淋巴細胞白血病(ALL) 的兒科患者和年輕人以及患有復發/難治性(RR) 的成人患者瀰漫性大 B 細胞淋巴瘤和 ciltacabtagene autoleucel (cilta-cel) 用於治療復發/難治性多發性骨髓瘤 (RRMM) 患者。此外,2022年8月,吉利德旗下公司Kite透過在巴西、新加坡和沙烏地阿拉伯開展業務來擴大業務。 Kite 已提交其 CAR T 細胞治療產品的監管申請。癌症和淋巴瘤病例的增加以及 T 細胞療法的應用和臨床試驗數量的增加預計將在未來幾年推動需求。
南美洲和中美洲 T 細胞治療市場收入及 2030 年預測(百萬美元)
南美洲和中美洲 T 細胞治療市場細分
南美洲和中美洲 T 細胞治療市場分為模式、治療類型、適應症和國家。
根據模式,南美洲和中美洲 T 細胞治療市場分為研究和商業化市場。 2022年,商業化細分市場將佔據更大的市場佔有率。
根據治療類型,南美洲和中美洲T細胞治療市場分為CAR T細胞療法和T細胞受體(TCR)療法。 2022年,CAR T細胞療法領域將佔據更大的市場佔有率。
根據適應症,南美洲和中美洲 T 細胞治療市場分為血液惡性腫瘤和實體腫瘤。 2022 年,血液惡性腫瘤細分市場佔據最大市場。
從國家來看,南美洲和中美洲 T 細胞治療市場僅限於巴西。 2022 年,巴西在南美洲和中美洲 T 細胞治療市場佔有率中佔據主導地位。
百時美施貴寶公司、吉利德科學公司、楊森全球服務有限責任公司和諾華公司是南美洲和中美洲 T 細胞治療市場的一些領導公司。
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.