![]() |
½ÃÀ庸°í¼
»óǰÄÚµå
1452637
Áß³²¹ÌÀÇ T¼¼Æ÷Ä¡·á ½ÃÀå ¿¹Ãø(-2030³â) : Áö¿ªº° ºÐ¼® : ¸ð´Þ¸®Æ¼º°, Ä¡·á À¯Çüº°(CAR T¼¼Æ÷Ä¡·á, T¼¼Æ÷ ¼ö¿ëü ±â¹Ý), ÀûÀÀÁõº°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) |
Áß³²¹ÌÀÇ T¼¼Æ÷Ä¡·á ½ÃÀåÀº 2022³â¿¡ 8,411¸¸ ´Þ·¯·Î Æò°¡µÇ¸ç, 2030³â¿¡´Â 2¾ï 6,559¸¸ ´Þ·¯¿¡ ´ÞÇÒ °ÍÀ¸·Î ¿¹ÃøµÇ¸ç, 2022-2030³âÀÇ CAGRÀº 15.5%·Î ¼ºÀåÇÒ °ÍÀ¸·Î ÃßÁ¤µË´Ï´Ù.
T¼¼Æ÷Ä¡·á ½ÂÀÎ °Ç¼ö Áõ°¡·Î Áß³²¹Ì T¼¼Æ÷Ä¡·á ½ÃÀå ¼ºÀå ÃËÁø
Ç¥ÀûÈµÈ Ä¡·á, ´õ ºü¸£°í È¿À²ÀûÀΠȸº¹, ºÎÀÛ¿ë °¨¼Ò µîÀÌ T¼¼Æ÷ Ä¡·áÀÇ ÀåÁ¡ÀÔ´Ï´Ù. Àü ¼¼°è¿¡¼ ¼¼Æ÷Ä¡·á´Â ´Ù¾çÇÑ ½ÂÀÎÀ¸·Î ÀÎÇØ ³Î¸® »ç¿ëµÇ°í ÀÖ½À´Ï´Ù.
2023³â ±æ¸®¾îµå ÄÄÆÛ´Ï(Gilead Company)ÀÇ ÀÚȸ»ç Kite´Â »ó¾÷Àû È®ÀåÀÇ ÀÏȯÀ¸·Î »ç¿ìµð¾Æ¶óºñ¾Æ, ½Ì°¡Æ÷¸£, ºê¶óÁú¿¡¼ »ç¾÷À» ½ÃÀÛÇÑ´Ù°í ¹ßÇ¥ÇßÀ¸¸ç, Kite´Â 3°³ ±¹°¡¿¡¼ CAR T ¼¼Æ÷ Ä¡·á Á¦Ç°ÀÇ ½ÂÀÎÀ» ½ÅûÇß½À´Ï´Ù.
¿¹¸¦ µé¾î ºê¸®½ºÅç ¸¶À̾ ½ºÄûºê(Bristol Myers Squibb)´Â 2022³â 6¿ù CD19 ÁöÇ⼺ Ű¸Þ¶ó Ç׿ø ¼ö¿ëü(CAR) T¼¼Æ÷ Ä¡·áÁ¦ÀÎ Breyanzi(lisocabtagene maraleucel)¿¡ ´ëÇØ ¼ºÀÎ ´ë¼¼Æ÷ B¼¼Æ÷ ¸²ÇÁÁ¾(LBCL) ȯÀÚÀÇ Ä¡·áÁ¦·Î¼ FDAÀÇ ½ÂÀÎÀ» ȹµæÇÏ¿´½À´Ï´Ù.
¹Ì ½ÄǰÀǾ౹(FDA)Àº Áö³ 2¿ù ¿¹½ºÄ«¸£Å¸(¿¹½ºÄ«¸£Å¸, axicabtagene ciloleucel)¸¦ 1Â÷ ÈÇи鿪¿ä¹ý¿¡ ºÒÀÀÇϰųª 1Â÷ ÈÇи鿪¿ä¹ý ÈÄ 12°³¿ù À̳»¿¡ Àç¹ßÇÑ ´ë¼¼Æ÷ B¼¼Æ÷ ¸²ÇÁÁ¾ ¼ºÀΠȯÀÚ¸¦ À§ÇÑ CAR T¼¼Æ÷ Ä¡·áÁ¦·Î ½ÂÀÎÇß½À´Ï´Ù. ¿¹½ºÄ«¸£Å¸´Â NCCN(National Comprehensive Cancer Network)ÀÇ Ä«Å×°í¸® 1 ±Ç°í¾ÈÀ» ¹ÞÀº ÃÖÃÊÀÇ CAR T¼¼Æ÷ Ä¡·áÁ¦ÀÔ´Ï´Ù.
2022³â 2¿ù, FDA´Â ciltacabtagene autoleucel(»óǰ¸í CARVYKTI)À» ÇÁ·ÎÅ×¾ÆÁ» ¾ïÁ¦Á¦, ¸é¿ªÁ¶ÀýÁ¦, Ç×CD38 ¸ð³ëŬ·Î³Î Ç×ü µî 4°¡Áö ÀÌ»óÀÇ Ä¡·á °æÇèÀÌ ÀÖ´Â Àç¹ß¼º ¶Ç´Â ºÒÀÀ¼º ´Ù¹ß¼º °ñ¼öÁ¾ ¼ºÀΠȯÀÚÀÇ Ä¡·áÁ¦·Î ½ÂÀÎ ½ÂÀεǾú½À´Ï´Ù.
2020³â 1¿ù, FDA´Â HLA-A*02:01 ¾ç¼ºÀÎ ÀýÁ¦ ºÒ°¡´ÉÇÑ ¶Ç´Â ÀüÀ̼º Æ÷µµ¸· Èæ»öÁ¾ ȯÀÚÀÇ Ä¡·áÁ¦·Î Å´Æ®·¢(tebentafusp-tebn)À» ½ÂÀÎÇß½À´Ï´Ù.
2021³â 3¿ù, ¾Æº£Äí¸¶(idecabtagene vicleucel)´Â Àç¹ß¼º ¶Ç´Â ºÒÀÀ¼º ´Ù¹ß¼º °ñ¼öÁ¾ Ä¡·áÁ¦·Î FDAÀÇ ½ÂÀÎÀ» ¹Þ¾Ò½À´Ï´Ù. ÀÌ Ä¡·áÁ¦´Â B ¼¼Æ÷ ¼º¼÷ Ç׿ø(BCMA) ÁöÇ⼺ À¯ÀüÀÚ ÀçÁ¶ÇÕ ÀÚ°¡ T ¼¼Æ÷ ¸é¿ª ¿ä¹ýÀ¸·Î ³Ä¡¼º ´Ù¹ß¼º °ñ¼öÁ¾ ¼ºÀΠȯÀÚ Ä¡·á¿¡ ÀûÀÀÁõÀ» °¡Áö°í ÀÖ½À´Ï´Ù.
µû¶ó¼ T ¼¼Æ÷ Ä¡·áÀÇ ½ÂÀÎ °Ç¼ö Áõ°¡°¡ ½ÃÀå ¼ºÀåÀ» ÃËÁøÇϰí ÀÖ½À´Ï´Ù.
Áß³²¹Ì T¼¼Æ÷Ä¡·á ½ÃÀå °³¿ä
Áß³²¹Ì T¼¼Æ÷Ä¡·á ½ÃÀåÀº ºê¶óÁú¿¡ ±¹ÇѵǾî ÀÖÀ¸¸ç, ºê¶óÁú¿¡¼¸¸ ½ÂÀÎµÇ¾î ½ÃÆÇµÇ°í ÀÖÀ¸¸ç, Brazilian Journal of Cancerology¿¡ µû¸£¸é 2023-2025³â »çÀÌ 70¸¸ 4,000¸íÀÇ ¾Ï ȯÀÚ°¡ »õ·Î ¹ß»ýÇÒ °ÍÀ¸·Î ¿¹»óµÇ°í ÀÖ½À´Ï´Ù. ¹ß»ýµÉ °ÍÀ¸·Î ¿¹»óµË´Ï´Ù. ºê¶óÁú¿¡¼´Â ¿¬°£ 12,000°Ç ÀÌ»óÀÇ ºñÈ£ÁöŲ¸²ÇÁÁ¾(NHL)ÀÌ Áø´ÜµÇ´Â °ÍÀ¸·Î ÃßÁ¤µË´Ï´Ù. ºê¶óÁú º¸°Ç±ÔÁ¦Ã»(ANVISA)Àº ºê¶óÁú¿¡¼ µÎ °¡Áö CAR T¼¼Æ÷ Ä¡·áÁ¦¸¦ ½ÂÀÎÇß½À´Ï´Ù. ¼Ò¾Æ ¹× ÀþÀº ¼ºÀÎ RR B¼¼Æ÷¼º ±Þ¼º ¸²ÇÁ¸ð±¸¹éÇ÷º´(ALL)°ú ¼ºÀÎ Àç¹ß ¹× ºÒÀÀ¼º ¹Ì¸¸¼º °Å´ë B¼¼Æ÷ ¸²ÇÁÁ¾(RRMM) ȯÀÚ¸¦ ´ë»óÀ¸·Î ÇÑ Æ¼½ê°Õ ·¹Å¬·ÎÀ̼¿(Novartis AG)°ú Àç¹ß ¹× ºÒÀÀ¼º ´Ù¹ß¼º °ñ¼öÁ¾(RRMM) ȯÀÚ¸¦ ´ë»óÀ¸·Î ÇÑ Àç¹ß¼º ¹× ºÒÀÀ¼º ´Ù¹ß¼º°ñ¼öÁ¾(RRMM) ȯÀÚ¸¦ ´ë»óÀ¸·Î ÇÑ Æ¿Å¸Ä«ºÎŸÁ¨ ¿ÀÅä·ÎÀ̼¿(ƿŸ¼¿)ÀÔ´Ï´Ù. ¶ÇÇÑ 2022³â 8¿ù, ±æ¸®¾îµå Ä«ÀÌÆ®´Â ºê¶óÁú, ½Ì°¡Æ÷¸£, »ç¿ìµð¾Æ¶óºñ¾Æ¿¡¼ »ç¾÷À» ½ÃÀÛÇÏ¸ç »ç¾÷À» È®ÀåÇß½À´Ï´Ù. Ä«ÀÌÆ®´Â CAR T¼¼Æ÷ Ä¡·á Á¦Ç°ÀÇ ½ÂÀÎÀ» ½ÅûÇÑ »óÅ´Ù. ¾Ï ¹× ¸²ÇÁÁ¾ ȯÀÚ ¼ö Áõ°¡, T¼¼Æ÷ Ä¡·á ½Åû °Ç¼ö ¹× ÀÓ»ó½ÃÇè °Ç¼ö Áõ°¡´Â ÇâÈÄ ¼ö³â°£ ¼ö¿ä¸¦ Áõ°¡½Ãų °ÍÀ¸·Î ¿¹»óµË´Ï´Ù.
Áß³²¹Ì T¼¼Æ÷Ä¡·á ½ÃÀå ¸ÅÃâ ¹× 2030³â±îÁöÀÇ ¿¹Ãø(US$Mn)
Áß³²¹Ì T ¼¼Æ÷ Ä¡·á ½ÃÀå ¼¼ºÐÈ
Áß³²¹Ì T ¼¼Æ÷ Ä¡·á ½ÃÀå ¼¼ºÐÈÁß³²¹Ì T¼¼Æ÷Ä¡·á ½ÃÀåÀº Ä¡·á¹ý, Ä¡·á À¯Çü, ÀûÀÀÁõ, ±¹°¡º°·Î ±¸ºÐµË´Ï´Ù.
¾ç½Äº°·Î Áß³²¹Ì T ¼¼Æ÷ Ä¡·á ½ÃÀåÀº ¿¬±¸¿ë°ú »ó¾÷¿ëÀ¸·Î ³ª´µ¸ç, 2022³â ½ÃÀå Á¡À¯À²Àº »ó¾÷È ºÎ¹®¿¡¼ ´õ Å« ºñÁßÀ» Â÷ÁöÇÒ °ÍÀ¸·Î ¿¹»óµË´Ï´Ù.
Ä¡·á À¯Çü¿¡ µû¶ó Áß³²¹Ì T ¼¼Æ÷ Ä¡·á ½ÃÀåÀº CAR T ¼¼Æ÷ Ä¡·á¿Í T ¼¼Æ÷ ¼ö¿ëü(TCR) ±â¹ÝÀ¸·Î ³ª´µ¸ç, 2022³â ½ÃÀå Á¡À¯À²Àº CAR T ¼¼Æ÷ Ä¡·á°¡ ´õ ³ôÀ» °ÍÀ¸·Î ¿¹»óµË´Ï´Ù.
ÀûÀÀÁõ¿¡ µû¶ó Áß³²¹Ì T ¼¼Æ÷ Ä¡·á ½ÃÀåÀº Ç÷¾× ¾Ç¼º Á¾¾ç°ú °íÇü Á¾¾çÀ¸·Î ³ª´µ¸ç, 2022³â Ç÷¾× ¾Ç¼º Á¾¾çÀÌ °¡Àå Å« ½ÃÀå Á¡À¯À²À» Â÷ÁöÇÒ °ÍÀÔ´Ï´Ù.
±¹°¡º°·Î´Â Áß³²¹Ì T ¼¼Æ÷ Ä¡·á ½ÃÀåÀº ºê¶óÁú¿¡ ±¹ÇѵǾî ÀÖÀ¸¸ç, 2022³â Áß³²¹Ì T ¼¼Æ÷ Ä¡·á ½ÃÀå Á¡À¯À²Àº ºê¶óÁúÀÌ µ¶Á¡Çß½À´Ï´Ù.
Bristol-Myers Squibb Co, Gilead Sciences Inc, Janssen Global Services LLC, Novartis AG´Â Áß³²¹Ì T¼¼Æ÷Ä¡·á ½ÃÀå¿¡¼ Ȱµ¿ÇÏ´Â ÁÖ¿ä ±â¾÷ÀÔ´Ï´Ù.
The South & Central America T cell therapy market was valued at US$ 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.