{"id":59191,"date":"2024-09-09T00:05:10","date_gmt":"2024-09-09T00:05:10","guid":{"rendered":"https:\/\/english.saigonbiz.com.vn\/2024\/09\/09\/hutchmed-highlights-clinical-data-to-be-presented-at-esmo-congress-2024-and-the-2024-world-conference-of-lung-cancer\/"},"modified":"2024-09-09T00:05:10","modified_gmt":"2024-09-09T00:05:10","slug":"hutchmed-highlights-clinical-data-to-be-presented-at-esmo-congress-2024-and-the-2024-world-conference-of-lung-cancer","status":"publish","type":"post","link":"https:\/\/english.saigonbiz.com\/vn\/hutchmed-highlights-clinical-data-to-be-presented-at-esmo-congress-2024-and-the-2024-world-conference-of-lung-cancer\/","title":{"rendered":"HUTCHMED Highlights Clinical Data to be Presented at ESMO Congress 2024 and the 2024 World Conference of Lung Cancer"},"content":{"rendered":"<div>\n<p align=\"justify\">HONG KONG and SHANGHAI and FLORHAM PARK, N.J., Sept.  09, 2024  (GLOBE NEWSWIRE) &#8212; HUTCHMED (China) Limited (\u201c<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=tOH8YgJ20vo_e2ADKDmd0t3L8NQhq_Su6tcj1YvMVTiIdrn4M281jIjBMtxcAZiSi9cRzu8FDXJ-54XiMXsHcQ==\" rel=\"nofollow noopener\" target=\"_blank\" title=\"HUTCHMED\">HUTCHMED<\/a>\u201d) (Nasdaq\/AIM:HCM; HKEX:13) today announces that new and updated data from several studies of compounds discovered by HUTCHMED will be presented at the 2024 World Conference on Lung Cancer (\u201cWCLC24\u201d) in San Diego, USA, and the European Society for Medical Oncology (\u201cESMO\u201d) Congress 2024, taking place in Barcelona, Spain.<\/p>\n<p align=\"justify\">Results from the FLOWERS study, a prospective, two-arm, randomized, multicenter Phase II clinical trial of osimertinib with or without savolitinib as first-line treatment in EGFRm, MET-aberrant advanced non-small cell lung cancer (\u201cNSCLC\u201d) patients, will be presented at WCLC24. As of May 28, 2024, the median follow-up was 8.2 months. Patients treated with osimertinib plus savolitinib (Cohort 2, N=21) showed deeper and more durable response over osimertinib monotherapy (Cohort 1, N=23) along the study follow-up. The confirmed objective response rate (ORR) in Cohort 1 and Cohort 2 were 60.9% and 90.5%, respectively, with disease control rate (DCR) of 87% and 95.2%, respectively. Immature progression-free survival (\u201cPFS\u201d) data also showed a positive trend in favor of the combination therapy, with median PFS of 9.3 months and 19.6 months in the cohort 1 and cohort 2 with maturity of 34.8% and 23.8%, respectively. Safety profiles of osimertinib monotherapy and osimertinib plus savolitinib were as expected, tolerable and manageable.<\/p>\n<table style=\"border-collapse: collapse; width:100%; border-collapse:collapse ;\">\n<tr>\n<td style=\"max-width:44%; width:44%; min-width:44%;;border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; text-align: center ;  vertical-align: middle; vertical-align: middle ; \"><strong>Abstract title<\/strong><\/td>\n<td style=\"max-width:28%; width:28%; min-width:28%;;border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; text-align: center ;  vertical-align: middle; vertical-align: middle ; \"><strong>Presenter \/ Lead author<\/strong><\/td>\n<td style=\"max-width:28%; width:28%; min-width:28%;;border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; text-align: center ;  vertical-align: middle; vertical-align: middle ; \"><strong>Presentation details<\/strong><\/td>\n<\/tr>\n<tr>\n<td colspan=\"3\" style=\"border-bottom: solid black 1pt ; vertical-align: middle ; \"><strong>WCLC24 &#8211; INVESTIGATOR-INITIATED STUDIES <\/strong><\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Osimertinib with or without savolitinib as 1L in de novo MET aberrant, EGFRm advanced NSCLC (CTONG 2008): A Phase II trial<\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Jinji Yang, <br \/>Guangdong Lung Cancer Institute, Guangdong Provincial People\u2019s Hospital, Southern Medical University, Guangzhou, China<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \"><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=EkPmgbZNbh9hfwHEoDgLh4e78v1BWQixn9dviKnz-3ss2l6KPaOprFpeBrWuLkXiq7sK4FlZkMyfBElI-KpPq8qVhB2rQYE4H3wQ7LPUxijvBubUpavFcSUz_SlLN_jG\" rel=\"nofollow noopener\" target=\"_blank\" title=\"PL04.10\">PL04.10<\/a><br \/>Plenary Session <br \/>PL04 Presidential Symposium 2, <br \/>Plenary Hall<br \/>Monday, September 9, 2024 at <br \/>8:30 AM PDT<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Study of Surufatinib Combined with Low Dose Topotecan in Second or Third-Line Multiple Distant Organ Metastatic ES-SCLC<\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Yingying Du, The First Affiliated Hospital of Anhui Medical University, Hefei, China; Hesheng Qian, Fuyang Cancer Hospital, Fuyang, China<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \"><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=ZPlXbLIhGaWvSbdYNeW_IvUwNE_-7aZ_EHwcHzYM9Mb0oUVa5QDJEc09VQKvZxYWVFK7D1LX2n1F856UnB2JhCbikrnpKXqhYgYby-x2WwZ6Q9rYmhur6aIAUsvFydPG\" rel=\"nofollow noopener\" target=\"_blank\" title=\"EP.13A.04A\">EP.13A.04A<\/a><br \/>ePoster<br \/>Saturday, September 7, 2024<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Surufatinib Plus Docetaxel in Patients with Relapsed Advanced Driver-Negative Non-Squamous NSCLC: A Phase Ib\/II Study <\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Qitao Yu, Wei Jiang, <br \/>Guangxi Medical University Cancer Hospital, Nanning, China<\/p>\n<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \"><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=zn3z-nTx_-Q4ZdRo15If4HZGXYNq6o1W2WIs36avQG3iUINcZlKCrPCOVAw3NpVuOa3vbxTwWMOHC5td8rsWvOOCF2bad4zK4pM0i3eH4Y8YSERdzXrPJBQ4ZghbXi0W\" rel=\"nofollow noopener\" target=\"_blank\" title=\"P3.12C.08\">P3.12C.08<\/a><br \/>Poster<br \/>Monday, September 9, 2024 at <br \/>8:30 AM PDT<\/td>\n<\/tr>\n<tr>\n<td style=\"vertical-align: top ; \">\u00a0<\/td>\n<td style=\"vertical-align: top ; \">\u00a0<\/td>\n<td style=\"vertical-align: top ; \">\u00a0<\/td>\n<\/tr>\n<\/table>\n<p align=\"justify\">Further analysis of fruquintinib\u2019s FRESCO-2 study in metastatic colorectal cancer and FRUTIGA study in gastric cancer, a biomarker study of savolitinib in gastric cancer as well as investigator-initiated studies of fruquintinib and surufatinib will be presented at the ESMO Congress 2024. Details of the presentations are as follows:<\/p>\n<table style=\"border-collapse: collapse; width:100%; border-collapse:collapse ;\">\n<tr>\n<td style=\"max-width:44%; width:44%; min-width:44%;;border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; text-align: center ;  vertical-align: middle; vertical-align: middle ; \"><strong>Abstract title<\/strong><\/td>\n<td style=\"max-width:28%; width:28%; min-width:28%;;border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; text-align: center ;  vertical-align: middle; vertical-align: middle ; \"><strong>Presenter \/ Lead author<\/strong><\/td>\n<td style=\"max-width:28%; width:28%; min-width:28%;;border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; text-align: center ;  vertical-align: middle; vertical-align: middle ; \"><strong>Presentation details<\/strong><\/td>\n<\/tr>\n<tr>\n<td colspan=\"3\" style=\"border-bottom: solid black 1pt ; vertical-align: middle ; \"><strong>ESMO 2024 &#8211; SPONSORED STUDIES<\/strong><\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Efficacy and safety of\u00a0fruquintinib\u00a0in patients with refractory metastatic colorectal cancer with and without liver metastasis: A subgroup analysis of the phase 3 FRESCO-2 trial<\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Rocio Garcia-Carbonero,<br \/>Hospital Universitario 12 de Octubre, lmas12, UCM, Madrid, Spain<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">520P <br \/>Poster Session \u2013 Colorectal cancer<br \/>Monday, 16 September 2024<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Efficacy and safety of fruquintinib in refractory metastatic colorectal cancer: A FRESCO-2 subgroup analysis by age<\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Maria Elena Elez Fernandez,<br \/>Vall d&#8217;Hebron Barcelona Hospital Campus, Universitat Aut\u00f2noma de Barcelona, Barcelona, Spain<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">526P<br \/>Poster Session \u2013 Colorectal cancer<br \/>Monday, 16 September 2024<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Efficacy of fruquintinib plus paclitaxel (F+PTX) in patients (pts) with prior immunotherapy (prior-IO): subgroup analysis from\u00a0FRUTIGA\u00a0study<\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Lin Shen,<br \/>Peking University Cancer Hospital &amp; Institute, Beijing, China<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">1410P<br \/>Poster Session \u2013 Oesophagogastric cancer<br \/>Monday, 16 September 2024<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Impact of subsequent anti-tumor therapies in patients (pts) with advanced gastric or gastroesophageal junction (G\/GEJ) adenocarcinoma receiving fruquintinib (F) plus paclitaxel (PTX) or placebo plus PTX in\u00a0FRUTIGA\u00a0study<\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Ruihua Xu,<br \/>Sun Yat-sen University Cancer Center, Guangzhou, China<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">1434P<br \/>Poster Session \u2013 Oesophagogastric cancer<br \/>Monday, 16 September 2024<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Association between Fruquintinib-induced Hypertension and Clinical Outcomes from FRUTIGA, a Phase 3 Study of Fruquintinib plus Paclitaxel in Previously Treated Advanced Gastric or Gastroesophageal Junction (G\/GEJ) Adenocarcinoma<\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Shukui Qin,<br \/>Chinese People&#8217;s Liberation Army Cancer Center of Nanjing Bayi Hospital, Nanjing, China<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">1443P<br \/>Poster Session \u2013 Oesophagogastric cancer<br \/>Monday, 16 September 2024<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Analysis of MET gene alterations in cfDNA samples from a phase II study of\u00a0savolitinib\u00a0in patients (pts) with MET-amplified gastroesophageal junction adenocarcinomas or gastric cancer (GEJ\/GC)<\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Zhi Peng,<br \/>Peking University Cancer Hospital &amp; Institute, Beijing, China<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">1461P<br \/>Poster Session \u2013 Oesophagogastric cancer<br \/>Monday, 16 September 2024<\/td>\n<\/tr>\n<tr>\n<td colspan=\"3\" style=\"border-top: solid black 1pt ; vertical-align: top ; \">\u00a0<\/td>\n<\/tr>\n<tr>\n<td colspan=\"3\" style=\"border-bottom: solid black 1pt ; vertical-align: middle ; \"><strong>ESMO 2024 &#8211; INVESTIGATOR-INITIATED STUDIES <\/strong><\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>A phase II clinical study of\u00a0fruquintinib\u00a0(Fru) combined with toripalimab (Tor) and short-course radiotherapy (SCRT) as neoadjuvant therapy for locally advanced rectal cancer (LARC)<\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Zhiping Li, Ye Chen,<br \/>West China Hospital of Sichuan University, Chengdu, China<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">570P<br \/>Poster Session \u2013 Colorectal cancer<br \/>Monday, 16 September 2024<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Stereotactic ablative radiotherapy combined with fruquintinib and tislelizumab in metastatic colorectal cancer: Updated findings from a single-arm, prospective phase II trial (RIFLE)<\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Zhen Zhang, Yajie Chen, <br \/>Fudan University Shanghai Cancer Center, Shanghai, China<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">537P\u00a0<br \/>Poster Session \u2013 Colorectal cancer<br \/>Monday, 16 September 2024<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Fruquintinib\u00a0combined with sintilimab and chemotherapy as the first-line treatment in advanced na\u00efve EGFR- and ALK-negative non-squamous non-small cell lung cancer (nsq-NSCLC): Updated results<\/strong><\/p>\n<\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Yongqian Shu, Pei Ma,<br \/>Jiangsu Province Hospital\/The First Affiliated Hospital of Nanjing Medical University, Nanjing, China<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">1329P\u00a0<br \/>Poster Session \u2013 NSCLC, metastatic<br \/>Saturday, 14 September 2024<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Fruquintinib in combination with sintilimab and CAPEOX as first-line treatment for advanced G\/GEJ cancer: A phase 1b\/2 clinical trial (FUNCTION)<\/strong><\/p>\n<\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Xiaobing Chen, Beibei Chen,<br \/>Henan Cancer Hospital\/ Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">1475TiP<br \/>Poster Session \u2013 Oesophagogastric cancer<br \/>Monday, 16 September 2024<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Fruquintinib combined with nab-paclitaxel and gemcitabine (AG) as the first-line treatment for pancreatic ductal adenocarcinoma (PDAC) with liver metastases: An open-label, single-arm, single-center phase II clinical study<\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Xianjun Yu, Miaoyan Wei,<br \/>Fudan University Shanghai Cancer Center, Shanghai, China<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">1529P\u00a0<br \/>Poster Session \u2013 Pancreatic cancer<br \/>Monday, 16 September 2024<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>A phase II study of\u00a0Fruquintinib\u00a0in the 1L or 2L treatment of unresectable metastatic soft tissue sarcoma<\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Zhiguo Luo, Xiaowei Zhang,<br \/>Fudan University Shanghai Cancer Center, Shanghai, China<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">1743P<br \/>Poster Session \u2013 Sarcoma<br \/>Saturday, 14 September 2024<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Surufatinib\u00a0combined with anti-PD-1\/PD-L1 antibody in the second line or monotherapy in third line treatment of advanced hepatocellular carcinoma: A single-arm, open-label, multi-center phase II study<\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Fuxiang Zhou,<br \/>Zhongnan Hospital, Wuhan University, Wuhan, China<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">974P<br \/>Poster Session \u2013 Hepatocellular carcinoma (HCC)<br \/>Monday, 16 September 2024<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Updated results of\u00a0Surufatinib\u00a0plus transarterial embolization versus\u00a0surufatinib\u00a0monotherapy in neuroendocrine tumor with liver metastasis: a prospective, randomized, controlled trial<\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Dan Cao, <br \/>West China Hospital, Sichuan University, Chengdu, China<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">1155P<br \/>Poster Session \u2013 Neuroendocrine tumours<br \/>Monday, 16 September 2024<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Surufatinib\u00a0plus toripalimab combined with pemetrexed (A), and platinum (P) in patients (pts) with advanced non-squamous non-small cell lung cancer (nsq-NSCLC): Updated results of a single-center, phase II trial<\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Li Zhang, Wenfeng Fang,<br \/>Sun Yat-Sen University Cancer Center, Guangzhou, China<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">1345P<br \/>Poster Session \u2013 NSCLC, metastatic<br \/>Saturday, 14 September 2024<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; vertical-align: top ; \"><strong>Surufatinib\u00a0combined with gemcitabine in soft tissue sarcoma (STS) patients failed with anthracyclines chemotherapy or monotherapy post-anlotinib progression: a multi-center, phase II trial<\/strong><\/td>\n<td style=\"border-top: solid black 1pt ; border-right: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">Xiaohui Niu, Yuhong Zhou,<br \/>Zhongshan Hospital, Fudan University, Shanghai, China<\/td>\n<td style=\"border-top: solid black 1pt ; border-bottom: solid black 1pt ; border-left: solid black 1pt ; vertical-align: top ; \">1740P<br \/>Poster Session \u2013 Sarcoma<br \/>Saturday, 14 September 2024<\/td>\n<\/tr>\n<tr>\n<td style=\"vertical-align: top ; \">\u00a0<\/td>\n<td style=\"vertical-align: top ; \">\u00a0<\/td>\n<td style=\"vertical-align: top ; \">\u00a0<\/td>\n<\/tr>\n<\/table>\n<p align=\"justify\"><strong>About HUTCHMED<\/strong><\/p>\n<p align=\"justify\">HUTCHMED (Nasdaq\/AIM:<strong>\u200b<\/strong>HCM; HKEX:<strong>\u200b<\/strong>13) is an innovative, commercial-stage, biopharmaceutical company. It is committed to the discovery, global development and commercialization of targeted therapies and immunotherapies for the treatment of cancer and immunological diseases. It has approximately 5,000 personnel across all its companies, at the center of which is a team of about 1,800 in oncology\/immunology. Since inception, HUTCHMED has focused on bringing cancer drug candidates from in-house discovery to patients around the world, with its first three medicines marketed in China, the first of which is also marketed in the US and Europe. For more information, please visit: <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=wDOEXX02YyfS7-G04GbwUde1xc2yhOcV5OxesiAwQngKt2dhy03MyWs3kT6f06-n0wkk7QKSD1Vn4P_nMerwsvI-4agO9PdZVx5Ohp155Yg=\" rel=\"nofollow noopener\" target=\"_blank\" title=\"www.hutch-med.com\">www.hutch-med.com<\/a> or follow us on <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=ij3UyR9iLf26nC4fnReZPmKEHb5UEi6iJwfiWFagNHGGayDJMV2kn0KGD-W8DgsMu5dyW-p0wJkQycTSphZ_OnVzcySe4MK-4EXA-e_KSpY=\" rel=\"nofollow noopener\" target=\"_blank\" title=\"LinkedIn\">LinkedIn<\/a>.<\/p>\n<p><strong><em>Forward-Looking Statements <\/em><\/strong><\/p>\n<p align=\"justify\"><em>This press release contains forward-looking statements within the meaning of the \u201csafe harbor\u201d provisions of the U.S. Private Securities Litigation Reform Act of 1995. These forward-looking statements reflect HUTCHMED\u2019s current expectations regarding future events, including but not limited to its expectations regarding the therapeutic potential of fruquintinib, savolitinib and surufatinib, the further clinical development for fruquintinib, savolitinib and surufatinib, its expectations as to whether any studies on fruquintinib, savolitinib and surufatinib, would meet their primary or secondary endpoints, and its expectations as to the timing of the completion and the release of results from such studies. Such risks and uncertainties include, among other things, assumptions regarding enrollment rates and the timing and availability of subjects meeting a study\u2019s inclusion and exclusion criteria; changes to clinical protocols or regulatory requirements; unexpected adverse events or safety issues; the ability of fruquintinib, savolitinib and surufatinib, including as combination therapies, to meet the primary or secondary endpoint of a study, to obtain regulatory approval in different jurisdictions and to gain commercial acceptance after obtaining regulatory approval; the potential markets of fruquintinib, savolitinib and surufatinib for a targeted indication, and the sufficiency of funding. In addition, as certain studies rely on the use of CAPEOX, docetaxel, gemcitabine, nab-paclitaxel, paclitaxel, pemetrexed, platinum, sintilimab, topotecan, tislelizumab or toripalimab as combination therapeutics, such risks and uncertainties include assumptions regarding their safety, efficacy, supply and continued regulatory approval. Existing and prospective investors are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. For further discussion of these and other risks, see HUTCHMED\u2019s filings with the U.S. Securities and Exchange Commission, The Stock Exchange of Hong Kong Limited and on AIM. HUTCHMED undertakes no obligation to update or revise the information contained in this press release, whether as a result of new information, future events or circumstances or otherwise.<\/em><\/p>\n<p><strong><em>Medical Information<\/em><\/strong><\/p>\n<p align=\"justify\"><em>This press release contains information about products that may not be available in all countries, or may be available under different trademarks, for different indications, in different dosages, or in different strengths. Nothing contained herein should be considered a solicitation, promotion or advertisement for any prescription drugs including the ones under development.<\/em><\/p>\n<p align=\"justify\"><strong>CONTACTS<\/strong><\/p>\n<table style=\"border-collapse: collapse; width:100%; border-collapse:collapse ;\">\n<tr>\n<td style=\"max-width:30%; width:30%; min-width:30%;;text-align: justify ;  vertical-align: middle; vertical-align: top ; \"><strong>Investor Enquiries<\/strong><\/td>\n<td style=\"max-width:70%; width:70%; min-width:70%;;vertical-align: top ; \">+852\u00a02121\u00a08200 \/ <a href=\"mailto:ir@hutch-med.com\" rel=\"nofollow noopener\" target=\"_blank\" title=\"ir@hutch-med.com\">ir@hutch-med.com<\/a><\/td>\n<\/tr>\n<tr>\n<td style=\"vertical-align: top ; \">\u00a0<\/td>\n<td style=\"vertical-align: top ; \">\u00a0<\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: justify ;  vertical-align: middle; vertical-align: top ; \"><strong>Media Enquiries<\/strong><\/td>\n<td style=\"vertical-align: top ; \">\u00a0<\/td>\n<\/tr>\n<tr>\n<td style=\"vertical-align: middle;   text-align: left;   padding-left: 15.0px; vertical-align: top ; \">Ben Atwell \/ Alex Shaw, FTI\u00a0Consulting<\/td>\n<td style=\"vertical-align: top ; \">+44\u00a020\u00a03727\u00a01030\u00a0\/ +44\u00a07771\u00a0913\u00a0902\u00a0(Mobile)\u00a0\/ +44\u00a07779\u00a0545\u00a0055\u00a0(Mobile)\u00a0\/ <a href=\"mailto:HUTCHMED@fticonsulting.com\" rel=\"nofollow noopener\" target=\"_blank\" title=\"HUTCHMED@fticonsulting.com\">HUTCHMED@fticonsulting.com<\/a><\/td>\n<\/tr>\n<tr>\n<td style=\"vertical-align: middle;   text-align: left;   padding-left: 15.0px; vertical-align: top ; \">Zhou Yi, Brunswick<\/td>\n<td style=\"vertical-align: top ; \">+852\u00a09783\u00a06894\u00a0(Mobile)\u00a0\/ <a href=\"mailto:HUTCHMED@brunswickgroup.com\" rel=\"nofollow noopener\" target=\"_blank\" title=\"HUTCHMED@brunswickgroup.com\">HUTCHMED@brunswickgroup.com<\/a><\/td>\n<\/tr>\n<tr>\n<td style=\"vertical-align: top ; \">\u00a0<\/td>\n<td style=\"vertical-align: top ; \">\u00a0<\/td>\n<\/tr>\n<tr>\n<td style=\"text-align: justify ;  vertical-align: middle; vertical-align: top ; \"><strong>Nominated Advisor<\/strong><\/td>\n<td style=\"vertical-align: top ; \">\u00a0<\/td>\n<\/tr>\n<tr>\n<td style=\"vertical-align: middle;   text-align: left;   padding-left: 15.0px; vertical-align: top ; \">Atholl Tweedie \/ Freddy Crossley \/<br \/>Rupert Dearden, Panmure Liberum<\/td>\n<td style=\"vertical-align: top ; \">+44\u00a0(20)\u00a07886\u00a02500<\/td>\n<\/tr>\n<\/table>\n<p><img decoding=\"async\" src=\"https:\/\/ml.globenewswire.com\/media\/YmI5YTQ0NDktYTc4Ni00OTVlLTg2NDQtYTQ4OTJmOTRjYTM0LTExMDgyODY=\/tiny\/HUTCHMED-China-Limited.png\" referrerpolicy=\"no-referrer-when-downgrade\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>HONG KONG and SHANGHAI and FLORHAM PARK, N.J., Sept. 09, 2024 (GLOBE NEWSWIRE) &#8212; HUTCHMED (China) Limited (\u201cHUTCHMED\u201d) (Nasdaq\/AIM:HCM; HKEX:13) today announces that new and updated data from several studies of compounds discovered by HUTCHMED will be presented at the 2024 World Conference on Lung Cancer (\u201cWCLC24\u201d) in San Diego, USA, and the European Society [&#8230;]\n","protected":false},"author":1,"featured_media":59192,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-59191","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-pr-newswire"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v21.6 (Yoast SEO v21.6) - 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