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Leaked documents suggest Philip Morris International's link to research activities. 泄露的文件显示菲利普莫里斯国际公司与研究活动有关联。
IF 41.6 1区 医学 Q1 ONCOLOGY Pub Date : 2024-08-01 Epub Date: 2024-07-14 DOI: 10.1016/S1470-2045(24)00393-0
Talha Burki
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引用次数: 0
Consensus guidelines and recommendations for the management and response assessment of chimeric antigen receptor T-cell therapy in clinical practice for relapsed and refractory multiple myeloma: a report from the International Myeloma Working Group Immunotherapy Committee. 针对复发和难治性多发性骨髓瘤临床实践中嵌合抗原受体 T 细胞疗法的管理和反应评估的共识指南和建议:国际骨髓瘤工作组免疫疗法委员会的报告。
IF 41.6 1区 医学 Q1 ONCOLOGY Pub Date : 2024-08-01 Epub Date: 2024-05-28 DOI: 10.1016/S1470-2045(24)00094-9
Yi Lin, Lugui Qiu, Saad Usmani, Chng Wee Joo, Luciano Costa, Benjamin Derman, Juan Du, Hermann Einsele, Carlos Fernandez de Larrea, Roman Hajek, P Joy Ho, Efstathios Kastritis, Joaquin Martinez-Lopez, Maria-Victoria Mateos, Joseph Mikhael, Philippe Moreau, Chandramouli Nagarajan, Ajay Nooka, Michael O'Dwyer, Fredrik Schjesvold, Surbhi Sidana, Niels Wcj van de Donk, Katja Weisel, Sonja Zweegman, Noopur Raje, Paula Rodriguez Otero, Larry D Anderson, Shaji Kumar, Tom Martin

Chimeric antigen receptor (CAR) T-cell therapy has shown promise in patients with late-line refractory multiple myeloma, with response rates ranging from 73 to 98%. To date, three products have been approved: Idecabtagene vicleucel (ide-cel) and ciltacabtagene autoleucel (cilta-cel), which are approved by the US Food and Drug Administration, the European Medicines Agency, Health Canada (ide-cel only), and Brazil ANVISA (cilta-cel only); and equecabtagene autoleucel (eque-cel), which was approved by the Chinese National Medical Products Administration. CAR T-cell therapy is different from previous anti-myeloma therapeutics with unique toxic effects that require distinct mitigation strategies. Thus, a panel of experts from the International Myeloma Working Group was assembled to provide guidance for clinical use of CAR T-cell therapy in myeloma. This consensus opinion is from experts in the field of haematopoietic cell transplantation, cell therapy, and multiple myeloma therapeutics.

嵌合抗原受体(CAR)T 细胞疗法已在晚期难治性多发性骨髓瘤患者中显示出前景,其反应率从 73% 到 98% 不等。迄今为止,已有三种产品获得批准:其中,Idecabtagene vicleucel(ide-cel)和ciltacabtagene autoleucel(cilta-cel)已获美国食品药品管理局、欧洲药品管理局、加拿大卫生部(仅ide-cel)和巴西ANVISA(仅cilta-cel)批准;equecabtagene autoleucel(eque-cel)已获中国国家医药产品管理局批准。CAR T 细胞疗法不同于以往的抗骨髓瘤疗法,具有独特的毒副作用,需要采取不同的缓解策略。因此,国际骨髓瘤工作组(International Myeloma Working Group)组建了一个专家小组,为CAR T细胞疗法在骨髓瘤中的临床应用提供指导。这份共识意见来自造血细胞移植、细胞疗法和多发性骨髓瘤疗法领域的专家。
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引用次数: 0
Closing the research gaps in obstetric health for survivors of cancer. 缩小癌症幸存者产科保健方面的研究差距。
IF 41.6 1区 医学 Q1 ONCOLOGY Pub Date : 2024-08-01 Epub Date: 2024-06-26 DOI: 10.1016/S1470-2045(24)00321-8
Ranjeet Bajpai, Jyoti Bajpai
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引用次数: 0
ImmunoPET in high-grade neuroendocrine tumours. 高分化神经内分泌肿瘤的免疫PET。
IF 41.6 1区 医学 Q1 ONCOLOGY Pub Date : 2024-08-01 Epub Date: 2024-06-28 DOI: 10.1016/S1470-2045(24)00314-0
Francesco Giammarile, Roberto C Delgado Bolton, Fuad Novruzov, Diana Paez
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引用次数: 0
Challenges and prospects for cancer treatment in prison settings. 监狱环境中癌症治疗的挑战和前景。
IF 41.6 1区 医学 Q1 ONCOLOGY Pub Date : 2024-08-01 DOI: 10.1016/S1470-2045(24)00272-9
Hujian Hong, Yanli Qu
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引用次数: 0
Challenges and prospects for cancer treatment in prison settings. 监狱环境中癌症治疗的挑战和前景。
IF 41.6 1区 医学 Q1 ONCOLOGY Pub Date : 2024-08-01 DOI: 10.1016/S1470-2045(24)00328-0
Feng Zhang
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引用次数: 0
Neoadjuvant camrelizumab plus apatinib for locally advanced microsatellite instability-high or mismatch repair-deficient colorectal cancer (NEOCAP): a single-arm, open-label, phase 2 study. 局部晚期微卫星不稳定性高或错配修复缺陷结直肠癌新辅助卡瑞珠单抗加阿帕替尼(NEOCAP):一项单臂、开放标签、2 期研究。
IF 41.6 1区 医学 Q1 ONCOLOGY Pub Date : 2024-07-01 Epub Date: 2024-06-06 DOI: 10.1016/S1470-2045(24)00203-1
Jie-Hai Yu, Bin-Yi Xiao, Dan-Dan Li, Wu Jiang, Ya Ding, Xiao-Jun Wu, Rong-Xin Zhang, Jun-Zhong Lin, Wei Wang, Kai Han, Ling-Heng Kong, Xin-Ke Zhang, Bi-Yun Chen, Wei-Jian Mei, Zhi-Zhong Pan, Jing-Hua Tang, Xiao-Shi Zhang, Pei-Rong Ding
<p><strong>Background: </strong>PD-1 blockade is highly efficacious for mismatch repair-deficient colorectal cancer in both metastatic and neoadjuvant settings. We aimed to explore the activity and safety of neoadjuvant therapy with PD-1 blockade plus an angiogenesis inhibitor and the feasibility of organ preservation in patients with locally advanced mismatch repair-deficient colorectal cancer.</p><p><strong>Methods: </strong>We initiated a single-arm, open-label, phase 2 trial (NEOCAP) at Sun Yat-sen University Cancer Center and the Provincial Hospital of Traditional Chinese Medicine, Guangzhou, China. Patients aged 18-75 years with untreated mismatch repair-deficient or microsatellite instability-high or POLE/POLD1-mutated locally advanced colorectal cancer (cT3 or N+ for rectal cancer, and T3 with invasion ≥5mm or T4, with or without N+ for colon cancer) and an Eastern Cooperative Oncology Group performance score of 0-1 were enrolled and given 200 mg camrelizumab intravenously on day 1 and 250 mg apatinib orally from day 1-14, every 3 weeks for 3 months followed by surgery or 6 months if patients did not have surgery. Patients who had a clinical complete response did not undergo surgery and proceeded with a watch-and-wait approach. The primary endpoint was the proportion of patients with a pathological or clinical complete response. Eligible enrolled patients who received at least one cycle of neoadjuvant treatment and had at least one tumour response assessment following the baseline assessment were included in the activity analysis, and patients who received at least one dose of study drug were included in the safety analysis. The study is registered with ClinicalTrials.gov (NCT04715633) and is ongoing.</p><p><strong>Findings: </strong>Between Sept 29, 2020, and Dec 15, 2022, 53 patients were enrolled; one patient was excluded from the activity analysis because they were found to be mismatch repair-proficient and microsatellite-stable. 23 (44%) patients were female and 29 (56%) were male. The median follow-up was 16·4 (IQR 10·5-23·5) months. 28 (54%; 95% CI 35-68) patients had a clinical complete response and 24 of these patients were managed with a watch-and-wait approach, including 20 patients with colon cancer and multiple primary colorectal cancer. 23 (44%) of 52 patients underwent surgery for the primary tumour, and 14 (61%; 95% CI 39-80) had a pathological complete response. 38 (73%; 95% CI 59-84) of 52 patients had a complete response. Grade 3-5 adverse events occurred in 20 (38%) of 53 patients; the most common were increased aminotransferase (six [11%]), bowel obstruction (four [8%]), and hypertension (four [8%]). Drug-related serious adverse events occurred in six (11%) of 53 patients. One patient died from treatment-related immune-related hepatitis.</p><p><strong>Interpretation: </strong>Neoadjuvant camrelizumab plus apatinib show promising antitumour activity in patients with locally advanced mismatch repair-deficient or microsa
背景PD-1阻断剂对错配修复缺陷结直肠癌的转移和新辅助治疗均有显著疗效。我们旨在探索 PD-1 阻断剂加血管生成抑制剂新辅助治疗的活性和安全性,以及局部晚期错配修复缺陷结直肠癌患者器官保留的可行性:我们在中山大学附属肿瘤医院和省中医院启动了一项单臂、开放标签的2期试验(NEOCAP)。年龄在18-75岁之间的错配修复缺陷或微卫星不稳定性高或POLE/POLD1突变的未经治疗的局部晚期结直肠癌患者(直肠癌为cT3或N+,T3且浸润≥5mm或T4、第 1 天静脉注射 200 毫克康瑞珠单抗,第 1-14 天口服 250 毫克阿帕替尼,每 3 周一次,持续 3 个月,然后进行手术;如果患者没有进行手术,则持续 6 个月。临床完全应答的患者不进行手术,而是采取观察和等待的方法。主要终点是获得病理或临床完全应答的患者比例。符合条件的入组患者如果接受了至少一个周期的新辅助治疗,并在基线评估后进行了至少一次肿瘤反应评估,则被纳入活性分析;接受了至少一剂研究药物的患者被纳入安全性分析。该研究已在ClinicalTrials.gov(NCT04715633)注册,目前正在进行中:2020年9月29日至2022年12月15日期间,53名患者入组;一名患者被排除在活动性分析之外,因为他们被发现具有错配修复能力和微卫星稳定性。23名(44%)患者为女性,29名(56%)患者为男性。中位随访时间为 16-4 个月(IQR 10-5-23-5)。28例(54%;95% CI 35-68)患者获得临床完全应答,其中24例患者采用观察和等待的方法进行治疗,包括20例结肠癌和多发性原发性结肠直肠癌患者。52 名患者中有 23 人(44%)接受了原发肿瘤手术,14 人(61%;95% CI 39-80)获得了病理完全反应。52例患者中有38例(73%;95% CI 59-84)完全应答。53例患者中有20例(38%)发生了3-5级不良反应;最常见的不良反应是转氨酶升高(6例[11%])、肠梗阻(4例[8%])和高血压(4例[8%])。在 53 例患者中,有 6 例(11%)发生了与药物相关的严重不良事件。一名患者死于与治疗相关的免疫相关肝炎:新辅助卡瑞珠单抗加阿帕替尼对局部晚期错配修复缺陷或微卫星不稳定性高的结直肠癌患者显示出良好的抗肿瘤活性。应高度警惕与免疫相关的不良事件。器官保留似乎不仅对直肠癌患者很有希望,而且对临床完全反应的结肠癌患者也很有希望。需要进行更长时间的随访,以评估观察-等待疗法的肿瘤学效果:国家自然科学基金、广东省基础与应用基础研究基金、中山大学肿瘤防治中心肿瘤创新研究项目:摘要中译本见补充材料部分。
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引用次数: 0
Tobacco and e-cigarette use in young people: an ongoing challenge. 青少年使用烟草和电子烟:一项持续的挑战。
IF 41.6 1区 医学 Q1 ONCOLOGY Pub Date : 2024-07-01 Epub Date: 2024-05-31 DOI: 10.1016/S1470-2045(24)00323-1
Talha Burki
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引用次数: 0
Correction to Lancet Oncol 2024; 25: e205-16. Lancet Oncol 2024; 25: e205-16 更正。
IF 41.6 1区 医学 Q1 ONCOLOGY Pub Date : 2024-07-01 DOI: 10.1016/S1470-2045(24)00288-2
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引用次数: 0
Overcoming barriers to early breast cancer presentation in Nigeria. 克服尼日利亚早期乳腺癌发病的障碍。
IF 41.6 1区 医学 Q1 ONCOLOGY Pub Date : 2024-07-01 DOI: 10.1016/S1470-2045(24)00319-X
Mercy Ofuya
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Lancet Oncology
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