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Primary diffuse large B-cell lymphoma of the CNS: a rare case of spontaneous remission. 中枢神经系统原发性弥漫性大b细胞淋巴瘤:一例罕见的自发缓解病例。
Pub Date : 2017-11-01 Epub Date: 2017-11-20 DOI: 10.2217/ijh-2017-0009
Fotini Debonera, Sunita Nasta, Maria Martinez-Lage, Stephen J Schuster, Donald E Tsai

There is no consensus on the optimal therapy for primary CNS lymphoma. Conventional treatment modalities include chemotherapy and radiation therapy, which carry significant risks of morbidity and mortality. In systemic lymphomas, there are situations where non-Hodgkin lymphomas have resolved spontaneously. We now report the case of a nonimmunocompromised patient with primary CNS lymphoma who underwent a spontaneous remission with a durable response. This case suggests that not all patients with primary CNS lymphomas require aggressive treatment with chemotherapy and radiation therapy.

对于原发性中枢神经系统淋巴瘤的最佳治疗方法尚无共识。传统的治疗方式包括化疗和放射治疗,它们有很大的发病率和死亡率风险。在全身性淋巴瘤中,有非霍奇金淋巴瘤自发消退的情况。我们现在报告的情况下,非免疫功能低下的患者原发性中枢神经系统淋巴瘤谁经历了自发缓解和持久的反应。本病例提示并非所有原发性中枢神经系统淋巴瘤患者都需要化疗和放疗等积极治疗。
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引用次数: 10
How can we better predict treatment outcomes in classical Hodgkin's lymphoma? 我们如何更好地预测经典霍奇金淋巴瘤的治疗结果?
Pub Date : 2017-11-01 Epub Date: 2017-11-20 DOI: 10.2217/ijh-2017-0010
Claudio Agostinelli
“ The results indicate that response-adapted therapy based on PET-2 results guarantees a PFS, in PET-2 positive patients and in the overall cohort, higher than PFS of historical controls treated with ABVD. ”
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引用次数: 0
Opportunities for targeting gene regulatory factors in B-cell acute lymphoblastic leukemia. 靶向b细胞急性淋巴细胞白血病基因调控因子的机会。
Pub Date : 2017-11-01 Epub Date: 2017-11-20 DOI: 10.2217/ijh-2017-0018
Christopher J Ott
“ there is intriguing experimental evidence to suggest targeting gene regulatory factors with pharmaceutical agents could be an effective therapeutic strategy for B-ALL. ” Modern chemotherapy regimens have had a profound impact on the prognosis of individuals diagnosed with B-cell acute lymphoblastic leukemia (B-ALL), especially children [1] . However these treatments achieve substantially poorer survival rates in adults, and are associated with significant short- and long-term toxicities. An advanced understanding of the genetic complexity that characterizes B-ALL allows for more precise patient stratification, and reveals disease subtypes that are at a high-risk for treatment relapse [2] . This genetic profiling has also revealed opportunities for the development of targeted therapies. For example, recurrent BCR–ABL1 translocations define a unique subtype of ALL found in 2–4% of pediatric and at least 25% of adult cases. The activity of this oncogene can be effectively inhibited with the tyrosine kinase inhibitor imatinib, with promising clinical results [3] . Intriguingly, many ALL oncogenes include gene fusions and translocations of transcription regulators and other chromatin associated factors (e.g., ETV6–RUNX1 , TCF3–PBX1 , MYC or MLL rearrangements), revealing the disease to be primarily one of disrupted gene expression control. The mechanistic aspects of these oncogenes are incompletely understood, yet remain an active area of research. These factors can unfortunately also often be viewed as intractable for therapeutics development. Yet much recent progress has been made in targeting gene regulatory complexes with small molecule pharmaceutical agents [4] . Additionally, promising preclinical and early clinical data in B-ALL
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引用次数: 0
Chronic lymphocytic leukemia: "The times they are a-changin". 慢性淋巴细胞白血病:“时代正在改变”。
Pub Date : 2017-06-01 Epub Date: 2017-11-17 DOI: 10.2217/ijh-2017-0007
Stefano Molica
“ the advent of targeted therapy in CLL requires the urgent introduction of revised clinical guidelines based not only on results of clinical trials but also including data from clinical practice and the assessment of drug-related toxicity according patients’ reported outcomes ”
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引用次数: 0
Updated classification and novel treatment prospective for nodal peripheral T-cell lymphomas. 淋巴结周围t细胞淋巴瘤的最新分类和新的治疗前景。
Pub Date : 2017-06-01 Epub Date: 2017-06-30 DOI: 10.2217/ijh-2017-0006
Pier Paolo Piccaluga
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引用次数: 0
Current challenges in the management of follicular lymphoma. 当前滤泡性淋巴瘤治疗面临的挑战。
Pub Date : 2017-06-01 Epub Date: 2017-06-30 DOI: 10.2217/ijh-2017-0003
Maryam Sarraf Yazdy, Chaitra Ujjani

Although typically indolent in nature, follicular lymphoma remains an ongoing challenge for practicing oncologists. While response rates >90% can be achieved with rituximab-based chemoimmunotherapy in advanced stage patients, the complete remission rates are substantially lower and patients inevitably relapse. The inability to achieve a complete remission and an early progression of disease have recently been determined to be indicative of poorer long-term outcomes. A greater understanding of the pathogenesis of follicular lymphoma has enabled the development of targeted therapies, which may improve standard treatment approaches. Examples include lenalidomide and obinutuzumab, which are currently in front-line Phase III investigation. Other therapies of interest include small molecule inhibitors, immune checkpoint inhibitors and chimeric antigen receptor T cells.

滤泡性淋巴瘤是一种典型的懒散性淋巴瘤,但对于肿瘤医生来说,它仍然是一项持续的挑战。虽然晚期患者使用利妥昔单抗化疗免疫疗法可获得大于90%的应答率,但完全缓解率却低得多,而且患者不可避免地会复发。无法实现完全缓解和疾病早期进展最近被确定为长期疗效较差的指标。随着人们对滤泡性淋巴瘤发病机理的进一步了解,靶向疗法得以开发,这可能会改善标准治疗方法。例如来那度胺和奥比奴珠单抗,这两种药物目前正处于前线III期研究阶段。其他值得关注的疗法包括小分子抑制剂、免疫检查点抑制剂和嵌合抗原受体 T 细胞。
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引用次数: 0
Survivors at risk: Hodgkin lymphoma survivors at high risk of second cancers. 高危幸存者:第二癌症高风险的霍奇金淋巴瘤幸存者。
Pub Date : 2017-06-01 Epub Date: 2017-06-30 DOI: 10.2217/ijh-2017-0008
Amit Sud

Amit Sud speaks to Sebastian Dennis-Beron, Commissioning Editor: Amit Sud is a clinical research fellow in Hematology at the Institute of Cancer Research, UK. He undertook his undergraduate medical training at the University of Manchester, gaining an honors degree. He completed his Masters in Medical Research at Manchester University, gaining a distinction. He continued his medical training in Manchester and London and started his specialization in Hematology in South West London. He was successful in obtaining a Cancer Research UK funded clinical research fellowship in Hematology under the supervision of Professor Richard Houlston at the Institute of Cancer Research. His current research focus is that of genetic susceptibility to Hodgkin lymphoma. He is a trainee member of the NCRI Lymphoma Clinical Studies Group.

Amit Sud与特约编辑Sebastian Dennis-Beron对话:Amit Sud是英国癌症研究所血液学临床研究员。他在曼彻斯特大学接受了本科医学培训,并获得了荣誉学位。他在曼彻斯特大学完成了医学研究硕士学位,并获得了优异的成绩。他在曼彻斯特和伦敦继续他的医学培训,并在伦敦西南部开始他的血液学专业。在癌症研究所Richard Houlston教授的指导下,他成功地获得了英国癌症研究中心资助的血液学临床研究奖学金。他目前的研究重点是霍奇金淋巴瘤的遗传易感性。他是NCRI淋巴瘤临床研究小组的实习成员。
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引用次数: 0
The bone marrow transplant clinical nurse specialist in hemato-oncology: an interview with Anthony Nolan Nurse Specialist Susan Paskar. 血液肿瘤学骨髓移植临床护士专家:采访安东尼·诺兰护士专家苏珊·帕斯卡。
Pub Date : 2017-06-01 Epub Date: 2017-06-30 DOI: 10.2217/ijh-2017-0014
Susan Paskar

Susan Paskar speaks to Sebastian Dennis-Beron, Commissioning Editor: Susan qualified in 1997 as a registered nurse and has 20 years of experience, in a range of specialties including hematology, medical and surgical oncology, general surgery, bariatric, breast, endocrine, head & neck, liver, urology and bone marrow/stem cell transplant. Working in both the UK and the USA, in regional transplant centers since 2002, she is considered expert in care of the bone marrow transplant patient from point of referral to long term follow-up care and palliation. She has been responsible for development and implementation of a Nurse-led late-effects post-bone marrow transplant service at the Freeman Hospital in Newcastle upon Tyne, as their Anthony Nolan Nurse Specialist.

苏珊于1997年获得注册护士资格,拥有20年的专业经验,包括血血学,内科和外科肿瘤学,普外科,减肥,乳腺,内分泌,头颈,肝脏,泌尿科和骨髓/干细胞移植。自2002年以来,她在英国和美国的地区移植中心工作,从转诊到长期随访护理和姑息治疗,她被认为是骨髓移植患者护理方面的专家。她在泰恩河畔纽卡斯尔的弗里曼医院负责开发和实施护士主导的骨髓移植后晚期效应服务,担任他们的安东尼诺兰护士专家。
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引用次数: 0
Targeting sphingosine kinase 1 in acute myeloid leukemia: translation to clinic. 针对鞘氨醇激酶1治疗急性髓系白血病的临床研究。
Pub Date : 2017-06-01 Epub Date: 2017-07-18 DOI: 10.2217/ijh-2017-0011
Jason A Powell, Craig T Wallington-Beddoe, Stuart M Pitson
Acute myeloid leukemia (AML) is an aggressive heterogeneous group of malignancies resulting from various oncogenic genetic lesions that presents as an accumulation of immature myeloid cells in the bone marrow and peripheral blood. Standard induction chemotherapeutics have remained the front line therapy for AML for over 30 years, and despite being often highly effective at achieving initial disease remission, these responses are often short-lived resulting in relapse and death. Indeed, the overall survival in young adults ( < 60 years) is < 30% [1] . Unlike the ever-increasing repertoire of targeted therapies for lymphoproliferative disorders, currently all- trans-retinoic-acid represents the only targeted therapy in routine clinical use for the treatment of one subclass of AML, acute promyelocytic leukemia, with this approach yielding a more favorable prognosis in this AML subtype than presently achievable in any other form of AML. No targeted therapies are in routine clinical use for the remaining subtypes of AML, which constitute about 90% of all AML patients, and thus, there is an enormous unmet need to develop such targeted therapies.
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引用次数: 5
Understanding the molecular basis of acute myeloid leukemias: where are we now? 了解急性髓性白血病的分子基础:我们现在在哪里?
Pub Date : 2017-06-01 Epub Date: 2017-11-17 DOI: 10.2217/ijh-2017-0002
Alicja M Gruszka, Debora Valli, Myriam Alcalay

Although the treatment modalities for acute myeloid leukemia (AML) have not changed much over the past 40 years, distinct progress has been made in deciphering the basic biology underlying the pathogenesis of this group of hematological disorders. Studies show that AML development is a multicause, multistep and multipathway process. Accordingly, AMLs constitute a heterogeneous group of diseases. The thorough understanding of the molecular basis of AML is paving the way for better therapeutic approaches. Multiple novel drugs are being introduced and new, more efficient and less toxic formulations of conventional therapeutics are becoming available. Here, we review the recent advances in the comprehension of the molecular processes that lead to the onset of AML and its translation into clinical practice.

尽管在过去的40年里,急性髓性白血病(AML)的治疗方式没有太大变化,但在解读这组血液疾病发病机制的基本生物学方面取得了明显的进展。研究表明AML的发展是一个多原因、多步骤、多途径的过程。因此,aml构成了一组异质性疾病。彻底了解AML的分子基础为更好的治疗方法铺平了道路。多种新药正在引进,新的、更有效的和毒性更小的传统治疗制剂正在出现。在这里,我们回顾了导致AML发病的分子过程及其转化为临床实践的最新进展。
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引用次数: 9
期刊
International Journal of Hematologic Oncology
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