June 30th 2025
Data support incorporating volumetric PET biomarkers into toxicity risk prediction for patients receiving CAR T-cell therapy for LBCL.
Medical Crossfire®: Harnessing the Power of Modern Therapies in Newly Diagnosed Multiple Myeloma
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Cases and Conversations™: Sorting Through the Expanding Treatment Options for Patients with Relapsed/Refractory Multiple Myeloma
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Cases & Conversations™: Transforming AML Care—Precision Strategies, Evolving Therapies, and Clinical Insights
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Medical Crossfire®: Improving Patient Outcomes in Myeloproliferative Neoplasms With Novel Therapeutic Approaches
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Fighting Disparities and Saving Lives: An Exploration of Challenges and Solutions in Cancer Care
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Community Practice Connections™: Selecting and Sequencing Therapy for Patients with DLBCL in an Era of Expanding Options
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BURST Expert Illustrations and Commentaries™: Exploring the Mechanistic Rationale for CSF-1R– Directed Treatment in Chronic GVHD
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(CME) Optimizing Management of Ocular Toxicity in Cancer Patients: The Role of Ophthalmologists in the Spectrum of Care
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(COPE) Optimizing Management of Ocular Toxicity in Cancer Patients: The Role of Ophthalmologists in the Spectrum of Care
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Community Practice Connections™: 6th Annual Precision Medicine Symposium – An Illustrated Tumor Board
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Medical Crossfire®: Expert Interpretations of the Latest Data in CLL Management – Understanding the Impact of Optimal Treatment Selection on Patient Outcomes
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Community Practice Connections™: Tailored Treatment Approaches for Older Patients With Advanced HR+/HER2– Breast Cancer
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High-Dose Chemo With GM-CSF May Help in Advanced Hodgkin’s Disease
February 1st 1999DUISBERG, Germany-High-dose chemotherapy (with colony stimulating factor support) significantly increased complete remission rates in advanced Hodgkin’s disease in a German randomized trial reported by Heinrich Gerhartz, MD, at the annual meeting of the American Society of Hematology.
Maxamine Appears to Increase Potency of Low-Dose IL-2 in Patients With AML
February 1st 1999GOTEBORG, Sweden-A postconsolidation regimen of low-dose interleukin-2 (IL-2) and the investigational agent histamine dihydrochloride (Maxamine) appears to increase leukemia-free survival in acute myelogenous leukemia (AML) patients in remission, Bo I. Nilsson, MD, PhD, reported at an ASH poster session.
Management of Mantle Cell Lymphoma
October 2nd 1998Manifestations of mantle cell lymphoma were recognized in the 1970s as distinct from those associated with the more readily classifiable lymphomas. It was not until the 1990s, however, that observation of a combination of immunologic, cytogenetic, and molecular genetic abnormalities characteristic of this new malignancy confirmed its existence. The clinical and pathologic entity was named mantle cell lymphoma and in 1994 was incorporated into the Revised European American Lymphoma Classification. Mantle cell lymphoma is a CD5 positive, B-cell lymphoma that usually displays the t(11;14). The lymphoma has a striking male predominance and is widely disseminated at diagnosis in 80% of patients. Mantle cell lymphoma responds poorly to available therapies, and the median survival is approximately 3 years.[ONCOLOGY 12(Suppl 8):49-55, 1998]
FDG-PET Finds Residual, Recurrent Hodgkin's Disease
September 1st 1998TORONTO--Residual masses are a frequent finding after treatment of Hodgkin’s disease. However, CT scans and MRI cannot reliably distinguish between scar tissue and viable tumor in these patients. A German study suggests that whole-body 18F-fluorodeoxyglucose positron emission tomography (FDG-PET) may be useful in determining the viability of these masses.
Octreotide Imaging Improves Staging of Hodgkin’s Disease
August 1st 1998TORONTO--In a study of newly diagnosed patients with Hodgkin’s disease, nuclear medicine imaging detected advanced disease in a significant portion of patients originally classified as having only stage I or II disease. These patients were imaged using indium-111 octreotide (OctreoScan), also known as somatostatin-receptor scintigraphy.
Individualizing Chemotherapy Dosage Improves Survival of Children With Acute Lymphoblastic Leukemia
May 1st 1998Individualizing the dosage of cancer chemotherapy can increase survival rates for children with acute lymphoblastic leukemia (ALL) without causing excessive toxicity, according to a recent study published in The New England Journal of Medicine.
Commentary (Armitage): Quality of Life in Low-Grade Non-Hodgkin’s Lymphoma
May 1st 1998The management of patients with the less aggressive subtypes of non-Hodgkin’s lymphoma remains a clinical challenge. As pointed out by Webster and Cella, this challenge relates, at least in part, to the comparatively long median survival that can be achieved in such patients with a wide variety of treatment approaches. However, it is very important to realize that not all patients with the indolent varieties of non-Hodgkin’s lymphoma are the same.
Commentary (Basen-Engquist/Cohen): Quality of Life in Low-Grade Non-Hodgkin’s Lymphoma
May 1st 1998Cancer treatment often has debilitating effects on the patients who receive it. Chemotherapy regimens can produce toxicities, such as gastrointestinal disturbances, hematologic deficiencies, fatigue, and neurotoxicity. Patients typically undergo these chemotherapy regimens to increase their disease-free survival time. Given that these therapies can negatively affect a patient’s quality of life (QOL), treatments need to provide clear curative potential and/or survival benefits to offset detrimental effects on QOL.
Cocaine Use May Double the Risk of Developing NHL
January 1st 1998Researchers found that men who use cocaine are twice as likely as abstainers to develop intermediate- or high-grade non-Hodgkin’s lymphoma (NHL). For those who use cocaine more frequently, ie, on at least nine occasions, the risk is more than triple what nonusers face, says Rebecca Nelson, a doctoral student in the preventive medicine department at the University of Southern California (USC) School of Medicine, in an article published recently in the British Journal of Cancer.
IFN May Affect CML Transplant Results
January 1st 1998ASH-Patients with chronic myelogenous leukemia (CML) who are eligible for transplant but lack a matched sibling donor should begin their search for an unrelated donor as soon as possible after diagnosis, A. James Morton, MD, said at the plenary session of the annual meeting of the American Society of Hematology (ASH) in San Diego.
Commentary (Giles/Kantarjian): Biology and Treatment of Chronic Myelogenous Leukemia
September 1st 1997Drs. Enright and McGlave succinctly review the biology of chronic myelogenous leukemia (CML) and highlight the therapeutic role of allogeneic stem-cell transplantation. Two points, however, warrant further discussion. The first is that a regimen containing interferon-alfa (Intron A, Roferon-A) is optimal front-line therapy for the great majority of CML patients.[1] The second is that use of an interferon-alfa-based regimen prior to allogeneic stem-cell transplantation does not adversely affect post-transplant mortality, morbidity, or anti-CML efficacy.
Cytogenetic Marker May Predict Second Cancer After Hodgkin's Disease
August 1st 1997NEW ORLEANS--A cytogenetic biomarker may be able to predict second cancers in patients with Hodgkin's disease, Sara Strom, PhD, of M.D. Anderson Cancer Center, reported at the American Society of Preventive Oncology (ASPO) annual meeting.
Delivery of Calicheamicin via New Antibody Is Promising in AML
July 1st 1997ASCO--Treatment with an investigational immunoconjugate, CMA-676, safely induced remissions in some patients with refractory or relapsed acute myelogenous leukemia (AML), Eric L. Sievers, MD, said in his poster presentation of the preliminary results at the American Society of Clinical Oncology annual meeting.
Milan Reports 18-Year Results of ABVD in Hodgkin's Disease
February 1st 1997VIENNA--The first Hodgkin's disease study updates to come out of the Milan Cancer Institute since 1989 have now confirmed that the therapeutic advantages of regimens containing ABVD (Adriamycin, bleomycin, vinblastine, dacarbazine) are sustained for nearly two decades.
Interferon Improves Survival in CML
January 1st 1997ORLANDO--Combination therapy utilizing interferon alfa-2b (Intron A) and cytarabine is associated with improved cytogenetic response and survival over interferon alone in patients with chronic myelogenous leukemia (CML), a French study, presented at the 38th Annual Meeting of the American Society of Hematology (ASH), has shown.
Radiolabeled Monoclonal Antibody Targets Bone Marrow in AML Transplant Patients
January 1st 1997ORLANDO--A preparative regimen employing a radiolabeled monoclonal antibody (MoAb), coupled with busulfan (Myleran) and cyclophosphamide (Cytoxan, Neosar), yielded a low relapse rate in patients with acute myelogenous leukemia (AML) undergoing bone marrow transplantation (BMT) while in first remission.
New Drug Treatment Discovered for CML
November 1st 1996Leukemia Society of America (LSA) scientist Dr. Brian Druker has described a drug that may be useful for combatting chronic myelogenous leukemia (CML). The new drug may be able to target leukemia cells, a much sought-after approach to cancer treatment.
Antisense Gene Therapy Trials Underway in Patients With CML
September 27th 1996Responding to the need for more efficacious and less toxic treatments for chronic myelogenous leukemia (CML), researchers at the University of Pennsylvania are exploring a novel form of gene therapy. By interfering with the transmission of a crucial message, they hope to prevent malignant cell growth without affecting normal hematopoietic cells.
New Donor Leukocyte Approaches May Improve Outcomes in Relapsed CML Post-transplant
September 1st 1996Following unmodified allogeneic bone marrow transplantation (BMT), up to 60% of patients with chronic myelogenous leukemia (CML) will relapse. The management of relapsed CML has proven especially difficult, because cytotoxic drugs and interferon-alfa (Intron A, Roferon-A) seldom cure the disease, and a second bone marrow transplant is associated with high mortality.
Lymphoma, Leukemia Patients Sought for Trial of MoAb
April 1st 1996BOSTON--Researchers at New England Deaconess Hospital are seeking patients with Hodgkin's disease, non-Hodgkin's lymphoma, acute myelogenous leukemia (AML), and chronic myelogenous leukemia (CML) for an FDA-sponsored study of a humanized anti-Tac (interleukin-2 receptor) monoclonal antibody. The phase Ib/II multidose trial will study tolerance, therapeutic efficacy, and biological efficacy.
ABMT Recommended for Relapsed Hodgkin's Disease, But Better Overall Survival Not Yet Proved
April 1st 1996The bulk of available evidence has made a persuasive case for early bone marrow transplantation as the treatment of choice for patients with relapsed Hodgkin's disease, Philip J. Bierman, MD, said at a lymphoma conference sponsored by the University of Texas M.D. Anderson Cancer Center.
Newer Strategies Aim to Improve Long-Term Remission Rates in AML
March 1st 1996SEATTLE--While about 65% of adults with newly diagnosed, acute myelogenous leukemia (AML) are able to achieve complete remission of their disease, this remission is often short-lived when conventional postremission regimens are used. However, new approaches to postremission therapy are proving beneficial to patients, Robert J. Mayer, MD, said at a symposium held in conjunction with the American Society of Hematology's 37th Annual Meeting.
Which Non-Hodgkin's Lymphoma Patients Benefit From ABMT?
February 1st 1996I would like to take issue with Dr. Bruce Cheson's response to a reader's question on the role of high-dose chemotherapy/autologous bone marrow transplantation (ABMT) in patients with non-Hodgkin's lymphoma (Oncology News International, December, 1995, page 25).
Commentary (Connors)-Hodgkin's Disease: Management of First Relapse
February 1st 1996The management of Hodgkin's disease presents the clinician with several separate opportunities to intervene effectively. Not only is it possible to treat newly diagnosed patients with the knowledge that the majority will be cured, but also one can approach relapse with cautious optimism. Unlike most human neoplasms, Hodgkin's disease can be regularly cured even after relapse has occurred. The article by Drs. Yuen and Horning reviews available data on the outcome of treatment of first relapse of Hodgkin's disease, and summarizes the evidence indicating that relapsed disease can still be cured.
Hodgkin's Disease: Management of First Relapse
February 1st 1996In most patients with newly diagnosed Hodgkin's disease, initial therapy is curative. However, a small portion of patients treated with radiotherapy alone for limited favorable disease, and a larger percentage of patients treated with combination chemotherapy, with or without radiotherapy, for advanced-stage or unfavorable disease relapse after initial remission. Patients relapsing after radiotherapy alone should do as well with salvage combination chemotherapy as patients with advanced disease who have never received radiation. In patients who relapse after combination chemotherapy, retreatment with the same regimen or employment of a non-cross-resistant regimen offers high response rates among those with favorable characteristics.
Commentary (Jain)-Hodgkin's Disease: Management of First Relapse
February 1st 1996Drs. Yuen and Horning provide an excellent, detailed review of the current status of salvage therapy for patients who have relapsed after initial treatment for Hodgkin's disease. The authors cover the various scenarios that confront the oncologist who manages patients with this illness. Most patients who present with early-stage Hodgkin's disease (stage IA and IIA) are still treated with primary radiation therapy, although there is an increasing trend toward combined-modality therapy in early-stage disease. As is mentioned in the article, despite excellent complete response rates with current treatment, there is still a substantial rate of relapse, which can be as high as 25%.
Risk of GI Cancer May Increase After Hodgkin's Disease Treatment
December 1st 1995MIAMI BEACH--Patients treated for Hodgkin's disease are at moderately increased risk of developing secondary gastrointestinal (GI) cancer, Sandra H. Birdwell, MD, said at the American Society for Therapeutic Radiology and Oncol-ogy (ASTRO) meeting.