ABVD Other Names: LYABVD
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Hodgkin Lymphoma Treatment Regimens
HODGKIN LYMPHOMA TREATMENT REGIMENS (Part 1 of 5) Clinical Trials: The National Comprehensive Cancer Network recommends cancer patient participation in clinical trials as the gold standard for treatment. Cancer therapy selection, dosing, administration, and the management of related adverse events can be a complex process that should be handled by an experienced health care team. Clinicians must choose and verify treatment options based on the individual patient; drug dose modifications and supportive care interventions should be administered accordingly. The cancer treatment regimens below may include both U.S. Food and Drug Administration-approved and unapproved indications/regimens. These regimens are provided only to supplement the latest treatment strategies. These Guidelines are a work in progress that may be refined as often as new significant data become available. The NCCN Guidelines® are a consensus statement of its authors regarding their views of currently accepted approaches to treatment. Any clinician seeking to apply or consult any NCCN Guidelines® is expected to use independent medical judgment in the context of individual clinical circumstances to determine any patient’s care or treatment. The NCCN makes no warranties of any kind whatsoever regarding their content, use, or application and disclaims any responsibility for their application or use in any way. Classical Hodgkin Lymphoma1 Note: All recommendations are Category 2A unless otherwise indicated. Primary Treatment Stage IA, IIA Favorable (No Bulky Disease, <3 Sites of Disease, ESR <50, and No E-lesions) REGIMEN DOSING Doxorubicin + Bleomycin + Days 1 and 15: Doxorubicin 25mg/m2 IV push + bleomycin 10units/m2 IV push + Vinblastine + Dacarbazine vinblastine 6mg/m2 IV over 5–10 minutes + dacarbazine 375mg/m2 IV over (ABVD) (Category 1)2-5 60 minutes. -
HODGKIN LYMPHOMA TREATMENT REGIMENS (Part 1 of 2)
HODGKIN LYMPHOMA TREATMENT REGIMENS (Part 1 of 2) The selection, dosing, and administration of anticancer agents and the management of associated toxicities are complex. Drug dose modifications and schedule and initiation of supportive care interventions are often necessary because of expected toxicities and because of individual patient variability, prior treatment, and comorbidities. Thus, the optimal delivery of anticancer agents requires a healthcare delivery team experienced in the use of such agents and the management of associated toxicities in patients with cancer. The cancer treatment regimens below may include both FDA-approved and unapproved uses/regimens and are provided as references only to the latest treatment strategies. Clinicians must choose and verify treatment options based on the individual patient. NOTE: GREY SHADED BOXES CONTAIN UPDATED REGIMENS. REGIMEN DOSING Classical Hodgkin Lymphoma—First-Line Treatment General treatment note: Routine use of growth factors is not recommended. Leukopenia is not a factor for treatment delay or dose reduction (except for escalated BEACOPP).1 CR=complete response IPS=International Prognostic Score PD=progressive disease PFTs=pulmonary function tests PR=partial response RT=radiation therapy SD=stable disease Stage IA, IIA Favorable ABVD (doxorubicin [Adriamycin] Days 1 and 15: Doxorubicin 25mg/m2 IV + bleomycin 10mg/m2 IV + vinblastine + bleomycin + vinblastine + 6mg/m2 IV + dacarbazine 375mg/m2 IV. dacarbazine [DTIC-Dome]) + Repeat cycle every 4 weeks for 2–4 cycles. involved-field radiotherapy (IFRT)1–4 Follow with IFRT after completion of chemotherapy. Abbreviated Stanford V Weeks 1, 3, 5 and 7: Vinblastine 6mg/m2 IV + doxorubicin 25mg/m2 IV. (doxorubicin + vinblastine + Weeks 1 and 5: Mechlorethamine 6mg/m2. -
Hodgkin Lymphoma
Hodgkin Lymphoma Erica, Hodgkin lymphoma survivor Revised 2016 Publication Update Hodgkin Lymphoma The Leukemia & Lymphoma Society wants you to have the most up-to-date information about blood cancer treatment. See below for important new information that was not available at the time this publication was printed. In May 2017, the Food and Drug Administration (FDA) approved nivolumab (Opdivo®) for the treatment of adult patients with classical Hodgkin lymphoma (HL) that has relapsed or progressed after 3 or more lines of systemic therapy that includes autologous hematopoietic stem cell transplantation (HSCT). It is also approved for the treatment of adult patients with classical HL that has relapsed or progressed after autologous HSCT and brentuximab vedotin. These indications are approved under accelerated approval based on overall response rate. Continued approval for this indication may be contingent upon verification and description of clinical benefit in confirmatory trials. In March 2017, the Food and Drug Administration (FDA) approved pembrolizumab (Keytruda®) for the treatment of adult and pediatric patients with refractory classical Hodgkin lymphoma (cHL), or who have relapsed after 3 or more prior lines of therapy. This indication is approved under accelerated approval based on tumor response rate and durability of response. Continued approval for this indication may be contingent upon verification and description of clinical benefit in the confirmatory trials. For more information, contact an Information Specialist at (800) 955-4572 or [email protected]. Information Specialists: 800.955.4572 I www.LLS.org PS57 A Message from Louis J. DeGennaro, PhD President and CEO of The Leukemia & Lymphoma Society The Leukemia & Lymphoma Society (LLS) is the world’s largest voluntary health organization dedicated to finding cures for blood cancer patients. -
Desmoid Tumors: Understanding Treatment Options in 2019
Desmoid Tumors: Understanding Treatment Options in 2019 Breelyn A. Wilky, MD Associate Professor Sarcoma Program, Division of Oncology A real desmoid story… 35 year old female physician who noted abdominal cramping and pain in her mid abdomen and a palpable mass in August 2018 She performed an ultrasound on herself in the ER which showed a 4.5 x 4.5 cm mass in her mid abdomen CT scan showed a mesenteric mass that was wrapped around and blocking the inferior mesenteric vein with multiple satellite nodules/lymph nodes. Biopsy confirmed the diagnosis of desmoid tumor A real desmoid story… Mother had a neuroendocrine cancer in the appendix, father had Hodgkins lymphoma The patient had a negative colonoscopy for any polyps She had no other medical problems but has three children, with the last baby born 4 months prior to her symptoms. This most recent baby was conceived with in vitro fertilization. Tumor board discussion… Ongoing pain likely related to venous outflow obstruction (confirmed on colonoscopy as well) Treatment options in 2019… Watch and Wait • Doxorubicin/ Dacarbazine Chemotherapy Attempt • MTX/vinblastine (IV) Surgery • Doxil • Sorafenib • Imatinib Targeted • Pazopanib treatments Radiation • Nirogacestat (chemo pills) • Tegavivint (IV) • Tamoxifen +/- sulindac Estrogen- Ablation • Aromatase blocking IRE/Nanoknife inhibitors Treatments HIFU • Celebrex Choosing a treatment approach . Anxiety over “doing nothing” . How long is acceptable to wait for Symptoms a response? Location . Can shrinkage or necrosis create a Risk to surrounding structures more definitive option? (surgery, and organs electroporation?) Growth pattern over time . What is the expected function or appearance after my desmoid Obvious estrogen exposure surgery? (pregnancy) . -
Older Patients
Older patients (aged ≥60 years) with previously untreated advanced-stage classical Hodgkin lymphoma: a detailed analysis from the phase III ECHELON-1 study by Andrew M. Evens, Joseph M. Connors, Anas Younes, Stephen M. Ansell, Won Seog Kim, John Radford, Tatyana Feldman, Joseph Tuscano, Kerry J. Savage, Yasuhiro Oki, Andrew Grigg, Christopher Pocock, Monika Dlugosz-Danecka, Keenan Fenton, Andres Forero-Torres, Rachael Liu, Hina Jolin, Ashish Gautam, and Andrea Gallamini Haematologica 2021 [Epub ahead of print] Citation: Andrew M. Evens, Joseph M. Connors, Anas Younes, Stephen M. Ansell, Won Seog Kim, John Radford, Tatyana Feldman, Joseph Tuscano, Kerry J. Savage, Yasuhiro Oki, Andrew Grigg, Christopher Pocock, Monika Dlugosz-Danecka, Keenan Fenton, Andres Forero-Torres, Rachael Liu, Hina Jolin, Ashish Gautam, and Andrea Gallamini. Older patients (aged ≥60 years) with previously untreated advanced-stage classical Hodgkin lymphoma: a detailed analysis from the phase III ECHELON-1 study. Haematologica. 2021; 106:xxx doi:10.3324/haematol.2021.278438 Publisher's Disclaimer. E-publishing ahead of print is increasingly important for the rapid dissemination of science. Haematologica is, therefore, E-publishing PDF files of an early version of manuscripts that have completed a regular peer review and have been accepted for publication. E-publishing of this PDF file has been approved by the authors. After having E-published Ahead of Print, manuscripts will then undergo technical and English editing, typesetting, proof correction and be presented for the authors' final approval; the final version of the manuscript will then appear in print on a regular issue of the journal. All legal disclaimers that apply to the journal also pertain to this production process. -
Systemic Therapy for Advanced Soft Tissue Sarcoma
Systemic Therapy for Advanced Soft Tissue Sarcoma a, b Jennifer Y. Sheng, MD *, Sujana Movva, MD KEYWORDS Advanced soft tissue sarcoma Chemotherapy Novel therapies KEY POINTS Survival for advanced soft tissue sarcomas has improved significantly over the last 20 years because of advancements in histologic classification, improved treatment ap- proaches, and novel agents. An important factor guiding choice of therapy is soft tissue sarcoma subtype, as drugs such as eribulin and trabectedin may have particular activity in leiomyosarcoma and liposarcoma. Focus on angiogenesis inhibition has led to the approval of pazopanib for soft tissue sar- coma, and the pathway continues to be investigated in this disease. Toxicity is an important area of investigation in soft tissue sarcoma, and new agents, such as aldoxorubicin, may be alternatives with better safety profiles. Future studies on treatment of advanced soft tissue sarcoma will continue to focus on identification of novel drug targets, personalization of therapy, and combination immunotherapies. BACKGROUND Sarcomas are rare tumors that arise from or are differentiated from tissues of meso- dermal origin. They comprise less than 1% of all adult malignancies.1 In 2015 there were approximately 14, 900 new cases diagnosed, with 6360 deaths in the United States. Sarcomas are grouped into 2 general categories: soft tissues sarcomas and primary bone sarcomas, which have different staging and treatment approaches. This article includes a discussion of chemotherapy in advanced or refractory soft tis- sue sarcoma. Patients with metastatic disease are usually best managed with chemo- therapy. Distant metastasis occurs in up to 10% of patients, with the lung being the most common site in 83% of cases.2 Systemic therapy can involve cytotoxic a Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins Uni- versity School of Medicine, Baltimore, MD, USA; b Department of Hematology/Oncology, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA 19111, USA * Corresponding author. -
Effective Treatment of Advanced Human Melanoma Metastasis In
Published OnlineFirst July 21, 2009; DOI: 10.1158/1078-0432.CCR-08-3275 Published Online First on July 21, 2009 as 10.1158/1078-0432.CCR-08-3275 Cancer Therapy: Preclinical Effective Treatment of Advanced Human Melanoma Metastasis in Immunodeficient Mice Using Combination Metronomic Chemotherapy Regimens William Cruz-Munoz, Shan Man, and Robert S. Kerbel Abstract Purpose: The development of effective therapeutic approaches for treatment of meta- static melanoma remains an immense challenge. Present therapies offer minimal ben- efit. Although dacarbazine chemotherapy remains the standard therapy, it mediates only low response rates, usually of short duration, even when combined with other chemotherapeutic agents. Thus, new therapeutic strategies are urgently needed. Experimental Design: Using a newly developed preclinical model, we evaluated the ef- ficacy of various doublet metronomic combination chemotherapy against established advanced melanoma metastasis and compared these with the standard maximum tol- erated dose dacarbazine (alone or in combination with chemotherapeutic agents or vascular endothelial growth factor receptor–blocking antibody). Results: Whereas maximum tolerated dose dacarbazine therapy did not cause signifi- cant improvement in median survival, a doublet combination of low-dose metronomic vinblastine and low-dose metronomic cyclophosphamide induced a significant increase in survival with only minimal toxicity. Furthermore, we show that the incorpo- ration of the low-dose metronomic vinblastine/low-dose metronomic -
CVD: Cisplatin, Vinblastine, and Dacarbazine
PATIENT EDUCATION patienteducation.osumc.edu CVD: Cisplatin, Vinblastine, and Dacarbazine What is CVD? It is the short name for the drugs used in this chemotherapy treatment. The three drugs you will receive during this treatment are Cisplatin (“C”), Vinblastine (“V”), and Dacarbazine (DTIC-DomeTM or “D”). This chemotherapy will be given daily for 5 days. What is Cisplatin (SIS-pla-tin) and how does it work? Cisplatin is a chemotherapy drug known as an “alkylating agent.” Cisplatin works to stop fast growing cancer cells from dividing and making new cells. This will be given daily on days 2 through 5. What is Vinblastine (vin-BLAS-teen) and how does it work? Vinblastine is a chemotherapy drug known as an “anti-microtubule inhibitor.” This drug fights cancer cells by stopping fast growing cancer cells from dividing and making new cancer cells. This drug will be given daily on days 1 through 5. What is Dacarbazine (da-KAR-ba-zeen) and how does it work? Dacarbazine is a chemotherapy drug known as an “alkylating agent.” Dacarbazine works to stop fast growing cancer cells from dividing and making new cells. This drug will be given on the first day. This handout is for informational purposes only. Talk with your doctor or health care team if you have any questions about your care. © September 10, 2020. The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute. Why am I getting three chemotherapy drugs for my cancer? These drugs work to stop fast growing cancer cells from dividing and making new cells, but they attack the cancer cells differently. -
Gemcitabine-Containing Chemotherapy for the Treatment of Metastatic Myxofibrosarcoma Refractory to Doxorubicin: a Case Series
Brief Report Gemcitabine-Containing Chemotherapy for the Treatment of Metastatic Myxofibrosarcoma Refractory to Doxorubicin: A Case Series 1, 2, 1,2, Arielle Elkrief y, Suzanne Kazandjian y and Thierry Alcindor * 1 Cedars Cancer Center, McGill University Health Centre, Montreal, QC H4A 3J1, Canada; [email protected] 2 Department of Medicine, McGill University Health Centre, Montreal, QC H4A 3J1, Canada; [email protected] * Correspondence: [email protected] These authors contributed equally to this paper. y Received: 7 December 2020; Accepted: 3 February 2021; Published: 5 February 2021 Abstract: Background: Myxofibrosarcoma is a type of soft-tissue sarcoma that is associated with high rates of local recurrence and distant metastases. The first-line treatment for metastatic soft-tissue sarcoma has conventionally been doxorubicin-based. Recent evidence suggests that myxofibrosarcoma may be molecularly similar to undifferentiated pleomorphic sarcoma (UPS), which is particularly sensitive to gemcitabine-based therapy. The goal of this study was to evaluate the activity of gemcitabine-containing regimens for the treatment of metastatic myxofibrosarcoma refractory to doxorubicin. Material and Methods: We retrospectively evaluated seven consecutive cases of metastatic myxofibrosarcoma at our institution treated with gemcitabine-based therapy in the second-line setting, after progression on doxorubicin. Baseline clinical and baseline characteristics were collected. Primary endpoints were objective response rate (ORR), progression-free survival (PFS) and overall survival (OS). Results: After progression on first-line doxorubicin, a partial, or complete radiological response was observed in four of seven patients who received gemcitabine-based chemotherapy. With a median follow-up of 14 months, median progression-free and overall survival were 8.5 months and 11.4 months, respectively. -
Efficacy, Safety, and Tolerability of Approved Combination BRAF and MEK Inhibitor Regimens for BRAF-Mutant Melanoma
Cancers 2019, 11, 1642; doi:10.3390/cancers11111642 S1 of S5 Supplementary Materials: Efficacy, Safety, and Tolerability of Approved Combination BRAF and MEK Inhibitor Regimens for BRAF-Mutant Melanoma Omid Hamid, C. Lance Cowey, Michelle Offner, Mark Faries and Richard D. Carvajal Table S1. Anticancer Treatment by Regimen Following Study Drug Discontinuation. Dabrafenib + Trametinib Vemurafenib + Encorafenib + [1,2] Cobimetinib [3] Binimetinib [4] COMBI-v † COMBI-d coBRIM COLUMBUS n = 352 n = 209 n = 183 n = 192 Any treatment 72 (20%) 101 (48%) 105 (57%) 80 (42%) Immunotherapy NR 117 (56%) 67 (37%) NR Any anti–PD-1/anti–PD-L1 NR NR 28 (15%) 39 (20%) Ipilimumab (anti-CTLA-4) 41 (12%) 86 (41%) 53 (29%) 33 (17%) Nivolumab (anti-PD-1) NR 15 (7%) NR NR Pembrolizumab (anti–PD-L1) 4 (1%) 27 (13%) NR NR anti-CTLA-4 + NR NR 4 (2%) 6 (3%) anti–PD-1/anti–PD-L1 ‡ Targeted therapies NR 21 (10%) § 32 (18%) NR BRAFi + MEKi NR NR 15 (8%) 10 (5%) ¶ BRAFi NR NR 19 (10%) 11 (6%) # MEKi NR NR 2 (1%) NR Chemotherapy NR 37 (18%) 30 (16%) 14 (7%) ** Other NR NR 2 (1%) †† 5 (3%) ‡‡ NR = not reported. Data are n (%). PD-1 = programmed death cell receptor 1. PD-L1 = programmed death cell ligand 1. † Multiple uses of a type of therapy for an individual patient were only counted once in the frequency for that treatment category; patients mght have received multiple lines of treatment. Received by ≥2% of patients. ‡ Ipilimumab + nivolumab or ipilimumab + pembrolizumab. § Small-molecule targeted therapy. -
Hodgkin Lymphoma
Hodgkin Lymphoma Zach, Hodgkin lymphoma survivor Revised 2013 A Message From John Walter President and CEO of The Leukemia & Lymphoma Society The Leukemia & Lymphoma Society (LLS) believes we are living at an extraordinary moment. LLS is committed to bringing you the most up-to-date blood cancer information. We know how important it is for you to have an accurate understanding of your diagnosis, treatment and support options. An important part of our mission is bringing you the latest information about advances in treatment for Hodgkin lymphoma, so you can work with your healthcare team to determine the best options for the best outcomes. Our vision is that one day the great majority of people who have been diagnosed with Hodgkin lymphoma will be cured or will be able to manage their disease with a good quality of life. We hope that the information in this publication will help you along your journey. LLS is the world’s largest voluntary health organization dedicated to funding blood cancer research, education and patient services. Since 1954, LLS has been a driving force behind almost every treatment breakthrough for patients with blood cancers, and we have awarded almost $1 billion to fund blood cancer research. Our commitment to pioneering science has contributed to an unprecedented rise in survival rates for people with many different blood cancers. Until there is a cure, LLS will continue to invest in research, patient support programs and services that improve the quality of life for patients and families. We wish you well. John -
NCCN Guidelines for Patients Hodgkin Lymphoma 2019
our Pleaseonline surveycomplete at NCCN.org/patients/survey NCCN GUIDELINES FOR PATIENTS® 2019 Hodgkin Lymphoma Presented with support from: Available online at NCCN.org/patients Ü Hodgkin Lymphoma It's easy to get lost in the cancer world Let Ü NCCN Guidelines for Patients® be your guide 9 Step-by-step guides to the cancer care options likely to have the best results 9 Based on treatment guidelines used by health care providers worldwide 9 Designed to help you discuss cancer treatment with your doctors NCCN Guidelines for Patients®: Hodgkin Lymphoma, 2019 1 About These NCCN Guidelines for Patients® are based on the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) for Hodgkin Lymphoma (Version 2.2019, July 15, 2019). © 2020 National Comprehensive Cancer Network, Inc. All rights reserved. NCCN Foundation® seeks to support the millions of patients and their families NCCN Guidelines for Patients® and illustrations herein may not be reproduced affected by a cancer diagnosis by funding and distributing NCCN Guidelines for in any form for any purpose without the express written permission of NCCN. No Patients®. NCCN Foundation is also committed to advancing cancer treatment one, including doctors or patients, may use the NCCN Guidelines for Patients for by funding the nation’s promising doctors at the center of innovation in cancer any commercial purpose and may not claim, represent, or imply that the NCCN research. For more details and the full library of patient and caregiver resources, Guidelines for Patients that have been modified in any manner are derived from, visit NCCN.org/patients. We rely solely on donations to fund the NCCN Guidelines based on, related to, or arise out of the NCCN Guidelines for Patients.