Difference between revisions of "How I Treat"

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==Plasma cell dyscrasias==
 
==Plasma cell dyscrasias==
 
===[[Light-chain (AL) amyloidosis]]===
 
===[[Light-chain (AL) amyloidosis]]===
*'''2022:''' Palladini & Merlini [https://doi.org/10.1182/blood.2020008737 How I treat AL amyloidosis]
+
*'''2022:''' Palladini & Merlini. [https://doi.org/10.1182/blood.2020008737 How I treat AL amyloidosis]
 +
*'''2012:''' Leung et al. [https://doi.org/10.1182/blood-2012-03-413682 How I treat amyloidosis: the importance of accurate diagnosis and amyloid typing] [https://pubmed.ncbi.nlm.nih.gov/22948045/ PubMed]
  
 
===[[Multiple myeloma]]===
 
===[[Multiple myeloma]]===
*'''2023:''' van de Donk [https://doi.org/10.1200/jco.22.02114 How We Manage Newly Diagnosed Multiple Myeloma With Circulating Tumor Cells]
+
*'''2023:''' van de Donk. [https://doi.org/10.1200/jco.22.02114 How We Manage Newly Diagnosed Multiple Myeloma With Circulating Tumor Cells]
 
*'''2022:''' Zamagni et al. [https://doi.org/10.1182/blood.2020008733 How I treat high-risk multiple myeloma]
 
*'''2022:''' Zamagni et al. [https://doi.org/10.1182/blood.2020008733 How I treat high-risk multiple myeloma]
 
*'''2022:''' Kastritis et al. [https://doi.org/10.1182/blood.2020008734 How I treat relapsed multiple myeloma]
 
*'''2022:''' Kastritis et al. [https://doi.org/10.1182/blood.2020008734 How I treat relapsed multiple myeloma]
*'''2022:''' Vaxman & Gertz [https://doi.org/10.1182/blood.2021011670 How I approach smoldering multiple myeloma]
+
*'''2022:''' Vaxman & Gertz. [https://doi.org/10.1182/blood.2021011670 How I approach smoldering multiple myeloma]
  
 
==Histiocytic disorders==
 
==Histiocytic disorders==

Revision as of 17:05, 21 September 2023

The "How I Treat" series has been published by Blood for several decades and covers a wide variety of topics in malignant and classical hematology. While these articles are not considered to be formal guidelines, they are considered highly reputable sources of expert opinion. They cover topics ranging from commonly encountered hematologic conditions with a large evidence base, to very rare conditions with only case reports to guide treatment. The purpose of this page is to consolidate the links to all known published How I Treat articles.

In the first two sections (malignant hematology and classical hematology), articles are presented by condition, in reverse chronological order. In the third section, articles are gathered under "special considerations" such as pregnancy and hematologic disease. Given the rapid change in evidence in many areas of hematology, readers are encouraged to consider any article published 5+ years ago to be for historical purposes, only.

Note: this page is currently under construction.

Malignant hematology

Myeloid neoplasms

Acute lymphoblastic leukemia (ALL)

Acute myeloid leukemia (AML)

Chronic myeloid leukemia (CML)

Essential thrombocythemia (ET)

Myelodysplastic syndrome (MDS)

Polycythemia vera (PV)

Lymphoid neoplasms

Adult T-cell leukemia-lymphoma (ATLL)

Burkitt lymphoma (BL)

Castleman disease

Chronic lymphocytic leukemia (CLL/SLL)

Cutaneous T-cell lymphoma (CTCL)

Hodgkin lymphoma

Diffuse large B-cell lymphoma (DLBCL)

Follicular lymphoma (FL)

Large granular lymphocytic leukemia (T-LGL)

NK- and T-cell lymphoma

Prolymphocytic leukemia (T-PLL)

Waldenström macroglobulinemia (WM)

Plasma cell dyscrasias

Light-chain (AL) amyloidosis

Multiple myeloma

Histiocytic disorders

Hemophagocytic lymphohistiocytosis (HLH)

Classical hematology

Hemostasis and thrombosis

Acquired thrombotic thrombocytopenic purpura (aTTP)

Antiphospholipid antibody syndrome (APS)

Arterial thromboembolism (ATE)

Hemophilia

Thrombotic microangiopathy (TMA)

Venous thromboembolism (VTE)

von Willebrand disease (vWD)

Cytopenias

Anemia

Autoimmune cytopenia

Immune thrombocytopenia (ITP)

Thrombocytopenia and platelet dysfunction

Hemoglobinopathies

Beta thalassemia

Sickle cell disease

Hemolytic disorders

Cold agglutinin disease (CAD)

Atypical hemolytic uremic syndrome (aHUS)

Paroxysmal nocturnal hemoglobinuria (PNH)

Warm autoimmune hemolytic anemia (WAIHA)

Special considerations

Age-based recommendations

Neonates

Children

Adolescents and young adults (AYA)

Older adults

Complications of treatment

Immune effector cells toxicity management

Infectious complications

Pregnancy

Transplatation

Allogeneic HSCT

Graft versus host disease (GVHD)