Leukemia & Lymphoma

Leukemia & Lymphoma

Published by Taylor & Francis

Online ISSN: 1029-2403

Journal websiteAuthor guidelines

Top-read articles

76 reads in the past 30 days

Real-world data of polatuzumab vedotin with bendamustine and rituximab for Japanese relapsed and refractory DLBCL: a multicenter retrospective study

March 2025

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115 Reads

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Aims and scope


Publishes research on hematological cancers, covering disease biology, novel agents, chemotherapy, pharmacology/pharmacogenomics, ethics and epidemiology.

  • Leukemia & Lymphoma is an international peer reviewed journal that publishes research on all aspects of hematological malignancies.
  • The journal aims to address the needs of physicians and scientists interested in clinical, translational, laboratory and basic science research, as well as clinical diagnosis and treatment of patients with malignant hematological disorders.
  • Leukemia & Lymphoma covers from clinical and clinico-pathological investigations to fundamental research in the following topics: disease biology; mechanisms of action of novel agents; development of combination chemotherapy; pharmacology and pharmacogenomics; ethics and epidemiology.
  • Submissions of unique clinical observations or confirmatory studies are considered and…

For a full list of the subject areas this journal covers, please visit the journal website.

Recent articles


Optimal timing of allogeneic hematopoietic stem cell transplant in MDS
  • Literature Review

June 2025

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5 Reads

Kristin Rathje

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Nicolaus Kröger



Lower-dose venetoclax (LoVe) based regimes in children with acute leukemia

June 2025

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15 Reads

Tablet venetoclax 100 mg along with tablet posaconazole 300 mg once a day for 7 days was used in 4 of the older children. The 2-year-old child received venetoclax 50 mg and posaconazole 100 mg once a day for 7 days. Posaconazole was added to use the drug interaction with venetoclax to the patient’s financial advantage where 100 mg is equivalent to 400 mg and to provide additional antifungal prophylaxis. Two children developed grade I transaminitis. None developed hyperbilirubinemia. All three children with ALL [2 Early T-cell precursor (ETP) ALL and 1 B-ALL) attained MRD-negative remission. None of the 2 children with acute myeloid leukemia (AML) showed any response. Both were shifted to best supportive care and quickly succumbed thereafter.
























Journal metrics


2.2 (2023)

Journal Impact Factor™


30%

Acceptance rate


4.1 (2023)

CiteScore™


16 days

Submission to first decision


0.629 (2023)

SNIP


0.790 (2023)

SJR

Editors