Combination Therapy in Lymphoma

A special issue of Cancers (ISSN 2072-6694). This special issue belongs to the section "Cancer Therapy".

Deadline for manuscript submissions: 31 August 2025 | Viewed by 3126

Special Issue Editors


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Guest Editor
Institute of Oncology Research, Faculty of Biomedical Sciences, USI, 6500 Bellinzona, Switzerland
Interests: lymphoma; lymphoma genomics; epigenetics; diffuse large B-cell lymphoma; marginal zone lymphoma; histone deacetylase inhibitors; anti-lymphoma agents; pre-clinical studies
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Guest Editor
Institute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera italiana, Via Vincenzo Vela, 66500 Bellinzona, Switzerland
Interests: B cell lymphoma biology; marginal zone lymphoma; drug response and resistance; multi-omics characterization

Special Issue Information

Dear Colleagues,

We are pleased to invite you to this Special Issue on “Combination therapy in lymphoma”.

Combination chemotherapy, comprising alkylating and immunosuppressive agents, was for decades the standard of care for patients with Hodgkin and non-Hodgkin lymphomas. Combination therapy is therefore not a new concept in lymphoma treatment. The potential novelty in this field comes from the increasing arsenal of drugs being developed to treat lymphomas, many of which target specific proteins or reactivate anti-tumour immunity. At the end of the last century, arguably one of the most, if not the most, explosive addition to the lymphoma drug arsenal was the monoclonal antibody rituximab. The addition of rituximab to standard of care combination chemotherapy marked a practise-changing shift in the treatment of NHL and significantly improved outcomes for a larger fraction of these patients, including more complete remissions. For Hodgkin lymphoma, which already responded well to combined chemotherapy regimens, the advent of antibody drug conjugates and immune checkpoint inhibitors less than a decade ago further improved patient outcomes, nudging response rates close to 100%. These advances in lymphoma treatment have taught us the value of attacking tumour cells using a multi-pronged approach. As such, this Special Issue on ‘Combination therapy in lymphoma’ aims to highlight pre-clinical and clinical research investigating drug combinations for the treatment of lymphomas. Original research articles and reviews are welcome. Research areas may include (but are not limited to) the following: non-Hodgkin lymphoma, Hodgkin lymphoma, targeted agents, antibody drug conjugates, bispecific agents, cellular therapies, immune checkpoint inhibitors and epigenetic agents.

We look forward to receiving your contributions.

Dr. Afua Adjeiwaa Mensah
Dr. Alberto Arribas
Guest Editors

Manuscript Submission Information

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Keywords

  • combination therapy
  • non-Hodgkin lymphoma
  • Hodgkin lymphoma
  • targeted agents
  • antibody drug conjugates
  • bispecific agents
  • cellular therapies, immune checkpoint inhibitors and epigenetic agents

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Published Papers (1 paper)

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Review

17 pages, 751 KiB  
Review
Updates on the Treatment of Richter’s Syndrome, Including Novel Combination Approaches
by Tanim Jain and Benjamin Heyman
Cancers 2025, 17(6), 943; https://doi.org/10.3390/cancers17060943 - 11 Mar 2025
Viewed by 2833
Abstract
Richter’s syndrome (RS) or transformation of chronic lymphocytic leukemia (CLL) into a more aggressive lymphoma (e.g., diffuse large B cell lymphoma, DLBCL) is a distinct disease that portends an overall poor prognosis and remains a challenge for clinicians to identify and treat effectively. [...] Read more.
Richter’s syndrome (RS) or transformation of chronic lymphocytic leukemia (CLL) into a more aggressive lymphoma (e.g., diffuse large B cell lymphoma, DLBCL) is a distinct disease that portends an overall poor prognosis and remains a challenge for clinicians to identify and treat effectively. This review of the current literature focuses on the pathology, diagnosis, and management of Richter’s syndrome. Clonally related RS has been found to have a worse prognosis than unrelated disease and the genomic profile of DLBCL-RS differs from that of de novo DLBCL. The standard of care therapy for RS has historically been chemoimmunotherapy; consolidative stem cell transplants have a role in improving durability of disease response. Given generally poor response rates to chemotherapy, there have been recent investigations into combination treatments with immune checkpoint inhibitors and small molecule targeted therapies, which have had mixed results. Additional studies are evaluating the use of bispecific antibodies, chimeric antigen receptor T cell therapy, and antibody drug conjugates. RS remains difficult to manage; however, advancements in the understanding of the underlying pathology of transformation and continued investigations into new therapies demonstrate promise for the future. Full article
(This article belongs to the Special Issue Combination Therapy in Lymphoma)
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