What is lymphoma?

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Last updated: April 24, 2025View editorial policy

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From the Guidelines

Lymphoma patients should be treated with rituximab in combination with chemotherapy regimens as the standard of care for first-line therapy, as it has been shown to improve progression-free survival. This approach is based on the recommendations outlined in the NCCN Guidelines for the diagnosis and management of patients with follicular lymphoma (FL), a common subtype of indolent non-Hodgkin's lymphoma (NHL) 1. The incorporation of rituximab into chemotherapy regimens has become a widely accepted standard of care for first-line therapy for patients with FL.

Some key points to consider in the management of lymphoma include:

  • The heterogeneity of non-Hodgkin's lymphomas, which originate in B lymphocytes, T lymphocytes, or natural killer cells 1
  • The importance of maintenance and consolidation therapy with rituximab and radioimmunotherapy to improve progression-free survival in patients experiencing response to first-line therapy 1
  • The chronic nature of follicular lymphoma, characterized by multiple recurrences with current therapies 1

In terms of symptoms and diagnosis, it is essential to be aware of:

  • Painless swollen lymph nodes, fever, night sweats, weight loss, and fatigue as common symptoms of lymphoma
  • The importance of early diagnosis for better outcomes, as many lymphomas are highly treatable or even curable, especially when detected in early stages.

From the FDA Drug Label

RITUXAN is a CD20-directed cytolytic antibody indicated for the treatment of: Adult patients with Non-Hodgkin's Lymphoma (NHL) Relapsed or refractory, low grade or follicular, CD20-positive B-cell NHL as a single agent. Previously untreated follicular, CD20-positive, B-cell NHL in combination with first line chemotherapy and, in patients achieving a complete or partial response to a rituximab product in combination with chemotherapy, as single-agent maintenance therapy Non-progressing (including stable disease), low-grade, CD20-positive, B-cell NHL as a single agent after first-line cyclophosphamide, vincristine, and prednisone (CVP) chemotherapy. Previously untreated diffuse large B-cell, CD20-positive NHL in combination with (cyclophosphamide, doxorubicin, vincristine, and prednisone) (CHOP) or other anthracycline-based chemotherapy regimens Pediatric patients aged 6 months and older with mature B-cell NHL and mature B-cell acute leukemia (B-AL) Previously untreated, advanced stage, CD20-positive, diffuse large B-cell lymphoma (DLBCL), Burkitt lymphoma (BL), Burkitt-like lymphoma (BLL) or mature B-cell acute leukemia (B-AL) in combination with chemotherapy.

Lymphoma Treatment: Rituximab (IV) is indicated for the treatment of various types of lymphoma, including:

  • Non-Hodgkin's Lymphoma (NHL)
  • Diffuse large B-cell lymphoma (DLBCL)
  • Burkitt lymphoma (BL)
  • Burkitt-like lymphoma (BLL)
  • Mature B-cell acute leukemia (B-AL) The recommended dose for adult and pediatric B-cell NHL is 375 mg/m2 2.

From the Research

Lymphoma Diagnosis and Treatment

  • Lymphoma is a group of malignant neoplasms of lymphocytes with more than 90 subtypes, traditionally classified as non-Hodgkin or Hodgkin lymphoma 3
  • The Lugano classification system incorporates symptoms and the extent of the disease as shown on positron emission tomography/computed tomography (PET/CT) to stage lymphoma, which is then used to determine treatment 3
  • Chemotherapy treatment plans differ between the main subtypes of lymphoma, with non-Hodgkin lymphoma treated with CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone) with or without rituximab (R-CHOP), and Hodgkin lymphoma treated with combined chemotherapy with ABVD (doxorubicin, bleomycin, vinblastine, and dacarbazine) 3

Role of PET/CT in Lymphoma Diagnosis and Treatment

  • 18F-FDG PET/CT is the imaging modality of choice for the accurate initial staging of most lymphomas, with high sensitivity in detecting nodal involvement and extra-nodal disease 4
  • PET/CT has excellent Negative Predictive Value (NPV>95%) in the detection of bone marrow involvement in Hodgkin's lymphoma, rendering bone marrow biopsy not absolutely necessary 4
  • Interim PET/CT shows high NPV for final treatment response and for increased progression-free survival in Hodgkin's lymphoma, and is also investigated in non-Hodgkin lymphomas 4
  • PET/CT is highly recommended for post-treatment assessment of lymphomas, with excellent NPV and superior diagnostic accuracy compared with CT 4

Comparison of Bone Marrow Biopsy and PET/CT

  • Bone marrow biopsy is the standard method for investigating bone marrow involvement, but PET/CT has been shown to be highly effective in detecting bone marrow involvement in lymphoma patients 5, 6, 7
  • PET/CT may replace bone marrow biopsy in detecting bone marrow involvement in aggressive lymphoma subtypes such as diffuse large B-cell lymphoma (DLBCL) and Hodgkin lymphoma (HL) 5, 6
  • The diagnostic accuracy of PET/CT in identifying bone marrow involvement in DLBCL patients has been shown to be high, with sensitivity, specificity, and overall diagnostic accuracy of 93.61%, 93.93%, and 93.84%, respectively 7

Survival and Prognosis

  • The presence of bone marrow involvement at the time of diagnosis is associated with poor prognosis and short overall survival (OS) in both PET/CT and bone marrow biopsy methods 5
  • PET/CT may be used to evaluate the response to treatment and predict survival in lymphoma patients, with a favorable PET response associated with better progression-free survival and overall survival 4, 5

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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