From the Guidelines
Lymphoma management should prioritize a comprehensive approach tailored to the specific lymphoma type, stage, and patient factors, with treatment options including chemotherapy regimens such as ABVD for Hodgkin lymphoma and R-CHOP for diffuse large B-cell lymphoma, as well as radiation therapy and stem cell transplantation for relapsed or refractory disease. When considering the management of lymphoma, it is essential to take into account the specific type and stage of the disease, as well as individual patient factors.
- For Hodgkin lymphoma, the standard of care for patients with early unfavorable disease is four cycles of ABVD followed by 30 Gy IF radiotherapy, resulting in tumor control and overall survival in excess of 85% or 90% at 5 years 1.
- For advanced-stage disease, the standard of care is currently under discussion, but multiagent chemotherapy with regimens such as MOPP/ABVD or ABVD have resulted in long-term cure rates of 50–60%, with BEACOPP escalated showing superior overall response, disease-free, and overall survival at 5 years 1.
- In the case of relapse, younger patients should receive high-dose chemotherapy and autologous stem-cell transplantation, with salvage regimens including DHAP, ESHAP, ICE, MiniBEAM, or gemcitabine combinations 1.
- Additionally, the Lymphoma Study Association guidelines recommend a risk-adapted strategy for transplant-eligible patients with relapsing or refractory Hodgkin’s lymphoma, based on three risk factors at progression and an early evaluation of salvage chemosensitivity using 18fluorodeoxy glucose-positron emission tomography 1.
- The use of targeted therapies, such as BTK inhibitors and checkpoint inhibitors, may also be considered for certain types of lymphoma, and supportive care should include antiemetics, growth factors, and prophylactic antimicrobials as needed.
- It is crucial to monitor treatment response with interim PET-CT scans and adjust therapy accordingly, with long-term monitoring essential due to potential late effects including secondary malignancies and cardiovascular complications.
From the FDA Drug Label
The trial was planned to enroll 600 patients with 1:1 randomization. The randomization was stopped early for efficacy after 362 patients had been enrolled (181 in each arm) according to the first planned interim analysis result A total of 328 randomized patients, aged 6 months and older, were included in the efficacy analyses, of which one patient under 3 years of age received intravenous RITUXAN or non-U.S. -licensed rituximab in combination with LMB chemotherapy Demographic and disease characteristics of the randomized trial population are displayed in Table 13: Table 13: Demographics and Disease Characteristics of the Randomized Trial Population - ITT RITUXAN + LMB ChemotherapyN = 164LMB ChemotherapyN = 164 BSA= Body Surface Area, B-AL=B-Cell Acute Leukemia, DLBCL= Diffuse Large B-cell Lymphoma, NHL= Non-Hodgkin's Lymphoma , CNS= Central Nervous System Male82%84% Female18%17% Age (years) Median (range)8 (2,17)7 (1,17) Age group 6 months to less than 3 years0.6%4% 3 to less than 12 years71%71% 12 to less than 18 years29%25% BSA (m2) Median (range)1.0 (0.6,2.3)0.97 (0.5,2. 7) Therapeutic group Group B high-risk49%51% Group C140%40% Group C311%10% Disease Type B-AL37%34% Burkitt or Burkitt-like NHL55%56% DLBCL8%8% Bone marrow involvement45%45% CNS involvement27%27% Efficacy was established based on event-free survival (EFS), where an event was defined as occurrence of progressive disease, relapse, second malignancy, death from any cause, or non-response as evidenced by detection of viable cells in residue after the second CYVE course, whichever occurs first. Efficacy analyses were performed in 328 randomized patients with a median follow-up of 3. 1 years. The results are described in Table 14. Table 14: Overview of Efficacy Results (ITT population) AnalysisLMB(N = 164)R-LMB(N=164) CI = confidence interval; EFS = event-free survival; HR = hazard ratio; ITT = intent-to-treat
- Event-free survival rate was calculated based on 38 event † two-sided unstratified log-rank test, testing null hypothesis of equality of event-free survivorship in randomization arms R-LMB and LMB against alternative hypothesis "event-free survivorship in group R-LMB is higher than in LMB." The analysis was based on 53% of information where the p-value boundary was 0. 014. ‡ R-LMB Versus LMB EFS*28 events10 events Two-sided unstratified log-rank test p-value 0.0012† Adjusted Cox HR‡ 0.32 (90% CI: 0.17,0.58) As of data cutoff date of 31 December 2017, there were 20 and 8 deaths reported in LMB arm and R-LMB arm, respectively, with an estimated overall survival (OS) HR of 0.36 (95% CI, 0.16 - 0. 81). No formal statistical test was conducted for overall survival and therefore the OS result is considered descriptive.
The management options for Lymphoma (Lymphatic system cancer) include:
- Rituximab in combination with chemotherapy, such as LMB chemotherapy or CHOP
- R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone)
- Other anthracycline-based chemotherapy regimens
- Rituximab as a single agent Key considerations for management include:
- Event-free survival (EFS): the time from randomization to the first of progressive disease, relapse, second malignancy, death from any cause, or non-response
- Overall survival (OS): the time from randomization to death from any cause
- Disease characteristics: such as DLBCL, NHL, B-AL, and CNS involvement
- Patient demographics: such as age, sex, and BSA These management options are based on the results of clinical trials, including those with rituximab in combination with chemotherapy, which have shown improved EFS and OS in patients with Lymphoma 2.
From the Research
Management Options for Lymphoma
The management options for lymphoma, a type of cancer that affects the lymphatic system, vary depending on the type and stage of the disease. The following are some of the management options for lymphoma:
- Chemotherapy: Chemotherapy is a common treatment for lymphoma, and the type of chemotherapy used depends on the type of lymphoma. For example, patients with Hodgkin lymphoma may receive chemotherapy regimens such as ABVD (doxorubicin, bleomycin, vinblastine, and dacarbazine) or BEACOPP (bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone) 3, 4.
- Radiation Therapy: Radiation therapy may be used in combination with chemotherapy to treat lymphoma, especially in patients with early-stage disease 5, 4.
- Immunotherapy: Immunotherapy, such as rituximab, may be used to treat certain types of lymphoma, including non-Hodgkin lymphoma 6, 4.
- Stem Cell Transplantation: Stem cell transplantation, either autologous or allogeneic, may be used to treat patients with relapsed or refractory lymphoma 5, 7.
- Salvage Chemotherapy: Salvage chemotherapy, such as R-DHAX (rituximab, dexamethasone, cytarabine, and oxaliplatin), may be used to treat patients with relapsed or refractory lymphoma 6.
- Palliative Care: Palliative care, including symptom management and supportive care, is an important part of lymphoma management, especially in patients with advanced disease 5, 4.
Treatment Regimens
Some common treatment regimens for lymphoma include:
- R-CHOP: Rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone, used to treat non-Hodgkin lymphoma 4, 7.
- ABVD: Doxorubicin, bleomycin, vinblastine, and dacarbazine, used to treat Hodgkin lymphoma 3, 4.
- BEACOPP: Bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone, used to treat Hodgkin lymphoma 3, 4.
- R-DHAX: Rituximab, dexamethasone, cytarabine, and oxaliplatin, used to treat relapsed or refractory non-Hodgkin lymphoma 6.
Special Considerations
Some special considerations in lymphoma management include:
- Risk Stratification: Patients with lymphoma should be risk-stratified to determine the best treatment approach 5, 3.
- Positron Emission Tomography (PET): PET scans may be used to assess treatment response and guide treatment decisions 5, 3.
- Supportive Care: Supportive care, including vaccination and infection prevention, is important in lymphoma management 4.