Follicular lymphoma (FL) is the second most common non-Hodgkin's lymphoma (NHL) in the Western world, representing 20% to 30% of all NHL cases and an annual incidence of 5/100,000.1,2 It is genetically characterized by an upregulation of B-cell lymphoma 2 (BCL2) of the originated B cell, which develops via the t(14;18) translocation to a proliferating clone.3 Patients usually presents with advanced and incurable disease; however, in the past 10 to 15 years, the introduction of new treatment approaches have remarkable improved the overall outcome of follicular lymphoma grade I-IIIa. Nowadays, there is a 5-year overall survival (OS) of more than 90% and a median OS approaching 20 years, making FL a chronic disease for the majority of patients.4,5 Despite these improvements, the major cause of death for patients with FL remains the lymphoma with a cumulative incidence of 10.3% at 10 years, followed by treatment-related mortality (3.0%).6 Certain subgroups still have a poor prognosis, and the optimal therapeutic approach in first line and relapsing disease is still a matter of debate. Major open questions in the treatment of FL are summarized in Table 1.
Stage I/II limited disease
Less than 20% of patients with FL are diagnosed with stage I/II disease, and the vast majority of these patients are treated out of the setting of a clinical trial. The reason for this is not only the limited number of patients with localized FL but also that it is considered as curable and often treated with radiotherapy alone (usually as involved field radiation therapy (IFRT)), making it less incentive for research. Recommended doses are in the range of 20 to 25 Gy, since higher doses failed to show improved efficacy.7 More important, in a recent analysis 5-year freedom from progression (FFP) was 74.1% for stage I but only 49.1% for stage II.8 These results may raise the question if radiotherapy alone reflects the best approach for all patients with limited disease. Furthermore, not all patients with early-stage FL receive radiotherapy, despite recommendation in international guidelines.9 The National Cancer Database documented a 13% decrease in the use of radiotherapy from 37% in 1999 to 24% in 2012.10 This is congruent with data from the National LymphoCare Study, a multicenter, prospective cohort trial, which reported radiotherapy as single treatment modality in 23% of patients, whereas 53% of patients received some form of systemic therapy, including 28% who received rituximab plus chemotherapy, 12% who received rituximab alone, and 13% who received radiation and chemotherapy.11,12 In a phase II trial combining IFRT with multiagent chemotherapy, the 10-year time to treatment failure (TTF) was 76% with an overall survival of 80%, which was superior to historical IFRT outcomes.13 In a recently published trial, 150 patients with stage I/II FL were randomized to either radiotherapy alone (30 Gy involved field) or to radiotherapy followed by six cycles of cyclophosphamide, vincristine, and prednisolone (CVP).14 A total of 31/75 patients received rituximab plus CVP. Progression-free survival (PFS) after 10 years was 59% with chemotherapy compared to 41% with radiotherapy alone. Adding rituximab to CVP, PFS further increased compared to radiotherapy alone (hazard ratio, 0.26; 95% CI, 0.07 to 0.97; p = 0.045). Fewer involved regions and PET staging were associated with better PFS. However, OS was around 90% at 10 years with no significant differences between both arms. Toxicities were higher with the use of chemotherapy.
In a multicenter study, two consecutive cohorts with a total of 94 patients with stage I/II FL, application of 4 cycles of rituximab before IFRT (group 2) was compared to IFRT alone (group 1).15 The 10-year PFS was significantly longer with the use of rituximab (64.4% vs 50.7%), but there was no effect on OS. In the German MIR study, 58 patients with early stage FL received 8 cycles of rituximab plus IFRT.16 PFS and OS at 5 years were 78% and 96% with a favorable toxicity profile.
It is not possible to draw a final conclusion on the best treatment approach in stage I/II follicular lymphoma. However, IFRT is well tolerated, and following adequate staging it achieves local lymphoma control and offers the possibility of cure for at least a portion of patients. Therefore, it is difficult to understand that a significant number of patients is deprived of IFRT. However, if patients will really benefit by adding rituximab or even chemotherapy to IFRT remains an open question.
Stage IIII/IV advanced disease
There is an overall agreement that a curative treatment in stage III/IV Fl is not established yet and that not all patients with stage III/IV FL will need immediate therapy. The decision to start or withhold treatment is mainly based on the occurrence of clinical symptoms and other signs of high tumor burden, as summarized in the GELF/BNLI cirteria.17,18 However, there is an increasing discussion about the role of so called “active surveillance” in asymptomatic patients. It is still unclear if transformation could be prevented by early treatment initiation. In this context, evidence suggests that baseline metabolic tumor volume (MTV) measured by positron emission tomography (PET) may predict PFS in patients with FL. In a very recent analysis, a correlation between baseline PET-derived MTV and outcome could not be demonstrated.19
In symptomatic patients with slow disease progression or in very old or comorbid patients, single agent rituximab might be a therapeutic option. Using rituximab alone, an event-free survival (EFS) of three to five years has been reported.20 However, in most patients requiring therapy, the combination of CD20 antibody and chemotherapy has become standard of care. Rituximab has been used for nearly two decades as CD20 antibody (and was initially approved for relapsed patients). Since 2017, Obinutuzumab is also approved in combination with chemotherapy in first-line FL. This compound is a type II CD20 antibody with a greater antibody-dependent cytotoxicity and direct apoptosis compared to rituximab.21,22 As chemotherapy backbone, most centers use bendamustine, CHOP (cyclophosphamide, vincristine, doxorubicin, prednisone), CVP, or, more and more rarely, FC(M) (fludarabine, cyclophosphamide, mitoxantrone). CHOP has been available since 1976 for the treatment of lymphomas, and its efficacy was impressively increased with the addition of rituximab (R-CHOP).23 In a randomized trial conducted by the Fondazione Italiana Linformi R-CHOP and R-FM were superior to R-CVP in terms of 8-year PFS (49% vs 52% vs 42%), but with no significant differences in OS.24 The authors observed a higher risk of dying as a result of causes unrelated to lymphoma progression with R-FM vs R-CVP. Furthermore, patients initially treated with R-CVP had a higher risk of lymphoma progression compared with those receiving R-CHOP, as well as a higher risk of requiring additional therapy. Based on these results, R-FM is used less frequently in FL, while R-CVP is often reserved to older or less fit patient populations.
The first time that R-CHOP was really challenged was in the STiL NHL 1-2003 trial which compared R-CHOP with bendamustine/rituximab (BR) without maintenance in a prospective, randomized fashion.25 In this study in a total of 535 patients, at a median follow-up of 45 months BR showed a significant better median PFS compared to R-CHOP (69.5 months vs 21.2 months; hazard ratio 0.58, 95% CI 0.44–0.74; p < 0.0001). The 10-year update was recently presented, which confirms a significant improvement regarding the time to next treatment for BR.26 Furthermore, BR was less toxic than R-CHOP. Similar results were reported in the BRIGHT study, which compared BR with either R-CHOP or R-CVP as first-line treatment of FL and mantle-cell lymphoma (MCL).27 At 5 years, PFS was 65.5% in the BR treatment group and 55.8% in the R-CHOP/R-CVP group (hazard ratio 0.61, 95% CI 0.45–0.85; p = 0.0025). There was no significant effect on OS between both groups. Safety profile was as expected with a higher number of secondary malignancies and infections in the BR treatment group. Overall, based on the better disease control using BR, the authors recommended BR as first-line treatment option in FL. In the GALLIUM trial in patients with untreated FL, obinutuzumab was combined with chemotherapy (CHOP, bendamustine, or CVP) and compared in a randomized, prospective fashion to rituximab plus chemotherapy, followed by maintenance in both arms.28 In this important study in 1202 patients, the estimated three-year rate of PFS was 80% for obinutuzumab plus chemotherapy and 73.3% for rituximab plus chemotherapy (hazard ratio 0.66, 95% CI 0.51–0.85; p = 0.0012). The same effect was also seen after a follow-up of almost 5 years.29 However, there was no effect on OS. The advantage of using Obinutuzumab compared to rituximab was independent of the selected chemotherapy, although the trial was not powered to show this difference.30 Furthermore, there was also a significant higher number of patients achieving minimal residual disease negativity with Obinutuzumab, which may explain the improved PFS.31 Adverse events, particular infusion-related events and neutropenia, were higher with obinutuzumab but manageable. According to chemotherapy, grade 3 to 5 adverse events, mainly cytopenias, were most frequent in patients treated with CHOP, whereas grade 3 to 5 infections and secondary malignancies were most frequent with bendamustine. These side effects of bendamustine have not been reported before and are explainable by the T cell suppression of bendamustine. Based on these data the use of bendamustine is discussed controversial, as part of induction therapy as well as maintenance.
In summary, at this time bendamustine or CHOP may be used as chemotherapy backbone in frontline FL. However, in rapidly growing FL or in patients with elevated LDH, CHOP may be the preferred treatment. Using bendamustine, investigors should be aware of possible side effects. Anti-infectious prophylaxis with cotrimoxazole should be considered. Obinutuzumab offers significant advantages compared to rituximab in terms of disease control.
There is still an ongoing discussion about the role of maintenance in FL. In the PRIMA trial, a total of 1018 patients received rituximab maintenance vs observation following initial therapy with R-CHOP, R-CVP, or R-FCM.32 PFS was significantly prolonged with rituximab maintenance. After nine years of follow-up, median PFS was 10.5 years in the rituximab maintenance arm vs 4.1 years in the observation arm (hazard ratio 0.61, 95% CI 0.52–0.73; p < 0.001).33 However, there was no effect on OS. These results were confirmed by another study.35 The RESORT trial sought to determine how to maximize the long-term benefit of using rituximab. This study enrolled 289 patients with low-tumor FL. Re-treatment with rituximab at each disease progression was compared to scheduled maintenance rituximab after single-agent rituximab.36 With a median follow-up of 4.5 years, median TTF was 3.9 years for patients receiving rituximab re-treatment and 4.3 years for those receiving maintenance (p = 0.54). The median doses of rituximab were 4 for re-treatment vs 18 for maintenance and the authors concluded that there was no benefit to rituximab maintainance over re-treatment. The Swiss Group for Clinical Cancer Research (SAKK) performed a trial randomizing 207 patients after four doses of rituximab to receive 8 months of rituximab maintenance vs 5 years of rituximab maintenance.20 It could be demonstrated that long-term rituximab maintenance therapy did not improve EFS or OS but was associated with increased toxicity. In the GALIUM trial, patients with bendamustine had a higher risk of dying compared to CHOP or CVP, independently of the CD20 antibody.28 Many of these events occurred during the maintenance phase, which may be due to the T cell suppression by bendamustine, which has also been reported also by other investigators. Given the fact that maintenance therapy has not shown prolonged OS yet but may be associated with increased risk of side effects, especially after the use of bendamustine, the role of maintenance in FL is at least questionable and requires further evaluation.
Since several years, investigators are confronted with a plethora of new compounds selectively targeting the cell surface, intracellular pathways and/or the microenvironment, which promise to be effective in FL (an overview is presented in Table 2). Most of these compounds are used in the relapsed or refractory situation, but there is also a discussion of the role of chemotherapy-free therapy in first line. The combination of rituximab and lenalidomide (R2) demonstrated promising efficacy in a phase II trial in untreated FL,37 and was consequently evaluated in a randomized phase III RELEVANCE trial.38 In this study, R2 was compared to rituximab plus chemotherapy, both followed by maintenance therapy, in untreated FL. A total of 1030 patients were enrolled. There was no difference in the response rate, 3-year PFS or 3-year OS between both arms. A higher percentage of patients receiving chemotherapy had grade 3 or 4 neutropenia and febrile neutropenia, whereas a higher percentage of patients receiving R2 had grade 3 or 4 cutaneous reactions. Although R2 failed to demonstrate superiority over standard immunochemotherapy and will not replace rituximab chemotherapy as first-line standard, this trial documents equivalence between immunochemotherapy and chemotherapy-free approach.
Relapsed follicular lymphoma
Early relapsed patients
There is an increasing understanding that the duration of response after first-line treatment greatly influenced overall prognosis. The National LymphoCare Study identified a group of 19% of patients who had early progression 2 years or less after initial immunochemotherapy (POD24 patients).5 Five-year OS was 50% in the POD24 group compared to 90% in patients without early relapse. In a detailed analysis the following risk factors were associated with increased risk of progression or death before 24 months: male gender, ECOG ≥2, high-risk Follicular Lymphoma International Prognostic Index, or baseline ß-2 microglobuline ≥ 3 mg/l.39 Factors associated with favorable outcome were achieving a CR and exposure to rituximab and/or anthracyclines. Furthermore, the regimen used as first-line therapy may influence the prognostic impact for OS of POD24. For example, the hazard ratio is 3.12 after rituximab or rituximab plus lenalidomide therapy but 6.44 following immunochemotherapy and antibody maintenance.5,40
Based on these results, treatment approaches have to be different for early relapsed patients compared to patients with late relapse, and several ongoing clinical trials are focusing on this point. Two essential questions are arising: What is the role of hematopoietic stem cell transplantation in this setting? And what is the best treatment approach for patients not fit enough for intensive regimens?
In a comprehensive analysis of two randomized trials from the German Low Grade Lymphoma Study Group, a total of 113 patients with POD24 received either salvage therapy including high-dose therapy followed by autologous stem cell transplantation (ASCT) or a transplant-free approach.41 The authors found a significant survival benefit associated with POD24 with a 5-year PFS for ASCT vs no transplant of 51% vs 19% (hazard ratio 0.38, 95% CI 0.24–0.62; p < 0.0001) and a 5-year OS of 77% vs 59% (hazard ratio 0.54, 95% CI 0.30–0.95; p = 0.031). In another analysis be the National LymphoCare Study and the Center for International Blood and Morrow Transplant Research (CIBMTR), 175 POD24 patients receiving ASCT were compared to 174 POD24-patients receiving non-ASCT.42 There was no difference in 5-year OS (ASCT, 67%; non-ASCT, 60%; p = 0.16). It is important to mention that among patients with ASCT, transplantation was not always performed at first relapse but after a median of 2 previous therapies. However, in a subgroup analysis in 123 patients receiving ASCT in the first year after treatment failure, 5-year OS with ASCT was 73% compared to 60% in patients without ASCT (p = 0.05). On multivariate analysis, early use of ASCT was associated with significantly reduced mortality (hazard ratio 0.63, 95% CI 0.42–0.94; p = 0.02). Therefore, salvage treatment with ASCT is strongly recommended in POD24 patients if possible.
The role of allogeneic stem cell transplantation (alloSCT) is much more controversial in FL, and there are only very limited data on alloSCT in POD24 patients. In 2013, the European Society for Blood and Marrow Transplantation (EBMT) published a consensus project summarizing indication for hematopoietic stem cell transplantation in patients with FL.43 Allo-SCT with preferable reduced conditioning should be considered at relapse after ASCT. However, the EBMT group did not reach a consensus in which situation an alloSCT should be preferred over ASCT. In an analysis of EBMT data and CIBMTR data, the 3-year OS following allogeneic transplantation was 66%; however, the transplant-related mortality remains high at 25% at three years.44 The CIBMTR retrospectively compared alloSCT with ASCT in POD24 patients.45 With a median follow-up of 69 to 73 months, the adjusted probability of 5-year OS was significantly higher after ASCT (70%; n = 240) or matched sibling donor alloSCT (73%; n = 105) vs matched unrelated donor alloSCT (49%; n = 95; p = 0.0008). The 5-year adjusted probability of non-relapsed mortality was significantly lower for ASCT (5%) vs matched sibling donor (17%) or matched unrelated donor alloSCT (33%; p < 0.0001). The role of alloSCT, given the early mortality, needs to be reevaluated in the light of newer treatment options. At this time, it is an option only for patients precluding use of ASCT (eg, with intensive bone marrow involvement) or after failed ASCT.
What will be the best approach to POD24 patients not suitable for any kind of transplantation? As reported by the LymphoCare study, standard immunochemotherapy is of limited efficacy. The phosphatidylinositol 3-kinase (PI3K)-inhibitor idelalisib has marked approval in multiple relapsed FL. Furthermore, idelalisib also showed antitumor activity in patients with high-risk FL relapsing within 24 months after initial immunochemotherapy.46 A total of 22/37 (59,4%) patients achieved a ≥50% decrease in the lymphoma mass. The median PFS was 11,1 months with no significant differences between “early-early” relapse patients (progressing in ≤12 months) and “late-early” relapse patients (progressing 12–24 months). These data clearly demonstrate the activity of idelalisib in POD24. Copanlisib, another PI3K-inhibitor, achieved a median PFS of 11.3 months in 93 POD24 patients.47 In a subgroup analysis of the AUGMENT trial (see below), 56 relapsed patients receiving R2 were identified as POD24.48 These patients had an ORR of 80%, with 30% CR and a median PFS of 30.4 months. In the MAGNIFY trial, R2 was also used in relapsed and refractory FL.49 The ORR of 370 patients was 74%, with 46% CR. Importantly, patients who were double refractory to both rituximab and alkylating agents achieved a median PFS of 15,5 months.50 POD24 patients had a median PFS of 23 months. PFS after one year was comparable for patients with less than two lines of previous therapies compared to patients with two or more lines of prior therapies.51 These data also demonstrate the efficacy of R2 in POD24 patients.
Since the vast majority of patients with POD24 are closely after rituximab treatment or even during rituximab maintenance, refractoriness to rituximab could be assumed in a subset of these. In the randomized GADOLIN trial, the anti-CD20 antibody obinutuzumab plus bendamustine followed by obinotuzumab maintenance was compared with bendamustine alone – without maintenance - in relapsed patients who were refractory to rituximab.52 Median PFS was significantly longer in the obinutuzumab/bendamustine arm (25.8 months) than in the bendamustine arm (14.1 months), with a hazard ratio for progression or death of 0.57 (95% CI 0.44–0.73; p < 0.001). A treatment benefit was also seen for OS (hazard ratio 0.67, 95% CI 0.47–0.96; p = 0.0269). Based on these results, obinutuzumab was approved for rituximab-refractory FL. In the GALLIUM trial, the use of obinutuzumab plus chemotherapy reduced the risk for POD24 compared to rituximab plus chemotherapy by 46%.53
Unfortunately, it is too early to give a final recommendation how to treat POD24 patients out of the transplant setting, but new compounds or chemotherapy-free combination could become an option and warrants further studies. In future, the treatment of patients with intermediate-early progresses (24–48 months) might also be challenging, since most of these patients will be rituximab refractory.
Late relapsed and multiple relapsed patients
The overall outcome for FL has impressively improved over the past few decades, and the majority of patients can anticipate a normal life expectancy, with an expected PFS after first-line therapy of up to 10 years.4,34 However, the relapsing nature of the disease necessitates serial treatment. ASCT is not recommended in first relapse outside POD24.43 In symptomatic patients with low tumor burden, rituximab monotherapy may be applied. For patients with low-risk profile and for those for whom conventional chemptherapies are not feasible, radioimmunotherapy offers an therapeutic option.9 In the vast majority of patients, investigators select immunochemotherapy as the appropriate treatment. However, new compounds are beginning to change the therapeutic landscape especially in multiple relapsed patients. Clinical trials in late relapsed should focus not only on efficacy but also on reducing toxicities.
The combination of lenalidomide and rituximab (R2) shows promising results both in first-line and early relapse patients as mentioned above but also in patients with late relapses and refractory FL. In the phase III, multicenter, randomized AUGMENT trail, R2 was compared to rituximab and placebo in indolent lymphoma patients.54 Of 358 patients enrolled, 82% had FL. The median number of prior therapies was one; however, 24% of patients had three or more systemic therapies. POD24 was seen in 33% of patients. PFS was significantly improved for R2 vs rituximab plus placebo, with a hazard ratio of 0.46 (95% CI 0.34–0.62; p < 0.001) and median duration of 39.4 months (95% CI 22.9 months to not reached) vs 14.1 months (95% CI 11.4–16.7 months), respectively. Estimated 2-year survival in the R2 arm was 93% (95% CI 87%–96%) vs 87% (95% CI 81%-92%) in the placebo plus rituximab arm. The safety profile was acceptable, though with significantly more infections, neutropenia, and cutaneous reactions using R2. Nevertheless, based on these results, market approval of R2 in relapsed FL has been granted in the US and is expected soon in Europe.
What can we learn from the AUGMENT trial? R2 is more effective compared to rituximab alone, what is not surprising. It is an excellent choice for patients who are refractory to chemotherapy or for patients with high tumor burden. However, rituximab monotherapy is also effective, as also shown by others,55 and remains a treatment options in comorbid patients or in patients with low tumor burden. Furthermore, since crossover was not allowed, we do not know if a R followed by R2 approach would be preferred with less toxicity than initial treatment with R2.
PI3K-inhibotors are a group of compounds with high activity in FL. Idelalisib is an inhibitor of the δ isoform of the PI3K. Approval was based on a phase II study, which showed a median PFS of 11 months and a median OS of 20.3 months in 125 patients with indolent lymphomas refractory to both alkylators and rituximab, 72 of them with FL.56 Patients had a median of four previous therapies. These results were recently approved by data from the British compassionate use program for idelalisib.57 However, investigators need to be aware of side effects. The most common adverse events reported were fatigue, diarrhea, nausea, rash, chills, and pyrexia, whereas the most frequent grade 3 and grade 4 adverse events were diarrhea, pneumonitis, and elevation of liver enzymes.58 Reports of deaths because of opportunistic infections with Pneumocystis jirovecii and CMV reactivation halted phase III studies with idelalisib,58 but with appropriate prophylaxis using cotrimoxazole and regularly CMV monitoring, idelalisib remains a clear treatment option.
There are further PI3K-Inhibitors that have been tested in phase II trials. Duvelisib, orally available, blocks the δ and γ isoforms of the PI3K. In the DYNAMO-trial, 129 patients with indolent lymphoma (83 of them with FL) refractory to rituximab and chemotherapy or radioimmunotherapy and with a median of three previous therapies achieved an ORR of 47.3%.59 The median PFS was 9.5 months and the median OS was 28.9 months. Duvelisib had a manageable safety profile. Most common grade III/IV adverse events were transient cytopenias and diarrhea.
Copanlisib is an intravenously available PI3K inhibitor blocking the α and δ isoforms of the PI3K. In the phase II CHRONOS-1 study of 142 patients (104 with FL), copanlisib showed an ORR of 61% with 17% CR.60 The median PFS was 12.5 months, the median OS was 42.6 months. Most frequent adverse events were transient hyperglycemia and hypertension with no evidence of worsening for patients treated long-term. Copanlisib has less severe toxicities compared to idelalisib, and received FDA approval for relapsed FL.
Ibrutinib is an orally available BTK-Inhibitor with high activity especially in chronic lymphocytic leukemia and mantle cell lymphoma. In the DAWN trial, ibrutinib was used as single agent in relapsed FL refractory to chemotherapy.61 A total of 110 patients had a median of 3 previous therapies. The ORR was 20.9% (CR 11%), with a median PFS of 4.6 months, and a 30-month OS of 61%. The most common adverse events were diarrhea, fatigue, cough, and muscle spasms. In a very recently published trial of 40 patients with recurrent FL, single agent ibrutinib achieved an ORR of 37.5%, with a median PFS of 14 months.62
Venetoclax inhibits BCL-2, normally overexpressed in FL. In a phase I trial, venetoclax was tested as single agent in various relapsed Non-Hodgkin lymphomas.63 In 29 patients with FL, the ORR was 38% (14% CR) with a median PFS of 11 months. Major toxicities were anemia, neutropenia, and fatigue. In the CONTRALTO trial, venetoclax was combined with rituximab or with BR and compared to BR in 154 FL patients with a median of three previous therapies.64 Addition of venetoclax to BR resulted in increased toxicity with consequent limitation of overall tolerability, but did not improve ORR compared to BR (venetoclax-BR, 84%; BR, 84%). Venetoclax plus rituximab achieved similar number of grade III/IV side effects compared to BR but lower ORR (venetoclax-R, 35%; BR, 84%).
At this time, the role of new compounds in FL is less promising than in other B cell lymphomas. PI3K-inhibitors are effective, but exhibit side effects which may preclude a wide application. Ibrutinib and venetoclax have only modest activity in relapsed FL. R2 will become a treatment option; however, the advantage over standard immunochemotherapy in the relapsed situation in uncertain. Table 2 summarizes clinical trials focusing on chemotherapy-free treatment in relapsed FL.
Chimeric antigen receptor (CAR) T cell therapy is a promising new class of cellular immunotherapy showing activity in several hematologic malignancies, especially in relapsed diffuse large B cell lymphoma and relapsed acute lymphocytic leukemia.65 In a recent trial involving 28 adult patients with relapsed or refractory lymphoma, 10 out of 14 with FL who received autologous CAR T cells achieved a CR, and at a median follow-up of 28.6 months, 89% of these maintained the response.66 In the entire cohort, 18% of patients developed a severe cytokine-release syndrome, and 11% developed serious encephalopathy. These data demonstrate the efficacy of CAR T cell therapy in FL, but much more patients have to be enrolled in clinical trials.
Although the majority of patients with FL have a life expectancy approaching that of healthy individuals, there are still significant controversies about the optimal treatment. Major challenges are the prevention and treatment of early relapses (POD24 patients), which is associated with a dismal prognosis. Furthermore, the implementation of new treatment options in present therapeutic algorithms in first-line and relapse /refractory patients will be a major requirement of future trials. These options include new compounds and chemotherapy-free regimens but also promising immunotherapy approaches as CAR T cell therapy.
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