Tackling mantle cell lymphoma (MCL): Potential benefit of allogeneic stem cell transplantation

Abstract

Mantle cell lymphoma (MCL) is a type of non-Hodgkins lymphoma (NHL) associated with poor progression-free and overall survival. There is a high relapse rate with conventional cytotoxic chemotherapy. Intensive combination chemotherapy including rituximab, dose intense CHOP- (cyclophosphamide-doxorubicin-vincristine-prednisone) like regimens, high dose cytarabine, and/or consolidation with autologous stem cell transplant (autoSCT) have shown promise in significantly prolonging remissions. Data from phase II studies show that even in patients with chemotherapy refractory MCL, allogeneic stem cell transplant (alloSCT) can lead to long term disease control. Most patients with MCL are not candidates for myeloablative alloSCT due to their age, comorbidities, and performance status. The advent of less toxic reduced intensity conditioning (RIC) regimens, which rely more on the graft-versus-lymphoma (GVL) effect, have expanded the population of patients who would be eligible for alloSCT. RIC regimens alter the balance of toxicity and efficacy favoring its use. Treatment decisions are complicated by introduction of novel agents which are attractive options for older, frail patients. Further studies are needed to determine the role and timing of alloSCT in MCL. Currently, for selected fit patients with chemotherapy resistant MCL or those who progress after autoSCT, alloSCT may provide long term survival.

Keywords:

• mantle cell lymphoma
• allogeneic SCT
• nonmyeloablative
• GVL

Mantle cell lymphoma (MCL) is a unique subtype of mature B-cell non-Hodgkin’s lymphomas (NHL) with a high response rate but an equally high relapse rate and relatively poor median survival. MCL can exhibit a spectrum of clinical courses. At one end of the spectrum is a chronic lymphocytic leukemia (CLL) like disease with a true chronic course where observation alone is warranted.¹ At the other end is an aggressive disease that displays rapid growth, relative chemoresistance, and early relapse. Generally, when treatment is necessary MCL usually exhibits shorter progression-free intervals compared to other indolent NHL. The wide variability in clinical behavior has increased treatment and prognostic uncertainty. This variability is reflected in its inclusion as an aggressive lymphoma in the Revised European-American Lymphoma (REAL) classification,² yet it remains included with indolent lymphomas in many current European and some US studies.

MCL has recently emerged as a separate clinicopathologic entity critically dependent on the dysregulation of cyclin D. The cytogenetic translocation t(11;14) (q13;q32) between the cyclin D1 (BCL-1 locus) and the immunoglobulin heavy chain (IgH) locus, which results in cyclin D1 dysregulation, is found in the majority of MCL cases. In the few cyclin D1 negative MCL, cyclin D2, D3, or both are overexpressed. MCL shares the CD5⁺ B-cell immunophenotype of CLL, but is differentiated from CLL by having bright CD20 with high levels of surface immunoglobulin and lack of CD23 expression. Morphologically, the appearance of MCL can vary from a small mature lymphocyte to a more blastoid larger cell that mirrors its protean behavior.

Mantle cell biology and behavior

Attempts have been made to subclassify MCL based on its histopathology, ie, classic, small cell, pleomorphic, and blastoid variants.³ Patients with the blastoid variant often have the worst outcomes and those with the small cell type of MCL seem to do the best, but this has not yet defined a treatment algorithm to address each subtype separately. Rosenwald et al used gene expression profiling by microarray to predict survival of patients with MCL. While no specific gene correlated with survival, expression of a panel of proliferation signature genes allowed separation into four quartiles of patients in which the first and fourth quartiles differed by more than 5 years in median survival.⁴ Reports of other gene panels to predict MCL outcome are intriguing and require validation in other patient populations.⁵

Proliferation assessed by Ki67 staining remains an effective, readily available prognostic indicator. More precise quantification may make it even more useful.⁶ A Cancer and Leukemia Group B (CALGB) phase II trial showed that >35% Ki-67 expression was associated with a shorter progression-free survival (PFS) and event-free survival (EFS) and PIM1 (a cell cycle-related gene) expression was associated with a shorter PFS.⁷ The German Low Grade Lymphoma study group (GLSG) developed the mantle cell lymphoma international prognostic index (MIPI) based on five prognostic factors: age, performance status, lactate dehydrogenase (LDH), leukocyte count, and Ki67 immunostaining index⁸ to classify MCL patients into three groups based on their overall survival (OS): low risk (median OS not reached), intermediate risk (51 months), and high risk groups (29 months).⁹ MIPI has, however, been variably predictive when applied to other intensively treated subsets of patients.^10,11

Current standard therapy

Analysis of outcomes data in MCL from trials conducted between 1975 to 1986 by the Kiel Lymphoma Study Group compared to trials conducted by the GLSG from 1996 to 2004 revealed an increase in median overall survival from 2.7 years to 4.8 years. Some of this improvement may be due to earlier and more specific diagnosis and better supportive care, but may also represent the improvements in MCL therapy with dose intense regimens and new therapeutic agents.¹²

The development of more intensive induction regimens, such as rituximab (a chimeric monoclonal anti-CD20 antibody) plus hyperfractionated cyclophosphamide and vincristine-doxorubicin-dexamethasone (R-HyperCVAD) with alternating dose intense chemotherapy combinations using high dose cytarabine, increased the reported percentage of complete responses (CR) and median PFS.¹³ Patient selection, however, may be an issue as two cooperative groups have been unable to effectively treat large numbers of patients with this regimen and there are no randomized data proving superior overall survival benefit compared to conventional anthracycline based chemotherapy (R-CHOP). Questions of improved long-term survival from dose intensification and addition of other cytotoxic agents remain unanswered, although recent evidence suggests there may be a subset of patients who gain a good long-term outlook with chemotherapy alone.¹³

The addition of rituximab has improved overall and complete response rates,^14,15 but not necessarily overall survival. Relatively small numbers of patients in recent trials may have limited statistical power to detect a difference, although in a relatively large MCL trial (122 patients) conducted by the GLSG, Lenz et al were unable to show a significant improvement in PFS from addition of rituximab to CHOP despite increased CR and overall response rates.¹⁵ A Cochrane meta-analysis in 2007 led to researchers concluded that adding rituximab did improve OS, although there were only three trials included and these were heterogenous.^16,17 Currently, the addition of rituximab has become a standard in the management of MCL first line in the United States (Table 1).

Table 1 First-line MCL regimens

Regimen	Year	n	RR%	CR%	PFS/TTF months
COP versus CHOP^Citation18	1989	37	84	41	7
		26	89	58	10
CHOP versus	2005	122	75	7	14
R-CHOP^Citation15			94	34	21
MCP versus CHOP^Citation19	2006	86	73	20	15
			87	15	21
R-CHOP^Citation14	2002	40	96	48	16.6
R-HyperCVAD-R-M/A^Citation13	2005	97	97	87	36 months FFS 73%
R-CHOP → RIT^Citation20	2007	56	88	55	27 months

Abbreviations: COP, cyclophosphamide-vincristine-prednisone; CHOP, cyclophosphamide-doxorubicin-vincristine-prednisone; MCP, mitoxantrone-chlorambucil-prednisone; RR, response rate; CR, complete response; PFS, progression-free survival; TTF, time to treatment failure; FFS, failure-free survival; HyperCVAD, hyperfractionated cyclophosphamide-vincristine-doxorubicin-dexamethasone; M/A, methotrexate/cytarabine; R, rituximab; R-CHOP, rituximab-cyclophosphamide-doxorubicin-vincristine-prednisone; RIT, radio immunotherapy; MCL, mantle cell lymphoma.

High-dose therapy with autologous stem-cell support

A natural extension of the dose intensification approach is the use of high-dose therapy requiring stem cell support. This has now been studied in multiple trials, which have predominantly been single arm Phase II trials evaluating response rates (Table 2). The European MCL network’s randomized trial comparing consolidation with myeloablative radiochemotherapy followed by autologous stem cell support (ASCT) to interferon-α maintenance in first remission showed a median PFS benefit (39 mos versus 17 mos, P = 0.01) with ASCT.²¹ The absence of minimal residual disease (MRD) after ASCT, assayed by quantitative real-time PCR of clonal IgH gene rearrangements, strongly predicted for longer failure free interval.²² Autotransplant in CR1 (complete response after first-line therapy) following R-CHOP or similar regimens is currently adopted as one standard approach in patients fit to undergo high dose therapy.

Table 2 Trials employing autologous Stem cell transplant consolidation

Regimen	Year	Author/institution	n	PFS/EFS	Remarks
Hyper-CVAD/MTX-Ara-C → Cy/TBI^Citation25	1998	Khouri/MD Anderson	45	3 yr EFS 42% Median PFS 39 mos	n = 25 1st line
Various^Citation26	2000	Vose/Univ Nebraska	40	2 year EFS 36%
RIT/cy/etop^Citation27	2002	Gopal/Univ WA Seattle	16	3 year PFS 61%	All relapsed
Various^Citation23	2003	Vandenberghe/EBBMT/ABMTR	195	2 year PFS 55% 5 year PFS 33%
CHOP like induction Dexa-BEAM → cy/TBI vs IFNα^Citation21	2005	Dreyling/European MCL network	62 (ASCT)	Median PFS 39 mos (ASCT) vs 17 mos (IFN)	First line
R-maxi-CHOP/HIDAC → BEAM^Citation28	2008	Geisler/Nordic Lymphoma group	160	6 year EFS 56%	First line
R-maxi-CHOP, eto, MTX/HIDAC → CEP, R^Citation7	2008	Hsi/CALGB	52	3 year PFS 52%, EFS 57%	Stratified by Ki-67 and PIM1

Abbreviations: Cy/TBI, cyclophosphamide/total body irradiation; RIT/cy/eto, radioimmunotherapy/cyclophosphamide/etoposide; HIDAC, high-dose cytarabine; BEAM, BCNU/etoposide/cytarabine/melphalan; CHOP, cyclophosphamide–doxorubicin–vincristine–prednisone; MTX, methotrexate; CEP, carmustine–etoposide–cyclophosphamide; mos, months; PFS, progression free survival; EFS, event free survival.

In a large retrospective study of the Autologous Blood and Marrow Transplant Registry (ABMTR) and European Blood and Bone Marrow Transplant (EBMT) registry, transplanted patients had a median survival of 59 months, which is longer than historical (1990s) series of patients treated conventionally with a median survival of 36 months.²³ Patients who received autotransplant in CR1 clearly did better than partial responders in the study. The addition of radioimmunotherapy holds promise in overcoming this difference by improving the degree of response prior to autoSCT.²⁴ Biologic markers are clearly needed to help stratify patients among treatment options and especially transplant options.

Allogeneic transplant in indolent non-Hodgkin’s lymphomas

Indolent lymphomas are currently considered incurable by cytotoxic chemotherapy alone even at high doses. In selected patients allogeneic transplant may offer the potential for longer remission and potentially cure. The significant toxicity, both high early mortality rate and graft-versus-host disease (GVHD), with myeloablative regimens and allogeneic stem cell transplant (alloSCT) has limited the use of this modality. The development of less toxic (nonmyeloablative or reduced intensity conditioning, RIC) regimens and improved supportive care with reduced early mortality and morbidity has led to renewed interest in allogeneic transplantation in indolent lymphomas where the challenge is to select appropriate patients with high enough risk of their disease to warrant the transplant risks.

In the early 1990s the European Bone Marrow Transplant Group (EBMTG) conducted a case-controlled study in NHL matching 101 alloSCT patients with 101 autologous stem cell transplant (autoSCT) patients. Although progression-free survival was similar (49% alloSCT versus 46% autoSCT), there was a trend to lower relapse rate for the alloSCT patients (23% vs 38%). Patients with chronic GVHD had a significantly lower relapse rate than those without (0% versus 35% P = 0.02) suggesting a strong graft-versus-lymphoma (GVL) effect.²⁹ An advantage in long term survival for patients who underwent allogeneic bone manow transplant (BMT) was suggested by other nonrandomized trials.^30,31 A Dutch trial involved 28 patients with recurrent or refractory low-grade NHL. The 18 patients with chemotherapy-sensitive disease underwent autoSCT and 10 patients, of whom seven were chemoresistant, underwent alloSCT. The 2 year PFS rates were 68% for alloSCT patients versus 22% for autoSCT patients (P = 0.049).³¹

Later trials concentrated on reduced intensity conditioning regimens. A fludarabine/cyclophosphamide-based regimen developed at the MD Anderson Cancer Center showed an actuarial probability for being alive and in remission at 2 years of 84%.³² An 8 year prospective study reported 47 patients treated with alloSCT using a fludarabine- cyclophosphamide-rituximab (FCR) conditioning regimen. The estimated PFS rate was 83% and survival of 85% at a median follow-up time of 60 months.³³ Other approaches with encouraging results include alemtuzumab-based regimens (Tables 3 and 4).^34,35

Table 3 Comparison of transplant strategies in indolent NHL and MCL

	Allo	Auto
Graft issues	Tumor free graft	Potential lymphoma contamination; graft purging benefit not yet proven
Mechanism of effect	GVL effect	High dose chemotherapy effect
Toxicity	Acute and chronic GVHD	Lower acute peritransplant morbidity and mortality
Efficacy	Prolonged remission; potential cure	Not generally curative
Graft quality	Healthy donor graft	Damage from prolonged chemotherapy – risk of myelodysplasia
Recipient factors	Limited patient population (age, performance status, comorbidities)	Safer in patients who are older and with comorbidities
Graft collection	Donor availability	Stem cell collection issues in heavily pretreated marrows

Abbreviations: GVL graft versus lymphoma; GVHD, graft-versus-host disease; allo, allogeneic transplant; auto, autologous transplant.

Table 4 Studies of fully myeloablative regimens in mantle cell lymphoma

Regimen	Graft source	Results	n	ORR	CR	Dz
Mostly cy/TBI^Citation36 MD Anderson Cancer Center	All sib donors	3 yr OS and FFP 55%	16		85.7%	11 rel/ref; 5 new Dx
Mostly cy/TBI^Citation37 Johns Hopkins	All T cell depleted bone marrow grafts from matched sib donors	EFS 50% at 25 mos median f/u; 46% TRM; Chronic GVHD 6%	9			7 chemosensitive
Mostly Bu/cy^Citation38 Princess Margaret Hospital	All matched sib donors; 5 BM and 1 PBSCT (non-myeloabl)	Median survival 4.3+ yrs No TRM	6	100%	66%	5 relapse/refractory
Mostly Cy/TBI^Citation39 Univ of Nebraska	88% PBSCT 100% Matched sib donor	5 yr RR 21% 5 yr EFS 44% 5 yr OS 49%	17	65% at D100	65% at D100	All chemosensitive

Abbreviations: Cy/TBI, cyclophosphamide/total body irradiation; OS, overall survival; FFP, freedom from progression; EFS, event free survival; TRM, transplant related mortality; Bu/cy, busulfan/cyclophosphamide; PBSCT, peripheral blood stem cell transplant; ORR, overall response rate; CR, complete response; Dz, disease charecteristics of patient enrolled; mos, months; GVHD, graft-versus-host disease.

Allogeneic transplant in MCL

Patients with relapsed or refractory MCL following con­ventional intensive chemotherapy or autoSCT have limited therapeutic options. Allogeneic transplant using myeloablative regimens was initially studied as a potentially curative approach for these patients. Because of the risks of early mortality and GVHD, allogeneic transplant is generally reserved for MCL patients who have relapsed after an autologous transplant and other intensive regimens. In cases of somewhat indolent progression of MCL, the less toxic RIC regimens, in which the GVL effect is thought to be the chief therapeutic effect, are attractive. However, the wide proliferative variation in MCL results in many patients whose highly proliferative disease outpaces the GVL effect following RIC regimens.

Case reports of patients with chemotherapy refractory MCL having prolonged remission after allogeneic transplant suggested a GVL effect.⁴⁰ Khouri et al reported results in 16 patients bolstering the hypothesis. Of the 16 patients, 11 were previously treated; 14 were treated with myeloablative regimens – either Cy/TBI (High-dose cyclophosphamide 120 mg/kg and total body irradiation-12 Gy given in four daily fractions) or BEAM (BCNU/Etoposide/Cytarabine/Melphalan). Overall survival and freedom from progression at 3 years was 55% and the results were even more encouraging for patients with chemotherapy sensitive disease.³⁶ Molecular studies demonstrated that three patients with disease detectable by PCR following transplant converted to negative status several months later, suggesting a GVL effect.

Berdeja et al reported results in 35 patients with MCL and low grade lymphoma showing a 50% event free survival at 25 months median follow-up. All grafts were from matched sibling donors and were T-cell depleted to reduce GVHD.³⁷ This strategy had encouraging results in patients with chemotherapy-sensitive disease showing transplant related mortality (TRM) of 14% and chronic GVHD of just 6%, but fared poorly in patients with resistant disease (TRM 86% and EFS of 0%). T-cell depletion, although effective for prevention of GVHD, severely compromises the beneficial GVL effect. A promising technique under investigation to control GVH without necessarily compromising GVL involves the use of suicide gene-modified human T-lymphocytes. Herpes simplex virus-thymidylate kinase modified donor T cells, which play a central role in the causation of GVHD, could potentially be controlled by the addition of an antiviral drug: ganciclovir.⁴¹

The University of Nebraska reported data on outcomes in patients with chemotherapy sensitive MCL undergoing autologous (n = 80) versus allogeneic (n = 17) stem cell transplant. Five year estimated event free survival (44% versus 39%) and overall survival (49% versus 47%) were similar in both groups. The five year relapse rate was lower at 21% in the alloSCT group, compared with 56% in the autoSCT group. This was balanced, however, by higher day 100 mortality rate in patients receiving allotransplant (19%). These data emphasize the dilemma of weighing the competing risks of progressive lymphoma versus treatment-related toxicity. The high early mortality limits the possibility of including allogeneic transplant in the initial treatment regimen for patients with chemotherapy sensitive MCL (Table 5).³⁹

Table 5 Results of alloSCT using reduced intensity regimens in mantle cell lymphoma

Regimen	Immuno-suppression	Results	N	CR	Dz
Various – mostly Flu based^Citation42 EBMT registry 2002	Various	OS at 1 yr 38% PFS at 1 yr 31% TRM at 1 yr 46%	22
FCR PFA^Citation43 MD Anderson Cancer Center 2003	Tacrolimus and methotrexate	Event free survival at 3 yrs 82% D100 mortality 0	18 4 MUD 13 MRD	94%	16 with chemosensitive dz
Flu/mel/CD52^Citation44 Univ College London 2004	Cyclosporine T cell – depleting conditioning regimen	OS at 3 yrs 60% PFS at 3 yrs 50%	10		20% NRM at D100 and 3 yrs
Fludarabine and 2 Gy TBI^Citation45 Fred Hutchinson Cancer Center 2004	Cyclosporine/mycophenolate mofetil	DFS 2 yrs 60% OS 2 yrs 65% NRM 2 yrs 24%	33 16 MRD 16 MUD	75%	Relapsed/refractory
Fludarabine +/−2 Gy TBI^Citation46 Fred Hutchinson Cancer Center 2008		5 yr NRM 27% 5 yr OS 58% 5 yr PFS 52%	53 MRD 28 MUD 25
FCR (86%) PFA (14%)^Citation47 MD Anderson Cancer Center 2009	Tacrolimus and methotrexate	Median PFS 60 mos Median OS NR 6 yr act PFS 46% 6 yr OS 53% TRM at 1 yr 9%	35		17% rel/ref 31% CR2 31% CR3

Abbreviations: FCR, fludarabine/cyclophosphamide/high-dose rituximab; PFA, cisplatin/fludarabine/cytarabine; Flu/melCD52, fludarabine, melphalan, alemtuzumab; NRM, nonrelapse mortality; MUD, matched unrelated donor; MRD, matched related donor; Dz, disease charecteristics of patients enrolled; TRM, transplant related mortality; OS, overall survival; PFS, progression free survival; CR, complete response; mos, months.

Fludarabine-based RIC regimens have gained precedence over myeloablative regimens in the last decade. Sorror et al updated the Seattle experience in 2008 with 33 patients with median follow up of 63 months and an additional 20 patients with shorter follow up. All patients received a fludarabine and 200 cGy TBI RIC regimen. This was a heavily pretreated population in which 40% of the patients had disease progression after prior autoSCT and an additional 11% had undergone planned autoSCT before alloSCT. Five year overall and progression free survival rates were 58% and 52% respectively, and there were no major differences between the use of related and matched unrelated donors.⁴⁶ At 5 years 44% were alive without GVHD, 14% with chronic GVHD requiring immunosuppression, and continued resolution of chronic GVHD was observed with time. Long term survival was achieved even in some chemotherapy-refractory patients, but those with bulky lymphadenopathy (≥5 cm) at the time of transplant invariably did poorly.

Tam et al published updated results of a risk adapted strategy at the MD Anderson Cancer Center. Of a total of 121 patients enrolled in sequential transplant protocols over a 17 year study period, 86 underwent autoSCT. The addition of rituximab resulted in a marked PFS improvement for those getting autoSCT in CR1. There were 35 patients (median age 58), all with relapsed or refractory MCL, who underwent nonmyeloablative allogeneic stem cell transplant. All patients were Stage 3 or 4 and 83% had chemosensitive disease at the time of transplant (46% in CR). With a median follow-up of 56 months the median PFS duration was 60 months, and the median OS had not yet been reached. Major determinants of disease control were use of peripheral blood stem cells (PBSC) versus bone marrow stem cells and achievement of >95% donor chimerism. Among 24 patients meeting both criteria, no lymphoma relapses had occurred at a median follow-up of 60 months.⁴⁷

In a retrospective study of 279 patients reported to the EBMT registry between 1998 and 2007 who had received RIC regimens in MCL, the Kaplan-Meier estimate of the PFS at 1 and 3 years was 49% and 29% respectively. The overall survival at 1 and 3 years was 60% and 43% respectively (Table 6).⁴⁸

Table 6 Characteristics of patients with mantle cell lymphoma receiving allogeneic hematopoietic cell transplants from 1998 to 2007 and registered to the CIBMTR

Variable	HLA-matched siblings		Unrelated
	N Eval	n (%)	N Eval	n (%)
Age (years)	525		203
<50		197 (38)		48 (24)
50–59		233 (44)		92 (45)
60–69		89 (17)		59 (29)
≥70		6 (1)		4 (2)
Male	524	421 (80)	203	163 (80)
Year of transplant	525		203
1998		46 (9)		2 (1)
1999		58 (11)		8 (4)
2000		65 (12)		15 (7)
2001		65 (12)		19 (9)
2002		43 (8)		16 (8)
2003		63 (12)		28 (14)
2004		45 (9)		26 (13)
2005		63 (12)		27 (13)
2006		45 (9)		35 (17)
2007		32 (6)		27 (13)
Conditioning regimen intensity	404		180
Myeloablative		213 (53)		84 (47)
Reduced intensity		191 (47)		96 (53)
Overall survival	525		203
100-days		85 (81–88)		78 (72–84)
1 year		65 (61–70)		53 (46–60)
3 years		54 (50–59)		37 (30–45)
Causes of death	230		121
Primary disease		60 (26)		39 (32)
New malignancy		3 (1)		0
GvHD		31 (13)		19 (16)
IPn		5 (2)		5 (4)
Infection		44 (19)		12 (10)
Organ failure		22 (10)		21 (17)
Other causes		48 (21)		20 (17)
Unknown		17 (7)		5 (4)

The data presented here are preliminary and were obtained from the Statistical Center of the Center for International Blood and Marrow Transplant Research. The analysis has not been reviewed or approved by the Advisory or Scientific Committee of the CIBMTR.

Data from the Center for International Blood and Marrow Transplant Research (CIBMTR) from 1998 to 2007 shows a steady use of related donors and increasing use of MUD donors in allogeneic transplants for MCL (written communication, January 2010). Roughly half of the 525 patients in the registry used RIC regimens for both related sibling and matched unrelated donors (MUD) donors and a major increase in the use of RIC regimens was seen in 2000 with roughly equal ablative and RIC regimens since that time. The median age for HLA-identical sibling donors was 53 (range 26–93) and for matched unrelated donors was 56 (range 23–72). The overall survival curves for this entire cohort are shown in Figure 1.

Figure 1 Probability of survival after transplants for Mantle Cell NHL 1998–2007.

The CIBMTR published outcomes of stem cell transplantation subdivided by donor type and conditioning regimen as shown in Figure 2.⁴⁹ Although it is difficult to make direct comparisons between the groups of patients who underwent auto versus allotransplant (selection bias – the allotransplant arm having more relapsed/refractory patients), it does give us an idea of real world outcomes. Patients who underwent autotransplant did better in the short run but seemed to have a continuing risk of relapse years post therapy. Patients undergoing allotransplant had worse survival immediately posttransplant due to short-term toxicity, but this early risk is balanced by the fact that the survival curves seem to plateau approximately 2 years later.

Figure 2 Probability of survival after transplants for mantle cell lymphoma, 1998–2007 by donor type and conditioning regimen.⁴⁹

Conclusions

The protean nature of MCL demands individualized treatment considerations. A small subset of MCL patients can be monitored for some years without therapy. It is unclear whether indicators such as a low MIPI score or low proliferation, whether by Ki67 or gene signature, can be a guide for this most indolent population. For most patients requiring treatment the current standard, if the patient is relatively young and fit, is a dose-intense or high-dose regimen. The optimal regimen, however, is currently unknown, though most current studies include a CHOP-like regimen as well as high dose cytarabine and rituximab. With the newer intensive regimens the place of high-dose therapy with autologous stem cell support continues to be debated, though there seems to be a progression-free survival advantage in most trials. Conclusions about the place of allogeneic transplant are complicated by the paucity of data, with only a few small phase II trials directing the field. Patients whose disease progressed after autoSCT have a very poor prognosis and, if they are suitable candidates, will likely benefit from an allogeneic approach. The current data, while encouraging, are limited by small numbers of highly selected patients, and whether there will be true long-term plateau suggesting cure is unclear in the current data from the CIBMTR and others.

Though it makes intuitive sense to consider patients with high MIPI scores as candidates for allogeneic transplant upfront, especially if they are relatively young and fit and have a sibling donor, this has not been tested in comparison to autologous transplant or intensive chemotherapy (such as R-HyperCVAD) in clinical trials to date. A very high risk population in which to consider allogeneic transplant would be patients with chemoresistant disease (ideally without bulky lymphadenopathy) where autologous transplant would not likely be of benefit.

In patients with relapsed MCL with lower proliferative behavior there may be time posttransplant for the GVL effect of a RIC allogeneic transplant to develop to overcome chemoresistance. Better biologic stratification of MCL in terms of proliferative rate will be important to define this group. Certain patients, particularly those with more rapid growth and higher tumor burdens, may require more intensive conditioning regimens to optimize disease control or even a planned tandem procedure of autoSCT followed soon after with an RIC allogeneic transplant, as reported in multiple myeloma.

The way forward

Therapeutic approaches in MCL must be individualized based on both host and disease characteristics. Clear definition of the lowest risk, indolent MCL subset are needed and recommended monitoring intervals defined for this indolent group. The optimal initial therapy of MCL for those requiring treatment has not been defined in clinical trials. This is now complicated by the many new agents available for trial including bendamustine, bortezomib, lenalidomide, and radioimmunotherapy. The evolving approach is to have separate trials for older, more frail patients that incorporate novel agents. These trials will test whether these new agents can be combined with, or replace, currently used chemotherapy combinations.

For young, fit patients trials will involve dose-dense or dose-intense regimens often requiring stem cell support. Autologous SCT is currently a favored approach as consolidation of first remission or, if not utilized until that point, as part of therapy for first relapse in appropriately selected patients. Trials should be designed to optimize conditioning regimens and investigate post transplant maintenance therapy, similar to evolving trials for multiple myeloma. Radioimmunotherapy is currently being investigated as part of the conditioning regimens for both autologous and allogeneic transplantation. Furthermore, the importance of disease burden at the time of transplant should be carefully defined systematically through imaging techniques. This would allow for stratification by MIPI or other prognostic risk groups and disease burden to permit comparison of autoSCT results. The prognostic importance of achieving a minimal residual disease state in the bone marrow, assayed by flow cytometric or PCR techniques, also needs to be evaluated, perhaps serving as a surrogate marker of outcome. While it is difficult to foresee use of even RIC alloSCT as consolidation therapy of first remission MCL until toxicity and early mortality is significantly reduced, the role of alloSCT in the relapsed setting merits further exploration. Once there is a greater consensus about the optimal autoSCT regimen for MCL, a randomized trial comparing autologous to allogeneic transplant using a RIC regimen could be undertaken in selected patients who have relapsed after their initial therapy. Better definition of high risk features that predict poor outcome with autoSCT would be very useful. At present, allogeneic transplant trials for MCL should be restricted to appropriately selected high risk patients whose disease is relapsed/refractory post autoSCT, or demonstrates chemotherapy resistance making autoSCT a poor option.

Disclosure

The authors report no conflicts of interest in this work.