Autologous Stem Cell Transplantation for T-Cell Lymphomas Perrone Giulia a and Paolo Corradini a,b Peripheral T-cell lymphomas (PTCLs) are a rare and heterogeneous group of T-cell malignancies characterized by a very poor outcome. The optimal treatment for PTCLs remains controversial. The role of stem cell transplantation in PTCLs has been investigated; however, no randomized control studies specifically dedicated to PTCLs are currently available. Several retrospective and prospective studies have suggested that high-dose chemotherapy (HDT) followed by autologous stem cell transplantation (ASCT) may improve the survival in patients with chemosensitive T-cell lymphoma, either upfront or as salvage treatment. This review provides a summary of the current literature with the intent to explore the role of ASCT in various clinical scenarios. Semin Hematol 51:59–66. C 2014 Elsevier Inc. All rights reserved.


eripheral T-cell lymphomas (PTCLs) are a heterogeneous group of aggressive non-Hodgkin lymphomas (NHLs) representing approximately 10%– 15% of lymphoid neoplasms in Western countries.1 Clinical appearance and manifestation sites vary widely among the different subgroups of PTCLs, and the classification by morphology only appears to be extremely difficult. The integration of morphologic, immunophenotypic, genetic, and clinical features let to identify four subgroups: cutaneous T-cell lymphomas, primary nodal PTCLs, extranodal lymphomas, and leukemic forms. This review will deal with the nodal and extranodal forms. Nodal PTCLs represent the most common and heterogeneous subtype of PTCL, including angioimmunoblastic T-cell lymphoma (AITL, 18%), anaplastic lymphoma kinasepositive (ALKþ, 7%) and anaplastic lymphoma kinasenegative (ALK–, 5%), anaplastic large cell lymphoma (ALCL), adult T-cell lymphoma (ATCL, 10%), and not otherwise specified (NOS, 26%). The extranodal form includes the rare but well-characterized form of T-cell lymphoma known as extranodal natural killer (NK)/T-cell lymphoma, nasal type (nasal NKTCL), as well as enteropathy type intestinal T-cell lymphoma (ENTL), and hepatosplenic T-cell lymphoma (HSL). The epidemiology of PTCLs shows important geographic variations, with a

Division of Hematology Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy. b Department of Hematology, University of Milan, Milano, Italy. Conflicts of interest: none. Address correspondence to Corradini Paolo, Department of Hematology and Pediatric Onco-Hematology, Division of Hematology and Stem Cell Transplantation, Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133 Milano, Italy. E-mail: [email protected] 0037-1963/$ - see front matter & 2014 Elsevier Inc. All rights reserved.

Seminars in Hematology, Vol 51, No 1, January 2014, pp 59–66

overall higher incidence in Asia and Central/South America than Western countries. The majority of patients are diagnosed in advance stage, with widespread disease.2 The median age at diagnosis is 60 years, with approximately 40% of cases occurring between the ages of 55 and 74, and only about 5% occurring after the age of 85. However, several subtypes had a median age that is much younger, including ALCL, ALKþ (33 years); hepatosplenic type (34 years); and subcutaneous panniculitis-like PTCL (33 years). It has been long recognized that the majority of PTCLs have a very poor prognosis compared to their B-cell counterpart.3Treatment outcomes for PTCLs are substantially inferior to B-cell lymphoma. T-cell phenotype per se is an independent negative prognostic factor.4 The International T-Cell Lymphoma Study reported an overall survival (OS) and failure-free survival (FFS) of only 10% at 10–15 years.5 Several prognostic scores have been evaluated to divide patients into low risk or high risk. The International Prognostic Index (IPI) appears to be prognostic for patients with PTCLs. Other prognostic models have been developed specifically for patients with PTCLs. The Prognostic Index for PTCLs (PIT score),6 based on age, lactate dehydrogenase (LDH), performance status, and bone marrow involvement, stratifies patients into more distinct prognostic groups compared to the IPI.7 Regarding the impact of histologic subtypes, the most important prognostic factor is the presence or absence of ALK in ALCL.8 The OS of ALKþ ALCL is substantially better than that seen for ALK- ALCL (70% v 49%, respectively). However, within the good prognostic category of ALKþ ALCL, survival was 90% for the low/low intermediate risk group and 33% for the high/high intermediate risk group. In multivariate analysis ALK expression and IPI were able to predict survival among ALCL patients. Currently, ALK positivity identifies the only histologic subtype with good prognosis. 59

P. Giulia and P. Corradini


Historically, the treatment of PTCL has been largely derived from that applied for B-NHL. Anthracyclinecontaining chemotherapy regimens were able to induce complete remission (CR) in 54% of the patients with T-cell lymphomas, with an OS of 41%.4 Comparative analysis with B-NHL showed no difference in response rate; however, T-cell lymphomas relapsed more frequently and earlier than B-cell lymphomas. When the main subgroups of T-cell lymphoma were analyzed, only ALKþ ALCL had an equivalent or even superior prognosis compared to aggressive B-NHL.4,8 A retrospective analysis on more than 1,300 newly diagnosed or relapsed/refractory PTCLs, evaluated in the International T-Cell Lymphoma Project, reported that the majority of patients with PTCLs did not clearly benefit from an anthracycline-containing regimen over a non– anthracycline-containing regimen.2 Moreover, from this study it emerged that about 30% of PTCLs are primary refractory and the survival curve does not reach a plateau, with a long-term survival rate of only 10%–30%. Neither intensified/escalated chemotherapeutic approaches9,10 nor the addition of a monoclonal antibody such as alemtuzumab11 has demonstrated a clear advantage in sustained remission and prolonged survival. In 2010 for the first time the incorporation of etoposide into the CHOP (cyclophosphamide, doxorubicin, vincristine, prednisone) treatment (CHOEP) was shown to improve event-free survival (EFS), at least in a subset of younger patients with PTCLs, without significant increasing the percentage of adverse events,12 suggesting a novel strategy to investigate further.

The discouraging results achieved with conventional therapies let to the investigation of new concepts, including high-dose chemotherapy (HD) followed by autologous stem cell transplantation (ASCT) or allogeneic stem cell transplantation (allo-SCT). So far, no randomized control trials exclusively dedicated to SCT in PTCL have been published; the majority of data derive from retrospective studies or phase II studies, often including both first-line and relapsed patients, therefore making it extremely difficult to obtain a conclusive analysis. Here, we review and comment on the role of ASCT in PTCLs based on the prospective and retrospective data currently available.

FRONTLINE AUTOLOGOUS STEM CELL TRANSPLANTATION Randomized trials on frontline ASCT are lacking, mainly because of the rarity of these diseases; therefore, no data are currently available to conclusively support the role of frontline ASCT. However, several phase II prospective trials have suggested the benefit of upfront ASCT, in particular for patients achieving at least a partial response (PR) after induction therapy (Table 1). In 2006, the long-term results of two Italian prospective phase II studies on sequential HDT, followed by ASCT, were reported.13 In an-intent-to-treat (ITT) analysis, only 46 of 62 patients (74%) completed the whole program. Progressive disease during the induction phase was the main obstacle for proceeding to the autografting

Table 1. Prospective Studies of Frontline ASCT in PTCL-Exclusive Patients



Status at Transplant Transplant Rate TRM

Response Rate


D’Amore et al17


ORR 82%



CR/u CR 78%

44% (5 yr) 51% (5 yr)

Reimer et al16


PD 16% CR1 47%



PR 8% CR 58%

36% (3 yr) 48% (3 yr)

PR1 24% 62 (19 ALKþ) CR1 56%



PR 8% CR 89%

30% (12 yr) 34% (12 yr)

Corradini et al13

Mercadal et al15


PR1 16% PD 24% CR1 49%

Rodriguez et al14


PR1 10% CR 46% PR 27%


PR11% 41%


CR 51%

30% (4 yr) 39% (4 yr)



PR 7% CR 89%

53% (3 yr) 73% (3 yr)

PR 5%

Abbreviations: ASCT, autologous stem cell transplantation; PTCL, peripheral T-cell lymphoma; TRM, transplant-related mortality; PFS, progression-free survival; OS, overall survival; ALK, alkaline kinase; ORR, overall response rate; CR, complete response; PR, partial response; PD, disease progression; uCR, unconfirmed CR; ND, not determined.

No. of First Author Patients Histology Rodriguez Song25 Blystad33




29 36 40

No data PTCL 56%, ALCL 25% PTCL 50%, ALCL 35%


PTCL 63%, ALCL 22%, NK/T 15%


PTCL 38%, ALCL 38%, EATL 14%

Median Status at Transplant Prior Lines

Response Rate

Follow-up (mo) PFS


CR 38%, PR 48% CR 42%, PR 50% CR1 27%, PR1 15% CR2/CR3 43%, PR2 15% CR1 32%, CR2/CR3 24%, PR 38% Ref. 5%

3 (1–4) 2 (1–3) No data

CR 79% No data CR 80%

43 42 36

32% (3 yr) 37% (3 yr) 48% (3 yr)

39% (3 yr) 48% (3 yr) 58% (3 yr)

No data

CR 86%


60% (5 yr)

56% (5 yr).

CR/PR1 49%, CR/ PR2 38%, Other 13%

2 (1-4)


44% (5 yr)

CR1 80%, CR2/3 50%, PR 46% 54% (5 yr)

PR 5% CR 76%

PR 5% Jagasia34


ALCL 54%, PTCL 21%, AITL 11%, NK/T 11%

CR1 3%, CR2 36%, PR1/2 50%, PD 11%

2 (1-3)

No data


CR/PR1 64%, CR/PR1 63%, Other 28% Other 45% 50% (3 yr) 69% (3 yr)

Kewalramani26 Kim31


PTCL 58%, ALCL ALK - 17%, AITL 17% PTCL 50%, NK/T 25%, ALCL 13%

CR 62%, PR 38%

No data

No data


24% (5 yr)

CR 28%, PR 63%, PD10%

2 (1-4);

CR 60%


Median 3.6 mo

Median 11.5 mo


PR 10% PD 20% CR 37%


34% (5 yr)

45% (5 yr)

PR 11% PD 16% No data


18% (5 yr)

34% (5 yr)

No data


25% (5 yr)

48% (5 yr)




PTCL 57%, ALCL 25%, AITL 8%


PTCL 34%, ALCL 66%



PTCL 30%, ALCL 34%, AITL 17%

CR1/PR1 19%, Ref. 2(1-4) 26%, Relapse 55% CR1/PR1 28%, CR2/ 2(1-5) PR2 49%, PD 19%

43% (6 yr) 33% (5 yr)



PR1 36%, CRZ2 36%, PRZ2 16% PD 9%

Autologous stem cell transplantation for T-cell lymphomas

Table 2. Retrospective Studies on ASCT as Salvage Strategy in PTCL Patients


Table 2 (continued ) No. of First Author Patients Histology



PTCL 100%

Median Status at Transplant Prior Lines

Response Rate

CR1/PR1 5/19%, CR2/PR2 5/39%, PD 9.4%

No data

No data

No data

CR 59%


No data

No data




PTCL 19%, ALCL 14%, AITL 17%, NK 11%



PTCL 45%, ALCL 45% , CR1/PR1 12%, CR2 AITL 10% 31%, PD 30%, Relapsed 21%

No data

Follow-up (mo) PFS



CR1/PR 51%, CR1/PR 76%, CR2/PR CR2/PR2 40%, 12%, Ref. Ref. 30% 0% 44% (3 yr) 53% (3 yr) CR1/PR1 60%, PR1 50%, CR2/PR2 38%, CR2 71% 61% (5 yr) 62% (5 yr) sens/ sens/ref. 68/ ref. 67/38% 29% 40% (5 yr) 54% (5 yr)

CR1/PR1 CR1/PR1 92%, 75%, Other Other 45% 32% Abbreviations: ASCT, autologous stem cell transplantation; PTCL, peripheral T-cell lymphoma; PFS, progression-free survival; OS, overall survival; ALCL, anaplastic large cell lymphoma; NK, natural killer cell; ALK, alkaline kinase; AITL, angioimmunoblastic T-cell lymphoma ; ORR, overall response rate; CR, complete response; PR, partial response; PD, disease progression; uCR, unconfirmed CR; sens./ref., sensitive/refractory.

P. Giulia and P. Corradini

Autologous stem cell transplantation for T-cell lymphomas

phase and the main cause of treatment failure. The high progression rate led to disappointing 12-year OS and disease-free survival (DFS) curves (34% and 55%, respectively). However, in multivariate analysis, achieving CR prior to transplant was strongly correlated with a superior 10-year EFS compared to less than CR; the 12-years DFS of this specific subgroup was projected at 60%, suggesting that consolidation of CR with ASCT can offer a greater chance of long-term survival. A separate analysis on ALKþ ALCL patients showed the most favorable OS and EFS for this specific histology subtype (62% and 54%, respectively, compared to 21% and 18% for non-ALKþ), with a further survival advantage for low-risk age-adjusted IPI (aaIPI) compared to intermediate–high risk categories. In 2007, the GELTAMO experience was reported by Rodriguez, et al.14 Twenty-six patients with nodal PTCL, excluding ALKþ ALCL, received three courses of MegaCHOP. Gallium scan–negative patients received one more course of treatment followed by ASCT, those remaining gallium scan–positive received two courses of salvage therapy (ifosfamide/etoposide treatment) and, patients with chemosensitive disease proceeded to ASCT. Overall, 73% of patients received ASCT and 89% were in CR after transplant. After a median follow-up of 3 years, OS and progression-free survival (PFS) of the entire cohort were 73% and 53%, respectively. In the subgroup of patients receiving transplant, 2-year OS and PFS were 84% and 56%, respectively. In univariate analysis, chemosensitive status after the first three cycles of treatment or at the time of transplant was the only prognostic factor for OS. Interestingly, to rescue primary resistant or early progressive patients, the investigators highlighted the role of alternative salvage treatment strategy before ASCT. In 2008 Mercadal, et al,15 on behalf of GELCAB, reported the data on 41 PTCL patients, excluding ALKþ ALCL and cutaneous forms, treated with intensive chemotherapy (three courses of high-dose CHOP alternating with three courses of ESHAP [etoposide, methylprednisolone, cytarabine, cisplatin]) followed by ASCT as consolidation. Only 59% of patients achieved a CR or PR, and an even lower proportion of patients (41%) eventually received ASCT. The investigators highlighted the high rate of severe hematologic toxicity and mobilization failure. After a median follow-up of 3.2 years, 4-year OS and PFS were 39% and 30%, respectively. No difference in term of OS was observed in CR patients who were candidates for ASCT according to whether ASCT was carried out or not. The impact of CHOP regimen before upfront ASCT was prospectively evaluated by Reimer, et al.16 From 2000 to 2006, 83 PTCLs (excluding ALKþ ALCL) patients were treated with four to six cycles of CHOP followed by stem cell collection preceded by a mobilizing cycle (DexaBEAM [dexamethasone BCNU, etoposide, cytarabine, melphalan] or ESHAP). Patients in CR or PR underwent myeloablative chemo-radiotherapy (fractionated total-body irradiation and high-dose cyclophosphamide) followed by ASCT. In this study, 66% of patients


received ASCT, while the remaining did not complete the study due to early progressive disease. In the ITT analysis, the overall response rate (ORR) after transplant was 66% (56% CR and 8% PR). The estimated 3-year OS and PFS for patients in CR were 48% and 36%, respectively. The 3-year OS and PFS for the entire population undergoing ASCT was 71%, whereas it was only 11% for those who did not undergo transplant. A trend for longer OS was observed in patients with low/intermediate low IPI (v high/intermediate high) who underwent transplantation in CR (v PR). The results of the study suggested that upfront ASCT is an effective treatment in PTCL; however, pretransplantation treatments need to be improved to increase both the response and transplantation rate. Based on the encouraging result reported by the German study on CHOEP treatment,12 the Nordic group designed a phase II study17 to evaluate the impact of a dose-intensified induction schedule (CHOEP-14 for six cycles) consolidated in first PR/CR with high-dose therapy (BEAM/ASCT). After induction, 82% of patients were in CR or PR. Disease refractory to induction treatment was observed in 16% of patients. Among the 70% of patients receiving ASCT, 78% were in CR after ASCT, 8% were in PR, and 7% experienced early disease progression. With a median follow-up of 60.5 months, 5-year OS and PFS were 51% and 44%, respectively. With respect to prognostic parameters, a significant correlation was observed between IPI (low/intermediate low v high/intermediate high) and OS. In multivariate analysis, ALK- ALCL showed a significantly better outcome as compared with other subtypes. The problem of the assessment of diagnosis by an expert pathologist was again raised in this study by the results of centralized review that modified 13% of original diagnoses. From the studies reported above, several important points emerge: (1) approximately one third of patients display primary resistant or early progressive disease becoming, therefore, not transplant eligible; (2) nevertheless, among the patients who are able to receive ASCT, the outcome seems to be superior to conventional chemotherapy; and (3) a treatment strategy including ASCT frontline can lead to long-term response in chemosensitive patients. The challenge is to make more patients able to receive the transplant and this group will be expanded by the use of new drugs such as pralatrexete and romidepsine.

AUTOLOGOUS STEM CELL TRANSPLANTATION IN RELAPSE/ REFRACTORY PTCLs In 1995, the PARMA study18 demonstrated that HDT followed by ASCT is the treatment of choice for patients with relapsed aggressive B-NHL, resulting in 40%–50% long-term DFS; on the contrary, the role of ASCT in T-cell NHL is less clear and still to be defined. Several retrospective studies have been published on the use of ASCT as salvage treatment (Table 2). It is important to consider that the majority of these retrospective studies are heterogeneous


in terms of histological subgroups, patient characteristics, prognostic factors, myeloablative regimens, and duration of follow-up. In addition, most of them contain some type of bias, largely due to patient selection and inclusion of the patients receiving either upfront or salvage ASCT. The two largest retrospective studies on ASCT in PTCL were reported by the GELTAMO group. In 2003, a series of 115 PTCLs patients,19 including ALCL (22%) and NK/T (15%) subtypes, treated from 1990 to 1999 was reported. At the time of transplant 32% of patients were in first CR and 24% in second or more CR. With a median follow-up of 37 months, the 5-years OS and DFS were 56% and 60%, respectively. The 5-years OS rates, according to disease status at transplantation, were 80%, 50%, and 46% for patients in CR1, CR2/ CR3, and PR, respectively. In multivariate analysis, only LDH level before transplantation predicted survival. Patients transplanted in first CR or with low aaIPI had a significantly longer DFS. In 2007, the GELTAMO20 reported a larger series of 123 patients who received ASCT as salvage treatment from 1990–2004. The 5-year OS and PFS were 45% and 34%, respectively. From multivariate analysis, three factors emerged as independent factors for outcome: having an aaIPI 41, a high β2-microglobulin level, or more than one extranodal disease site. Patients with no pretransplant adverse factors had an OS and PFS at 5 years of 60% and 43%, respectively. Moreover, PFS and OS of patients in second or subsequent CR at transplant (35% and 57%, respectively) were superior compared to those in second PR (23% and 33%) or with refractory disease (10% and 9%). As in other retrospective studies,21,22 the importance of being in CR at the time of transplant to achieve a long-term survival was emphasized. Several studies have specifically described the outcome of ASCT in patients with chemosensitive disease. In 2001 Blystad, et al23 reported a double-institution Scandinavian study on 40 patients with chemosensitive disease who underwent ASCT, either frontline (CR1 27%, PR1 155) or as salvage treatment (CR2/CR3 43%, PR2 15%) from 1990 over a period of 10 years. With a median follow-up of 36 months, 3-years PFS and OS rates were 48% and 58%, respectively. Interestingly, purging of the autograft was performed in 13 of the 40 patients; however, no conclusive data on its effect on outcome can be acquired. With a follow-up of 60 months, Chen, et al24 reported the experience of the Stanford University on 53 PTCL patients with chemosensitive disease treated with ASCT from 1989–2006. The 5-year OS was 76% for patients receiving consolidative ASCT in first CR, compared to 48% for patients in second remission or beyond. In multivariate analysis, CR status at þ90 days after ASCT was predictive of longer OS and PFS. In this study, no benefit was observed with T-cell–purged graft. Also, the Japan registry22 demonstrated better long-term outcome in PTCL patients transplanted in first CR or PR compared to other disease status (5-year OS 72.9% v 45.8%, PFS 73.1% v 42.2%). From the database of the Cleveland

P. Giulia and P. Corradini Clinic, Smith, et al24 evaluated 32 patients with relapsed disease uniformly treated with the same preparative regimens (busulfan/etoposide/cyclophosphamide). Their 5-year OS and relapse-free survival (RFS) rates were 34% and 18%, respectively, lower than what has been published in other studies. Several publications have retrospectively compared the outcome of aggressive T- and B-cell lymphoma with chemosensitive relapsed treated with ASCT. Song, et al25 reviewed 36 patients with relapsed or refractory PTCLs undergoing ASCT and matched them to patients with aggressive B-NHL treated at the same institution. Patients were similar for age, stage at relapse, presence of extranodal disease, and chemosensitivity to salvage treatment. The 3-year EFS rates of patients with the PTCLs, ALCL, and diffuse large B-cell lymphoma (DLBCL) were 37%, 67%, and 48%, respectively. The 3-year OS rates of patients with the PTCLs, ALCL, and DLBCL were 37%, 67%, and 48%, respectively. This study showed inferior outcomes following ASCT in patients with PTCL NOS compared to ALCL and DLBCL. In 2006 Kewalramani, et al26 evaluated 24 patients undergoing ASCT with relapsed or refractory PTCL (ALKþ ALCL or not documented ALK expression were excluded) who responded to first-line or second-line chemotherapy and compared them with 86 consecutive patients with chemosensitive relapsed or primary refractory DLBCL (before the rituximab era). Five-year PFS rates for PTCL and DLBCL were 24% and 34%, respectively (P ¼ .14); the corresponding OS rates were 33% and 39%, respectively. No significant differences were found between the two groups with respect to time to disease progression and survival after progression, but rituximab was not yet available. Most of the published data includes heterogeneous subtypes of T-cell NHL; however, more recently some efforts have been made to define the role of ASCT in specific subtypes. Federico, et al27 retrospectively analyzed 243 AITL patients on behalf of the International Peripheral T-Cell Lymphoma Project. Only 17% of patients were treated with ASCT. Five-year OS was 32% in the whole population, confirming the poor outcome of AITL. However, no data were specifically reported on the outcome of patients receiving ASCT. A retrospective analysis of the European Bone Marrow Transplant registry (EBMT)28 on 146 AITL patients demonstrated an OS and PFS of 59% and 42% at 4 years. The PFS was higher in patients who received ASCT in CR, achieving 56% at 4 years versus 23% in the case of chemorefractory disease. Also, extranodal T-cell lymphoma can benefit from ASCT. In a prospective observational study, EATL treated frontline with alternating courses of IVE (ifosfamide, vincristine, etoposide) and methotrexate followed by ASCT showed a 5-year OS of 60% compared to a historical control of 22% with conventional chemotherapy,29 which supports the role of intense upfront regimens as a bridge to transplant. The retrospective study from the EBMT30 on 44 patients with EATL treated with ASCT showed 4-year PFS and OS of 54% and 59%, respectively, confirming the possibility of long-term disease control.

Autologous stem cell transplantation for T-cell lymphomas

Taken together, these data show that the ASCT as salvage strategy appears feasible and safe with a low morbidity and mortality. Disease status at the time of transplantation is critical. A better long-term survival in patients transplanted in CR is described, compared to patients with other disease status. However, since all data in this setting are generated retrospectively, the value of this observation needs further confirmation.

CONCLUSIONS Across all retrospective and prospective trials that have addressed the role of ASCT in PTCLs, the procedure was considered safe and feasible, but unfortunately resulted in an unavoidable poor outcome in chemorefractory disease. The role of frontline ASCT remains to be fully delineated. We currently do not know if achieving CR versus PR before transplant, or normalized functional imaging, significantly improves long-term outcome. In general, patients in CR at transplantation had a better long-term outcome compared with patients achieving less than CR or less than PR.20,21,24,31 In conclusion, all of the prospective trials of upfront ASCT demonstrated that chemosensitive disease is the strongest predictor of outcome; thus, the emerging key message is that only chemosensitive disease seems to benefit from autografting and that there is no reason to perform ASCT in refractory patients. In addition, due to the absence of a phase III trial, we do not know for sure if patients in CR really need consolidation with ASCT. It seems that this is the case if we compare the results of conventional chemotherapy with ASCT, but this is just speculation. Early progressive disease (PD) after induction treatment, which entails about one third of patients, is the major limitation to proceeding with transplant and represents a treatment failure with currently no alternative effective strategies. In this context, the use of novel agents may potentially improve rate and duration of response and clinical trials are therefore essential, either frontline to evaluate if a larger number of patients can retain a chemosensitive disease, or in chemorefractory patients before transplant to induce a possible response in this subgroup. In conclusion, regarding the role of SCT, a definitive statement is still to be defined. Therefore it is strongly recommended that patients should be entered into clinical trials designed to evaluate novel therapeutic strategies.


3. 4.




8. 9.








Acknowledgement The study was supported in part by AIRC.

REFERENCES 1. Petrich AM, Helenowski I, Galamaga RW, et al. Trends in incidence and outcome in T-cell lymphoma since 1992: a SEER database analysis. Blood. 2012;120:4264. 2. Vose J, Armitage J, Weisenburger D. International peripheral T-cell and natural killer/T-cell lymphoma study:



pathology findings and clinical outcomes. J Clin Oncol. 2008;26:4124-30. Vose JM. Peripheral T-cell non-Hodgkin's lymphoma. Hematol Oncol Clin North Am. 2008;22:997-1005. Gisselbrecht C, Gaulard P, Lepage E, et al. Prognostic significance of T-cell phenotype in aggressive non-Hodgkin's lymphomas. Groupe d'Etudes des Lymphomes de l'Adulte (GELA). Blood. 1998;92:76-82. A predictive model for aggressive non-Hodgkin's lymphoma. The International Non-Hodgkin's Lymphoma Prognostic Factors Project. N Engl J Med. 1993;329:987-94. Gallamini A, Stelitano C, Calvi R, et al. Peripheral T-cell lymphoma unspecified (PTCL-U): a new prognostic model from a retrospective multicentric clinical study. Blood. 2004; 103:2474-9. Went P, Agostinelli C, Gallamini A, et al. Marker expression in peripheral T-cell lymphoma: a proposed clinical-pathologic prognostic score. J Clin Oncol. 2006;24:2472-9. Falini B, Pileri S, Zinzani PL, et al. ALKþ lymphoma: clinicopathological findings and outcome. Blood. 1999;93:2697-706. Mounier N, Simon D, Haioun C, Gaulard P, Gisselbrecht C. Impact of high-dose chemotherapy on peripheral T-cell lymphomas. J Clin Oncol. 2002;20:1426-7. Simon A, Peoch M, Casassus P, et al. Upfront VIPreinforced-ABVD (VIP-rABVD) is not superior to CHOP/ 21 in newly diagnosed peripheral T cell lymphoma. Results of the randomized phase III trial GOELAMS-LTP95. Br J Haematol. 2010;151:159-66. Gallamini A, Zaja F, Patti C, et al. Alemtuzumab (Campath1H) and CHOP chemotherapy as first-line treatment of peripheral T-cell lymphoma: results of a GITIL (Gruppo Italiano Terapie Innovative nei Linfomi) prospective multicenter trial. Blood. 2007;110:2316-23. Schmitz N, Trumper L, Ziepert M, et al. Treatment and prognosis of mature T-cell and NK-cell lymphoma: an analysis of patients with T-cell lymphoma treated in studies of the German High-Grade Non-Hodgkin Lymphoma Study Group. Blood. 2010;116:3418-25. Corradini P, Tarella C, Zallio F, et al. Long-term follow-up of patients with peripheral T-cell lymphomas treated up-front with high-dose chemotherapy followed by autologous stem cell transplantation. Leukemia. 2006;20:1533-8. Rodriguez J, Conde E, Gutierrez A, et al. Frontline autologous stem cell transplantation in high-risk peripheral T-cell lymphoma: a prospective study from The Gel-Tamo Study Group. Eur J Haematol. 2007;79:32-8. Mercadal S, Briones J, Xicoy B, et al. Intensive chemotherapy (high-dose CHOP/ESHAP regimen) followed by autologous stem-cell transplantation in previously untreated patients with peripheral T-cell lymphoma. Ann Oncol. 2008;19:958-63. Reimer P, Rudiger T, Geissinger E, et al. Autologous stemcell transplantation as first-line therapy in peripheral T-cell lymphomas: results of a prospective multicenter study. J Clin Oncol. 2009;27:106-13. D'amore F, Relander T, Lauritzsen Gf, et al. Up-front autologous stem-cell transplantation in peripheral T-cell lymphoma: NLG-T-01. J Clin Oncol. 2012;30:3093-9. Philip T, Guglielmi C, Hagenbeek A, et al. Autologous bone marrow transplantation as compared with salvage chemotherapy in relapses of chemotherapy-sensitive non-Hodgkin's lymphoma. N Engl J Med. 1995;333:1540-5.


19. Rodriguez J, Caballero Md, Gutierrez A, et al. High-dose chemotherapy and autologous stem cell transplantation in peripheral T-cell lymphoma: the GEL-TAMO experience. Ann Oncol. 2003;14:1768-75. 20. Rodriguez J, Conde E, Gutierrez A, et al. The adjusted International Prognostic Index and beta-2-microglobulin predict the outcome after autologous stem cell transplantation in relapsing/refractory peripheral T-cell lymphoma. Haematologica. 2007;92:1067-74. 21. Yang DH, Kim WS, Kim SJ, et al. Prognostic factors and clinical outcomes of high-dose chemotherapy followed by autologous stem cell transplantation in patients with peripheral T cell lymphoma, unspecified: complete remission at transplantation and the prognostic index of peripheral T cell lymphoma are the major factors predictive of outcome. Biol Blood Marrow Transplant. 2009;15:118-25. 22. Numata A, Miyamoto T, Ohno Y, et al. Long-term outcomes of autologous PBSCT for peripheral T-cell lymphoma: retrospective analysis of the experience of the Fukuoka BMT group. Bone Marrow Transplant. 2010;45:311-6. 23. Blystad AK, Enblad G, Kvaloy S, et al. High-dose therapy with autologous stem cell transplantation in patients with peripheral T cell lymphomas. Bone Marrow Transplant. 2001;27:711-6. 24. Chen AI, Mcmillan A, Negrin RS, Horning SJ, Laport GG. Long-term results of autologous hematopoietic cell transplantation for peripheral T cell lymphoma: the Stanford experience. Biol Blood Marrow Transplant. 2008;14:741-7. 25. Song KW, Mollee P, Keating A, Crump M. Autologous stem cell transplant for relapsed and refractory peripheral T-cell lymphoma: variable outcome according to pathological subtype. Br J Haematol. 2003;120:978-85. 26. Kewalramani T, Zelenetz AD, Teruya-Feldstein J, et al. Autologous transplantation for relapsed or primary refractory peripheral T-cell lymphoma. Br J Haematol. 2006;134:202-7. 27. Federico M, Rudiger T, Bellei M, et al. Clinicopathologic characteristics of angioimmunoblastic T-cell lymphoma: analysis of the International Peripheral T-Cell Lymphoma Project. J Clin Oncol. 2013;31:240-6.

P. Giulia and P. Corradini

28. Kyriakou C, Canals C, Goldstone A, et al. High-dose therapy and autologous stem-cell transplantation in angioimmunoblastic lymphoma: complete remission at transplantation is the major determinant of Outcome-Lymphoma Working Party of the European Group for Blood and Marrow Transplantation. J Clin Oncol. 2008;26:218-24. 29. Sieniawski M, Angamuthu N, Boyd K, et al. Evaluation of enteropathy-associated T-cell lymphoma comparing standard therapies with a novel regimen including autologous stem cell transplantation. Blood. 2010;115:3664-70. 30. Jantunen E, Boumendil A, Finel H, et al. Autologous stem cell transplantation for enteropathy-associated T-cell lymphoma: a retrospective study by the EBMT. Blood. 2013; 121:2529-32. 31. Kim MK, Kim S, Lee SS, et al. High-dose chemotherapy and autologous stem cell transplantation for peripheral T-cell lymphoma: complete response at transplant predicts survival. Ann Hematol. 2007;86:435-42. 32. Rodriguez J, Munsell M, Yazji S, et al. Impact of high-dose chemotherapy on peripheral T-cell lymphomas. J Clin Oncol. 2001;19:3766-70. 33. Blystad AK, Holte H, Kvaloy S, Smeland E, Delabie J, Kvalheim G. High-dose therapy in patients with Hodgkin's disease: the use of selected CD34(þ) cells is as safe as unmanipulated peripheral blood progenitor cells. Bone Marrow Transplant. 2001;28:849-57. 34. Jagasia M, Morgan D, Goodman S, et al. Histology impacts the outcome of peripheral T-cell lymphomas after high dose chemotherapy and stem cell transplant. Leuk Lymphoma. 2004;45:2261-7. 35. Smith SD, Bolwell BJ, Rybicki LA, et al. Autologous hematopoietic stem cell transplantation in peripheral T-cell lymphoma using a uniform high-dose regimen. Bone Marrow Transplant. 2007;40:239-43. 36. Nademanee A, Palmer JM, Popplewell L, et al. Highdose therapy and autologous hematopoietic cell transplantation in peripheral T cell lymphoma (PTCL): analysis of prognostic factors. Biol Blood Marrow Transplant. 2011;17: 1481-9.

Autologous stem cell transplantation for T-cell lymphomas.

Peripheral T-cell lymphomas (PTCLs) are a rare and heterogeneous group of T-cell malignancies characterized by a very poor outcome. The optimal treatm...
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