The Different Treatment Approaches in Younger Patients with Angioimmunoblastic T-Cell Lymphoma
Introduction: Angioimmunoblastic T-cell lymphoma (AITL) is characterized by low response rate to standard therapy and relapses in the course of treatment. CHOP-like therapy shows 70-80 % of overall response rate, though 2-year progression-free survival is observed only in 30-40 % of patients. Older...
Saved in:
Published in | Blood Vol. 128; no. 22; p. 5345 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
02.12.2016
|
Online Access | Get full text |
Cover
Loading…
Abstract | Introduction: Angioimmunoblastic T-cell lymphoma (AITL) is characterized by low response rate to standard therapy and relapses in the course of treatment. CHOP-like therapy shows 70-80 % of overall response rate, though 2-year progression-free survival is observed only in 30-40 % of patients. Older patients are more frequently diagnosed with AITL than younger subjects. Usually the median age of those patients is 60 years. A search for new approaches to treatment of AITL has an important medical and social aspect.
Aim: The aim of our study is to define rational approaches to treatment of younger patients with AITL, to assess the overall and progression-free survival depending on the type of therapy.
Patients and methods: 45 patients with AITL were treated between 2002 and 2016 in our center. The diagnosis was verified according to WHO classification. We analyzed clinical outcomes in 17 (38%) patients younger than 55 years treated by different protocols.
Results: Of 17 patients there were 9 men and 8 women with a median age of 41 (range, 29-55) years. 14 of 17 patients had Ann Arbor stage IV. Bone marrow involvement was detected in 7 of 17 cases by histological tests. Lung involvement was observed in 10 cases. B symptoms and elevated LDH level were present in all patients. Despite the younger age of the patients, 12 of 17 were classified as having an intermediate-high (n=5) and high (n=7) risk IPI score. There were 5 of 17 patients, who received CHOP-like therapy; other 12 patients were treated by longed therapy. There were 4 of 5 patients after CHOP-like therapy, who showed the progression from 1 to 4 (median 2) months, one achieved partial remission. There were 12 of 17 patients who were treated by the longed therapy according to RALL-2009 protocol (ClinicalTrials.gov public site; NCT01193933), successfully used for treatment of acute lymphoblastic leukemia in Russia. The program is based on non-intensive but uninterrupted treatment. After induction + consolidation phases (150 days) patients received maintenance therapy by interferon-A and thalidomide over 2 years. All 12 patients achieved complete remission, none of them showed disease progression. Two patients received autologous stem cell transplant (Auto-SCT) as first line consolidation treatment, conditioning regimen was CEAM (CCNU, etoposide, Ara-C, melphalan). One patient died after Auto-SCT from infection complications without disease progression. 11 (92%) of 12 patients treated by RALL-2009 protocol are alive, follow-up survival varies from 3 to 73 (median 19) months. A univariate analysis of overall and progression-free survival curves showed that longed therapy is more effective than CHOP-like therapy (Fig.1).
Conclusion: Though, the study is small, the results show that higher efficiency of RALL-2009 protocol than CHOP-like therapy in younger patients withAITL. It is particularly important for working patients. The principle of non-intensive but uninterrupted usage cytostatic drugs and longed maintenance therapy by immunomodulators allows to avoid the early treatment failures and provides optimistic long-term results.
[Display omitted]
No relevant conflicts of interest to declare. |
---|---|
AbstractList | Introduction: Angioimmunoblastic T-cell lymphoma (AITL) is characterized by low response rate to standard therapy and relapses in the course of treatment. CHOP-like therapy shows 70-80 % of overall response rate, though 2-year progression-free survival is observed only in 30-40 % of patients. Older patients are more frequently diagnosed with AITL than younger subjects. Usually the median age of those patients is 60 years. A search for new approaches to treatment of AITL has an important medical and social aspect.
Aim: The aim of our study is to define rational approaches to treatment of younger patients with AITL, to assess the overall and progression-free survival depending on the type of therapy.
Patients and methods: 45 patients with AITL were treated between 2002 and 2016 in our center. The diagnosis was verified according to WHO classification. We analyzed clinical outcomes in 17 (38%) patients younger than 55 years treated by different protocols.
Results: Of 17 patients there were 9 men and 8 women with a median age of 41 (range, 29-55) years. 14 of 17 patients had Ann Arbor stage IV. Bone marrow involvement was detected in 7 of 17 cases by histological tests. Lung involvement was observed in 10 cases. B symptoms and elevated LDH level were present in all patients. Despite the younger age of the patients, 12 of 17 were classified as having an intermediate-high (n=5) and high (n=7) risk IPI score. There were 5 of 17 patients, who received CHOP-like therapy; other 12 patients were treated by longed therapy. There were 4 of 5 patients after CHOP-like therapy, who showed the progression from 1 to 4 (median 2) months, one achieved partial remission. There were 12 of 17 patients who were treated by the longed therapy according to RALL-2009 protocol (ClinicalTrials.gov public site; NCT01193933), successfully used for treatment of acute lymphoblastic leukemia in Russia. The program is based on non-intensive but uninterrupted treatment. After induction + consolidation phases (150 days) patients received maintenance therapy by interferon-A and thalidomide over 2 years. All 12 patients achieved complete remission, none of them showed disease progression. Two patients received autologous stem cell transplant (Auto-SCT) as first line consolidation treatment, conditioning regimen was CEAM (CCNU, etoposide, Ara-C, melphalan). One patient died after Auto-SCT from infection complications without disease progression. 11 (92%) of 12 patients treated by RALL-2009 protocol are alive, follow-up survival varies from 3 to 73 (median 19) months. A univariate analysis of overall and progression-free survival curves showed that longed therapy is more effective than CHOP-like therapy (Fig.1).
Conclusion: Though, the study is small, the results show that higher efficiency of RALL-2009 protocol than CHOP-like therapy in younger patients withAITL. It is particularly important for working patients. The principle of non-intensive but uninterrupted usage cytostatic drugs and longed maintenance therapy by immunomodulators allows to avoid the early treatment failures and provides optimistic long-term results.
[Display omitted]
No relevant conflicts of interest to declare. Introduction: Angioimmunoblastic T-cell lymphoma (AITL) is characterized by low response rate to standard therapy and relapses in the course of treatment. CHOP-like therapy shows 70-80 % of overall response rate, though 2-year progression-free survival is observed only in 30-40 % of patients. Older patients are more frequently diagnosed with AITL than younger subjects. Usually the median age of those patients is 60 years. A search for new approaches to treatment of AITL has an important medical and social aspect. Aim: The aim of our study is to define rational approaches to treatment of younger patients with AITL, to assess the overall and progression-free survival depending on the type of therapy. Patients and methods: 45 patients with AITL were treated between 2002 and 2016 in our center. The diagnosis was verified according to WHO classification. We analyzed clinical outcomes in 17 (38%) patients younger than 55 years treated by different protocols. Results: Of 17 patients there were 9 men and 8 women with a median age of 41 (range, 29-55) years. 14 of 17 patients had Ann Arbor stage IV. Bone marrow involvement was detected in 7 of 17 cases by histological tests. Lung involvement was observed in 10 cases. B symptoms and elevated LDH level were present in all patients. Despite the younger age of the patients, 12 of 17 were classified as having an intermediate-high (n=5) and high (n=7) risk IPI score. There were 5 of 17 patients, who received CHOP-like therapy; other 12 patients were treated by longed therapy. There were 4 of 5 patients after CHOP-like therapy, who showed the progression from 1 to 4 (median 2) months, one achieved partial remission. There were 12 of 17 patients who were treated by the longed therapy according to RALL-2009 protocol (ClinicalTrials.gov public site; NCT01193933), successfully used for treatment of acute lymphoblastic leukemia in Russia. The program is based on non-intensive but uninterrupted treatment. After induction + consolidation phases (150 days) patients received maintenance therapy by interferon-A and thalidomide over 2 years. All 12 patients achieved complete remission, none of them showed disease progression. Two patients received autologous stem cell transplant (Auto-SCT) as first line consolidation treatment, conditioning regimen was CEAM (CCNU, etoposide, Ara-C, melphalan). One patient died after Auto-SCT from infection complications without disease progression. 11 (92%) of 12 patients treated by RALL-2009 protocol are alive, follow-up survival varies from 3 to 73 (median 19) months. A univariate analysis of overall and progression-free survival curves showed that longed therapy is more effective than CHOP-like therapy (Fig.1). Conclusion: Though, the study is small, the results show that higher efficiency of RALL-2009 protocol than CHOP-like therapy in younger patients withAITL. It is particularly important for working patients. The principle of non-intensive but uninterrupted usage cytostatic drugs and longed maintenance therapy by immunomodulators allows to avoid the early treatment failures and provides optimistic long-term results. Figure 1 (A) Overall and (B) progression-free survival of younger patients with AITL depending on the type of therapy. Figure 1. (A) Overall and (B) progression-free survival of younger patients with AITL depending on the type of therapy. |
Author | Savchenko, Valeri G. Kovrigina, Alla Vinogradova, Yulia E. Parovichnikova, Elena N. Zvonkov, Eugene E. Chernova, Natalia G. Sidorova, Yulia V. |
Author_xml | – sequence: 1 givenname: Natalia G. surname: Chernova fullname: Chernova, Natalia G. organization: Department Chemotherapy of Lymphomas, National Research Center for Hematology, Moscow, Russia – sequence: 2 givenname: Yulia E. surname: Vinogradova fullname: Vinogradova, Yulia E. organization: I.M. Sechenov First Moscow State Medical University, Moscow, Russia, Moscow, Russia – sequence: 3 givenname: Eugene E. surname: Zvonkov fullname: Zvonkov, Eugene E. organization: Department Chemotherapy of lymphomas, National Research Center for Hematology, Moscow, Russia – sequence: 4 givenname: Yulia V. surname: Sidorova fullname: Sidorova, Yulia V. organization: Department of Molecular Hematology, National Research Center for Hematology, Moscow, Russia – sequence: 5 givenname: Alla surname: Kovrigina fullname: Kovrigina, Alla organization: National Research Center for Hematology, Moscow, Russian Federation – sequence: 7 givenname: Elena N. surname: Parovichnikova fullname: Parovichnikova, Elena N. organization: Bone Marrow Transplantation Department, National Research Center for Hematology, Moscow, Russian Federation – sequence: 9 givenname: Valeri G. surname: Savchenko fullname: Savchenko, Valeri G. organization: National Research Center for Hematology, Moscow, Russia |
BookMark | eNqFkMtOwzAQRS1UJErhG_APJPgR57GMylOqBIuAxAbLtSeNURJHdgrq35O07NncGenqXs2cS7ToXQ8I3VASU5qz223rnInfKctjxmLBE3GUM7SkguURIYws0JIQkkZJkdELdBnCFyE04Uws0WfVAL6zdQ0e-hFXHtTYzVs5DN4p3UDAtscfbt_vwONXNdrJDfjHjg0u-511tuv2vdu2KoxW4ypaQ9vizaEbGtepK3ReqzbA9d9cobeH-2r9FG1eHp_X5SbSlKQiMqkquDa1AQ1aEW4UV0azRNECGFOKJ1DzjJrJFdyQHLRmmTCpFkXCM8L4CmWnXu1dCB5qOXjbKX-QlMgZkzxikjMmyZicCR1lSpanJEznfVvwMujpRQ3GetCjNM7-2_ELvF93GA |
ContentType | Journal Article |
Copyright | 2016 American Society of Hematology |
Copyright_xml | – notice: 2016 American Society of Hematology |
DBID | 6I. AAFTH AAYXX CITATION |
DOI | 10.1182/blood.V128.22.5345.5345 |
DatabaseName | ScienceDirect Open Access Titles Elsevier:ScienceDirect:Open Access CrossRef |
DatabaseTitle | CrossRef |
DatabaseTitleList | CrossRef |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine Chemistry Biology Anatomy & Physiology |
EISSN | 1528-0020 |
EndPage | 5345 |
ExternalDocumentID | 10_1182_blood_V128_22_5345_5345 S0006497119353467 |
GroupedDBID | --- -~X .55 1CY 23N 2WC 34G 39C 4.4 53G 5GY 5RE 5VS 6I. 6J9 AAEDW AAFTH AAXUO ABOCM ABVKL ACGFO ADBBV AENEX AFOSN AHPSJ ALMA_UNASSIGNED_HOLDINGS BAWUL BTFSW CS3 DIK DU5 E3Z EBS EJD EX3 F5P FDB FRP GS5 GX1 IH2 K-O KQ8 L7B LSO MJL N9A OK1 P2P R.V RHF RHI ROL SJN THE TR2 TWZ W2D W8F WH7 WOQ WOW X7M YHG YKV ZA5 0R~ AALRI AAYXX ACVFH ADCNI ADVLN AEUPX AFETI AFPUW AGCQF AIGII AITUG AKBMS AKRWK AKYEP AMRAJ CITATION H13 |
ID | FETCH-LOGICAL-c1065-d6a93cdfdececa03da3adc24a19e22aa34ef371dcec53d08ecc275d6c59437023 |
ISSN | 0006-4971 |
IngestDate | Tue Jul 01 00:15:54 EDT 2025 Fri Feb 23 02:36:50 EST 2024 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 22 |
Language | English |
License | This article is made available under the Elsevier license. |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c1065-d6a93cdfdececa03da3adc24a19e22aa34ef371dcec53d08ecc275d6c59437023 |
OpenAccessLink | https://dx.doi.org/10.1182/blood.V128.22.5345.5345 |
PageCount | 1 |
ParticipantIDs | crossref_primary_10_1182_blood_V128_22_5345_5345 elsevier_sciencedirect_doi_10_1182_blood_V128_22_5345_5345 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2016-12-02 |
PublicationDateYYYYMMDD | 2016-12-02 |
PublicationDate_xml | – month: 12 year: 2016 text: 2016-12-02 day: 02 |
PublicationDecade | 2010 |
PublicationTitle | Blood |
PublicationYear | 2016 |
Publisher | Elsevier Inc |
Publisher_xml | – name: Elsevier Inc |
SSID | ssj0014325 |
Score | 2.2040818 |
Snippet | Introduction: Angioimmunoblastic T-cell lymphoma (AITL) is characterized by low response rate to standard therapy and relapses in the course of treatment.... |
SourceID | crossref elsevier |
SourceType | Index Database Publisher |
StartPage | 5345 |
Title | The Different Treatment Approaches in Younger Patients with Angioimmunoblastic T-Cell Lymphoma |
URI | https://dx.doi.org/10.1182/blood.V128.22.5345.5345 |
Volume | 128 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwELaWIh4XBFsQ5SUfEJdVQmI7L27LUqiAIiG2q8KByLEdFLUkaJWtVP4Of5TxI9ksLSrlYiVxMnnMl8k4_mYGoacFE5SnZeYpoojHQhV6BVfcK6h2ZgvBU1PrcP9DvHfA3h5Gh6PRrwFradUWvvh5blzJ_2gVtoFedZTsJTTbC4UNsAz6hRY0DO0_6_iVq3DSTuY9Z3zqEoUbstXEvNBqqbPxV-t4tmn9rWoqHR3SFOBB67ytc2-m_-S9PwUNN85ed_O9x66ovKUCqKWupWqts06hyCdv_K53UdWa8iXdDp9Xunu37_5y0tRHzYkNsoE7U4O-T5VslhvHLfzhb4nQFPMJyIapjXX5Ogsc5ayrTocdkGDD_JJ0gDMbpOysaURtqkn3Ze5Wz1r9VGeRNUx_fwHyfEJ8vbO_FjDMs_3H969nJZrxUEpyIyjXgnJCci3DNFfQVQJjEV0m493H9VQVo8SWyXD360iEIOj5X67ofBdo4NbMb6NbbjyCpxZcd9BI1WO0Pa1523w_xc-wYQibqZcxuvayW7ox6-oEjtH1fUfP2EZfAZC4ByTuAYnXgMRVjR0gcQdIrAGJzwISW0DiDpB30cHr3flsz3MFPDwRgmvryZhnVMhSKqEED6jklEtBGA8zRQjnlKmSJqGE3ojKIAVzQpJIxiLKGE3Am7yHtuqmVvcRjkIRhzxhESlKVqqkkBErOQ8CKQOVZcUOCrpnmv-weVryC_S5g150zz537qZ1I3PA1UUHP7j8-R6im-sX5RHaapcr9Rg82rZ4YhD1G2nUn2s |
linkProvider | Colorado Alliance of Research Libraries |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=The+Different+Treatment+Approaches+in+Younger+Patients+with+Angioimmunoblastic+T-Cell+Lymphoma&rft.jtitle=Blood&rft.au=Chernova%2C+Natalia+G.&rft.au=Vinogradova%2C+Yulia+E.&rft.au=Zvonkov%2C+Eugene+E.&rft.au=Sidorova%2C+Yulia+V.&rft.date=2016-12-02&rft.issn=0006-4971&rft.eissn=1528-0020&rft.volume=128&rft.issue=22&rft.spage=5345&rft.epage=5345&rft_id=info:doi/10.1182%2Fblood.V128.22.5345.5345&rft.externalDBID=n%2Fa&rft.externalDocID=10_1182_blood_V128_22_5345_5345 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0006-4971&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0006-4971&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0006-4971&client=summon |