Impact of Front-Line Treatment Interim PET/CT in Peripheral T-Cell Lymphoma Patients' Survival: Experience of a Single Center
Introduction: The introduction of PET/CT in the staging and response assessment to therapy has changed the clinical evaluation of most lymphomas, especially Hodgkin lymphoma and aggressive B-cell lymphomas. The use of PET/CT in the staging of peripheral T-cell lymphomas (PTCL) is already a standard...
Saved in:
Published in: | Blood Vol. 142; no. Supplement 1; p. 6216 |
---|---|
Main Authors: | , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Elsevier Inc
02-11-2023
|
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Abstract | Introduction: The introduction of PET/CT in the staging and response assessment to therapy has changed the clinical evaluation of most lymphomas, especially Hodgkin lymphoma and aggressive B-cell lymphomas. The use of PET/CT in the staging of peripheral T-cell lymphomas (PTCL) is already a standard of care in many centers, although its decisional role in course of chemotherapy or at the end of treatment remains unclear.
Objective: The aim of this study is to evaluate the predictive role of interim PET/CT in newly diagnosed PTCL patients.
Methods: We retrospectively analyzed the clinical data of adult patients diagnosed with PTCL and actively treated between 2014 and 2023 at our center. All patients were evaluated with PET/CT at different timepoints (baseline, interim and end of treatment).
Results: We evaluated 49 patients, with a median age at diagnosis of 59 years (range: 18-83), and a slight predominance of females (54%) (table 1). Almost half of the patients were diagnosed of angioimmunoblastic/T-follicular helper lymphoma (AITL/TFHL) 23(47%), followed by anaplastic large cell lymphoma (ALCL) in 17 cases [9 ALK+ (18%) and 8 ALK- (17%))] and peripheral T-cell lymphoma NOS (PTCL-NOS) in 9 (18%). Seven (14%) patients had ECOG ≥ 2, 47 (90%) had stage III-IV disease, among them, 42 (84%) with extranodal involvement. Bone marrow was involved in 14 out of 36 (39%) evaluated patients. Twenty-seven (54%) patients had IPI score 3-5. Front-line treatment consisted in CHOP in 32 (65%) patients and brentuximab vedotin+CHP in 17 (35%). Interim evaluation was performed after 3 cycles in 32 (65%) and after 4 cycles in 16 (33%) patients. Only one patient was evaluated after 2 cycles due to suspected disease progression. At this time point, 31 (63%) patients were considered in complete metabolic response (CMR) with a Deauville Score (DS) 1-3, 12 (25%) in partial metabolic response (PMR) with a DS 4 and 6 (12%) patients with progressive disease (PD) with DS5. Among the latter's, 4 patients were treated with 2 nd line treatment, while 2 completed the planed 6 cycles due to significant tumor burden . Among 48 patients evaluated after 3 and 4 cycles of therapy, CMR was achieved in 18 (56%) and 13 (81%), respectively (p=0,088). Eleven (34%) and one (6%) pts were in PMR at iPET after 3 and 4 cycles, respectively.
Forty-five (92%) patients completed front-line therapy and were evaluated with EOT PET/. CMR (DS1-3) was reported in 32 (71%) patients, PMR in 8 (18%) and PD in 5 (%). Among patients with CMR at iPET, 25 (81%) maintained CMR, 5 (16%) converted to PMR and only 1 (3%) progressed. Among patients with PMR at iPET, 5 (42%) converted to CMR, 4 (33%) maintained PMR and 3 (25%) progressed. Eighteen (37%) patients were consolidated with autologous stem cell transplantation, all in CMR at EOT, except for 1 patient with PMR DS4.
With a median follow-up of 28 months (range: 2-107 months), 25 (51%) patients relapsed or progressed. Median progression-free survival (PFS) of the entire population was 24 months. According to interim response, median PFS of DS1-3, DS4 and DS5 were 28, 10 and 2 months, respectively (Figure 1). In univariate analysis, along traditional prognostic factors as advance stage (p=0.0324), increased LDH (0.0211), IPI ≥ 3 (0.0198) and bone marrow infiltration (0.0475), interim PET/CT (iPET) impacted on PFS (DS1-3 vs DS4 vs DS5, p=0.004; DS1-3 vs DS4-5, p=0.0233). When considering the exact timing, iPET after 4 cycles seemed to relate better with PFS (DS1-3 vs DS4 vs DS5, p=0.0009) than after 3 cycles (DS1-3 vs DS4 vs DS5, p=0.32).
In the multivariate analysis, iPET/CT response maintained its prognostic significance (for DS1-3 vs DS4 vs DS5: HR 2.37, 95% CI 1,44-3,89, p=0,).
Median OS was not reached. The estimated 2-year OS for the entire population was 75% (95% CI, 58-86). According to iPET, the estimated 2-year OS for DS1-3, DS4 and DS5 were 85% (60-95), 64% (30-85) and 63% (14-90), respectively. No impact of iPET was documented on .
Conclusion: Our study highlights the potential role of interim PET/CT in the management of PTCL. Reaching an early metabolic complete remission seems to be associated with longer PFS. Patients with a DS4 at interim evaluation remain challenging for clinicians, since also in our study half of them converted to CMR at the end of . Further radiomics analysis may help to better identify patients at higher risk of progression and offer a more tailored treatment.
De Oliveira:Janssen: Other: Travel Expenses; Janssen, Alexion: Consultancy. Gonzalez Barca:Janssen, Abbvie, Takeda, EUSAPharma, AstraZeneca, Lilly: Speakers Bureau; Janssen, Abbvie, Kiowa, EUSA Pharma, Beigene, Sobi: Consultancy; Janssen, Abbvie, AstraZeneca: Other: Travel. Sureda Balari:Takeda: Consultancy, Speakers Bureau; Kite: Consultancy, Speakers Bureau. Domingo Domenech:BeiGene: Consultancy; BMS: Speakers Bureau; Takeda: Consultancy, Honoraria, Speakers Bureau.
[Display omitted] |
---|---|
AbstractList | Introduction: The introduction of PET/CT in the staging and response assessment to therapy has changed the clinical evaluation of most lymphomas, especially Hodgkin lymphoma and aggressive B-cell lymphomas. The use of PET/CT in the staging of peripheral T-cell lymphomas (PTCL) is already a standard of care in many centers, although its decisional role in course of chemotherapy or at the end of treatment remains unclear.
Objective: The aim of this study is to evaluate the predictive role of interim PET/CT in newly diagnosed PTCL patients.
Methods: We retrospectively analyzed the clinical data of adult patients diagnosed with PTCL and actively treated between 2014 and 2023 at our center. All patients were evaluated with PET/CT at different timepoints (baseline, interim and end of treatment).
Results: We evaluated 49 patients, with a median age at diagnosis of 59 years (range: 18-83), and a slight predominance of females (54%) (table 1). Almost half of the patients were diagnosed of angioimmunoblastic/T-follicular helper lymphoma (AITL/TFHL) 23(47%), followed by anaplastic large cell lymphoma (ALCL) in 17 cases [9 ALK+ (18%) and 8 ALK- (17%))] and peripheral T-cell lymphoma NOS (PTCL-NOS) in 9 (18%). Seven (14%) patients had ECOG ≥ 2, 47 (90%) had stage III-IV disease, among them, 42 (84%) with extranodal involvement. Bone marrow was involved in 14 out of 36 (39%) evaluated patients. Twenty-seven (54%) patients had IPI score 3-5. Front-line treatment consisted in CHOP in 32 (65%) patients and brentuximab vedotin+CHP in 17 (35%). Interim evaluation was performed after 3 cycles in 32 (65%) and after 4 cycles in 16 (33%) patients. Only one patient was evaluated after 2 cycles due to suspected disease progression. At this time point, 31 (63%) patients were considered in complete metabolic response (CMR) with a Deauville Score (DS) 1-3, 12 (25%) in partial metabolic response (PMR) with a DS 4 and 6 (12%) patients with progressive disease (PD) with DS5. Among the latter's, 4 patients were treated with 2 nd line treatment, while 2 completed the planed 6 cycles due to significant tumor burden . Among 48 patients evaluated after 3 and 4 cycles of therapy, CMR was achieved in 18 (56%) and 13 (81%), respectively (p=0,088). Eleven (34%) and one (6%) pts were in PMR at iPET after 3 and 4 cycles, respectively.
Forty-five (92%) patients completed front-line therapy and were evaluated with EOT PET/. CMR (DS1-3) was reported in 32 (71%) patients, PMR in 8 (18%) and PD in 5 (%). Among patients with CMR at iPET, 25 (81%) maintained CMR, 5 (16%) converted to PMR and only 1 (3%) progressed. Among patients with PMR at iPET, 5 (42%) converted to CMR, 4 (33%) maintained PMR and 3 (25%) progressed. Eighteen (37%) patients were consolidated with autologous stem cell transplantation, all in CMR at EOT, except for 1 patient with PMR DS4.
With a median follow-up of 28 months (range: 2-107 months), 25 (51%) patients relapsed or progressed. Median progression-free survival (PFS) of the entire population was 24 months. According to interim response, median PFS of DS1-3, DS4 and DS5 were 28, 10 and 2 months, respectively (Figure 1). In univariate analysis, along traditional prognostic factors as advance stage (p=0.0324), increased LDH (0.0211), IPI ≥ 3 (0.0198) and bone marrow infiltration (0.0475), interim PET/CT (iPET) impacted on PFS (DS1-3 vs DS4 vs DS5, p=0.004; DS1-3 vs DS4-5, p=0.0233). When considering the exact timing, iPET after 4 cycles seemed to relate better with PFS (DS1-3 vs DS4 vs DS5, p=0.0009) than after 3 cycles (DS1-3 vs DS4 vs DS5, p=0.32).
In the multivariate analysis, iPET/CT response maintained its prognostic significance (for DS1-3 vs DS4 vs DS5: HR 2.37, 95% CI 1,44-3,89, p=0,).
Median OS was not reached. The estimated 2-year OS for the entire population was 75% (95% CI, 58-86). According to iPET, the estimated 2-year OS for DS1-3, DS4 and DS5 were 85% (60-95), 64% (30-85) and 63% (14-90), respectively. No impact of iPET was documented on .
Conclusion: Our study highlights the potential role of interim PET/CT in the management of PTCL. Reaching an early metabolic complete remission seems to be associated with longer PFS. Patients with a DS4 at interim evaluation remain challenging for clinicians, since also in our study half of them converted to CMR at the end of . Further radiomics analysis may help to better identify patients at higher risk of progression and offer a more tailored treatment. Introduction: The introduction of PET/CT in the staging and response assessment to therapy has changed the clinical evaluation of most lymphomas, especially Hodgkin lymphoma and aggressive B-cell lymphomas. The use of PET/CT in the staging of peripheral T-cell lymphomas (PTCL) is already a standard of care in many centers, although its decisional role in course of chemotherapy or at the end of treatment remains unclear. Objective: The aim of this study is to evaluate the predictive role of interim PET/CT in newly diagnosed PTCL patients. Methods: We retrospectively analyzed the clinical data of adult patients diagnosed with PTCL and actively treated between 2014 and 2023 at our center. All patients were evaluated with PET/CT at different timepoints (baseline, interim and end of treatment). Results: We evaluated 49 patients, with a median age at diagnosis of 59 years (range: 18-83), and a slight predominance of females (54%) (table 1). Almost half of the patients were diagnosed of angioimmunoblastic/T-follicular helper lymphoma (AITL/TFHL) 23(47%), followed by anaplastic large cell lymphoma (ALCL) in 17 cases [9 ALK+ (18%) and 8 ALK- (17%))] and peripheral T-cell lymphoma NOS (PTCL-NOS) in 9 (18%). Seven (14%) patients had ECOG ≥ 2, 47 (90%) had stage III-IV disease, among them, 42 (84%) with extranodal involvement. Bone marrow was involved in 14 out of 36 (39%) evaluated patients. Twenty-seven (54%) patients had IPI score 3-5. Front-line treatment consisted in CHOP in 32 (65%) patients and brentuximab vedotin+CHP in 17 (35%). Interim evaluation was performed after 3 cycles in 32 (65%) and after 4 cycles in 16 (33%) patients. Only one patient was evaluated after 2 cycles due to suspected disease progression. At this time point, 31 (63%) patients were considered in complete metabolic response (CMR) with a Deauville Score (DS) 1-3, 12 (25%) in partial metabolic response (PMR) with a DS 4 and 6 (12%) patients with progressive disease (PD) with DS5. Among the latter's, 4 patients were treated with 2 nd line treatment, while 2 completed the planed 6 cycles due to significant tumor burden . Among 48 patients evaluated after 3 and 4 cycles of therapy, CMR was achieved in 18 (56%) and 13 (81%), respectively (p=0,088). Eleven (34%) and one (6%) pts were in PMR at iPET after 3 and 4 cycles, respectively. Forty-five (92%) patients completed front-line therapy and were evaluated with EOT PET/. CMR (DS1-3) was reported in 32 (71%) patients, PMR in 8 (18%) and PD in 5 (%). Among patients with CMR at iPET, 25 (81%) maintained CMR, 5 (16%) converted to PMR and only 1 (3%) progressed. Among patients with PMR at iPET, 5 (42%) converted to CMR, 4 (33%) maintained PMR and 3 (25%) progressed. Eighteen (37%) patients were consolidated with autologous stem cell transplantation, all in CMR at EOT, except for 1 patient with PMR DS4. With a median follow-up of 28 months (range: 2-107 months), 25 (51%) patients relapsed or progressed. Median progression-free survival (PFS) of the entire population was 24 months. According to interim response, median PFS of DS1-3, DS4 and DS5 were 28, 10 and 2 months, respectively (Figure 1). In univariate analysis, along traditional prognostic factors as advance stage (p=0.0324), increased LDH (0.0211), IPI ≥ 3 (0.0198) and bone marrow infiltration (0.0475), interim PET/CT (iPET) impacted on PFS (DS1-3 vs DS4 vs DS5, p=0.004; DS1-3 vs DS4-5, p=0.0233). When considering the exact timing, iPET after 4 cycles seemed to relate better with PFS (DS1-3 vs DS4 vs DS5, p=0.0009) than after 3 cycles (DS1-3 vs DS4 vs DS5, p=0.32). In the multivariate analysis, iPET/CT response maintained its prognostic significance (for DS1-3 vs DS4 vs DS5: HR 2.37, 95% CI 1,44-3,89, p=0,). Median OS was not reached. The estimated 2-year OS for the entire population was 75% (95% CI, 58-86). According to iPET, the estimated 2-year OS for DS1-3, DS4 and DS5 were 85% (60-95), 64% (30-85) and 63% (14-90), respectively. No impact of iPET was documented on . Conclusion: Our study highlights the potential role of interim PET/CT in the management of PTCL. Reaching an early metabolic complete remission seems to be associated with longer PFS. Patients with a DS4 at interim evaluation remain challenging for clinicians, since also in our study half of them converted to CMR at the end of . Further radiomics analysis may help to better identify patients at higher risk of progression and offer a more tailored treatment. De Oliveira:Janssen: Other: Travel Expenses; Janssen, Alexion: Consultancy. Gonzalez Barca:Janssen, Abbvie, Takeda, EUSAPharma, AstraZeneca, Lilly: Speakers Bureau; Janssen, Abbvie, Kiowa, EUSA Pharma, Beigene, Sobi: Consultancy; Janssen, Abbvie, AstraZeneca: Other: Travel. Sureda Balari:Takeda: Consultancy, Speakers Bureau; Kite: Consultancy, Speakers Bureau. Domingo Domenech:BeiGene: Consultancy; BMS: Speakers Bureau; Takeda: Consultancy, Honoraria, Speakers Bureau. [Display omitted] |
Author | Montane Carbo, Clara Rampi, Nicolo De Oliveira, Ana C. Arevalo Leon, Carolina Esther Lopez-Pereira, Patricia Gonzalez Barca, Eva Maria Cortes-Romera, Montserrat Sureda Balari, Anna Maria Domingo Domenech, Eva Martinez-Ramos, Carolina |
Author_xml | – sequence: 1 givenname: Nicolo surname: Rampi fullname: Rampi, Nicolo organization: Department of Oncology and Oncohaematology, University of Milan, Vigevano, Italy – sequence: 2 givenname: Montserrat surname: Cortes-Romera fullname: Cortes-Romera, Montserrat organization: Department of Nuclear Medicine, IDI, Hospital Universitari de Bellvitge, Barcelona, Spain – sequence: 3 givenname: Patricia surname: Lopez-Pereira fullname: Lopez-Pereira, Patricia organization: Clinical Hematology Department, Institut Català d'Oncologia, Hospital Duran i Reynals, IDIBELL, Barcelona, Spain – sequence: 4 givenname: Carolina surname: Martinez-Ramos fullname: Martinez-Ramos, Carolina organization: Department of Nuclear Medicine. IDI. Hospital Universitari de Bellvitge, Barcelona, Spain – sequence: 5 givenname: Clara surname: Montane Carbo fullname: Montane Carbo, Clara organization: Clinical Hematology Department, Institut Català d'Oncologia, Hospital Duran i Reynals, IDIBELL, Barcelona, Spain – sequence: 6 givenname: Carolina Esther surname: Arevalo Leon fullname: Arevalo Leon, Carolina Esther organization: Clinical Hematology Department, Institut Català d'Oncologia, Hospital Duran i Reynals, IDIBELL, Barcelona, Spain – sequence: 7 givenname: Ana C. surname: De Oliveira fullname: De Oliveira, Ana C. organization: Clinical Hematology Department. Institut Català d'Oncologia, Hospital Duran i Reynals, IDIBELL, Universitat de Barcelona, Barcelona, Spain – sequence: 8 givenname: Eva Maria surname: Gonzalez Barca fullname: Gonzalez Barca, Eva Maria organization: Department of Hematology, Department of Clinical Sciences, Institut Català d'Oncologia, Hospitalet de Llobregat, Barcelona University, Barcelona, Spain – sequence: 9 givenname: Anna Maria surname: Sureda Balari fullname: Sureda Balari, Anna Maria organization: Clinical Hematology Department, Institut Català d'Oncologia, Hospital Duran i Reynals, IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain – sequence: 10 givenname: Eva surname: Domingo Domenech fullname: Domingo Domenech, Eva organization: Clinical Hematology Department, Institut Català d'Oncologia, Hospital Duran i Reynals, IDIBELL, Barcelona, Spain |
BookMark | eNp9kD1PwzAQhi1UJErhB7B5YzK1HecLJhS1UCkSlRpmy3HO1ChxIidUdOC_k7TMTKcbnvfufa7RzLUOELpj9IGxhC_Lum0rwikPCEsiloYXaM5CnhBKOZ2hOaU0IiKN2RW67vtPSpkIeDhHP5umU3rArcFr37qB5NYBLjyooQE34I0bwNsGb1fFMiuwdXg77t0evKpxQTKoa5wfm27fNgpv1WBHqL_Huy9_sAdVP-LVdzcC4DRMNxTeWfdRA85gCr5Bl0bVPdz-zQV6X6-K7JXkby-b7DknmgVxSCKTaqahCllZxSylsWBUKRFrnZiwjIRIRMhMmfIgoVUqKqONCcqIgzZRbLQKFoidc7Vv-96Dkd1YSvmjZFRO_uTJn5z8ybO_kXk6MzA-drDgZa9PPSrrQQ-yau0_9C_TnXsX |
ContentType | Journal Article |
Copyright | 2023 The American Society of Hematology |
Copyright_xml | – notice: 2023 The American Society of Hematology |
DBID | AAYXX CITATION |
DOI | 10.1182/blood-2023-186195 |
DatabaseName | CrossRef |
DatabaseTitle | CrossRef |
DatabaseTitleList | CrossRef |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine Chemistry Biology Anatomy & Physiology |
EISSN | 1528-0020 |
EndPage | 6216 |
ExternalDocumentID | 10_1182_blood_2023_186195 S0006497123128138 |
GroupedDBID | --- -~X .55 0R~ 1CY 23N 2WC 34G 39C 4.4 53G 5GY 5RE 6J9 AAEDW AALRI AAXUO ABOCM ACGFO ADBBV AENEX AFETI AFOSN AITUG AKRWK ALMA_UNASSIGNED_HOLDINGS AMRAJ 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 WH7 WOQ WOW X7M YHG YKV 5VS AAYXX ABVKL CITATION W8F |
ID | FETCH-LOGICAL-c1375-6f9c1ced51bd71907410aa47cc8f5b6448451fb92380d94dfcff3b62ecf67fca3 |
ISSN | 0006-4971 |
IngestDate | Thu Nov 21 22:14:11 EST 2024 Sat Oct 26 15:42:31 EDT 2024 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | Supplement 1 |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c1375-6f9c1ced51bd71907410aa47cc8f5b6448451fb92380d94dfcff3b62ecf67fca3 |
OpenAccessLink | https://doi.org/10.1182/blood-2023-186195 |
PageCount | 1 |
ParticipantIDs | crossref_primary_10_1182_blood_2023_186195 elsevier_sciencedirect_doi_10_1182_blood_2023_186195 |
PublicationCentury | 2000 |
PublicationDate | 2023-11-02 |
PublicationDateYYYYMMDD | 2023-11-02 |
PublicationDate_xml | – month: 11 year: 2023 text: 2023-11-02 day: 02 |
PublicationDecade | 2020 |
PublicationTitle | Blood |
PublicationYear | 2023 |
Publisher | Elsevier Inc |
Publisher_xml | – name: Elsevier Inc |
SSID | ssj0014325 |
Score | 2.4827697 |
Snippet | Introduction: The introduction of PET/CT in the staging and response assessment to therapy has changed the clinical evaluation of most lymphomas, especially... |
SourceID | crossref elsevier |
SourceType | Aggregation Database Publisher |
StartPage | 6216 |
Title | Impact of Front-Line Treatment Interim PET/CT in Peripheral T-Cell Lymphoma Patients' Survival: Experience of a Single Center |
URI | https://dx.doi.org/10.1182/blood-2023-186195 |
Volume | 142 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1ba9RAFB62FS8volvF1gvzIAqWoTuZXCa-1bilxSrFjeBbSCYzENjdLLb70IL_3TPXbK2CCr6EZDbZM-R8mXOdcxB6OZFtxlPKScNrRuI6bUnOUjBWMsZqkSdJZALtx7Ps01f-fhpPRyPfe28Y-6-chjHgtd45-xfcDn8KA3AOPIcjcB2Of8T3k7Dt8UjXJiCnWo0sQzq58QB2i_2zaalL45ba33EGI6a6wHy_JIV25p1eApP7Ra0r-Hc-1WK2hmUFpqqdCEOFZLvBcgYScC6Nr9il-_pA8dx1o7fBpMWqC_jrQ_xDJ_yek8-9dpAZDy1MHF4WgDPkC_UreUVgorKzt9jWAl0QKrYcAtwDNGzmYOEaEm36NSJmNvgNVnDYcHMtH1RLV90Uj15bwG19LrcEpxFNN8S5v7wpKrguPWu3B1j6gFnb8POnCtwzo7gBUdCFI04Z30K3IljXjAV_8iEErWIW2YYZbo4uiA6EDm6Q-bUatKHalA_QfWeT4EMLpodoJJdjtHO4rC_6xSV-hU2WsAm_jNHtd_7sbuF7BY7RnY8uRWMHfbcAxL3CAwBxACB2AMQAwIOixN0SD_DDFn7Yww97-L3GHnxv8QA9TaPGFnrYQu8R-nI0LYtj4np8EEFZlpBU5YIK2Sa0aTOqPTV0UtdxJgRXSaOdB3FCVQNmCJ-0edwqoRRr0kgKlWZK1Owx2l72S_kEYdqKFH7LZQ5mQSSyvGlbkU8kbxQFQRPvojf-lVcrW8qlMiYwjyrDn0rzp7L82UWxZ0rldFGrY1aAn98_tvdvjz1F94ZP4Bnavvi2ls_R1nm7fmEg9gOuGaoc |
link.rule.ids | 315,782,786,27933,27934 |
linkProvider | Flying Publisher |
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=Impact+of+Front-Line+Treatment+Interim+PET%2FCT+in+Peripheral+T-Cell+Lymphoma+Patients%27+Survival%3A+Experience+of+a+Single+Center&rft.jtitle=Blood&rft.au=Rampi%2C+Nicolo&rft.au=Cortes-Romera%2C+Montserrat&rft.au=Lopez-Pereira%2C+Patricia&rft.au=Martinez-Ramos%2C+Carolina&rft.date=2023-11-02&rft.pub=Elsevier+Inc&rft.issn=0006-4971&rft.volume=142&rft.spage=6216&rft.epage=6216&rft_id=info:doi/10.1182%2Fblood-2023-186195&rft.externalDocID=S0006497123128138 |
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 |