Evidence map›Paper›PMID 34292324›Full record

Trial reportBlood2021

Outcomes and prognostic factors in angioimmunoblastic T-cell lymphoma: final report from the international T-cell Project.

Ranjana H Advani, Tetiana Skrypets, Monica Civallero, Michael A Spinner, Martina Manni, Won Seog Kim, Andrei R Shustov, Steven M Horwitz, Felicitas Hitz, Maria Elena Cabrera and 9 more

Registry-linked trialAbstract readClinical Trial
In one paragraph

Trial report in Blood, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01142674 (Prospective Collection of Data in Pts With Peripheral T-Cell Lymphoma), which is not on this map. Cited by 84 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01142674 completednot on this map

Prospective Collection of Data in Pts With Peripheral T-Cell Lymphoma: PTCL,NOS;AITL; Extranodal NK/T-cell;Enteropathy-type; Hepatosplenic γ-δ; Subcutaneous Panniculitis-like; ALCL,Primary Systemic Type. By the Intl. T-Cell Lymphoma Project

TypeobservationalSponsorAssociazione Angela Serra per la ricerca sul cancroRan2006 to 2018Enrolled1,650ConditionsLymphoma, T-Cell, Peripheral
3 · Its place in the literature

Who cites it

84 citing papers in PubMed, 1 synthesis or guideline pooled it.

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24 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Ranjana H AdvaniDivision of Oncology, Department of Medicine, Stanford University, Stanford, CA.
Tetiana SkrypetsDepartment of Surgery, Medicine, Dentistry and Morphological Sciences with Transplant Surgery, Oncology and Regenerative Medicine Relevance (CHIMOMO), University of Modena and Reggio Emilia, Modena, Italy.ORCID 0000-0002-2276-869X
Monica CivalleroDepartment of Surgery, Medicine, Dentistry and Morphological Sciences with Transplant Surgery, Oncology and Regenerative Medicine Relevance (CHIMOMO), University of Modena and Reggio Emilia, Modena, Italy.ORCID 0000-0001-8606-5806
Michael A SpinnerDivision of Oncology, Department of Medicine, Stanford University, Stanford, CA.
Martina ManniDepartment of Surgery, Medicine, Dentistry and Morphological Sciences with Transplant Surgery, Oncology and Regenerative Medicine Relevance (CHIMOMO), University of Modena and Reggio Emilia, Modena, Italy.
Won Seog KimSungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, South Korea.
Andrei R ShustovDivision of Hematology, Fred Hutchinson Cancer Research Center, University of Washington Medical Center, Seattle, WA.
Steven M HorwitzDepartment of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY.
Felicitas HitzThe Swiss Group for Clinical Cancer Research, Department of Oncology/Haematology, Cantonal Hospital, St Gallen, Switzerland.
Maria Elena CabreraSección Hematología, Hospital del Salvador, Universidad de Chile, Santiago, Chile.
Ivan DlouhyHematology Department, Hospital Clinic de Barcelona, Barcelona, Spain.
José VassalloA.C. Camargo Cancer Center, Universidade Estadual de Campinas (Unicamp), Campinas, São Paulo, Brazil.ORCID 0000-0002-2192-4865
Stefano A PileriDivision of Haematopathology, Istituto Europeo di Oncologia Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Milano, Italy.ORCID 0000-0001-8032-5128
Giorgio InghiramiDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY.ORCID 0000-0001-5566-0864
Silvia MontotoDepartment of Haemato-oncology, Barts Health NHS Trust, London, United Kingdom.ORCID 0000-0002-3006-9725
Umberto VitoloHematology, Città della Salute e della Scienza Hospital and University, Turin, Italy.ORCID 0000-0001-7772-2747
John RadfordChristie NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom; and.ORCID 0000-0001-7898-2786
Julie M VoseUniversity of Nebraska Medical Center, Omaha, NE.ORCID 0000-0003-1015-7434
Massimo FedericoDepartment of Surgery, Medicine, Dentistry and Morphological Sciences with Transplant Surgery, Oncology and Regenerative Medicine Relevance (CHIMOMO), University of Modena and Reggio Emilia, Modena, Italy.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Preclinical Models and Therapeutics CoreP01CA229100 · NCI · MAYO CLINIC ARIZONA · PI SCOTT, DAVID WILLIAM · 2018 to 2022
$10.2M
NCI NIH HHS P01 CA229100NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Angioimmunoblastic T-cell lymphoma (AITL) is a unique subtype of peripheral T-cell lymphoma (PTCL) with distinct clinicopathologic features and poor prognosis. We performed a subset analysis of 282 patients with AITL enrolled between 2006 and 2018 in the international prospective T-cell Project (NCT01142674). The primary and secondary end points were 5-year overall survival (OS) and progression-free survival (PFS), respectively. We analyzed the prognostic impact of clinical covariates and progression of disease within 24 months (POD24) and developed a novel prognostic score. The median age was 64 years, and 90% of patients had advanced-stage disease. Eighty-one percent received anthracycline-based regimens, and 13% underwent consolidative autologous stem cell transplant (ASCT) in first complete remission (CR1). Five-year OS and PFS estimates were 44% and 32%, respectively, with improved outcomes for patients who underwent ASCT in CR1. In multivariate analysis, age ≥60 years, Eastern Cooperative Oncology Group performance status >2, elevated C-reactive protein, and elevated β2 microglobulin were associated with inferior outcomes. A novel prognostic score (AITL score) combining these factors defined low-, intermediate-, and high-risk subgroups with 5-year OS estimates of 63%, 54%, and 21%, respectively, with greater discriminant power than established prognostic indices. Finally, POD24 was a powerful prognostic factor with 5-year OS of 63% for patients without POD24 compared with only 6% for patients with POD24 (P < .0001). These data will require validation in a prospective cohort of homogeneously treated patients. Optimal treatment of AITL continues to be an unmet need, and novel therapeutic approaches are required.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsDisease ProgressionFemaleHumansImmunoblastic LymphadenopathyLymphoma, T-Cell, PeripheralMaleMiddle AgedPrognosisStem Cell TransplantationT-LymphocytesTransplantation, AutologousTreatment Outcome

Identifiers

PMID34292324
PMCPMC8493974

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.