Evidence map›Paper›PMID 33188164›Full record

Trial reportBlood cancer journal2020

Updated risk-oriented strategy for acute lymphoblastic leukemia in adult patients 18-65 years: NILG ALL 10/07.

Renato Bassan, Chiara Pavoni, Tamara Intermesoli, Orietta Spinelli, Manuela Tosi, Ernesta Audisio, Filippo Marmont, Chiara Cattaneo, Erika Borlenghi, Sergio Cortelazzo and 13 more

Open access · goldAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Blood cancer journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 3 pooled it
5.0field-weighted citation impact, top 4% of its field
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 3 syntheses or guidelines pooled it, 43 citations in OpenAlex.

  1. Guideline
  2. Pooled it
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  14. Article
  15. How I treat newly diagnosed acute lymphoblastic leukemia.Clinical hematology international · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 11 institutions in 1 country.

Renato BassanU.O.C. Ematologia, Ospedale dell'Angelo, Mestre-Venezia, Italy. renato.bassan@aulss3.veneto.it.ORCID 0000-0001-8214-2894
Chiara PavoniU.O.C. Ematologia, Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy.
Tamara IntermesoliU.O.C. Ematologia, Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy.
Orietta SpinelliU.O.C. Ematologia, Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy.ORCID 0000-0003-0374-1536
Manuela TosiU.O.C. Ematologia, Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy.
Ernesta AudisioEmatologia 2, Presidio Ospedaliero Molinette, A.O.U. Città della Salute e della Scienza, Torino, Italy.
Filippo MarmontEmatologia 2, Presidio Ospedaliero Molinette, A.O.U. Città della Salute e della Scienza, Torino, Italy.
Chiara CattaneoDivisione di Ematologia, Spedali Civili, Brescia, Italy.
Erika BorlenghiDivisione di Ematologia, Spedali Civili, Brescia, Italy.ORCID 0000-0002-4666-3817
Sergio CortelazzoDivisione di Ematologia e TMO, Ospedale S. Maurizio, Bolzano, Italy.
Irene CavattoniDivisione di Ematologia e TMO, Ospedale S. Maurizio, Bolzano, Italy.
Monica FumagalliU.O. di Ematologia e TMO, Ospedale S. Gerardo, Monza Brianza, Italy.
Daniele MatteiS.C. Ematologia, Azienda Ospedaliera S. Croce e Carle, Cuneo, Italy.
Claudio RomaniU.O. Ematologia e Centro TMO, Ospedale Armando Businco, Cagliari, Italy.
Agostino CortelezziU.O. Ematologia e TMO, Fondazione IRCSS Cà Granda, Ospedale Maggiore Policlinico, Milano, Italy.
Nicola FracchiollaU.O. Ematologia e TMO, Fondazione IRCSS Cà Granda, Ospedale Maggiore Policlinico, Milano, Italy.
Fabio CiceriEmatologia e TMO, Ospedale S. Raffaele, Milano, Italy.
Massimo BernardiEmatologia e TMO, Ospedale S. Raffaele, Milano, Italy.ORCID 0000-0002-1334-0851
Anna Maria ScattolinU.O.C. Ematologia, Ospedale dell'Angelo, Mestre-Venezia, Italy.
Lorella DepaoliDipartimento di Ematologia e Medicina Trasfusionale, Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo, Alessandria, Italy.
Arianna MasciulliFROM, Fondazione per la Ricerca, Ospedale Papa Giovanni XXIII, Bergamo, Italy.
Elena OldaniU.O.C. Ematologia, Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy.
Alessandro RambaldiU.O.C. Ematologia, Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy.ORCID 0000-0002-3739-7502
Ospedale Papa Giovanni XXIII · ITAzienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITIRCCS Ospedale San Raffaele · ITOspedale dell' Angelo · ITOspedale di Bolzano · ITPresidio Ospedaliero · ITAzienda Ospedaliera Nazionale SS. Antonio e Biagio e Cesare Arrigo · ITAzienda Ospedaliera San Gerardo · ITAzienda Sanitaria Ospedaliera S.Croce e Carle Cuneo · ITUniversity of Milan · IT

Funding

Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research) AIRC IG 2008 code 6105
6 · The paper itself

Abstract

An updated strategy combining pediatric-based chemotherapy with risk-oriented allogeneic hematopoietic cell transplantation (HCT) was evaluated in Philadelphia chromosome-negative acute lymphoblastic leukemia (Ph- ALL) and compared with a published control series. Following induction-consolidation chemotherapy, responsive patients were assigned to receive maintenance chemotherapy or undergo early HCT according to the risk stratification criteria and minimal residual disease (MRD) status. Of the 203 study patients (median age 41 years, range 17-67), 140/161 with Ph- ALL achieved complete remission (86.9%; 91.6% ≤55 years, P = 0.0002), with complete MRD clearing in 68/109; 55 patients were assigned to maintenance chemotherapy, and 85 to HCT due to very high-risk characteristics (hyperleukocytosis, adverse genetics, early/mature T-precursor ALL, and MRD persistence). The 5-year relapse incidence was 36%, and the treatment-related mortality rate was 18%. Median overall and relapse-free survival were 7.4 and 6.2 years, with rates of 54 and 53% at 5 years, respectively, which were significantly better than those obtained with the historical protocol (P = 0.001 and P = 0.005, respectively), without significant differences between maintenance and HCT cohorts. In prognostic analysis, MRD negativity and age ≤55 years were the most favorable independent prognostic factors. A reduction in treatment toxicity and further improvements in the risk definitions and risk-oriented design are the focuses of this ongoing research.

Indexed as

Hematopoietic Stem Cell TransplantationMaintenance ChemotherapyAdolescentAdultAgedAllograftsDisease-Free SurvivalFemaleHumansMaleMiddle AgedNeoplasm, ResidualPrecursor Cell Lymphoblastic Leukemia-LymphomaSurvival Rate

Identifiers

PMID33188164
PMCPMC7666128
OpenAlexW3106278547

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Registered trials

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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.