Evidence map›Paper›PMID 37026799›Full record

Trial reportBlood advances2023

A fixed-duration immunochemotherapy approach in CLL: 5.5-year results from the phase 2 ICLL-07 FILO trial.

Anne-Sophie Michallet, Rémi Letestu, Magali Le Garff-Tavernier, Lydia Campos, Michel Ticchioni, Marie-Sarah Dilhuydy, Stephane Morisset, Valérie Rouille, Béatrice Mahé, Kamel Laribi and 23 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Blood advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02666898 (Phase II, Multicenter, Trial, Exploring "Chemo-free" Treatment), which is not on this map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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.

NCT02666898 phase2completednot on this map

Phase II, Multicenter, Trial, Exploring "Chemo-free" Treatment (GA101+Ibrutinib) and MRD-driven Strategy in Previously Untreated Symptomatic B-chronic Lymphocytic Leukemia Medically Fit. A FILO Study. A Study From the Goelams/GCFLLC/MW Intergroup

TypeinterventionalSponsorFrench Innovative Leukemia OrganisationRan2015 to 2023Enrolled135ConditionsLeukemia, Lymphocytic, Chronic, B-CellArmsGA101, Ibrutinib, Cyclophosphamide, Fludarabine
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
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

33 authors at 20 institutions in 1 country.

Anne-Sophie MichalletDepartment of Hematology, Centre Léon Bérard, Lyon, France.
Rémi LetestuHematology Laboratory, Avicenne Hospital, Hôpitaux universitaires Paris Seine Saint-Denis (HUPSSD), Assistance Publique-Hôpitaux de Paris (AP-HP), Bobigny, France.ORCID 0000-0002-2437-2656
Magali Le Garff-TavernierDepartment of Hematology Biology, AP-HP, Hôpital Pitié Salpêtrière, Paris, France.ORCID 0000-0002-3131-3240
Lydia CamposDepartment of Hematology Biology, Le Centre Hospitalier Universitaire (CHU) Saint Etienne, Saint Etienne, France.ORCID 0000-0001-7971-4476
Michel TicchioniDepartment of Immunology, CHU Nice, Nice, France.
Marie-Sarah DilhuydyDepartment of Hematology, CHU Bordeaux, Pessac, France.
Stephane MorissetDepartment of Hematology, Centre Léon Bérard, Lyon, France.ORCID 0000-0002-7747-113X
Valérie RouilleDepartment of Hematology, CHU Montpellier, Montpellier, France.
Béatrice MahéDepartment of Hematology, Nantes University Hospital, Nantes, France.
Kamel LaribiDepartment of Hematology, CH Le Mans, Le Mans, France.
Bruno VillemagneDepartment of Hematology, CHD Vendée, La Roche-sur-Yon, France.ORCID 0000-0003-4093-6463
Emmanuelle FerrantDepartment of Hematology and Oncology, CH Lyon-Sud, Hospices Civils de Lyon, Université Claude Bernard, Pierre-Benite, Lyon, France.
Olivier TournilhacDepartment of Hematology and Cellular Therapy, CHU Hotel Dieu Hématologie, Clermont-Ferrand, France.ORCID 0000-0002-9438-621X
Alain DelmerDepartment of Hematology, CHU Reims, Reims, France.ORCID 0000-0002-1430-2574
Lysiane MolinaDepartment of Hematology, CHU Grenoble, La Tronche, France.
Véronique LeblondDepartment of Hematology, AP-HP, Hôpital Pitié Salpêtrière, Paris, France.
Cécile TomowiakDepartment of Hematology, CHU Poitiers, Poitiers, France.
Sophie de GuibertDepartment of Hematology, CHU Rennes, Rennes, France.
Frederique Orsini-PiocelleHematology Service, CH Annecy, Annecy, France.
Anne BanosDepartment of Hematology, CH Côte Basque, Bayonne, France.
Philippe CarassouDepartment of Hematology, CH Metz, Metz, France.
Guillaume CartronDepartment of Hematology, CHU Montpellier, Montpellier, France.ORCID 0000-0003-0659-9635
Luc Mathieu ForneckerDepartment of Hematology, Strasbourg University Hospital, Strasbourg, France.
Loic YsebaertInstitut Universitaire du Cancer Toulouse-Oncopole, Toulouse, France.
Caroline DartigeasDepartment of Hematology, CHU Tours, Hôpital Bretonneau, Tours, France.
Margot Truchan-GraczykDepartment of Hematology, CHU Angers, Angers, France.
Jean-Pierre VilqueInstitut d'Hématologie de Basse-Normandie, Centre François Baclesse, Caen, France.
Thérèse Aurran SchleinitzDepartment of Hematology, Institut Paoli Calmettes, Marseille, Marseille France.
Florence CymbalistaDepartment of Hematology, Avicenne Hospital, HUPSSD, AP-HP, Bobigny, France.
Stéphane LeprêtreInserm U1245 and Department of Hematology, Centre Centre Henri-Becquerel and Normandie University UNIROUEN, Rouen, France.
Vincent LévyDepartment of Clinical Research, Avicenne Hospital, HUPSSD, AP-HP, Bobigny, France.
Florence Nguyen-KhacDepartment of Hematology, AP-HP, Hôpital Pitié Salpêtrière, Paris, France.ORCID 0000-0003-3107-6668
Pierre FeugierDepartment of Hematology, Centre Hospitalier Régional Universitaire de Nancy, Hôpitaux de Brabois, Vandoeuvre-lès-Nancy, France.
Assistance Publique – Hôpitaux de Paris · FRSorbonne Université · FRCentre Léon Bérard · FRCentre Hospitalier de la Côte Basque · FRCentre Hospitalier du Mans · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Bordeaux · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de Montpellier · FRCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Nice · FRCentre Hospitalier Universitaire de Poitiers · FRCentre Hospitalier Universitaire de Reims · FRCentre Hospitalier Universitaire de Rennes · FRCentre Hospitalier Universitaire de Saint-Étienne · FRCentre Hospitalier Universitaire de Tours · FRInserm · FRInstitut Paoli-Calmettes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In previously untreated, medically fit patients with chronic lymphocytic leukemia (CLL), research is focused on developing fixed-duration strategies to improve long-term outcomes while sparing patients from serious toxicities. The ICLL-07 trial evaluated a fixed-duration (15-month) immunochemotherapy approach in which after obinutuzumab-ibrutinib induction for 9 months, patients (n = 10) in complete remission (CR) with bone marrow (BM) measurable residual disease (MRD) <0.01% continued only ibrutinib 420 mg/day for 6 additional months (I arm), whereas the majority (n = 115) received up to 4 cycles of fludarabine/cyclophosphamide-obinutuzumab 1000 mg alongside the ibrutinib (I-FCG arm). Primary analysis at month 16 showed that 84 of 135 (62.2%) patients enrolled achieved CR with a BM MRD <0.01%. Here, we report follow-up at median 63 months. Peripheral blood (PB) MRD was assessed 6 monthly beyond the end of treatment using a highly sensitive (10-6) flow cytometry technique. In the I-FCG arm, the PB MRD <0.01% rate (low-level positive <0.01% or undetectable with limit of detection ≤10-4) in evaluable patients was still 92.5% (74/80) at month 40 and 80.6% (50/62) at month 64. No differences in the PB MRD status were apparent per to the IGHV mutational status. In the overall population, 4-year progression-free and overall survival rates were 95.5% and 96.2%, respectively. Twelve deaths occurred overall. Fourteen serious adverse events occurred beyond the end of treatment. Thus, our fixed-duration immunochemotherapy approach produced deep and sustained PB MRD responses, high survival rates, and low long-term toxicity. A randomized trial is needed to compare our immunochemotherapy approach with a chemotherapy-free strategy. This trial was registered at www.clinicaltrials.gov as #NCT02666898.

Indexed as

Leukemia, Lymphocytic, Chronic, B-CellBone MarrowCyclophosphamideHumansNeoplasm, ResidualRemission InductionRituximabCyclophosphamideRituximab

Identifiers

PMID37026799
PMCPMC10410135
OpenAlexW4362691868

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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.