Evidence map›Paper›PMID 30850381›Full record

Trial reportBlood2019

Venetoclax plus R- or G-CHOP in non-Hodgkin lymphoma: results from the CAVALLI phase 1b trial.

Andrew D Zelenetz, Gilles Salles, Kylie D Mason, Carla Casulo, Steven Le Gouill, Laurie H Sehn, Herve Tilly, Guillaume Cartron, Martine E D Chamuleau, Andre Goy and 13 more

Registry-linked trialOpen access · bronzeAbstract readClinical Trial, Phase IClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Blood, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02055820 (A Phase Ib/II, Open-Label Study Evaluating the Safety, Efficacy and Pharmacokinetics of GDC-0199), which is not on this map. Cited by 74 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 3 pooled it
14.8field-weighted citation impact, top 1% 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.

NCT02055820 phase1 / phase2completednot on this map

A Phase Ib/II, Open-Label Study Evaluating the Safety, Efficacy and Pharmacokinetics of GDC-0199 (ABT-199) in Combination With Rituximab (R) or Obinutuzumab (G) Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (CHOP) in Patients With B-Cell Non-Hodgkin's Lymphoma (NHL) and DLBCL

TypeinterventionalSponsorHoffmann-La RocheRan2013 to 2019Enrolled267ConditionsLymphoma, Non-HodgkinArmsVenetoclax, Cyclophosphamide, Obinutuzumab, Rituximab, Doxorubicin
3 · Its place in the literature

Who cites it

74 citing papers in PubMed, 3 syntheses or guidelines pooled it, 134 citations in OpenAlex.

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  9. Targeting protein-protein interactions in the BCL-2 family: opportunities for precision oncology.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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14 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 16 institutions in 7 countries.

Andrew D ZelenetzMemorial Sloan Kettering Cancer Center, New York, NY.
Gilles SallesHospices Civils de Lyon, Lyon, France.
Kylie D MasonRoyal Melbourne Hospital, Melbourne, VIC, Australia.
Carla CasuloWilmot Cancer Institute, University of Rochester, Rochester, NY.
Steven Le GouillService d'Hématologie, CHU de Nantes, Nantes, France.
Laurie H SehnCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada.
Herve TillyCentre Henri Becquerel, Rouen, France.
Guillaume CartronDepartment of Hematology, University of Montpellier, Montpellier, France.
Martine E D ChamuleauHOVON Lunenburg Lymphoma Phase I-II Consortium, VU University Medical Center, Amsterdam, The Netherlands.
Andre GoyHackensack University Medical Center, Hackensack, NJ.
Constantine S TamPeter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Pieternella J LugtenburgHOVON Lunenburg Lymphoma Phase I-II Consortium, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Adam M PetrichAbbVie, North Chicago, IL.
Arijit SinhaRoche Products Ltd, Welwyn Garden City, United Kingdom.
Divya SamineniGenentech Inc, South San Francisco, CA.
Sylvia HerterRoche Pharmaceutical Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
Ellen IngallaGenentech Inc, South San Francisco, CA.
Edith Szafer-GlusmanGenentech Inc, South San Francisco, CA.
Christian KleinRoche Pharmaceutical Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
Deepak SampathGenentech Inc, South San Francisco, CA.
Martin KornackerF. Hoffmann-La Roche Ltd, Basel, Switzerland; and.
Mehrdad MobasherGenentech Inc, South San Francisco, CA.
Franck MorschhauserUniversité de Lille, CHU Lille, Groupe de Recherche sur les Formes Injectables et les Technologies Associées, Lille, France.
Roche (Switzerland) · CHAbbVie (United States) · USAmsterdam UMC Location VUmc · NLBC Cancer Agency · CACentre Henri BecquerelCentre Hospitalier Universitaire de Nantes · FRErasmus MC Cancer Institute · NLHackensack University Medical Center · USHospices Civils de Lyon · FRMemorial Sloan Kettering Cancer Center · USPeter MacCallum Cancer Centre · AURoche (United Kingdom) · GBThe Royal Melbourne Hospital · AUUniversité de Lille · FRUniversité de Montpellier · FRUniversity of Rochester · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Novel strategies, such as chemosensitization with targeted agents, that build on the success of standard immunochemotherapy show promise for the treatment of non-Hodgkin lymphoma (NHL). Here, we report a phase 1b study investigating dose escalation of the BCL2 inhibitor, venetoclax, in combination with rituximab or obinutuzumab and cyclophosphamide, doxorubicin, vincristine, and prednisone (R-/G-CHOP) chemotherapy in B-cell NHL. Objectives included safety assessment and determination of a recommended phase 2 dose (RP2D). Fifty-six patients were enrolled, most with follicular lymphoma (43%) or diffuse large B-cell lymphoma (DLBCL; 32%). Dose-limiting toxicities were reported in 3/14 patients at the first venetoclax dose (200 mg/d), after which dosing was changed from daily to 10 days per cycle and escalated to 800 mg. A further reduction to 5 days per cycle occurred at the 800-mg dose level in the G-CHOP arm. Cytopenias were predominant among grade 3/4 events and reported at a higher rate than expected, particularly in the G-CHOP arm; however, safety was manageable. Overall response rates were 87.5% (R-CHOP and G-CHOP combinations); complete response (CR) rates were 79.2% and 78.1%, respectively. Most double-expressor (BCL2

Indexed as

AgedAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsBridged Bicyclo Compounds, HeterocyclicCyclophosphamideDisease-Free SurvivalDoxorubicinFemaleHumansLymphoma, Non-HodgkinMaleMaximum Tolerated DoseMiddle AgedPrednisoneRituximabSulfonamidesAntibodies, Monoclonal, HumanizedBridged Bicyclo Compounds, HeterocyclicCyclophosphamideDoxorubicinobinutuzumabPrednisoneR-CHOP protocolRituximabSulfonamidesvenetoclaxVincristine

Identifiers

PMID30850381
PMCPMC6497517
OpenAlexW2922237910

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.