Evidence map›Paper›PMID 28971900›Full record

Trial reportHaematologica2017

Pan-phosphatidylinositol 3-kinase inhibition with buparlisib in patients with relapsed or refractory non-Hodgkin lymphoma.

Anas Younes, Gilles Salles, Giovanni Martinelli, Robert Gregory Bociek, Dolores Caballero Barrigon, Eva González Barca, Mehmet Turgut, John Gerecitano, Oliver Kong, Chaitali Babanrao Pisal and 2 more

Open access · goldAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Haematologica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
4.4field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Phase I/Ib Study of the Efficacy and Safety of Buparlisib and Ibrutinib Therapy in MCL, FL, and DLBCL with Serial Cell-Free DNA Monitoring.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
  6. PI3K Inhibitors in Cancer: Clinical Implications and Adverse Effects.International journal of molecular sciences · 2021
    Review
  7. Review
  8. Targeted Treatment of Follicular Lymphoma.Journal of personalized medicine · 2021
    Review
  9. Review
  10. Review
  11. Article
  12. Genetic alterations and their clinical implications in DLBCL.Nature reviews. Clinical oncology · 2019
    Review
  13. The Role of PI3K Inhibition in Lymphoid Malignancies.Current hematologic malignancy reports · 2019
    Review
  14. Review
  15. Review
  16. Targeting the "undruggable" RAS - new strategies - new hope?Cancer drug resistance (Alhambra, Calif.) · 2019
    Review
  17. Novel therapies for relapsed/refractory aggressive lymphomas.Hematology. American Society of Hematology. Education Program · 2018
    Review
  18. Review
  19. 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

12 authors at 10 institutions in 7 countries.

Anas YounesMemorial Sloan Kettering Cancer Center, New York, NY, USA; Weill Cornell Medical College, Cornell University, New York, NY, USA younesa@mskcc.org wskimsmc@skku.edu.
Gilles SallesCentre Hospitalier Lyon-Sud, Pierre Bénite, Lyon, France.
Giovanni MartinelliEuropean Institute of Oncology, Milan, Italy.
Robert Gregory BociekUniversity of Nebraska Medical Center, Omaha, NE, USA.
Dolores Caballero BarrigonHospital Universitario de Salamanca, Spain.
Eva González BarcaHospital Duran i Reynals-ICO, Barcelona, Spain.
Mehmet TurgutOndokuz Mayis University, Samsun, Turkey.
John GerecitanoMemorial Sloan Kettering Cancer Center, New York, NY, USA; Weill Cornell Medical College, Cornell University, New York, NY, USA.
Oliver KongNovartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
Chaitali Babanrao PisalNovartis Healthcare Pvt. Ltd., Hyderabad, India.
Ranjana TavorathNovartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
Won Seog KimSamsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea younesa@mskcc.org wskimsmc@skku.edu.
Memorial Sloan Kettering Cancer Center · USNovartis (United States) · USComplejo Hospitalario de Salamanca · ESDuran i Reynals Hospital · ESEuropean Institute of Oncology · ITHôpital Lyon Sud · FRNovartis (India) · INOndokuz Mayıs University · TRSungkyunkwan University · KRUniversity of Nebraska Medical Center · 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

Activation of the phosphatidylinositol 3-kinase/mechanistic target of rapamycin pathway plays a role in the pathogenesis of non-Hodgkin lymphoma. This multicenter, open-label phase 2 study evaluated buparlisib (BKM120), a pan-class I phosphatidylinositol 3-kinase inhibitor, in patients with relapsed or refractory non-Hodgkin lymphoma. Three separate cohorts of patients (with diffuse large B-cell lymphoma, mantle cell lymphoma, or follicular lymphoma) received buparlisib 100 mg once daily until progression, intolerance, or withdrawal of consent. The primary endpoint was overall response rate based on a 6-month best overall response by cohort; secondary endpoints included progression-free survival, duration of response, overall survival, safety, and tolerability. Overall, 72 patients (26 with diffuse large B-cell lymphoma, 22 with mantle cell lymphoma, and 24 with follicular lymphoma) were treated. The overall response rates were 11.5%, 22.7%, and 25.0% in patients with diffuse large B-cell lymphoma, mantle cell lymphoma, and follicular lymphoma, respectively; two patients (one each with diffuse large B-cell lymphoma and mantle cell lymphoma) achieved a complete response. The most frequently reported (>20%) adverse events of any grade in the population in which safety was studied were hyperglycemia, fatigue, and nausea (36.1% each), depression (29.2%), diarrhea (27.8%), and anxiety (25.0%). The most common grade 3/4 adverse events included hyperglycemia (11.1%) and neutropenia (5.6%). Buparlisib showed activity in relapsed or refractory non-Hodgkin lymphoma, with disease stabilization and sustained tumor burden reduction in some patients, and acceptable toxicity. Development of mechanism-based combination regimens with buparlisib is warranted. (This study was funded by Novartis Pharmaceuticals Corporation and registered with

Indexed as

Phosphoinositide-3 Kinase InhibitorsAdultAgedAged, 80 and overAminopyridinesFemaleHumansLymphoma, FollicularLymphoma, Large B-Cell, DiffuseLymphoma, Mantle-CellLymphoma, Non-HodgkinMaleMiddle AgedMorpholinesRecurrenceRemission InductionAminopyridinesMorpholinesNVP-BKM120Phosphoinositide-3 Kinase Inhibitors

Identifiers

PMID28971900
PMCPMC5709110
OpenAlexW2763994374

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.