Evidence map›Paper›PMID 28522441›Full record

Trial reportBlood2017

Encouraging activity for R-CHOP in advanced stage nodular lymphocyte-predominant Hodgkin lymphoma.

Michelle A Fanale, Chan Yoon Cheah, Amy Rich, L Jeffrey Medeiros, Chao-Ming Lai, Yasuhiro Oki, Jorge E Romaguera, Luis E Fayad, F B Hagemeister, Felipe Samaniego and 14 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Blood, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

31 citing papers in PubMed, 83 citations in OpenAlex.

  1. Trial
  2. ABVD plus rituximabHaematologica · 2019
    Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Individualized patient care in nodular lymphocyte-predominant Hodgkin lymphoma.Hematology. American Society of Hematology. Education Program · 2022
    Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 3 institutions in 2 countries.

Michelle A FanaleDepartment of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.ORCID 0000-0003-3880-0866
Chan Yoon CheahDepartment of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-7988-1565
Amy RichDepartment of Hematopathology.
L Jeffrey MedeirosDepartment of Hematopathology.ORCID 0000-0001-6577-8006
Chao-Ming LaiDepartment of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.
Yasuhiro OkiDepartment of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.
Jorge E RomagueraDepartment of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.
Luis E FayadDepartment of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.
F B HagemeisterDepartment of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.
Felipe SamaniegoDepartment of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.
Maria A RodriguezDepartment of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.
Sattva S NeelapuDepartment of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.
Hun J LeeDepartment of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.
Loretta NastoupilDepartment of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-6071-8610
Nathan H FowlerDepartment of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-9494-1877
Francesco TurturroDepartment of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.
Jason R WestinDepartment of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-1824-2337
Michael L WangDepartment of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center, Houston, TX.
Peter McLaughlinPhysicians Network.
Chelsea C PinnixDepartment of Radiation Oncology, and.
Sarah A MilgromDepartment of Radiation Oncology, and.
Bouthaina DabajaDepartment of Radiation Oncology, and.ORCID 0000-0002-1226-0681
Sandra B HorowitzDepartment of Pharmacy Clinical Programs, University of Texas MD Anderson Cancer Center, Houston, TX; and.
Anas YounesLymphoma Department, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-0001-4133
The University of Texas MD Anderson Cancer Center · USDayton Physicians Network · USMemorial Sloan Kettering Cancer Center · US

Funding

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

Abstract

Nodular lymphocyte Hodgkin lymphoma (NLPHL) is a rare disease for which the optimal therapy is unknown. We hypothesized that rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) could decrease rates of relapse and transformation. We retrospectively reviewed patients with NLPHL diagnosed between 1995 and 2015 confirmed by central pathologic review. Fifty-nine had sufficient treatment and follow-up data for analysis. We described progression-free survival (PFS), overall survival (OS), and histologic transformation according to treatment strategy and explored prognostic factors for PFS and OS. The median age at diagnosis was 41 years; 75% were male, and 61% had a typical growth pattern. Twenty-seven patients were treated with R-CHOP with an overall response rate of 100% (complete responses 89%). The median follow-up was 6.7 years, and the estimated 5- and 10-year PFS rates for patients treated with R-CHOP were 88.5% (95% confidence interval [CI], 68.4% to 96.1%) and 59.3 (95% CI, 25.3% to 89.1%), respectively. Excluding patients with histologic transformation at diagnosis, the 5-year cumulative incidence of histologic transformation was 2% (95% CI, 87% to 100%). No patient treated with R-CHOP experienced transformation. A high-risk score from the German Hodgkin Study Group was adversely prognostic for OS (

Indexed as

AdolescentAdultAgedAntibodies, Monoclonal, Murine-DerivedAntineoplastic Combined Chemotherapy ProtocolsCyclophosphamideDisease-Free SurvivalDoxorubicinFemaleFollow-Up StudiesHodgkin DiseaseHumansMaleMiddle AgedPrednisoneRetrospective StudiesAntibodies, Monoclonal, Murine-DerivedCyclophosphamideDoxorubicinPrednisoneR-CHOP protocolRituximabVincristine

Identifiers

PMID28522441
PMCPMC5578726
OpenAlexW2614289524

What OpenQuestion holds

Textmetadata
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.