Evidence map›Paper›PMID 34477816›Full record

Trial reportBlood advances2021

Long-term efficacy and safety of CT-P10 or rituximab in untreated advanced follicular lymphoma: a randomized phase 3 study.

Christian Buske, Wojciech Jurczak, Juan-Manuel Sancho, Edvard Zhavrid, Jin Seok Kim, José-Ángel Hernández-Rivas, Aliaksandr Prokharau, Mariana Vasilica, Rajnish Nagarkar, Larry Kwak and 5 more

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

Trial report in Blood advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02162771 (A Phase 3, Randomised, Parallel-Group, Active-Controlled, Double-Blind Study to Demonstrate Equivalence of Pharmacokinetics and Noninferiority of Efficacy for CT-P10 in Comparison With Rituxan, Each Administered in Combination With Cyclophosphamide, Vincristine, and Prednisone), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 24% 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.

NCT02162771 phase3completednot on this map

A Phase 3, Randomised, Parallel-Group, Active-Controlled, Double-Blind Study to Demonstrate Equivalence of Pharmacokinetics and Noninferiority of Efficacy for CT-P10 in Comparison With Rituxan, Each Administered in Combination With Cyclophosphamide, Vincristine, and Prednisone (CVP) in Patients With Advanced Follicular Lymphoma

TypeinterventionalSponsorCelltrionRan2014 to 2018Enrolled140ConditionsLymphoma, FollicularArmsRituxan, CT-P10, Cyclophosphamide, Vincristine, Prednisone
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Analysis of 78 Cases of Primary Gastrointestinal Lymphoma.Journal of healthcare engineering · 2022
    Article
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

15 authors at 13 institutions in 9 countries.

Christian BuskeComprehensive Cancer Center Ulm, Institute of Experimental Cancer Research, University Hospital of Ulm, Ulm, Germany.
Wojciech JurczakMaria Sklodowska-Curie National Research Institute of Oncology, Kraków, Poland.ORCID 0000-0003-1879-8084
Juan-Manuel SanchoCatalan Institute of Oncology-Josep Carreras Leukaemia Research Institute - Hospital Germans Trias i Pujol, Badalona, Spain.ORCID 0000-0001-7168-6538
Edvard ZhavridDepartment of Chemotherapy, Alexandrov National Cancer Centre of Belarus, Minsk, Belarus.
Jin Seok KimDepartment of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.ORCID 0000-0001-8986-8436
José-Ángel Hernández-RivasDepartment of Hematology, Hospital Universitario Infanta Leonor, Universidad Complutense, Madrid, Spain.ORCID 0000-0003-4550-757X
Aliaksandr ProkharauDepartment of Oncology, Minsk City Clinical Oncology Dispensary, Minsk, Belarus.ORCID 0000-0002-9429-0138
Mariana VasilicaHematology Department, Fundeni Clinical Institute, Bucharest, Romania.
Rajnish NagarkarCurie Manavata Cancer Centre, Nashik, India.
Larry KwakDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA.
Won-Seog KimDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University, Seoul, South Korea.
SangJoon LeeCelltrion, Inc., Incheon, South Korea; and.ORCID 0000-0001-9897-2163
SungHyun KimCelltrion, Inc., Incheon, South Korea; and.
KeumYoung AhnCelltrion, Inc., Incheon, South Korea; and.
Michinori OguraDepartment of Hematology and Oncology, Kasugai Municipal Hospital, Kasugai, Japan.ORCID 0000-0002-6853-4688
Celltrion (South Korea) · KR9th City Clinical Hospital · BYCity of Hope · USHCG Cancer Centre · INHospital Universitario Infanta Leonor · ESInstitutul Clinic Fundeni · ROJosep Carreras Leukaemia Research Institute · ESKasugai Municipal Hospital · JPN.N. Alexandrov National Cancer Centre · BYSamsung Medical Center · KRThe Maria Sklodowska-Curie National Research Institute of Oncology · PLUniversity Hospital Ulm · DEYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rituximab biosimilars are a cornerstone of treatment of advanced-stage follicular lymphoma (FL). This double-blind, parallel-group, phase 3 trial randomized (1:1) adults (≥18 years) with stage III to IV indolent B-cell lymphoma, including grades 1 to 3a FL, to receive CT-P10 or rituximab (375 mg/m2 IV), with cyclophosphamide, vincristine, and prednisone, every 3 weeks for 8 cycles (induction period). Patients achieving complete response (CR), unconfirmed CR, or partial response (PR) received CT-P10 or rituximab maintenance for 2 years (375 mg/m2, every 8 weeks). Primary end points were previously reported, proving noninferiority of efficacy and pharmacokinetic equivalence of CT-P10 to rituximab. Secondary end points included overall response rate (PR+CR) during the induction period per 2007 International Working Group (IWG) criteria, survival analyses, and overall safety. Between 28 July 2014 and 29 December 2015, 140 patients were randomized (70 per group). Median follow-up was 39.9 months (interquartile range, 36.7-43.5). Per 1999 IWG criteria, 4-year Kaplan-Meier estimates (95% confidence interval [CI]) for CT-P10 and rituximab were 61% (47% to 73%) and 55% (36% to 70%) for progression-free survival (hazard ratio, 1.33 [95% CI, 0.67-2.63]; P=.409), respectively, and 88% (77% to 94%) and 93% (83% to 97%) for overall survival (5.29 [0.84-33.53]; P=.077). Overall, 90% (CT-P10) and 86% (rituximab) of patients experienced treatment-emergent adverse events. Long-term safety profiles were similar between groups. Findings confirm favorable outcomes for CT-P10-treated patients with advanced-stage FL and demonstrate comparable long-term efficacy and overall safety between CT-P10 and rituximab. This trial was registered at www.clinicaltrials.gov as #NCT02162771.

Indexed as

Biosimilar PharmaceuticalsLymphoma, FollicularAntibodies, Monoclonal, Murine-DerivedHumansRituximabAntibodies, Monoclonal, Murine-DerivedBiosimilar PharmaceuticalsCT-P10Rituximab

Identifiers

PMID34477816
PMCPMC8525228
OpenAlexW3198467013

What OpenQuestion holds

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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.