Evidence map›Paper›PMID 32777066›Full record

Trial reportBlood advances2020

Prospective long-term follow-up after first-line subcutaneous cladribine in hairy cell leukemia: a SAKK trial.

Rudolf Benz, Kornelius Arn, Martin Andres, Thomas Pabst, Michael Baumann, Urban Novak, Felicitas Hitz, Urs Hess, Reinhard Zenhaeusern, Yves Chalandon and 14 more

Open access · goldAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Blood advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Guideline
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Skin changes in hairy cell leukemia.Annals of hematology · 2021
    Review
  13. Review
  14. 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

24 authors at 16 institutions in 1 country.

Rudolf BenzDivision of Hematology and Oncology, Kantonsspital Muensterlingen, Muensterlingen, Switzerland.
Kornelius ArnDepartment of Hematology, Kantonsspital Luzern, Luzern, Switzerland.
Martin AndresDepartment of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Thomas PabstDepartment of Medical Oncology, Inselspital Bern, Bern, Switzerland.
Michael BaumannCenter for Laboratory Medicine St. Gallen, St. Gallen, Switzerland.
Urban NovakDepartment of Medical Oncology, Inselspital Bern, Bern, Switzerland.
Felicitas HitzDepartment of Oncology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Urs HessDepartment of Oncology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Reinhard ZenhaeusernDepartment of Oncology Spitalzentrum Oberwallis, Brig, Switzerland.
Yves ChalandonHematology Division, University Hospital Geneva and Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Ulrich MeyOncology and Hematology, Kantonsspital Graubuenden, Graubuenden, Switzerland.
Sabine BlumService of Hematology, University Hospital Lausanne, Lausanne, Switzerland.
Daniel RauchDepartment of Oncology, Spital Thun, Thun, Switzerland.
Alix O'Meara SternDepartment of Oncology, Kantonsspital Neuchatel, Neuchatel, Switzerland.
Nathan CantoniDivision of Hematology and Transfusionmedicine, Kantonsspital Aarau, Aarau, Switzerland.
Mario BargetziDivision of Hematology and Transfusionmedicine, Kantonsspital Aarau, Aarau, Switzerland.
Elena Bianchi-PapinaDepartment of Hematology, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
Davide RossiDepartment of Hematology, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
Jakob PasswegDepartment of Hematology, University Hospital Basel, Basel, Switzerland.
Andreas LohriDepartment of Oncology, Kantonsspital Baselland Liestal, Liestal, Switzerland.
Simona BerardiSwiss Group for Clinical Cancer Research (SAKK) Coordinating Center, Bern, Switzerland; and.
Qiyu LiSwiss Group for Clinical Cancer Research (SAKK) Coordinating Center, Bern, Switzerland; and.
Anita FellerFoundation National Institute for Cancer Epidemiology and Registration, University of Zurich, Zurich, Switzerland.
Georg StussiDepartment of Hematology, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
Institute of Oncology Research · CHKantonsspital Aarau · CHKantonsspital St. Gallen · CHSwiss Group For Clinical Cancer Research · CHUniversity Hospital of Bern · CHHospital Neuchâtel · CHKantonsspital Baselland · CHKantonsspital Graubünden · CHKantonsspital Münsterlingen · CHLuzerner Kantonsspital · CHSpital Thurgau (Switzerland) · CHUniversity Hospital of Basel · CHUniversity of Bern · CHUniversity of Geneva · CHUniversity of St.Gallen · CHUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hairy cell leukemia (HCL) remains an incurable disease. However, first-line treatment with either intravenous or subcutaneous cladribine generally leads to long-lasting remissions. Although there are excellent long-term data for intravenous application, similar data regarding subcutaneous administration are lacking. We therefore analyzed the long-term outcome of 3 prospective multicenter clinical trials on subcutaneous cladribine performed by the Swiss Group for Clinical Cancer Research (SAKK), which recruited 221 patients with classical HCL between 1993 and 2005. Median overall survival from start of treatment was not reached. Pretreatment anemia, higher Eastern Cooperative Oncology Group score, and higher age were associated with poorer overall survival in multivariable analysis, whereas early progression at 24 and 36 months had no significant impact on overall survival. Second-line treatment was necessary in 53 (23.7%) patients after a median of 5 (range, 0.2-20.4) years, and first retreatment was mainly monotherapy with cladribine (66%) or rituximab (15.1%) or a combination of these drugs (15.1%). A total of 44 (19.9%) patients developed second primary malignancies with a median time to occurrence of 5.7 (range, 0.01-17.5) years. Second primary malignancies were the main cause for death (14; 27.5%). Compared with a matched normal Swiss population, the incidence of second primary malignancies was not increased. However, survival of patients with HCL was slightly inferior by comparison (P = .036). In conclusion, the outcome of HCL patients treated with subcutaneous cladribine is excellent, and in most patients, 1 cycle of subcutaneous cladribine is sufficient for long-term disease control.

Indexed as

Antineoplastic AgentsLeukemia, Hairy CellChild, PreschoolCladribineFollow-Up StudiesHumansProspective StudiesAntineoplastic AgentsCladribine

Identifiers

PMID32777066
PMCPMC7422123
OpenAlexW3048088359

What OpenQuestion holds

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Registered trials

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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.