Evidence map›Paper›PMID 27066340›Full record

ArticleSpringerPlus2016

Response-adapted treatment with upfront high-dose chemotherapy followed by autologous stem-cell transplantation rescue or consolidation phase high-dose methotrexate for primary central nervous system lymphoma: a long-term mono-center study.

Yoko Nakasu, Koichi Mitsuya, Nakamasa Hayashi, Ikue Okamura, Keita Mori, Terukazu Enami, Raine Tatara, Satoshi Nakasu, Takashi Ikeda

Abstract read
In one paragraph

Article in SpringerPlus, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
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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

9 authors.

Yoko NakasuDivision of Neurosurgery, Shizuoka Cancer Center, Nagaizumi, Sunto, Shizuoka, 4118777 Japan.
Koichi MitsuyaDivision of Neurosurgery, Shizuoka Cancer Center, Nagaizumi, Sunto, Shizuoka, 4118777 Japan.
Nakamasa HayashiDivision of Neurosurgery, Shizuoka Cancer Center, Nagaizumi, Sunto, Shizuoka, 4118777 Japan.
Ikue OkamuraDivision of Stem Cell Transplantation, Shizuoka Cancer Center, Nagaizumi, Sunto, Shizuoka, 4118777 Japan.
Keita MoriDivision of Biostatics, Shizuoka Cancer Center, Nagaizumi, Sunto, Shizuoka, 4118777 Japan.
Terukazu EnamiDivision of Stem Cell Transplantation, Shizuoka Cancer Center, Nagaizumi, Sunto, Shizuoka, 4118777 Japan.
Raine TataraDivision of Stem Cell Transplantation, Shizuoka Cancer Center, Nagaizumi, Sunto, Shizuoka, 4118777 Japan.
Satoshi NakasuDivision of Neurooncology, Kusatsu General Hospital, Yabase, Kusatsu, Shiga, 5250066 Japan.
Takashi IkedaDivision of Stem Cell Transplantation, Shizuoka Cancer Center, Nagaizumi, Sunto, Shizuoka, 4118777 Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment regimens for primary central nervous system lymphoma (PCNSL) include high-dose methotrexate (HD-MTX)-based chemotherapy, with or without radiotherapy and are based on studies of selected patient groups. This retrospective study assessed a consistent strategy of response-adapted protocol applied for patients including age >65 years in a cancer center for 10 years longitudinally. Case notes were studied of 61 consecutively treated patients with PCNSL histologically diagnosed between 2003 and 2013. Clinical follow-up during and after treatment included neurologic examination and magnetic resonance imaging. Of the patients studied, 14.8 % (9/61) were clinically unfit for chemotherapy; the remaining 85.2 % (52/61) of patients were treated with HD-MTX. Of these patients, 58 % (30/52) achieved an initial complete response, with a median survival of 100.1 months. Of these response-adapted patients, 33 % (10/30) were <65 years and were treated with upfront high-dose chemotherapy and autologous stem-cell transplantation (HDC-ASCT). The remaining response-adapted patients included 53 % (16/30) who were ≥65 years underwent consolidation with HD-MTX, and 14 % (4/30) who chose radiotherapy. The median survival of patients with HDC-ASCT had not yet been reached compared with 67.6 months for patients with HD-MTX consolidation treatment (p = 0.26). At the end of the study, 75 % (39/52) of patients had died mainly owing to progression or relapse of PCNSL. Multivariate analysis showed that age younger than 65 years (p = 0.02) and complete response for up-front HD-MTX (p = 0.001) were independent prognostic indicators of overall survival. In conclusion, this single-center retrospective clinical study has shown that treatment of PCNSL with upfront HDC-ASCT and consolidation phase HD-MTX monotherapy may be feasible, even for elderly patients in a routine clinical setting, using the three-step selection by eligibility and response to initial HD-MTX, and age threshold of 65 years for ASCT.

Indexed as

Autologous stem-cell transplantChemotherapyMethotrexatePrimary central nervous system lymphomaRadiotherapyRituximab

Identifiers

PMID27066340
PMCPMC4786507

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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.