Hydrogenology
Hydrogenology editorial study record

Two weeks of hydrogen inhalation can significantly reverse adaptive and innate immune system senescence patients with advanced non-small cell lung cancer: a self-controlled study

Chen JB et al. · Med Gas Res. 2020;10(4):149–154.

HumanInhaled H₂Published 2020
Study record, not medical adviceThis page reports one source and Hydrogenology’s source-text extraction. It does not establish that molecular hydrogen is effective, safe or appropriate for any person. Human, animal and laboratory evidence must not be treated as equivalent.
Source and classification

What kind of evidence is this?

Evidence stream

Human

Reported design

Uncontrolled self-comparison study

Research topic

Cancer research

Administration classification

Inhaled H₂

Study result signal

Not reported in this record.

Outcome type

Not reported in this record.

Reported in the source

Methods at a glance

Population or model

Adults with advanced non-small cell lung cancer awaiting standard treatment

Sample

20 participants

Duration

4 hours daily for 2 weeks

Intervention

Nasal cannula or mask inhalation at 3,000 mL/min for 4 hours daily

Hydrogen form

Brown’s gas / oxyhydrogen — H₂ and O₂ co-delivered, not H₂ alone.

H₂ specification

66.7% H₂ + 33.3% O₂ by volume.

H₂ flow

2,001 mL/min H₂, calculated as 3,000 mL/min total mixed-gas flow × 66.7% H₂.

O₂ delivered with H₂

999 mL/min O₂, calculated as 3,000 mL/min × 33.3% O₂.

Comparator

No concurrent control group; each participant was compared with their own baseline

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Peripheral-blood adaptive and innate lymphocyte subsets

Reported result

Multiple immune-cell subset measures moved toward the ranges used by the authors after two weeks. No tumor response, progression or survival outcome was tested.

Results-extraction completeness

Gas composition, flow, methods, principal results, funding and conflict statement checked in the open-access full text; independent appraisal remains incomplete.

A reported association, difference or mechanism is not automatically a clinical benefit. Null findings, outcome type, study design and precision all matter.

Interpretation limits

Cautions and applicability

Design and reporting cautions

Uncontrolled 20-person biomarker study with many lymphocyte measures and only two weeks of follow-up. It does not establish cancer treatment benefit. Authors reported no financial support or conflicts.

Applies directly to

Adults with advanced NSCLC awaiting standard treatment; not evidence for tumor control or improved survival.

Preliminary appraisal framework

Not reported in this record.

Preliminary risk-of-bias status

Not reported in this record.

Appraisal rationale

Not reported in this record.

No single-study GRADE certainty rating is assigned. Certainty is assessed by important outcome across a complete eligible evidence set, not by attaching a final grade to one source.

Provenance

Sources and record status

Identifiers

PMID: 33380580 · DOI: 10.4103/2045-9912.304221

Publisher access

Open-access full text is available through PMC.

Extraction basis

Open-access PMC full text and PubMed bibliographic record.

Record revision

2026-08-10