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RecruitingNCT06389201Updated Feb 18, 2025

Pretreatment With HCQ Before Radiotherapy and Chemotherapy in Advanced NPC Patients

An interventional study of HCQ and Placebo in Nasopharyngeal Carcinoma, sponsored by Affiliated Hospital of Nantong University. Recruiting at 1 site in China. Open to participants aged 20 Years to 70 Years. Per ClinicalTrials.gov, last updated 2025-02-18.

Sponsored by Affiliated Hospital of Nantong University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Aug 2024; still recruiting 2 years 2 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
20 Years to 70 Years
Sex
All
01

Study summary

Dormant cancer cells that survive anti-cancer therapy can lead to cancer recurrence and disseminated metastases that prove fatal in most cases. Recently, specific dormant polyploid giant cancer cells (PGCC) have drawn the investigators' attention because of their association with the clinical risk of nasopharyngeal carcinoma (NPC) recurrence, as demonstrated by previous clinical data. In study, the investigators report the biological properties of PGCC, and reveal that autophagy is a critical mechanism of PGCC induction. Moreover, pharmacological inhibition of autophagy greatly impaired PGCC formation, significantly suppressing metastasis and improving survival in a mouse model. Mechanistically, chemotherapeutic drugs partly damaged mitochondria, and activated autophagy to promote PGCC formation. High numbers of PGCCs correlated with shorter recurrence time and worse survival outcomes in NPC patients. Collectively, these findings suggest a therapeutic approach of targeting dormant PGCCs in cancer.

Pretreatment with an autophagy inhibitor (HCQ) before chemotherapy and radiotherapy could prevent formation of therapy-induced dormant polyploid giant cancer cells, thereby reducing recurrence and metastasis of nasopharyngeal carcinoma.

Read the detailed description

Although the majority of patients with nasopharyngeal carcinoma (NPC) do not present with overt metastases at diagnosis, a significant number succumb to disseminated disease years after the successful treatment of the primary tumor. Thus, late NPC recurrence may be the result of rare and elusive dormant cancer cells hiding in specialized niches being reactivated by specific signals. The concept of cancer dormancy has been described for the most common solid and hematological cancers; however, the dormant cancer cells in NPC remain largely uncharacterized.

Although many factors contribute toward cancer cell dormancy, recent studies have demonstrated that cancer therapy can induce cellular dormancy. Indeed, therapy-induced dormancy has been shown to lead to durable proliferation arrest, resulting in the formation of polyploid giant cancer cells (PGCCs), which are a unique sub-population of cancer cells that contribute toward the heterogeneity of solid tumors. Unlike regular-sized diploid cancer cells, PGCCs display distinct morphological features, including a large cytoplasmic area and a high genomic content contained within a single highly enlarged nucleus or multiple nuclei. Despite being present in low numbers, the frequency of PGCCs increases markedly after exposure to hypoxia and therapeutic interventions such as radiotherapy and chemotherapies.

The investigators' findings, which used a highly relevant clinical orthotopic model of imageable NPC and clinical data, suggest that autophagy inhibition (HCQ) prevents therapy-induced dormant PGCC formation and thereby prevents NPC metastasis.

02

Conditions studied

  • Nasopharyngeal Carcinoma

Keywords

  • autophagy
  • tumor dormancy
  • nasopharyngeal carcinoma
  • recurrence
  • metastasis
03

In context

Nasopharyngeal Carcinoma

816 studies on the registry are indexed under Nasopharyngeal Carcinoma; 282 are open to participants now.

This study's planned enrollment of 30 is below the median of 84 across 668 interventional studies indexed under Nasopharyngeal Carcinoma.

Browse Nasopharyngeal Carcinoma studies →

Lead sponsor

Affiliated Hospital of Nantong University is the lead sponsor of 92 studies on the registry; 53 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Clinical diagnosis of NPC.
  • Have not received any cancer therapies
  • Must provide informed consent

Exclusion criteria

Exclusion Criteria:

  • With metastasis before the first treatment.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Pretreatment with an autophagy inhibitor (HCQ) before chemotherapy and radiotherapy

    Hydroxychloroquine (HCQ), is used one day before chemotherapy and radiotherapy, 400-600mg, oral tablet, once. During chemotherapy and radiotherapy, HCQ maintenance dose is 200-400mg daily.

    Drug: HCQ

  • Placebo comparator
    Receive placebo before and during chemotherapy and radiotherapy

    Placebos are used one day before chemotherapy and radiotherapy, and during the therapy.

    Other: Placebo

Interventions

  • DrugHCQ

    HCQ, 400-600mg, oral tablet, once, one day before chemotherapy and radiotherapy. During therapy, HCQ maintenance dose is 200-400mg daily.

    Also known as: Hydroxychloroquine

  • OtherPlacebo

    Placebo, oral tablet, once, one day before chemotherapy and radiotherapy. During therapy, placebo maintenance oral tablet once daily.

06

What researchers measure

Primary outcomes

  1. Recurrence and metastasis

    After the patients are diagnosed and treated, CT scans is used semi-annually to determine the progression, recurrence and metastasis of tumor.

    Time frame: Five to Ten years.

07

Study locations

1 of 1 sites recruiting
  • Bo You
    Nantong, Jiangsu 226000, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — Study protocol, statistical analysis plan, informed consent form, clinical study report, and analytic code will be shared to other researchers.

Supporting information: Study protocol, Sap, Icf, Csr, Analytic code

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 18, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06389201
Lead sponsor
Affiliated Hospital of Nantong University
Responsible party
Sponsor
First posted
Apr 29, 2024
Start date
Aug 1, 2024
Primary completion
Aug 1, 2029 (estimated)
Completion
Aug 1, 2034 (estimated)
Last update
Feb 18, 2025

Study contacts

Bo You, Doctor
Contact
youbo19891014@163.com
+8615851358688 ext. +8615851358688
Bo You, Doctor
principal investigator · Department of Otorhinolaryngology-Head and Neck Surgery, Affiliated Hospital of Nantong University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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