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NCT Number: NCT06427447

Adjuvant Chemoradiotherapy Versus Chemotherapy for Pancreatic Cancer (ADJUPANC)

In this trial, we aim to compare the outcomes of adjuvant chemoradiotherapy with chemotherapy for patients with resected pancreatic cancer who are at high risk of disease progressions.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Huojun Zhang

Shanghai, Shanghai Municipality, 200433, China

Location status: Recruiting

Location contact

Huojun Zhang, M.D.

PRINCIPAL_INVESTIGATOR

Xiaofei Zhu, M.D.

CONTACT

[email protected]

86-021-31162222

About this study

Pancreatic cancer is a lethal malignancy with the lowest 5-year overall survival rate of 9% and an increasing incidence. In China, the mortality of pancreatic cancer ranked the sixth among all cancers. Although surgical resection is the only radical treatment, only less than 20% patients could receive upfront surgery at the initial diagnosis. Even though patients have surgery, the incidence of disease progressions, including local progression and metastasis, is about 80-90%. In NCCN guidelines and Chinese guidelines, adjuvant chemotherapy is recommended for post-operative pancreatic cancer, while adjuvant chemoradiotherapy could also be used. However, it has not been clarified that which patients may benefit from adjuvant chemoradiotherapy, and no high-level evidence has shown the advantages of adjuvant chemoradiotherapy over chemotherapy. In meta-analyses, it was demonstrated that patients with lymph nodes metastases, R1 or R2 resection or lymphovascular invasion could achieve longer survival after adjuvant chemoradiotherapy compared with chemotherapy. Therefore, we aim to compare the outcomes of adjuvant chemoradiotherapy with those of chemotherapy in patients with lymph nodes metastases, R1 or R2 resection or lymphovascular invasion after surgical resection of pancreatic cancer.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 18-75 years
  • Pathologically confirmed pancreatic ductal adenocarcinoma
  • Pathologically confirmed lymph node metastasis, R1 or R2 resection or lymphovascular invasion (one of the risk factors)
  • No history of cancer treatment after surgical resection
  • No disease progression confirmed by imaging examinations
  • ECOG 0 to1 point
  • No abnormality in blood routine test, liver and kidney function test and coagulation test (White blood cell count ≥4.0×10^9/L, neutrophil count ≥2.0×10^9, hemoglobin level ≥100g/L, platelet count ≥100×10^9/L, ALT and AST level < 2.5 times the upper limit of normal, total bilirubin and creatinine level within the normal, international normalized ratio <2)

Exclusion criteria

  • History of cancer treatment after surgical resection
  • History of other cancers within 5 years
  • Disease progression, including local pprogression or metastasis, confirmed by imaging examinations
  • ECOG ≥2 points
  • Significant abnormality in blood routine test, liver and kidney function test and coagulation test
  • Active inflammatory bowel disease
  • Gastrointestinal bleeding or perforation within 6 months
  • Infections requiring antibiotics
  • Heart or respirotory insufficiency
  • Pregnant women or breastfeeding women

Treatment and study plan

Adjuvant chemoradiotherapy

Combination Product

Upfront chemotherapy (gemcitabine plus capecitabine) followed chemoradiotherapy (radiotherapy with concurrent capecitabine)

Adjuvant chemotherapy

Drug

Chemotherapy (gemcitabine plus capecitabine)

Primary outcomes

  1. Disease progression free survival will be determined.

    Time frame: 3 years

    The time from the start of treatment until documentation of any clinical or radiological disease progression or death, whichever occurred first. Progression is assessed by the Response Evaluation Criteria in Solid Tumors (RECIST; version 1.1), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions.

Secondary outcomes

  1. Overall survival will be determined.

    Time frame: 3 years

    The time from the randomization to death.

  2. Treatment-related adverse events will be determined.

    Time frame: 3 years

    Treatment-related adverse effects are determined by National Cancer Institute Common Toxicity Criteria for Adverse Events (CTCAE) version 5.0.

  3. Quality of life will be determined.

    Time frame: 3 years

    The analysis of quality of life is based on European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (QLQ-C30). All scales and subscales range from 0 to 100. Regarding physical functioning, role functioning, emotional functioning, cognitive functioning, social functioning and global health, higher scores may indicate better outcomes. In the case of fatigue, nausea and vomitting, pain, dyspnea, insomina, appetite loss, constipation, diarrhea and financial difficulties, lower scores may indicate better outcomes. Scales of all items are independent and not combined to compute a total score.

Study contacts

Contact information is provided by the study sponsor or research team.

Xiaofei Zhu

CONTACT

[email protected]

86-021-31162222

Sponsors and collaborators

Lead sponsor

Changhai Hospital

Other

Registry information

Official study title

Adjuvant Chemoradiotherapy Versus Chemotherapy for Post-operative Pancreatic Cancer

Acronym: ADJUPANC

Important dates

Study start
2024
Primary completion
2028
Study completion
2029
First posted
May 23, 2024
Registry last updated
Feb 4, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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