Actively Recruiting

Phase 2
Age: 18Years - 70Years
FEMALE
NCT03101995

Assessment of Gemcitabine as Chemoradiotherapy in Patients With Locally Advanced Carcinoma of Cervix and Renal Disease

Led by National Institute of Cancerología · Updated on 2025-05-28

18

Participants Needed

1

Research Sites

406 weeks

Total Duration

On this page

Sponsors

N

National Institute of Cancerología

Lead Sponsor

I

Instituto Nacional de Cardiologia Ignacio Chavez

Collaborating Sponsor

AI-Summary

What this Trial Is About

From the global burden of Cervical Cancer (CC), 85% occurs in developing countries, representing 12% of cancer in women. In Mexico CC ranks second in incidence and mortality among women. The National Institute of Cancer in Mexico (lNCAN) receives annually about 500 patients with CC, 80% of which are diagnosed with locally advanced disease. Furthermore, 10 to 20% of these present kidney deterioration. The main reason for kidney disease is ureteral obstruction, other causes include age and comorbidities, such as diabetes and hypertension. The standard treatment for locally advanced disease consists in concomitant chemo-radiotherapy based on cisplatin (QT-RT), followed by brachytherapy, with an absolute benefit of 10%. However, the use of cisplatin in patients with renal disease may be questionable, considering it is a nephrotoxic treatment. Given that renal dysfunction limits the standard treatment efficiency because of the widely known nephrotoxicity of cisplatin, in most Cancer Centers of our country, patients with renal dysfunction receive only radiation therapy, even though it has proven less effective than concomitant QT-RT, limiting disease-free and overall survival of these patients. Venook et al. used gemcitabine as a radiosensitizer in patients with cancer and renal dysfunction. Our group, has observed encouraging results using gemcitabine as an alternative to cisplatin in concomitant treatment with radiotherapy, in CC patients with renal insufficiency. 89% of patients had complete response and improvement in renal function, with an enhanced creatinine clearance after treatment. Therefore, it is necessary to explore the safety of gemcitabine as an alternative treatment for CC patients with locally advanced disease and renal deterioration. We propose this clinical trial to assess the safety of treatment with gemcitabine and specifically on renal function in patients with renal deterioration. It is important to take into consideration that CC in advanced stages produces pain, transvaginal fetid discharge and general discomfort. It also causes side effects secondary to renal failure such as nausea, vomiting, fatigue, anemia, among others. These effects have a significant impact on the quality of life of these patients. Cancer treatment and its side effects, besides the implications of a nephrostomy catheter or ileostomy bag, determine the deterioration in the quality of life of the patient, during and sometimes after treatment. Thus it is of utmost importance to evaluate the factors that could help improve the quality of life of patients and explore the factors that deteriorate it. This clinical trial aims to generate scientific evidence to help make the best decisions concerning the treatment of patients with cervical cancer and renal impairment, and the impact on their quality of life.

CONDITIONS

Official Title

Assessment of Gemcitabine as Chemoradiotherapy in Patients With Locally Advanced Carcinoma of Cervix and Renal Disease

Who Can Participate

Age: 18Years - 70Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women aged 18 to 70 years who provide written consent
  • Negative pregnancy test for women of childbearing age before treatment
  • Agrees to use approved contraception during study and 12 weeks after treatment
  • Postmenopausal women with prior bilateral oophorectomy, or age ≥60, or amenorrhea ≥12 months with hormonal confirmation
  • Diagnosed with cervical cancer stage IB2 to IVA, with or without small retroperitoneal lymph nodes
  • Histologic confirmation of squamous, adenosquamous, adenocarcinoma, or glassy cell carcinoma
  • No prior treatment and medically fit for gemcitabine
  • Measurable disease by CT or MRI according to RECIST criteria
  • Functional status 0-3 by WHO criteria
  • Renal dysfunction defined as glomerular filtration rate <60 ml/min/1.73m2
  • Normal blood counts and liver function (hemoglobin >10 g/L, leucocytes >4000/mm3, platelets >100,000/mm3, bilirubin ≤1.5x upper normal limit, transaminases <1.5x upper normal limit)
  • Normal chest X-ray
Not Eligible

You will not qualify if you...

  • Prior or concurrent cancers except non-melanoma skin cancer
  • Diabetes or hypertension with retinopathy or albuminuria >300
  • Active tuberculosis infection
  • HIV infection
  • History of systemic lupus erythematosus or other rheumatologic kidney diseases
  • Presence of vesicovaginal or vesicorectal fistula at diagnosis
  • Uncontrolled diseases including active infections, heart failure, unstable angina, arrhythmia, decompensated diabetes, difficult-to-control hypertension, or psychiatric illness
  • Concurrent treatment with other experimental drugs
  • Social, family, or geographic factors suggesting poor study adherence
  • Pregnancy
  • Disease progression or unacceptable toxicity during study
  • Inappropriate inclusion violating starting criteria

AI-Screening

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Trial Site Locations

Total: 1 location

1

National Institute of Cancer

Mexico City, Mexico City, Mexico, 14080

Actively Recruiting

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Research Team

L

Lucely C Cetina, MD, M.Sc.

CONTACT

R

Roberto Jiménez, MD, M.Sc.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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