Overview

Carboplatin-Paclitaxel Adjuvant Chemotherapy in the Treatment of Locally Advanced Cervical Cancer

Status:
Recruiting
Trial end date:
2023-12-01
Target enrollment:
0
Participant gender:
Female
Summary
This is a mutlicentric, open-label non-randomized, national, 1-stage phase II trial to assess efficacy and safety of a weekly Carboplatin-Paclitaxel adjuvant chemotherapy after intensity modulated extended-field chemoradiation in patient suffering from of locally advanced cervical cancer with para-aortic positive nodes.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Centre Oscar Lambret
Treatments:
Albumin-Bound Paclitaxel
Carboplatin
Paclitaxel
Criteria
PART 1:

Inclusion Criteria:

- Female patient aged more than 18 years old

- Histological diagnosis of squamous cell carcinoma, adenocarcinoma or adenosquamous
cell carcinoma of the cervix

- With locally advanced cervical cancer (FIGO stage IB1, IB2, II, IIIB or IVA disease)

- With para-aortic or iliac common nodes positive on PET-scan or after laparoscopic
surgical staging if PET-scan negative

- ECOG Performance Status ≤ 2

- Adequate hematologic function: Absolute Neutrophil Count (ANC) ≥ 1,500/mm3, platelets
≥ 100,000/mm3, hemoglobin ≥ 10g/dL

- Adequate renal function: creatinine clearance (estimated according to MDRD formula) ≥
60ml/min/1.73m²

- Adequate hepatic function: Aspartate aminotransferase (ALT)/ Alanine aminotransferase
(ALT) ≤ 2.5 × upper normal limit (UNL); Total bilirubin ≤ 1.5 x UNL (except in case of
Gilbert's disease)

- Negative serum pregnancy test within 7 days prior to treatment for women of
childbearing potential. For non-menopaused women, if not surgically sterilized,
willing to accept the use of an effective contraceptive regimen during the treatment
period and at least 6 months after the end of treatment

- Absence of contraindication to receive the products used in this study (products used
in concomitant/ adjuvant chemotherapy) according to the most recent SmPC of these
products (available at http://base-donnees-publique.medicaments.gouv.fr/)

- Patient is willing and able to comply with the protocol for the duration of the study
including undergoing treatment and scheduled visits and examinations including
follow-up

- Patient covered by the French "Social Security" regime

- Signed informed consent form

Exclusion Criteria:

- Histological diagnosis of sarcoma

- Previous hysterectomy or planned hysterectomy as part of their initial cervix cancer
therapy,

- Presence of distant metastases other than lombo-aortic lymph nodes

- Patient with other invasive malignancies, with the exception of non-melanoma skin
cancer, who had (or have) any evidence of the other cancer present within the last 5
years

- Patient with bilateral hydronephrosis unless at least one side has been stented

- Prior diagnosis of Crohn's disease or ulcerative colitis or sclerodermia

- Other uncontrolled intercurrent disease including, but not limited to: active
infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac
arrhythmia

- Known hypersensitivity to any of the study drugs, study drug classes, or excipients in
the formulation

- Pregnant or breastfeeding woman,

- Participation in another therapeutic trial with an experimental molecule for the
current disease

- Psychiatric illness or social situation that would limit compliance with study
requirement, substantially increase the risk of side effects, or compromise the
ability of the patient to give written informed consent

- Inability to comply with medical follow-up of the trial (geographical, social or
psychic reasons)

- Person under guardianship or curatorship

PART 2:

Inclusion Criteria:

- Maintained consent

- Adequate hematologic function: Absolute Neutrophil Count (ANC) ≥ 1,500/mm3, platelets
≥ 100,000/mm3, hemoglobin ≥ 10g/dL

- Adequate renal function: creatinine clearance (estimated according to MDRD formula) ≥
60ml/min/1.73m2

- Adequate hepatic function: Aspartate aminotransferase (ALT)/ Alanine aminotransferase
(ALT) ≤ 2.5 × upper normal limit (UNL); Total bilirubin ≤ 1.5 x UNL (except in case of
Gilbert's disease)

- Patient having received curative intent chemo-radiation therapy with the following
recommendations:

- extended field CT-RT delivered by IMRT: 45-50Gy according the dosimetry
limitation histogram dose volume (HDV) in whole pelvis and Para Aortic volumes +
concomitant boost on macroscopic nodes defined as PET-positive

- associated with weekly Cisplatin (40mg/m²)

- followed by image guided brachytherapy. Patient will be eligible even in case of
temporary stop of radiation therapy, provided she has received a total dose of
45Gy and a concomitant boost. Patient should have received at least 3 injections
of Cisplatin 40mg/m² during radiation therapy.

Exclusion Criteria:

- Progression during Part 1,

- Contraindication for one of the study drug in particular the residual toxicity of Part
1 (radio-chemotherapy) such as:

- Renal failure (defined as creatinine clearance according to MDRD formula < 60 mL/
min/1.73m2),

- Any clinical residual toxicity (including peripheral neuropathy) ≥ grade 2 (as
per CTCAE v5),

- Radiation therapy prematurely stopped (total dose on whole pelvis and on nodes not
received)

- Cumulative dose of Cisplatin received less than 120 mg/m².