A Study of Additional Chemotherapy After Surgery for People With Malignant Peritoneal Mesothelioma

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorMemorial Sloan Kettering Cancer Center

About this trial

The purpose of this study is to find out whether intraperitoneal or intravenous chemotherapy given after cytoreductive surgery and HIPEC are effective treatments for people with malignant peritoneal mesothelioma. Outcomes will be compared by observing intraperitoneal versus intravenous treatments to analyze if one is better than the other.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patient age 18 years or older, both sexes.

Clinical diagnosis of MPM at enrolling institution.

Prior to randomization, intraoperative pathologic confirmation of epithelioid MPM at enrolling institution.

Complete or near-complete CRS achieved.

Disqualifiers

Subjects who have previously undergone intraperitoneal chemotherapy or systemic chemotherapy/immunotherapy for peritoneal mesothelioma.

Subjects who have previously received platinum-containing chemotherapy regimens.

Subjects with preoperative or intraoperative biopsy consistent with sarcomatoid mesothelioma, well-differentiated papillary mesothelioma, or benign multicystic mesothelioma.

Other prior malignancies, except for cured non-melanoma skin cancer, curatively treated in situ carcinoma of the cervix, adequately treated malignancies for which there has been no evidence of activity for more than three years, or indolent tumors for which observation over two years is a reasonable option.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Pemetrexed

    Drug

    Pemetrexed will be administered intravenously

  • Cisplatin

    Drug

    Cisplatin will be administered intravenously

  • Carboplatin

    Drug

    Possible substitution with carboplatin based on clinician discretion

Treatment groups

64 Participants
are divided into 2 treatment groups
Group A: IVC armExperimental treatment 3 interventions
Group B: NIPC armActive comparator 3 interventions

Trial outcomes

Primary outcomes

1

Progression Free Survival

Progression Free Survival in the two treatment arms.

Time frame
up to 24 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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