Chemotherapy for Lung Cancer in HIV-positive Patients

Non-small Cell Lung Cancer Clinical Trial

— CHIVA  

Official title:

Phase II Trial Evaluating the Efficacy and Safety of Carboplatin Plus Pemetrexed in Human Immunodeficiency Virus Positive (HIV+) Patients With Stage III (Not Amenable to Radiation or Inoperable) or Stage IV Nonsquamous Non Small Cell Lung Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01296113
• Other study ID #: IFCT-1001
• Status: Completed
• Phase: Phase 2
• Start date: May 2011
• Est. completion date: July 2017

Study information

• Verified date: March 2023
• Source: Intergroupe Francophone de Cancerologie Thoracique
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a phase II, multicenter, non-randomized, open-label study evaluating the combination of pemetrexed plus carboplatin in HIV-positive patients with lung cancer.

Description:

The use of tritherapy in developed countries starting in 1996 led to a considerable reduction in AIDS mortality due to opportunistic infections and AIDS-defining cancers. However, increased life expectancies were accompanied by a diversification of the causes of death in HIV-infected individuals. In France between 2000 and 2005, non-AIDS-defining mortality rose from 53% to 64%: non-AIDS-defining cancers (apart from hepatocellular carcinoma) had the highest mortality rates, increasing from 11% to 17% in 2005, followed by liver disease (15% in 2005), cardiovascular disease (8% in 2005) and suicide (5%). Among all cancer-related deaths (AIDS- and non-AIDS-defining), the proportion due to non-AIDS-defining cancers (apart from hepatocellular carcinoma) increased from 38% to 50% and lung cancer (LC) accounted for 65% of deaths. Many epidemiological studies have demonstrated an elevated risk of LC in HIV-infected individuals HIV-positive subjects are younger at diagnosis of LC than the general population (45 versus 62 years). In the most recent studies, adenocarcinoma comprised 70% of cases. The prognosis of LC is worse in HIV-positive individuals. Some authors suggest that these poor outcomes may be related to interactions and additive toxicities of the cytotoxic and antiretroviral drugs. It is also likely that the disease is particularly aggressive. In the general population with a PS of 0 or 1 and under 70 years of age, bitherapy improves survival as compared to monotherapy. Survival is higher when the doublet comprises a platin. Since HIV-positive subjects with LC tend to be young, it is logical to offer them the best treatment which has demonstrated efficacy in the general population. In comparison to cisplatin, carboplatin causes less vomiting, nephrotoxicity and neurotoxicity. Survival is very slightly higher with cisplatin, but this comes at the cost of greater toxicity. Carboplatin is better tolerated in subjects with PS=2 or who are over 70 years of age The HIV-positive population is specific in that: - PS is more often altered but the subjects are young, which calls for a platin-based doublet. - HAART is essential and its absorption should not be compromised by repeated vomiting which is more severe with cisplatin. - Nephropathy occurs in 15-38% of cases; the causes are multifactorial and include the HIV virus itself and the antiretroviral drugs (Tenofovir®). - Peripheral neuropathy is frequently related to HIV or to the antiretroviral treatments (especially didanosine or stavudine (2010 YENI report)). - Premature ageing is seen in HIV-positive subjects; this exposes them to increased cardiovascular risk and a higher frequency of heart disease which can restrict the hyper-hydration required when using cisplatin. - In 2010, virtually all patients are treated on an ambulatory basis whereas in the past they would have been hospitalized. Carboplatin is administered in the day hospital of all the centers, but not cisplatin. - It is important to preserve an optimal quality of life during the first line of therapy in these patients whose life expectancy is such that very few will be eligible for a second round of therapy. Scagliotti published a phase III trial comparing cisplatin plus pemetrexed with cisplatin plus gemcitabine in subjects < 70 years old with advanced-stage NSCLC. Overall survival was identical in both arms but the toxicity profile was in favor of the pemetrexed arm. The combination of first-line carboplatin plus pemetrexed has been evaluated in several phase II trials, particularly in subjects with a poor PS. In contrast to the taxanes or vinorelbine, for example, pemetrexed is not metabolized by CYP450, which facilitates its use in combination with protease inhibitors and NNRTI, which respectively inhibit or induce the CYP450 system. Ancillary study BIO-IFCT-1001 will be made. Since the samples will be small, focus will be on the biomarkers associated with multiple or specific resistance to platinum salts or to pemetrexed, particularly those more specifically found in NSCLC of nonsquamous histology. Similarly, biomarkers for which IFCT pathologists have acquired an expertise will also be favored. This expertise mainly involves, on the one hand, detecting K-Ras mutations (15-25% of ADC) and RasSF1 methylation as well as TubIII expression by immunohistochemistry (IHC) and testing for mucosecretion by PAS diastase-resistant staining, and on the other hand, evaluating ERCC1 and/or MSH2 expression and thymidylate synthase (TS) expression by IHC.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 61
• Est. completion date: July 2017
• Est. primary completion date: January 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• NSCLC histologically (highly recommended) and/or cytologically confirmed, stage III (non-irradiable or inoperable) or stage IV (according to 2009 TNM classification), with other than predominantly squamous histology
• HIV seropositivity (previous or inaugural), irrespective of CD4 count or viral load
• Presence of at least one measurable lesion (RECIST v1.1)
• Subject having signed the informed consent form,
• Subject who, in the investigator's opinion, will be able to comply with the requirements and constraints of the study
• Age = 18 years = 75 years,
• WHO performance status: 0, 1 or 2
• Weight loss = 10% of total body weight in the month before inclusion
• Estimated life expectancy = 1 month,
• Covered by health insurance

Exclusion Criteria:

• Bronchial cancer already treated (other than endoscopic deobstruction)
• Cancer which is amenable to surgery or radiation (curative),
• Squamous cell lung cancer or mixed small cell and non-small cell cancer, small cell lung cancer
• Creatinine clearance (MDRD) < 45 mL/min
• Severe hypersensitivity to any of the study products or excipients
• Severe disease or uncontrolled systemic disease (unstable or decompensated respiratory disease, cardiac, hepatic or renal disease, uncontrolled opportunistic infection)
• Significant abnormality in CBC-platelets (Hb <9 g/dL, PNN <1500 / mm3, platelets < 100,000 / mm3)
• Significant abnormality in liver tests (AST, ALT > 3x ULN, and <5 in case of liver metastases),
• Women of childbearing age without effective contraception; pregnant or breastfeeding women
• Subject who cannot take vitamin B12, folic acid or corticosteroids
• Diffuse interstitial pneumonia
• Any geographical situation or psychological condition that precludes full understanding and compliance with the protocol

Related Conditions & MeSH terms

• Carcinoma, Non-Small-Cell Lung
• HIV Seropositivity
• Hiv-positive
• Lung Neoplasms
• Non-small Cell Lung Cancer

Intervention

Drug:
• Chemotherapy
Pemetrexed + Carboplatin On D1 of a 21-day cycle: Pemetrexed 500 mg/m² IV in 10 minutes followed 30 minutes later by: Carboplatin AUC 5 in 30 minutes in 100 ml sterile water or 5% glucose or physiological serum. The carboplatin dose will be calculated by the Calvert formula with a target AUC of 5 mg/mL.min as follows: Carboplatin dose in mg = 5 x (GFR + 25) GFR is estimated according to the MDRD equation for creatinine clearance • 4 cycles total

Locations

Country	Name	City	State
France	Centre Hospitalier du Pays d'Aix	Aix-en-Provence
France	Annemasse - CH	Ambilly
France	Annecy - CH	Annecy
France	Avignon - CH	Avignon
France	CH de la Côte Basque	Bayonne
France	CHU Besancon - Pneumologie	Besancon
France	Caen - CHU Côte de Nacre	Caen
France	CH Cahors	Cahors
France	CHU	Clermont-Ferrand
France	CH	Colmar
France	CH Compiègne - Pneumologie	Compiègne
France	Créteil - CHI	Créteil
France	CHU Grenoble - pneumologie	Grenoble
France	Le Mans - Centre Hospitalier	Le Mans
France	CH	Longjumeau
France	Hôpital de la Croix Rousse	Lyon
France	Hôpital Louis Pradel	Lyon
France	APHM - Hôpital Nord	Marseille
France	Montpellier - CHRU	Montpellier
France	Nevers - CH	Nevers
France	Centre Antoine Lacassagne	Nice
France	CHR d'Orléans La Source	Orléans
France	APHP - Hopital Tenon - Pneumologie	Paris
France	GH Paris Saint-Joseph	Paris
France	Hôpital Saint Antoine	Paris
France	Paris - Pitié-salpêtrière	Paris
France	Pau - CH	Pau
France	Centre François Magendie - hôpital du Haut-Lévèque	Pessac
France	HCL - Lyon Sud (Pneumologie)	Pierre Bénite
France	Reims - CHU	Reims
France	Rennes - CHU	Rennes
France	Saint Brieuc - CHG	Saint Brieuc
France	NHC - Pneumologie	Strasbourg
France	Suresnes - Hopital Foch	Suresnes
France	Thonon les bains - CH	Thonon les bains
France	Toulon - CHI	Toulon
France	CHU Toulouse - Pneumologie	Toulouse
France	Tourcoing - CH	Tourcoing
France	Tours - CHU	Tours
France	CH Valence	Valence

Sponsors (1)

Lead Sponsor	Collaborator
Intergroupe Francophone de Cancerologie Thoracique

Country where clinical trial is conducted

France, 

References & Publications (2)

Lavole A, Chouaid C, Baudrin L, Wislez M, Raguin G, Pialoux G, Girard PM, Milleron B, Cadranel J. Effect of highly active antiretroviral therapy on survival of HIV infected patients with non-small-cell lung cancer. Lung Cancer. 2009 Sep;65(3):345-50. doi: 10.1016/j.lungcan.2008.11.018. Epub 2009 Jan 9. — View Citation

Lavole A, Greillier L, Mazieres J, Monnet I, Kiakouama-Maleka L, Quantin X, Spano JP, Lena H, Fraisse P, Janicot H, Audigier-Valette C, Langlais A, Morin F, Makinson A, Cadranel J; French Cooperative Thoracic Intergroup (IFCT). First-line carboplatin plus — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Disease-Control rate after 4 cycles		3-weeks

External Links

•   IFCT official website