Lung cancer patients harboring epidermal growth factor receptor mutation among those infected by human immunodeficiency virus

Abstract

With the advent of antiretroviral therapy, lung cancer has become a crucial health problem among individuals living with human immunodeficiency virus (HIV). In East Asian populations, the frequency of lung cancer patients harboring epidermal growth factor receptor (EGFR) mutations is greater than in other populations. Herein, we present two cases of advanced non-small cell lung cancer with EGFR mutations in patients treated with EGFR-tyrosine kinase inhibitors. Both patients were male, 67 and 59 years of age, with known HIV infection and immunologically stable disease with antiretroviral therapy. Case 1 was treated with erlotinib for recurrent adenocarcinoma metastasizing to the liver and brain harboring EGFR mutation in exon 21 L858R. The duration of treatment efficacy was 9.7 months. Case 2 had an EGFR mutation exon 19 in-frame deletion with bone metastasis and was treated with gefitinib for 22.1 months in combination with antiretroviral therapy. These advanced lung cancer patients living with HIV with EGFR mutations demonstrate the promising effectiveness and safety of EGFR-tyrosine kinase inhibitors concomitant with antiretroviral therapy for an extended period.

Introduction

Patients living with human immunodeficiency virus (HIV) survive longer following the advent of antiretroviral therapy.^1,2 Consequently, an increased incidence of non-AIDS-defining cancers is recognized as a crucial factor among individuals living with HIV.³ Today, roughly one third of HIV-infected patients die of malignancies, and lung cancer is a leading cause of death among non-AIDS-defining cancers.⁴ In general, lung cancer patients living with HIV have a poor prognosis, with a life expectancy of 5 months in contrast with more than 12 months among non-HIV patients.⁵ Individuals living with HIV are considered to be too fragile for chemotherapy and have a poor bone marrow reserve;⁶ therefore, the benefit of cytotoxic chemotherapy is uncertain because these patients are excluded from clinical trials.

Epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs), such as gefitinib and erlotinib, are promising targeted agents for lung cancer harboring EGFR mutations. The response rate to EGFR-TKIs in EGFR mutated lung cancer is 60%–80% and increases survival two-fold.^7,8 The patient characteristics of those with lung cancer harboring EGFR mutations include being female, adenocarcinoma, non-smoker, and East Asian.⁹ Moreover, the frequency of mutated EGFR non-small cell lung cancers (NSCLCs) is 30% in East Asian populations,¹⁰ whereas it is less than 10% in Western countries.¹¹ Although the prevalence of EGFR mutations among the lung cancer patients living with HIV is uncertain, it will likely be greater than what is estimated because patients who have been reported to date are almost all from the United States and Europe. Also, individuals living with HIV are more likely to be smokers.^12–14 Therefore, only one reported lung cancer patient living with HIV has been published previously.¹⁵

Herein, we present two lung cancer patients harboring EGFR mutations living with HIV and treated with EGFR-TKIs.

Case presentation

Case 1

A 67 year old homosexual male patient treated with antiretroviral therapy for 3 years presented with locally advanced adenocarcinoma (stage IIIB) in the left lower lobe and synchronous early adenocarcinoma (stage IA) in the right upper lobe with different EGFR mutations (exon 19 E746-A750 del in the left lower lobe and exon 19 L747-S752 del in the right upper lobe). The category according to the United States Center for Disease Control and Prevention (CDC) Classification System for HIV was B2 (CD4 cell count 404 cells/μL and viral load not detectable) and had a history of heavy cigarette smoking. The antiretroviral therapy included tenofovir/emtricitabine and raltegravir. First-line chemoradiotherapy maintained stable disease for 11 months; however, subsequent recurrence of liver and brain metastasis was evident (Figure 1A). The patient was treated with erlotinib and achieved a partial response (Figure 1B) for 9.7 months. Mild rash and anorexia occurred during treatment. After erlotinib failure, the patient underwent two lines of singlet chemotherapy (docetaxel and pemetrexed) and died 39.0 months after the lung cancer diagnosis.

Figure 1.

Computed tomography (CT) before and after treatment.

Notes: CT before treatment with erlotinib demonstrated hepatic metastasis (A) and efficacy after 3 months of treatment (B).

Case 2

A 59 year old male patient underwent surgery for early lung cancer of T2aN0M0 before surgery and was diagnosed with T2aN2M0 stage IIIA pathologically. The patient underwent antiretroviral therapy (emtricitabine/tenofovir/darunavir) for 1 month before lung cancer was suspected. He was previously a light smoker. His CDC classification system for HIV was A3 (CD4 cell count 120 cells/μL and viral load 2.1×10⁴ copies/μL). His EGFR mutation status was exon 21 L858R. He was treated with adjuvant chemotherapy (cisplatin/vinorelbine). His antiretroviral therapy was changed from danavir, a protease inhibitor, to raltegravir before adjuvant chemotherapy. He completed four subsequent cycles of chemotherapy; however, he suffered from disseminated varicella zoster during his last cycle. Six months later, recurrent left femoral bone metastasis with pathological fracture appeared; therefore, he underwent artificial femoral head replacement followed by radiotherapy to the femoral bone at a dose of 37.5 Gy. However, 3 months later, multiple recurrences appeared in the left hip along the surgical scar (Figure 2A). He began treatment with gefitinib with poor performance status. A mild rash appeared, but he continued gefitinib treatment for 22.1 months (Figure 2B) until disease progression.

Figure 2.

Multiple metastases in the hip muscle along the surgical incision.

Notes: (A) At the time of the recurrence. (B) Three months later, shrinkage was sustained for more than 19 months with gefitinib treatment.

The clinical outcomes of the present cases are shown in Table 1.

Table 1.

Summary of patients’ characteristics including a reported case

Author	Age	Sex	Stage	Histology	Treatment line	EGFR mutation	Response to EGFR-TKI	Duration of response (months)
Erickson et al15	52	F	IV	BAC (Adeno)	1st-line	exon 19	response	14
Present case 1	67	M	rec	Adeno	2nd-line	exon 19	PR	9.7
Present case 2	59	M	rec	Adeno	1st-line	exon 21	PR	22.1

Abbreviations: EGFR, epidermal growth factor receptor; EGFR-TKI, epidermal growth factor receptor-tyrosine kinase inhibitor; BAC, bronchioloalveolar carcinoma; Adeno, adenocarcinoma; rec, recurrence; PR, partial response.

Discussion

The two patients living with HIV of recurrent NSCLC harboring mutated EGFR reported herein demonstrate the efficacy of EGFR-TKI treatment.

The number of HIV-infected patients with lung cancer has recently been increasing in the United States because of the change of disease spectrum from opportunistic infections to other diseases, a result of the introduction of antiretroviral therapy which strongly inhibits HIV and restores immunity of the patients.^16,17 Lung cancer in HIV-infected patients is characterized by a younger age at onset, more rapid disease progression, and shorter survival compared to non-infected patients.⁵ There are several studies on the prognosis of HIV-infected patients with lung cancer treated with or without antiretroviral therapy, and the majority of studies conclude that there is additional benefit to concomitant therapy.^18–20 Among advanced NSCLC patients with HIV infection having CD4 cell counts greater than 200 cells/μL, 75%–90% of reported patients benefited from standard chemotherapy and had a median survival of 11.5 months, a similar prognosis to that of advanced NSCLC patients without HIV infection.¹⁹ On the other hand, patients with a CD4 count less than 200 cells/μL had a shorter median survival of 3.4 months.¹⁸

In the general population, the prognosis of advanced NSCLC has increased from two- to three-fold from 1995 to 2013. The treatment options are now diverse, and they have changed the strategy for treatment, especially with the discovery of driver oncogenes and molecular targeted treatment. Whether chemotherapy in HIV-infected patients with lung cancer is beneficial, and if so, details regarding the appropriate dose, remain unclear. Drug interactions between antiretroviral therapy and anticancer agents have been considered a possible issue, despite limited in vivo or in vitro data.²¹ In AIDS-associated lymphoma, ever since the advent of antiretroviral therapy, conventional-dose chemotherapy is recommended for patients with good performance status. Wang et al reported similar efficacies and toxicity profiles of CODOX-M/IVAC among patients with Burkitt’s lymphoma with or without AIDS.²² Furthermore, the prognosis of patients treated with chemotherapy for Burkitt’s lymphoma was similar to non-AIDS patients.^23,24 Further prospective investigations are required to determine whether the management of HIV patients with malignancies treated with chemotherapy is identical to non-HIV individuals. The standard treatment for lung cancer is evaluated and determined by clinical trials, but individuals living with HIV are excluded from these trials. Physicians should pay more attention to complications to avoid severe toxicities in these patients. Finally, the possibility of pharmacodynamic interactions or bone marrow fragility remains a concern due to the risk of myelosuppression caused by HIV.⁶ In fact, a recent Phase I/pharmacokinetic study of sunitinib with antiretroviral therapy for patients living with HIV demonstrated that a ritonavir (protease inhibitor)-based regimen required a reduced dose of sunitinib due to higher toxicities, whereas non-ritonavir-based regimens were more efficacious with standard sunitinib dosing.²⁵

Advanced lung cancer cases with EGFR mutations treated with EGFR-TKIs are anticipated to have twice the survival than EGFR wild type patients.^6,7 In East Asian females, non-or light-smoking patients, 30%–35% have EGFR mutations, while only ~10% of all NSCLC cases in the Caucasian population were found to have EGFR mutations.¹¹ Limited data demonstrating the rate of EGFR mutation among lung cancer patients living with HIV was 35.7% in Japan.²⁶ Therefore, a specific ethnic group; East Asian patients with concomitant HIV and lung cancer will require different clinical management and policies than Caucasian patients.

Conclusion

We report two lung cancer patients living with HIV and harboring EGFR mutations were active for EGFR-TKI with safety and long-term duration of response.