The Combined Use of Chemotherapy and Radiotherapy with PD-1 Inhibitor, Pembrolizumab, in Advanced Cervical Cancer: A Case Report.

As a result of the limited therapeutic options, advanced cervical cancer is difficult to treat, making the prognosis poor. Therefore, new therapeutic modalities or combinations need to be explored. We herein reported a case of stage IVB cervical cancer which was irresponsive to chemotherapy alone. Based on previous studies and after patient's consent was obtained, we made a therapeutic plan: chemotherapy (albumin-bound paclitaxel and carboplatin) combined with immunotherapy (PD-1 inhibitor pembrolizumab). After 6 cycles of combined treatment, the patient got almost complete resolution with slight advent event. The treatment was further supported by local radiotherapy combined with immunotherapy. During the treatment period, disease was relatively stable, but the patient suffered severe grade 4 myelosuppression. We were therefore left with no other choice than to interrupt both chemotheraphy and radiotherapy. Before long, the tumor grew explosively again. These guided us to conclude that the combination use of albumin-bound paclitaxel (nab-paclitaxel) and carboplatin and pembrolizumab is effective and well tolerated in the treatment of advanced cervical cancer. The combined use of radiotherapy and pembrolizumab may also be effective. However, the combination use of chemotherapy, radiotherapy and immunotherapy in advanced cancer has not been well studied, and there are still many unsolved queries.

Introduction

With the use of HPV (Human Papillomavirus) vaccines and cervical cancer screening, the incidence and the mortality rate of cervical cancer have been decreased in many countries worldwide.1,2 However, cervical cancer still ranks fourth for both incidence and mortality in female cancers and is the most common gynecological tumor, with an incidence of 569847 new cases and 311365 deaths reported in the year 2018 worldwide as estimated by GLOBOCAN.2 Patients with localized disease could select radical and surgical treatment, while the treatment options for patients with advanced disease including metastatic (ie FIGO stage IVB) and recurrent cervical cancer is limited, and the prognosis is poor.3,4 A common option for patients with advanced cervical cancer is palliative chemotherapy mainly based on cisplatin. The combination use of vascular endothelial growth factor inhibitors is also found to be functional. However, the response rate is not satisfactory.5–8 New treatment modalities are needed to be developed. With the development of immunotherapy, the effect of the Programmed cell death-1/programmed cell death-ligand 1 (PD-1/PD-L1) inhibitors, one of the most well-known immune-checkpoint inhibitors, has been researched in cervical cancer.

The PD-1/PD-L1 inhibitors have proven to be beneficial in various tumors including cervical cancer.9 Briefly, PD-1 expresses on the surface of T cells, while PD-L1 expresses itself on the surface of tumor cells. The binding of PD-1 and PD-L1 triggers immune tolerance to tumor cells and promotes tumor growth. PD-1/PD-L1 inhibitors re-energize the immune response by blocking PD-1/PD-L1 binding.10 The antitumor activity and manageable safety of PD-1/PD-L1 inhibitors including pembrolizumab and nivolumab was verified by Clinical trial KEYNOTE-028, KEYNOTE-158 and CheckMate 358 in advanced cervical cancer.11–13 And the FDA has approved pembrolizumab for patients with recurrent or metastatic cervical cancer with disease progression during or after chemotherapy.9 However, the response rate of monotherapy of PD-1/PD-L1 inhibitors for advanced cervical cancer was not high, the overall response rate was 17%, 13.3% and 26.3% respectively for clinical trial KEY-NOTE028, KEYNOTE-158 and CheckMate 358.11–13 Many ongoing clinical trials investigated the combination use of PD-1/PD-L1 inhibitors with chemotherapy including Platinum, Vinorelbine, radiotherapy and vascular endothelial growth factor inhibitors, in an aim to enhance the efficacy of PD-1/PD-L1 inhibitors treatment.9

Here, we reported a case of advanced cervical cancer of FIGO stage IVB. The patient reached almost complete remission after receiving combination treatment of chemotherapy (nab-paclitaxel and carboplatin) and immunotherapy (pembrolizumab). As the systemic metastasis was under control, the patient was transferred to local pelvic palliative radiotherapy combined with immunotherapy. The disease remained stable, however, severe adverse events occurred during this period and both chemotherapy and radiotherapy had to be interrupted. The tumor explosively grew again. We herewith want to share the successful combination use of nab-paclitaxel and carboplatin, and PD-1inhibitor together, and discuss the clinical thinking brought by this case.

Case Presentation

A 55-year-old female patient with no past medical histories went to hospital with chief complaint of increasing amount of watery vaginal discharge for the past one month. Following cervical biopsy done in August 2018, the woman was diagnosed with cervical malignant tumor. Histopathological report showed that it was a poorly or moderately differentiated invasive squamous cell carcinoma with locally visible adenoid structure. The patient received one course of chemotherapy with cisplatin and paclitaxel. However, three weeks later, the cervical lesion was found to be larger, and the patient was transferred to our hospital. The treatment timeline is shown in Figure 1.

Figure 1

Timeline of different treatments and disease status.

When the patient attended our hospital, gynecological examination showed that the anterior wall of the vagina was invaded up to the lower third. The cervical tumor was ulcerated, with a diameter of 4 cm. The bilateral parametrium was infiltrated up to the pelvis. A comprehensive inspection including CT and PET-CT was performed in our hospital. Computed tomography (CT) scan (Figure 2A) of the chest and abdomen revealed an irregular cervical mass measuring 4.16*4.15cm, with invasion of the vagina, and infiltration of the bilateral parametrium up to the pelvis. Dense masses were seen in bilateral adnexa (3.18*2.19cm in the right side and 2.62*2.77cm in the left side) favoring the risk of metastasis. Multiple nodules were observed in the uterine rectal fossa indicating multiple implants. And the enhanced mass showed liver metastases (the largest one measuring 1.23*1.27cm). Multiple enlarged lymph nodes were observed in the retroperitoneal area, around the left iliac vessels and pelvic wall. The left supraclavicular lymph nodes presented swelling measuring 1.32*1.05cm. The positron emission tomography-computed tomography (PET/CT) (Figure 2A) showed cervical cancer with invasion in lower uterus and vaginal invasion. The PET/CT also showed positive metastatic evidence in the left supraclavicular region, bilateral parametrium, liver, retroperitoneal lymph nodes, areas around the iliac vessels and pelvic wall. Tumor biomarker CA-125 and CEA were high, while SCC was normal (Figure 3). And the patient was diagnosed with cervical cancer IVB according to FIGO staging with a TNM classification established as T3bN1M1.

Figure 2

PET-CT and CT images of the patient. (A) The patient transferred to our hospital, (B) after chemotherapy of other regimens, (C) after two cycles of combination treatment of nab-paclitaxel and carboplatin and pembrolizumab, (D) after 6 cycles of combination treatment of nab-paclitaxel and carboplatin and pembrolizumab, (E) explosive growth of the tumor.

Figure 3

Changes in tumor index values. The ordinate is displayed on a logarithmic scale. (A) The patient started combination treatment of chemotherapy and immunotherapy. (B) The patient was transferred to radiotherapy combined with immunotherapy. (C) Radiotherapy was interrupted and the patient started single use of pembrolizumab.

The clinical characteristics of the disease resembled that of small cell neuroendocrine cervical carcinoma (SCNECC), by having a systemic metastasis, by being a rapid progressing tumor, and by not being sensitive to chemotherapy regimen of cisplatin and Paclitaxel.14 The pathological type of SCNESS was suspected, and we empirically used the chemotherapy regimen of etoposide and cisplatin (EP) in September 2018. At the same time, we added the immunohistochemical examination of the cervical biopsy tissue and PD-L1 examination. PD-L1 status was positive, PD-L1 was presented in 10% of tumoral cells. And the blood tumor mutation burden was 12.0Muts/Mb. Immunohistochemical work-up revealed positive expression CK5/6-, P63±, P40-, P16+, CK7++, WT-1±, P53++90%, Ki67+70%. The histopathological report indicated poorly differentiated adenocarcinoma (Figure 4). After one session of the EP chemotherapy, the cervical lesion upon gynecological examination was found to be slightly reduced, and bevacizumab was added to the EP regimen in October 2018. The combination use of bevacizumab was reported to improve the survival data of advanced cervical cancer and was recommended by NCCN guideline.9,15 However, after two sessions of the EP chemotherapy, the tumor biomarkers showed increased expression of CEA, CA-125, CA19-9 (Figure 3). The CT (2018–11) (Figure 2B) showed that the treatment outcome was not satisfactory. The CT image showed that part of the lesions including the left supraclavicular lymph nodes, cervix lesions and pelvic lymph node decreased in size while others including bilateral adnexal, implants in the uterine rectal fossa and liver metastases continued to progress.

Figure 4

Representative picture of immunohistochemical staining. The picture revealed positive CK7 staining which showed brown color (magnification, ×400).

Considering the poor effect of tumor treatment, we considered that the use of PD-1 inhibitor may be beneficial. After consultation with the patient, we formulated a treatment plan, whereby the chemotherapy regimen of nab-paclitaxel and carboplatin was combined with PD-1inhibitor. Pembrolizumab was used as estimated in dose of 2mg/kg, every 3 weeks following the Chinese clinical trial (KEYNOTE 151).16 Nab-paclitaxel and carboplatin were used with proper reduction dose of 260mg/m2 and AUC=5. On 2018-11-15, 12–10, the patient used pembrolizumab 100mg d1, nab-paclitaxel 300mgd2 and carboplatin 400mgd2. Two cycles after the treatment, the biomarker CA-125 became more than four times lower than before, CEA decreased to almost three times lower than before, and other biomarkers returned to normal value (Figure 3). The gynecological examination suggested that the cervical tumor decreased in size, and the invasion tumor of the vagina was almost completely resolved. The CT scan (Figure 2C) depicted resolved lesions in almost all initial tumor including cervix, the invasion of the vagina, left adnexa, the left supraclavicular lymph nodes, and liver. As the disease got a partial response, this treatment plan was continued for four more sessions, on 2019-1-7, 2019-1-28, 2019-2-21 and 2019-3-31. The values of the biomarkers gradually decreased, and at the end of the four cycles, only CEA was slightly high (Figure 3). PET/CT (Figure 2D) obtained before the last session (2019-3-15) demonstrated almost complete resolution of all lesions. During the treatment, the patient had no obvious side effects, only suffered grade1–2 myelosuppression, with decreased expression of leukocyte and thrombocyte.

As the systematic metastases controlled, pelvic palliative radiotherapy combined with immunotherapy was administered after a multidisciplinary consultation with an aim to control the primary local disease. Chemotherapy was haltered because the patient suffered from grade 1–2 myelosuppression after receiving multiple cycles of chemotherapy. As a consequence, only radiotherapy and immunotherapy were administered to ensure the successful completion of the radiotherapy session. The initial plan of radiotherapy used consisted of whole pelvic field external beam radiotherapy followed with intracavitary brachytherapy. The total dose for external beam radiotherapy was 49.4Gy with a fraction size of 1.9 Gy. As for the brachytherapy, the total dose used was 24 Gy to point A with a fraction size of 6Gy. From 2019-4-11, the patient received Pelvic external beam radiotherapy 1.9Gy daily. After the completion of 43.7Gy of external beam radiotherapy, it was noted that the woman suffered grade3 myelosuppression with thrombocytopenia. Platelets were thus transfused and the planned dose of pelvic external beam radiotherapy was completed. Then, after the patient underwent one brachytherapy of 6Gy, the level of blood platelets dropped to grade4 myelosuppression. At this time, radiotherapy had to be stopped and therefore, the brachytherapy was not completed as planned. The last session of radiotherapy was administered on 2019-05-27. During this period, pembrolizumab was continued to be used Q21days on 4–2, 4–23, 5–16. The myelosuppression persisted and stayed severe, platelet-related drugs were not useful and the patient relied solely on blood transfusion therapy to get a temporary remission. As such, the use of chemotherapy could not be continued. The biomarkers tested on 2019-06-26 showed a rapid increase to an even higher level than what they were before the treatment. Single therapy of pembrolizumab was continued used Q21days on 6–6, 6–23, 7–19 and 8–12. However, the biomarkers kept on increasing. No obvious lesions were observed in the cervix (Figure 5). CT scan showed (Figure 2E) reduced lesion in cervix, the vagina and bilateral adnexa, but with an extensive growth in the liver, supraclavicular lymph nodes, retroperitoneal lymph nodes, and many new lesions were noted in thoracic and peritoneal lymph nodes. Immunotherapy had no effect on the patient anymore and the treatment was interrupted and limited to only maintenance treatment.

Figure 5

Image of the cervix at the end of therapy.

Discussion

Stage IVB cervical cancer is defined as a tumor that metastasizes to distant organs or lymph nodes.17,18 These patients are often mixed with recurrent cervical cancer in clinical trials, and therapeutic options are limited. The recommended treatment is based on prior chemotherapy, with cisplatin plus paclitaxel and bevacizumab.19 After discussing with a multidisciplinary team, a more specific and adapted treatment can be sought.20 However, the prognosis of stage IVB cervical cancer patients remains poor, with 5-year overall survival of about 10%.20 The advent of PD1/PD-L1 inhibitors breaks through the therapeutic bottle neck and may change the traditional treatment model.9,21

The combination of chemotherapy and immunotherapy has been shown to improve treatment effects. Some studies suggested a synergistic interrelation of chemo and immunotherapy.22,23 Especially, in randomized clinical trials, combined PD-L1 blockade with chemotherapy demonstrated significantly increased overall survival and progression-free survival compared to chemotherapy alone with no change in adverse events in non-small cell lung carcinoma.24 In addition, preclinical data also suggest a synergistic interaction between radiation therapy and immune checkpoint inhibitors.25,26 In stage III non-small cell lung carcinoma, the use of Durvalumab, a PD-L1 inhibitor, following chemo-radiotherapy was found to improve overall survival.25

As previously reported, except for some ongoing clinical trials, there are relatively few studies on the application of chemotherapy combined with PD-1/PD-L1 inhibitors in cervical cancer. Here, we presented an innovative case of a patient with cervical cancer stage IVB who was not sensitive to two chemotherapy regimens. Unexpected result happened when the patient turned to use nab-paclitaxel and carboplatin combined with PD-1inhibitor pembrolizumab. After two cycles of treatment, the biomarker decreased significantly, and the imaging report suggested obvious resolution of lesions in almost all initial tumor. After additional four cycles of the regimen, the biomarkers almost returned to normal, and the PET-CT result suggested an almost complete resolution of all lesions. Until the end of the six cycles, the patient had no complaints of any obvious side effects and suffered from only grade1-2 myelosuppression This suggested a positive effect of the combination use of chemotherapy (nab-paclitaxel and carboplatin) and pembrolizumab in this stage IVB cervical cancer patient. Also, this treatment regimen appears to be safe. This is consistent with many clinical trials, as the safety combination use of PD-1/PD-L1 inhibitors with chemotherapy was verified by some articles.24,27 Of course, this situation does not rule out the separate effect of albumin paclitaxel. It has been documented that albumin paclitaxel has also proven to be an effective chemotherapy drug for cervical cancer and has been recommended as the second-line therapy for recurrent or metastatic cervical cancer by NCCN guideline.15,28

As the systemic metastasis was controlled, local radiotherapy was administered with combination of immunotherapy. Unfortunately, the patient suffered severe grade 4 myelosuppression during this period. Thus, radiotherapy was interrupted and the brachytherapy was not completed. As myelosuppression was not a common adverse event for immunotherapy,29 we concluded that radiation therapy triggered off the severe myelosuppression. However, since the patient already received many cycles of chemotherapy which is known to disrupt the platelet-making function, radiotherapy may just aggravate this condition. The combination of radiotherapy and immunotherapy was proved to be effective to this patient as the tumor index indicated a stable condition. However, the safety and proper dose of radiotherapy for patients after cycles of chemotherapy and immunotherapy needs to be attentively administered and monitored. Most of the research of radiotherapy and immunotherapy were preclinical trials, the optimal timing of radiation therapy and immune checkpoint inhibitors is unclear.30 Many queries remain to be solved such as optimal dose, scheduling and so on.

The tumor index increased significantly after interrupting the use of chemotherapy and radiotherapy. This indicated that the single use of the immune checkpoint inhibitors could not function anymore. The possible reason may be the single effect of immunotherapy was not effective enough. Another possible reason may be the patient developed acquired resistance to immunotherapy. Resistance to immunotherapy is a known phenomenon; however, knowledge is rather limited as to the mechanisms of acquired resistance in patients under treatment.31,32

Conclusion

From this case, we can see a positive effect and good tolerance of the combination use of nab-paclitaxel and carboplatin and pembrolizumab. Radiotherapy with pembrolizumab may also be effective. However, special consideration is needed, as to when be the optimal time for systematic treatment turning to local therapy, how to adjust the dose of chemotherapy and radiotherapy with immunotherapy, and how to avoid acquired resistance of immunotherapy.