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Erschienen in: International Journal of Clinical Oncology 5/2020

23.09.2019 | Invited Review Article

Combination therapy with PD-1 or PD-L1 inhibitors for cancer

verfasst von: Hidetoshi Hayashi, Kazuhiko Nakagawa

Erschienen in: International Journal of Clinical Oncology | Ausgabe 5/2020

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Abstract

Immune checkpoint inhibitors (ICIs)—such as antibodies to programmed cell death–1 (PD-1), to its ligand PD-L1, or to cytotoxic T lymphocyte-associated protein–4 (CTLA-4)—are an evolving treatment option for several types of cancer, but only a limited number of patients benefit from such therapy. Preclinical studies have suggested that the combination of PD-1 or PD-L1 inhibitors with either cytotoxic chemotherapy or antibodies to CTLA-4 is a promising treatment strategy for advanced cancer. Indeed, combinations of cytotoxic chemotherapy and PD-1/PD-L1 inhibitors have been approved and are now used in clinical practice for the treatment of advanced non-small cell lung cancer and small cell lung cancer on the basis of positive results of large-scale clinical trials. In addition, the combination of antibodies to CTLA-4 (ipilimumab) and to PD-1 (nivolumab) has been found to confer a survival benefit in patients with melanoma or renal cell carcinoma. Several ongoing clinical trials are also investigating ICI combination therapy in comparison with standard therapy for other tumor types. The identification of patients likely to achieve a sufficient benefit from PD-1/PD-L1 inhibitor monotherapy remains a challenge; however, with the establishment of novel complementary biomarkers being needed. Preclinical and clinical investigations of immune-related adverse events of ICI combination therapy are also warranted to establish management strategies. In this review, we summarize the current landscape of combination therapy with PD-1/PD-L1 inhibitors plus either cytotoxic chemotherapy or CTLA-4 inhibitors to clarify the benefits of and outstanding clinical issues related to such treatment.
Literatur
1.
Zurück zum Zitat Ishida Y, Agata Y, Shibahara K et al (1992) Induced expression of PD-1, a novel member of the immunoglobulin gene superfamily, upon programmed cell death. EMBO J 11(11):3887–3895CrossRefPubMedPubMedCentral Ishida Y, Agata Y, Shibahara K et al (1992) Induced expression of PD-1, a novel member of the immunoglobulin gene superfamily, upon programmed cell death. EMBO J 11(11):3887–3895CrossRefPubMedPubMedCentral
2.
Zurück zum Zitat Freeman GJ, Long AJ, Iwai Y et al (2000) Engagement of the PD-1 immunoinhibitory receptor by a novel B7 family member leads to negative regulation of lymphocyte activation. J Exp Med 192(7):1027–1034CrossRefPubMedPubMedCentral Freeman GJ, Long AJ, Iwai Y et al (2000) Engagement of the PD-1 immunoinhibitory receptor by a novel B7 family member leads to negative regulation of lymphocyte activation. J Exp Med 192(7):1027–1034CrossRefPubMedPubMedCentral
39.
Zurück zum Zitat Zinner RG, Obasaju CK, Spigel DR et al (2015) PRONOUNCE: randomized, open-label, phase III study of first-line pemetrexed + carboplatin followed by maintenance pemetrexed versus paclitaxel + carboplatin + bevacizumab followed by maintenance bevacizumab in patients ith advanced nonsquamous non-small-cell lung cancer. J Thorac Oncol 10(1):134–142. https://doi.org/10.1097/JTO.0000000000000366 CrossRefPubMed Zinner RG, Obasaju CK, Spigel DR et al (2015) PRONOUNCE: randomized, open-label, phase III study of first-line pemetrexed + carboplatin followed by maintenance pemetrexed versus paclitaxel + carboplatin + bevacizumab followed by maintenance bevacizumab in patients ith advanced nonsquamous non-small-cell lung cancer. J Thorac Oncol 10(1):134–142. https://​doi.​org/​10.​1097/​JTO.​0000000000000366​ CrossRefPubMed
42.
Zurück zum Zitat Patel JD, Socinski MA, Garon EB et al (2013) PointBreak: a randomized phase III study of pemetrexed plus carboplatin and bevacizumab followed by maintenance pemetrexed and bevacizumab versus paclitaxel plus carboplatin and bevacizumab followed by maintenance bevacizumab in patients with stage IIIB or IV nonsquamous non-small-cell lung cancer. J Clin Oncol 31(34):4349–4357. https://doi.org/10.1200/JCO.2012.47.9626 CrossRefPubMedPubMedCentral Patel JD, Socinski MA, Garon EB et al (2013) PointBreak: a randomized phase III study of pemetrexed plus carboplatin and bevacizumab followed by maintenance pemetrexed and bevacizumab versus paclitaxel plus carboplatin and bevacizumab followed by maintenance bevacizumab in patients with stage IIIB or IV nonsquamous non-small-cell lung cancer. J Clin Oncol 31(34):4349–4357. https://​doi.​org/​10.​1200/​JCO.​2012.​47.​9626 CrossRefPubMedPubMedCentral
56.
Zurück zum Zitat Collins AV, Brodie DW, Gilbert RJ et al (2002) The interaction properties of costimulatory molecules revisited. Immunity 17(2):201–210CrossRefPubMed Collins AV, Brodie DW, Gilbert RJ et al (2002) The interaction properties of costimulatory molecules revisited. Immunity 17(2):201–210CrossRefPubMed
59.
Zurück zum Zitat Takahashi T, Tagami T, Yamazaki S et al (2000) Immunologic self-tolerance maintained by CD25(+)CD4(+) regulatory T cells constitutively expressing cytotoxic T lymphocyte-associated antigen 4. J Exp Med 192(2):303–310CrossRefPubMedPubMedCentral Takahashi T, Tagami T, Yamazaki S et al (2000) Immunologic self-tolerance maintained by CD25(+)CD4(+) regulatory T cells constitutively expressing cytotoxic T lymphocyte-associated antigen 4. J Exp Med 192(2):303–310CrossRefPubMedPubMedCentral
61.
Zurück zum Zitat Warner AB, Postow MA (2018) Combination controversies: checkpoint inhibition alone or in combination for the treatment of melanoma? Oncology (Williston Park) 32(5):228–234 Warner AB, Postow MA (2018) Combination controversies: checkpoint inhibition alone or in combination for the treatment of melanoma? Oncology (Williston Park) 32(5):228–234
Metadaten
Titel
Combination therapy with PD-1 or PD-L1 inhibitors for cancer
verfasst von
Hidetoshi Hayashi
Kazuhiko Nakagawa
Publikationsdatum
23.09.2019
Verlag
Springer Singapore
Erschienen in
International Journal of Clinical Oncology / Ausgabe 5/2020
Print ISSN: 1341-9625
Elektronische ISSN: 1437-7772
DOI
https://doi.org/10.1007/s10147-019-01548-1

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